Food Coloring and Packaging Ink Contamination: A Review

By Lewis Perdue on January 14, 2026 in Featured, Uncategorized

By Lewis Perdue, January 14, 2026

1. Introduction to Synthetic Food Dyes

Synthetic food dyes are widely used in processed foods, beverages, confectionery, and pharmaceuticals to enhance visual appeal. The primary dyes approved for use in the United States include FD&C Red No. 3 (Erythrosine), Red No. 40 (Allura Red AC), Yellow No. 5 (Tartrazine), Yellow No. 6 (Sunset Yellow FCF), Blue No. 1 (Brilliant Blue FCF), Blue No. 2 (Indigo Carmine), and Green No. 3 (Fast Green FCF). In the European Union, similar synthetic colorants are approved under E-number designations. These azo dyes, characterized by the presence of one or more nitrogen-nitrogen double bonds (-N=N-), represent the largest class of synthetic food colorants. [Citations 1-3]

The safety of synthetic food dyes has been scrutinized since the 1970s when pediatric allergist Benjamin Feingold first hypothesized that food additives, including synthetic colorings, may contribute to attentional problems in children. This hypothesis prompted decades of research examining associations between synthetic food dye consumption and neurobehavioral outcomes in children. [Citations 4-5]

2. Neurobehavioral Effects in Children

2.1 The Southampton Studies

The landmark 2007 Southampton study (McCann et al.) represents the largest and most rigorous investigation of food additives and child behavior. This randomized, double-blinded, placebo-controlled crossover trial enrolled 153 three-year-old and 144 eight/nine-year-old children from the general population. Children were given drinks containing either artificial food colorings plus sodium benzoate or placebo. The results demonstrated that consumption of the additive mixtures resulted in increased hyperactive behavior in both age groups, with effects observed in children without pre-existing behavioral disorders. [Citation 6]

Following this study, the European Food Safety Authority (EFSA) concluded that the study provided limited evidence of a small effect on activity and attention in some children, though effects were not consistent across age groups and dye mixtures. The EU subsequently required warning labels on foods containing specific synthetic dyes stating they “may have an adverse effect on activity and attention in children.” [Citations 7-8]

2.2 Meta-Analyses and Systematic Reviews

The California Office of Environmental Health Hazard Assessment (OEHHA) conducted a comprehensive systematic review in 2021, identifying 27 clinical trials examining synthetic food dyes and neurobehavioral outcomes. The review found that synthetic food dyes can affect activity and attention in some children, with OEHHA identifying 1 mg tartrazine as the lowest observed adverse effect level. The review also examined animal studies, finding altered motor activity in 17 of 21 studies and learning/memory effects in 12 of 18 studies. [Citations 9-10]

A 2012 meta-analysis by Nigg et al. concluded that color additives have an effect on hyperactive behavior in children, with a small subset showing more extreme behavioral responses. The analysis suggested that restricting synthetic food dye consumption would benefit some children with ADHD, potentially affecting tens of thousands of children in the United States. [Citation 11]

2.3 Genetic Moderation of Effects

Research by Stevenson et al. (2010) demonstrated that polymorphisms in histamine degradation genes (HNMT Thr105Ile and HNMT T939C) and dopamine transporter genes (DAT1) moderated children’s responses to synthetic food dyes. Children lacking the protective C allele in HNMT T939C—approximately 60% of children studied—showed greater adverse responses to food dyes. This suggests a biological basis for individual variation in sensitivity to synthetic colorants. [Citation 12]

3. Azo Dye Metabolism by Gut Microbiota

Azo dyes undergo reductive cleavage of the nitrogen-nitrogen double bond by intestinal bacteria, producing aromatic amine metabolites. This azoreduction occurs through NAD(P)H-dependent azoreductase enzymes expressed by multiple bacterial species including Bacteroides vulgatus, one of the most abundant species in the human colon. Three types of bacterial azoreductases have been characterized: flavin-dependent NADH-preferred, flavin-dependent NADPH-preferred, and flavin-free NADPH-preferred enzymes. [Citations 13-14]

A 2023 study surveyed 206 bacterial strains representative of 124 species and found that several groups of gut bacteria, including ones not previously associated with azoreduction, could reduce common food azo dyes including Allura Red, Amaranth, Sunset Yellow, and Tartrazine. Importantly, some bacterial strains showed effects on growth related to the presence of azo dyes or their reduction products, suggesting potential impacts on gut microbial ecosystems. [Citation 15]

3.1 Carcinogenic Aromatic Amine Metabolites

By the 1940s, aromatic amines such as benzidine and 2-naphthylamine, used in azo dye synthesis, were established as human and rodent carcinogens. Intestinal bacteria can reduce benzidine-based dyes (Direct Black 38, Direct Red 2, Direct Blue 15) to release free benzidine, 3,3′-dimethylbenzidine, and 3,3′-dimethoxybenzidine—all known carcinogens. The metabolites were confirmed by gas chromatography/mass spectrometry. [Citations 16-17]

Some metabolites produced by intestinal microbiota are carcinogenic to humans even when the parent azo dye is not classified as carcinogenic. Studies have shown that benzidine can induce tumors in the gastrointestinal tract, pancreas, liver, and gallbladder. The EU has classified azo dyes based on benzidine, 3,3′-dimethoxybenzidine, and 3,3′-dimethylbenzidine as Category 2 carcinogens. [Citation 18]

4. Individual Dye Safety Profiles

4.1 Red No. 3 (Erythrosine) — Now Banned

On January 15, 2025, the FDA revoked authorization for Red No. 3 (erythrosine) in food and pharmaceuticals, citing the Delaney Clause which prohibits FDA authorization of any food or color additive found to induce cancer in humans or animals. Studies from the 1980s linked Red No. 3 to thyroid tumors in male rats, leading to its 1990 ban in cosmetics. Although the FDA stated that the mechanism by which Red No. 3 causes thyroid cancer in male rats—increased circulating TSH—is not relevant to humans at typical exposure levels, the Delaney Clause mandated the ban regardless. Food manufacturers must reformulate by January 2027; drug manufacturers by January 2028. [Citations 19-21]

4.2 Red No. 40 (Allura Red AC)

Red No. 40 is the most widely consumed food colorant globally, with annual production exceeding 2.3 million kg. While OECD-guideline compliant studies found no evidence of in vivo genotoxic potential, a 2023 study found that Red 40 causes DNA damage in colorectal cancer cell lines and in living mice, promotes colonic inflammation, and impacts the gut microbiome. The incidence of early-onset colorectal cancer has risen concurrently with increased synthetic food dye consumption over the past 40 years, raising concerns about potential associations. [Citations 22-24]

Red 40 has been found to be contaminated with benzidine and other carcinogens during manufacturing. A 2024 review in Carcinogenesis noted that although no governing agencies classify Allura Red AC as a carcinogen, its interactions with key contributors to colorectal carcinogenesis—inflammatory mediators, the microbiome, and DNA damage pathways—make it suspect and worthy of further investigation. [Citations 25-26]

4.3 Yellow No. 5 (Tartrazine)

Tartrazine has been linked to behavioral effects in children and shows genotoxicity in multiple studies. The OEHHA review identified 1 mg tartrazine as inducing significant behavioral responses in children. Challenge studies found that 22 of 34 hyperactive children (65%) clearly reacted to tartrazine with irritability, restlessness, and sleep disturbance. In vitro studies have demonstrated tartrazine is toxic to DNA at all concentration levels tested. Chronic consumption has been found to impair memory and learning in rodents through mechanisms involving gut microbiota degradation, free radical release, and oxidative stress. [Citations 27-29]

5. Titanium Dioxide (E171)

Titanium dioxide (E171) has been widely used as a white pigment and opacifier in foods. Food-grade E171 contains particles predominantly in the 200-300 nm range but with a nano-sized fraction (<100 nm) comprising up to 50% of particles by number. In May 2021, EFSA concluded that E171 could no longer be considered safe as a food additive because a concern for genotoxicity could not be ruled out. The EU banned E171 in food as of August 2022 through Regulation (EU) 2022/63. [Citations 30-32]

Studies have shown that TiO2 nanoparticles can accumulate in the liver and intestine, with significant titanium accumulation associated with necroinflammatory foci. Animal studies demonstrated increased superoxide production and inflammation in the stomach and intestine following E171 exposure. French researchers found that E171 nanoparticles absorb quickly through the mouth into the bloodstream, damaging DNA and hindering cell regeneration. [Citations 33-34]

Despite the EU ban, regulatory agencies in the United States (FDA), Canada, Australia/New Zealand (FSANZ), Japan, and the United Kingdom continue to permit titanium dioxide in food. The US FDA permits its use at no more than 1% by weight of food. The contrasting regulatory approaches reflect different interpretations of the precautionary principle and requirements for demonstrating safety. [Citation 35]

6. Packaging Ink Photoinitiators

Photoinitiators are essential components of UV-curing printing inks used on food packaging, particularly cartonboard. These compounds absorb UV energy and generate free radicals to initiate polymerization. After UV ink curing, residual photoinitiators can migrate from the printed surface to food through set-off (transfer to the food-contact side during stacking), direct penetration through porous substrates, and vapor-phase transfer. [Citations 36-37]

6.1 The 2005 ITX Incident

In 2005, isopropylthioxanthone (ITX) was detected at 120-300 µg/L in Nestlé infant formula in Europe, leading to the recall of over 30 million liters of dairy products across the continent. The contamination occurred through migration of photoinitiators from printed beverage cartons. This incident triggered more than 100 RASFF (Rapid Alert System for Food and Feed) alerts within subsequent years regarding photoinitiator migration from food contact materials. [Citation 38]

6.2 Benzophenone and Derivatives

Benzophenone (BP) and 4-methylbenzophenone (4-MBP) are among the most widely used and studied photoinitiators. A German study detected benzophenone in 49% of packaging samples, with 20 food products exceeding legal limits. In cereals packaged in cartonboard, concentrations up to 3,729 µg/kg of 4-methylbenzophenone and 4,210 µg/kg of benzophenone were reported. EFSA recommends a combined limit of 0.6 mg/kg for BP and 4-MBP, though there is no specific EU legislation covering printing inks for food contact use. [Citations 39-40]

A 2024 study found total photoinitiator concentrations in paper food packaging ranging from 48.3 to 111,000 ng/g, dominated by benzophenones (77.1% of total). Benzophenone was the dominant congener in corrugated paper at concentrations up to 36,600 ng/g. Migration quantity increased time-dependently over the first 13 days before reaching equilibrium. Photoinitiators have demonstrated skin contact toxicity, reproductive toxicity, endocrine disrupting activity, and potential carcinogenicity. [Citation 41]

6.3 Barrier Effectiveness and Migration Dynamics

Research has demonstrated a six-order-of-magnitude difference in diffusion coefficients between materials, with low-density polyethylene (LDPE) providing the worst barrier and polyethylene terephthalate (PET) the best. Polyethylene provides at best a temporary barrier effect, slowing but not preventing migration. Surface-to-food-mass ratios in actual packaging were found to be up to 6 times higher than the default value (6 dm²/kg) specified in EU legislation, indicating that standard migration limits likely underestimate actual exposure. [Citations 42-43]

7. Mineral Oil Hydrocarbons (MOSH/MOAH)

Mineral oil hydrocarbons (MOH) are divided into mineral oil saturated hydrocarbons (MOSH) and mineral oil aromatic hydrocarbons (MOAH). They contaminate food through environmental sources, machinery lubricants, processing aids, food additives, and migration from food contact materials—particularly recycled paperboard. Printing inks used on food packaging are a predominant source, with migration from printed paper considerably higher than from unprinted paper. [Citations 44-45]

7.1 EFSA Risk Assessment

EFSA’s 2023 updated risk assessment found MOSH detected in 82.6% and MOAH in 50.4% of food contact paper samples from China. Migration of MOSH from 47.9% of samples exceeded 2 mg/kg, and MOAH from 32.2% exceeded 0.5 mg/kg under worst-case conditions. For infants, estimated MOAH exposure ranged from 0.8 to 44.6 µg/kg body weight per day at average levels and up to 78.8 µg/kg bw/day at the 95th percentile. EFSA concluded these exposure levels are of concern due to the possible presence of genotoxic and carcinogenic compounds in MOAH fractions. [Citations 46-47]

7.2 Human Tissue Accumulation

Autopsy studies dating to the 1960s demonstrated that MOH exposure causes deposits in human tissues, specifically in mesenteric lymph nodes, spleen, and liver. A 2023 re-analysis of biopsy and autopsy data found that MOSH concentrations in mesenteric lymph nodes and adipose tissue showed a 1.2-1.4-fold increase per decade of life, indicating very long-term accumulation. The German BfR recommends preliminary migration limits of 12 mg/kg for MOSH C10-C16 and 4 mg/kg for MOSH C16-C20. [Citations 48-49]

In pasta packed in recycled paperboard, MOSH and MOAH migration continued over two years of storage. Egg pasta stored on shelves reached 14.5 mg/kg MOSH and 2.0 mg/kg MOAH after two years. Aluminum foil barriers significantly reduced migration, with egg pasta reaching approximately 8 mg/kg MOSH within two months when protected. [Citation 50]

8. Regulatory Landscape

Regulatory approaches to synthetic food dyes differ significantly between jurisdictions. The European Union requires warning labels on foods containing six specific dyes (tartrazine, quinoline yellow, sunset yellow, carmoisine, ponceau 4R, and allura red) stating they “may have an adverse effect on activity and attention in children.” The EU has also banned titanium dioxide (E171) as a food additive as of 2022 and restricted Red No. 3 (erythrosine) to only certain processed cherries since 1994. [Citations 51-52]

In the United States, the FDA maintains that approved food dyes are safe at current exposure levels. However, the January 2025 ban on Red No. 3 under the Delaney Clause demonstrates that animal carcinogenicity data can mandate regulatory action regardless of human relevance assessments. California passed a 2023 law banning Red No. 3, potassium bromate, brominated vegetable oil, and propylparaben in food products, effective 2027—the first state-level action of this kind. [Citations 53-54]

For printing inks and photoinitiators, no harmonized EU legislation specifically covers their use in food contact materials, though general food contact regulations (EC 1935/2004, EC 178/2002) apply. Industry guidelines recommend polymeric multifunctional photoinitiators (molecular weight >1000 Da) to reduce migration potential compared to conventional low-molecular-weight photoinitiators (typically <500 Da). [Citation 55]

9. Summary and Conclusions

The scientific literature supports several conclusions regarding food coloring and packaging ink contamination:

Synthetic food dyes can affect activity and attention in some children, with effects demonstrated in randomized, double-blinded, placebo-controlled trials. Genetic polymorphisms in histamine and dopamine-related genes moderate individual susceptibility. The effect size, while statistically small, may affect tens of thousands of children and represents a public health concern.

Azo dyes undergo gut microbial metabolism to produce aromatic amine metabolites, some of which are established human carcinogens (benzidine, related congeners). This metabolic activation pathway represents a mechanism for carcinogenic potential independent of the parent dye’s direct toxicity.

Packaging-derived contamination from photoinitiators (benzophenone, ITX) and mineral oil hydrocarbons (MOSH/MOAH) represents an underappreciated exposure pathway. Migration occurs through set-off, direct penetration, and vapor-phase transfer, with standard regulatory migration limits potentially underestimating actual exposure by six-fold.

MOSH accumulates in human tissues over decades, with concentration increases of 1.2-1.4-fold per decade observed in mesenteric lymph nodes and adipose tissue. MOAH fractions containing three or more aromatic rings are of particular concern due to genotoxic and carcinogenic potential.

Regulatory approaches remain fragmented, with the EU applying more precautionary standards (warning labels, titanium dioxide ban) compared to the United States. The 2025 US ban on Red No. 3, 35 years after evidence of animal carcinogenicity, illustrates the lag between scientific evidence and regulatory action.

References

1. Amchova P, Siska F, Ruda-Kucerova J. “Food Safety and Health Concerns of Synthetic Food Colors: An Update.” Toxics 12(7):466, 2024. https://www.mdpi.com/2305-6304/12/7/466 [Accessed January 11, 2026]

2. Silva MM, Reboredo FH, Lidon FC. “Food Colour Additives: A Synoptical Overview on Their Chemical Properties, Applications in Food Products, and Health Side Effects.” Foods 11(3):379, 2022. https://www.mdpi.com/2304-8158/11/3/379 [Accessed January 11, 2026]

3. Kobylewski S, Jacobson MF. “Toxicology of food dyes.” International Journal of Occupational and Environmental Health 18(3):220-246, 2012. https://pubmed.ncbi.nlm.nih.gov/23026007/ [Accessed January 11, 2026]

4. Miller MD, Marty MA, et al. “Potential impacts of synthetic food dyes on activity and attention in children: a review of the human and animal evidence.” Environmental Health 21:45, 2022. https://link.springer.com/article/10.1186/s12940-022-00849-9 [Accessed January 11, 2026]

5. California OEHHA. “Health Effects Assessment: Potential Neurobehavioral Effects of Synthetic Food Dyes in Children.” California Office of Environmental Health Hazard Assessment, 2021. https://oehha.ca.gov/sites/default/files/media/downloads/risk-assessment/report/healthefftsassess041621.pdf [Accessed January 11, 2026]

6. McCann D, Barrett A, Cooper A, et al. “Food additives and hyperactive behaviour in 3-year-old and 8/9-year-old children in the community: a randomised, double-blinded, placebo-controlled trial.” Lancet 370(9598):1560-1567, 2007. https://pubmed.ncbi.nlm.nih.gov/17825405/ [Accessed January 11, 2026]

7. EFSA Panel on Food Additives, Flavourings, Processing Aids and Food Contact Materials. “Assessment of the results of the study by McCann et al. (2007) on the effect of some colours and sodium benzoate on children’s behaviour.” EFSA Journal 660:1-54, 2008. https://www.efsa.europa.eu/en/news/efsa-evaluates-southampton-study-food-additives-and-child-behaviour [Accessed January 11, 2026]

8. Arnold LE, Lofthouse N, Hurt E. “Artificial Food Colors and Attention-Deficit/Hyperactivity Symptoms: Conclusions to Dye for.” Neurotherapeutics 9(3):599-609, 2012. https://pmc.ncbi.nlm.nih.gov/articles/PMC3441937/ [Accessed January 11, 2026]

9. Llewellyn GC, Penberthy JK, Parker JM. “Food Color Additives in the US Food Supply: Review of Neurobehavioral Safety.” Journal of Pediatric Neurology and Neuroscience 4(1):55-72, 2020. https://scholars.direct/Articles/pediatric-neurology/jpnn-4-015.php?jid=pediatric-neurology [Accessed January 11, 2026]

10. Weiss B. “Synthetic Food Colors and Neurobehavioral Hazards: The View from Environmental Health Research.” Environmental Health Perspectives 120(1):1-5, 2012. https://pmc.ncbi.nlm.nih.gov/articles/PMC3261946/ [Accessed January 11, 2026]

11. Nigg J, Lewis K, Edinger T, Falk M. “Meta-Analysis of Attention-Deficit/Hyperactivity Disorder or Attention-Deficit/Hyperactivity Disorder Symptoms, Restriction Diet, and Synthetic Food Color Additives.” Journal of the American Academy of Child & Adolescent Psychiatry 51(1):86-97, 2012. https://www.scientificamerican.com/article/does-artificial-food-coloring-contribute-to-adhd-in-children/ [Accessed January 11, 2026]

12. Stevenson J, Sonuga-Barke E, McCann D, et al. “The role of histamine degradation gene polymorphisms in moderating the effects of food additives on children’s ADHD symptoms.” American Journal of Psychiatry 167(9):1108-1115, 2010. https://pmc.ncbi.nlm.nih.gov/articles/PMC3441937/ [Accessed January 11, 2026]

13. Chen H. “Toxicological significance of azo dye metabolism by human intestinal microbiota.” Frontiers in Bioscience 4:568-586, 2012. https://pmc.ncbi.nlm.nih.gov/articles/PMC5870118/ [Accessed January 11, 2026]

14. Ryan A, Kaplan E, Allen-Vercoe E. “Reductive metabolism of azo dyes and drugs: Toxicological implications.” Food and Chemical Toxicology 178:113877, 2023. https://www.sciencedirect.com/science/article/abs/pii/S0278691523003344 [Accessed January 11, 2026]

15. Zahran SA, Ali-Tammam M, Hashem AM, et al. “Metabolism of azo food dyes by bacterial members of the human gut microbiome.” Anaerobe 83:102783, 2023. https://pubmed.ncbi.nlm.nih.gov/37769703/ [Accessed January 11, 2026]

16. Cerniglia CE, Freeman JP, Franklin W, Pack LD. “Metabolism of azo dyes derived from benzidine, 3,3′-dimethyl-benzidine and 3,3′-dimethoxybenzidine to potentially carcinogenic aromatic amines by intestinal bacteria.” Carcinogenesis 3(11):1255-1260, 1982. https://pubmed.ncbi.nlm.nih.gov/7151244/ [Accessed January 11, 2026]

17. Chung KT. “Azo dyes and human health: A review.” Journal of Environmental Science and Health Part C 34(4):233-261, 2016. https://pubmed.ncbi.nlm.nih.gov/27635691/ [Accessed January 11, 2026]

18. Ito T, Ochi T, Yamazaki K, et al. “Microbial Degradation of Azo Dyes: Approaches and Prospects for a Hazard-Free Conversion by Microorganisms.” International Journal of Molecular Sciences 23(9):4639, 2022. https://pmc.ncbi.nlm.nih.gov/articles/PMC9026373/ [Accessed January 11, 2026]

19. US Food and Drug Administration. “FDA to Revoke Authorization for the Use of Red No. 3 in Food and Ingested Drugs.” FDA Constituent Update, 2025. https://www.fda.gov/food/hfp-constituent-updates/fda-revoke-authorization-use-red-no-3-food-and-ingested-drugs [Accessed January 11, 2026]

20. Hofseth LJ. “The FDA banned Red 3 food coloring. A scientist explains the dye’s history and health risks.” PBS News / The Conversation, 2025. https://www.pbs.org/newshour/health/the-fda-banned-red-3-food-coloring-a-scientist-explains-the-dyes-history-and-health-risks [Accessed January 11, 2026]

21. US FDA Federal Register. “Color Additive Petition From Center for Science in the Public Interest, et al.; Request To Revoke Color Additive Listing for Use of FD&C Red No. 3.” Federal Register 90:4628, 2025. https://public-inspection.federalregister.gov/2025-00830.pdf [Accessed January 11, 2026]

22. Bastaki M, Farrell T, Bhusari S, et al. “Lack of genotoxicity in vivo for food color additive Allura Red AC.” Food and Chemical Toxicology 105:308-314, 2017. https://pubmed.ncbi.nlm.nih.gov/28458012/ [Accessed January 11, 2026]

23. Honma M. “Evaluation of the in vivo genotoxicity of Allura Red AC (Food Red No. 40).” Food and Chemical Toxicology 84:270-275, 2015. https://pubmed.ncbi.nlm.nih.gov/26364875/ [Accessed January 11, 2026]

24. Harris Q, Vikas A, Trauner E, et al. “The synthetic food dye, Red 40, causes DNA damage, causes colonic inflammation, and impacts the microbiome in mice.” Toxicology Reports 11:221-232, 2023. https://pmc.ncbi.nlm.nih.gov/articles/PMC10502305/ [Accessed January 11, 2026]

25. Hofseth LJ, Hebert JR, Murphy EA, et al. “Allura Red AC is a xenobiotic. Is it also a carcinogen?.” Carcinogenesis 45(10):711-720, 2024. https://pmc.ncbi.nlm.nih.gov/articles/PMC11464682/ [Accessed January 11, 2026]

26. Hashem AS, et al. “Food Color Additives in Hazardous Consequences of Human Health: An Overview.” Current Nutrition & Food Science 19(9):867-878, 2023. https://pubmed.ncbi.nlm.nih.gov/36650651/ [Accessed January 11, 2026]

27. Rowe KS, Rowe KJ. “Synthetic food coloring and behavior: A dose response effect in a double-blind, placebo-controlled, repeated-measures study.” Journal of Pediatrics 125(5 Pt 1):691-698, 1994. https://pmc.ncbi.nlm.nih.gov/articles/PMC9052604/ [Accessed January 11, 2026]

28. El Golli N, et al. “Coloring outside the lines: Exploring the dysbiotic impact of azo dyes on gut health and inflammation.” Probiologists, 2024. https://www.probiologists.com/article/coloring-outside-the-lines-exploring-the-dysbiotic-impact-of-azo-dyes-on-gut-health-and-inflammation [Accessed January 11, 2026]

29. Doguc DK, Ceyhan BM, Ozturk M, Gultekin F. “Effects of maternally exposed colouring food additives on cognitive performance in rats.” Toxicology and Industrial Health 29(7):616-623, 2013. https://link.springer.com/article/10.1186/s12940-022-00849-9 [Accessed January 11, 2026]

30. EFSA Panel on Food Additives and Flavourings. “Safety assessment of titanium dioxide (E171) as a food additive.” EFSA Journal 19(5):6585, 2021. https://www.efsa.europa.eu/en/news/titanium-dioxide-e171-no-longer-considered-safe-when-used-food-additive [Accessed January 11, 2026]

31. European Commission DG SANTE. “Goodbye E171: The EU bans titanium dioxide as a food additive.” European Commission Newsroom, 2022. https://ec.europa.eu/newsroom/sante/items/732079/en [Accessed January 11, 2026]

32. Warheit DB, Brill R, et al. “Safety of titanium dioxide (E171) as a food additive for humans.” Frontiers in Toxicology 6:1439320, 2024. https://pmc.ncbi.nlm.nih.gov/articles/PMC11295244/ [Accessed January 11, 2026]

33. Pinget G, et al. “Impact of the food additive titanium dioxide (E171) on gut microbiota-host interaction.” Frontiers in Nutrition 6:57, 2019. https://usrtk.org/chemicals/titanium-dioxide/ [Accessed January 11, 2026]

34. Pele LC, et al. “Titanium dioxide nanoparticles in food packaging and human health.” ScienceDirect Toxicology, 2025. https://www.sciencedirect.com/science/article/abs/pii/S0300483X25000459 [Accessed January 11, 2026]

35. UK Committee on Toxicity. “COT Statement on the Safety of Titanium dioxide (E171) as a Food Additive.” UK Food Standards Agency, 2024. https://cot.food.gov.uk/COT%20Statement%20on%20the%20Safety%20of%20Titanium%20dioxide%20(E171)%20as%20a%20Food%20Additive%20-%20Lay%20Summary [Accessed January 11, 2026]

36. Lago MA, Rodriguez-Bernaldo de Quiros A, et al. “Photoinitiators: a food safety review.” Food Additives & Contaminants Part A 32(5):779-798, 2015. https://www.researchgate.net/publication/272080012_Photoinitiators_a_food_safety_review [Accessed January 11, 2026]

37. Mohapatra SK. “Photoinitiator Selection for Food Packaging Inks and Coatings – Concerns and Opportunities.” LinkedIn Article, 2020. https://www.linkedin.com/pulse/photoinitiator-selection-food-packaging-inks-coatings-mohapatra [Accessed January 11, 2026]

38. Jung T, Simat TJ, Kimmel J, Fiedler D. “Occurrence of photoinitiators in carton board packaging materials.” Food Packaging Forum, 2013. https://foodpackagingforum.org/news/printing-ink-exposure-from-fcm-significantly-underestimated [Accessed January 11, 2026]

39. Shen M, Liu G, Yin H, et al. “Occurrences and migration characteristics of photoinitiators in paper food packaging: Implication for human exposure.” Journal of the Chinese Institute of Engineers, 2024. https://www.sciencedirect.com/science/article/abs/pii/S1001074224004765 [Accessed January 11, 2026]

40. Kim S, Lee S, Shin D, et al. “Cumulative Dietary Risk Assessment of Benzophenone-Type Photoinitiators from Packaged Foodstuffs.” Toxics 10(1):19, 2022. https://pmc.ncbi.nlm.nih.gov/articles/PMC8774600/ [Accessed January 11, 2026]

41. Anderson WAC, Castle L. “Benzophenone in cartonboard packaging materials and the factors that influence its migration into food.” Food Additives & Contaminants 20(6):607-618, 2003. https://www.researchgate.net/publication/300478350_Benzophenone_UV-Photoinitiators_Used_in_Food_Packaging_Potential_for_Human_Exposure_and_Health_Risk_Considerations [Accessed January 11, 2026]

42. US FDA. “Hazard Identification of Printing Ink Substances Used on the Exterior of Food Packaging.” FDA Technical Report, 2023. https://www.fda.gov/media/168846/download [Accessed January 11, 2026]

43. Sagratini G, Caprioli G, et al. “Determination of ink photoinitiators in packaged beverages by gas chromatography-mass spectrometry.” Journal of Chromatography A 1194(2):213-220, 2008. https://pubmed.ncbi.nlm.nih.gov/21847975/ [Accessed January 11, 2026]

44. EFSA CONTAM Panel. “Update of the risk assessment of mineral oil hydrocarbons in food.” EFSA Journal 21(9):8215, 2023. https://pmc.ncbi.nlm.nih.gov/articles/PMC10498375/ [Accessed January 11, 2026]

45. Weber S, Schrag K, Mildau G, et al. “Analytical Methods for the Determination of Mineral Oil Saturated Hydrocarbons (MOSH) and Mineral Oil Aromatic Hydrocarbons (MOAH)—A Short Review.” Analytical Chemistry Insights 13:1177390118777757, 2018. https://journals.sagepub.com/doi/10.1177/1177390118777757 [Accessed January 11, 2026]

46. Li S, Gao Y, Li S, et al. “Migration of mineral oil hydrocarbons from food contact papers into food simulants and extraction from their raw materials.” Food Additives & Contaminants Part A 38(6):924-937, 2021. https://pubmed.ncbi.nlm.nih.gov/33818316/ [Accessed January 11, 2026]

47. Grob K. “Mineral oil in food, cosmetic products, and in products regulated by other legislations.” Critical Reviews in Toxicology 50(1):1-36, 2020. https://www.tandfonline.com/doi/full/10.1080/10408444.2019.1694862 [Accessed January 11, 2026]

48. Cravedi JP, Boudry G, et al. “Evidence for an accumulation of mineral oil saturated hydrocarbons (MOSH) in human tissues: a re-evaluation of biopsy and autopsy data.” Journal of Consumer Protection and Food Safety 18:401-411, 2023. https://link.springer.com/article/10.1007/s00003-023-01458-5 [Accessed January 11, 2026]

49. UC Davis Food Quality. “Mineral Oil (MOSH – MOAH) Food Contamination.” UC Food Quality Resource, 2024. https://ucfoodquality.ucdavis.edu/chemical-contaminants/mineral-oil-mosh-moah [Accessed January 11, 2026]

50. Barp L, et al. “Migration of selected hydrocarbon contaminants into dry pasta packaged in direct contact with recycled paperboard.” Food Additives & Contaminants Part A 32(2):271-283, 2015. https://foodpackagingforum.org/news/hydrocarbon-contaminants-in-pasta-packed-in-recycled-paperboard [Accessed January 11, 2026]

51. European Parliament and Council. “Regulation (EC) No 1333/2008 on food additives.” Official Journal of the European Union L354:16-33, 2008. https://pmc.ncbi.nlm.nih.gov/articles/PMC3441937/ [Accessed January 11, 2026]

52. European Commission. “Commission Regulation (EU) 2022/63 amending Annexes II and III to Regulation (EC) No 1333/2008 on titanium dioxide.” Official Journal of the European Union, 2022. https://essfeed.com/why-titanium-dioxide-was-banned-as-a-food-additive-in-the-eu/ [Accessed January 11, 2026]

53. Center for Science in the Public Interest. “Food Dyes: A Rainbow of Risks.” CSPI Report, 2010. https://www.cspi.org/sites/default/files/attachment/food-dyes-rainbow-of-risks.pdf [Accessed January 11, 2026]

54. California Legislature. “California Food Safety Act (AB 418).” California State Legislature, 2023. https://www.healthline.com/health/red-dye-3 [Accessed January 11, 2026]

55. Bradley EL, Stratton JS, et al. “Printing ink compounds in foods: UK survey results.” Food Additives & Contaminants Part B 6(2):73-83, 2013. https://www.researchgate.net/publication/265605623_Migration_of_Photoinitiators_in_Food_Packaging_A_Review [Accessed January 11, 2026]

Conflict-of-Interest Signals in Key BPA Biomonitoring and Toxicokinetic Studies

Supplemental Information – Best Practices Index

Food and beverage sourcing and selections: background
Food selections for both legs of the study were patterned after a “typical American diet”as defined by the United States Department of Agriculture (USDA). In addition, identical (or extremely similar) foods chosen for each leg needed to be widely available in the United States in a practical manner convenient to other investigators. Absent an unrealistically massive budget that would allow LC/MS testing on every food component in both legs of this study, certain assumptions needed to be made regarding food sourcing and the effects on replicability. Investigators based those assumptions on (among many considerations) on how food processing adds plastic-derived chemical (PDC) contamination and the ways that PDCs infiltrate the food chain. Baseline leg For the “typical” plastic-contaminated baseline leg, food was sourced from national brands available at a large chain store, Safeway. While there are no truly national food chains[x], large regional chains such as Kroger, Safeway and others offer many of the same national brands. Because national brands are processed according to consistent corporate manufacturing standards [x] investigators gave them preference. This is preference based on an unverifiable assumption that, for example, Oreo cookies purchased at a California Safeway are likely to have the identical (or close to) nutritional composition and plastic-derived chemical contamination as Oreo cookies purchased in Ohio, New York or Florida. In addition, processed foods provide nutrition information that is likely to be relatively accurate and probably consistent regardless of the purchase location. Further, these foods experience a higher degree of processing than fresh foods which exposes them to numerous additives and polymer surfaces[x]. lastly, these national brands are frozen, canned, and packaged in other extended-shelf life materials which are substantially plastic-based[x]. That set of assumptions also postulates that these foods are likely to provide sufficient plastic-based contamination levels to contrast with levels in the intervention leg. It’s important to acknowledge that many items in chain stores — such as fresh fruit, vegetables and milk — are obtained from local or regional sources whose contamination levels likely vary widely. Investigators in this study, therefore, relied upon frozen fruit and vegetables for the contamination leg. Because milk is sourced locally or regionally even by large chains we had milk samples analyzed via LC-MS/MS which offers future investigators the advantage of choosing milk with the same or similar BPA quantification. This testing was also performed because our original protocol called for using the least contaminated milk to produce our own cheese. Time constraints and other issues of practicality make that unfeasible. We elected to select cheese from a nationally available dairy brand whose milk scored below LOQ in the LC-MS/MS tests. Food Sourcing: Intervention leg For the intervention leg, food was sourced as close as possible in the food chain to its actual production from a vendor capable of shipping nationally. Investigators developed detailed standards for intervention food selections based on literature searches detailing detected or projected contamination sources. Special attention was devoted to the health effects of micro- and nanoplastics and to minimizing exposure to those particles. Key for these considerations were that the producer: Either dry-farmed or used well water for irrigation No irrigation with recycled wastewater or biosolids (sewage plant sludge) Adhered — as a minimum — to USDA organic standards Food was sourced by the ability to trace items to the source of production, and vetting of the source for complying with standards according to food type. The exhaustively detailed standards used are described in Appendix 2 of the Revised Stealth Syndromes Human Study Protocol, If the absence of contamination could not be determined, then specific foods were considered contaminated and eliminated from the intervention diet. Some entire classes of food — such as fish and seafood –were excluded because the constant environmental pollution variability makes it impossible to assess contamination potential (fish).
Basic Scientific Lab Standards — Best Practices for a Replicable Dietary Intervention
NOTES: All of the best practices described below have been developed and hands-on tested in an actual dietary intervention study as feasible and minimally disruptive in a commercial-standard kitchen. The kitchen must be treated as a laboratory; a recipe is a protocol; foods are reagents; every item used in preparation and cooking is equipment and instrumentation; detailed notes must be captured on every item, step, and procedure. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. CARDINAL COROLLARY#1: You must know, and disclose: the exact composition and source of every ingredient, item, and piece of equipment. CARDINAL COROLLARY #2: The exact ingredients, items, and pieces of equipment must be readily available to the broadest geographical spectrum of investigators. CARDINAL COROLLARY #3: The preparation environment must be precisely and completely described in a manner that it can be duplicated by other investigators. CARDINAL COROLLARY #4: Rely only on data that you have observed and collected. Do not use self-reported or memory-based information or rely on un-monitored test subject compliance. Accuracy and replicability depend upon using precise methods under identical conditions using identical materials, reagents, apparatus, and test subjects. Unfortunately, human dietary intervention studies located in a search of the scientific literature are fatally confounded by the failure to employ basic scientific methods that are standard in bench experiments. In addition to these shortcomings, dietary intervention studies treat the kitchen as a black box to be provided by caterers, institutional kitchens, or even test subject memories. (Black Box meals: A look at five dietary intervention studies. ) Most studies involving BPA and phthalates have given general instructions to food preparers to use only “fresh” ingredients and to avoid any plastic contact. However, specific food sources and the details of their production are not available. Neither are specific cooking protocols nor the identities of the utensils, pots, pans, cleaning regimen (surfactants an issue), recipes, or ingredients (processing & methyl contributors an issue). Data regarding those conditions cannot account for the wide variability of contamination in the growing, processing, and sourcing stages. As a result, instructions in previous dietary studies account only for contamination transfer from food packaging materials and preparation. No studies have been found that succeed in quantitatively parsing the growing, production, and processing contamination from that of food contact materials and preparation. Unlike clinical blood panels and mass spectrometer tests which have accepted standards, meals — even those using the same recipes — are rife with confounding factors to which no laboratory-quality standards have ever been addressed. Few chefs, other than bakers, adhere to the precise requirements of recipes. And even bakers can be confounded by variations in measurements, sourced materials, timing, and baking temperatures. This is a first effort at applying the basic principals of laboratory bench science protocols and practices to a kitchen responsible for dietary intervention meals. Best bench science practices in the kitchen developed in a study of the effects of Bisphenol A and Inflammation. Non-food exposures Numerous non-food sources of BPA are present in the environment and likely pose significant “background” contamination which will vary depending upon the test subjects’ lifestyles and environments. This is particularly critical because major health effects including estrogen/testosterone disruptions, inflammation, and metabolic events such as insulin resistance and lipid imbalance, can be affected by low doses of scores of chemicals. For more on this see: Reducing Non-Food Exposures. Sanitation/Hygiene As with all appropriate bench science work, preparation surfaces should be non-reactive, non-porous, resistant to chemicals, heat, and easy to clean. Stone or ceramic tiles can accumulate contaminants in grout. Sealants will contain polymers. Polymer-based surfaces cannot be used. Dietary interventions also require that preparation surfaces must be efficient to maintain hygiene in the event that food makes incidental contact. Stainless steel offers all of those characteristics which is why professional and health-department approved kitchens are almost totally stainless steel. Environment – Floor, walls, ventilation PM2.5 Constant ventilation of HEPA-filtered air is vital to prevent contamination of food with polymer-based particles which can confound results. Air should be constantly monitored throughout the trial and records kept. The type and age of the HVAC system should be noted as well as the type of filter used and the ducting materials (metal versus plastic). Immediately after dusting, the HVAC filter should be changed and the system fan run continuously for four hours to collect as much dust as possible which has been stirred up from cleaning. A fresh filter should then be installed. HEPA-class air purifier use should report the make, model, capacity, and whether it is portable or installed with the HVAC system. If portable, the location should be noted along with the distance from the HVAC air return. PurpleAir is an accurate and cost-effective solution for monitoring. Other than the cost of the sensor ($179), monitoring is free and historical data can be downloaded and saved. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Cleaning Protocol – Floors Polymer-based materials are universally found in professional and institutional kitchens given to their durability and ease of cleaning. However, friction against the floor caused by shoes and rolling carts inevitably creates ultra-fine particles many of which qualify as PM2.5 which — regardless of chemical composition — cause inflammation when inhaled. Significantly, many of the polymers from which flooring is made (such as polyvinyl chloride) have known health effects and can contaminate food destined for test subjects. For this and standard hygiene reasons, floors should be wet-mopped with at the end of every food preparation day. The cleaner for this task and food preparation surfaces should be hypochlorite-based and free of surfactants such as ethoxylates that have been shown to cause health effects. Spills and other unanticipated incidents should be cleaned with water — minus cleaning agents — when possible. […]
Why a Dormitory Setting is Needed for Replication and Valid Causal Conclusions in Dietary Intervention Studies
Non-food-exposures (NFEs) — including environmental conditions — are so numerous and variable that a precise replication of those is impractical and, perhaps, impossible. See: Reducing Non-Food Exposures in dietary intervention studies. Plastic contamination is also inescapable. Plastic micro-and nanoparticles — as well as the chemical compounds used to produce the polymers — are ubiquitous in the environment and present formidable confounding factors for replicability and causality. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Expense and Practicality Issues As we proceeded to implement our original study protocol, we were continually confronted with a self-reinforcing cascade of confounding factors. Among these confounding factors are: Extreme variations among published studies that measured BPA and phthalate concentrations in many common food items.[i],[ii],[iii],[iv],[v],[vi],[vii] Evidence of inherent contamination in production and processing and not solely from food contact materials.[viii],[ix],[x],[xi],[xii],[xiii],[xiv] Ubiquitous contamination of all commonly available foods. See Appendix 3. The necessity to test every food ingredient for nutrition and contamination levels. Substantial controls that needed to be imposed on non-food contamination sources. Lengthy testing regime a barrier to subject compliance. Those chemicals exist in, and are mostly inseparable from: the air, food, dishes, non-stick coatings, water, clothing, surroundings (floors, walls, draperies, fabric coverings etc.), polymer gloves, thermal cash register receipts and an unknowable number of other sources. What’s more, the consistency of those contaminants change over time and place and will vary from person to person. Given the vast nature of confounding factors, it is not surprising that dietary intervention studies studying the effects of Bisphenol A (BPA) are inconsistent, not replicable and, on the whole, incapable of supporting a causal relationship. Without a valid, causal relationship, it is not possible for a clinician or other health professional to make fact-based recommendations to their patients and clients. Likewise, regulatory decisions based upon those are not based on solid science and subject to endless arguments among scientists. What factors need to be considered? Within the bounds of the possible, a proper dormitory environment will will minimize confounding factors by providing the same environment — air, water, food — for all study participants. Minimize the use of, and contact with plastic. Towels, napkins and all other cloth material will be 100% cotton. All cotton fabric will be sourced from that which is grown organically, without pesticides. All items will be laboratory tested for pesticide and plastic residues. Bedding will be 100% cotton. Multiple layers will be installed to minimize migration of plastic from sanitary mattress covers which are expected to block migration from mattress materials. Subjects will be provided with a choice of all-cotton under-garments (possibly scrubs). All cotton outerwear will be provided. All garments will be pre-washed multiple (TBD) times to reduce/remove sizing or possible plastics contamination. All garments will be changed daily. Study-issued socks and slippers will be issued. Exercise shoes and cotton socks to be allowed in the ventilated exercise area only. Shoes must not be worn outside that area. Rooms will be identically equipped and all surfaces cleaned with an acceptable detergent and implements. If dormitory flooring is vinyl or polymer based, all chair legs will be covered with a sock-like cotton covering to reduce microplastic contamination. No chairs with rolling wheels will be permitted. Air monitoring for PM 2.5 New HVAC air filters will be installed. Portable HEPA air filters will be employed. Number TBD Access to the dormitory will be restricted to study-related personnel Tub bathing will be allowed every 2 days. No showers will be allowed due to aerosolization of plastic chemicals and nanoparticles. Opportunities for exercise must be investigated, but remain problematic because of the use of plastics in exercise equipment. This may be possible by the use of proper ventilation to remove plastic contamination from leaching and frictional shedding of micro/nanoplastics. Psychological factors must be considered and resolved including need for privacy, minimum stress (to reduce cortisol levels), possible conflicts among study participants. This will be particularly important for sleeping arrangements unless it’s possible to provide a private room for each participant. Creative partitioning in multiple-occupant rooms might provide a solution. In addition to other screening requirements for potential participants, should study subjects be screened psychologically for their suitability to comply with the protocol and to interface appropriately with other subjects. Broadband internet access [i] Fasano, E., Bono-Blay, F., Cirillo, T., Montuori, P., and Lacorte, S. 2012. Migration of phthalates, alkylphenols, bisphenol A and di(2-ethylhexyl)adipate from food packaging. Food Control 27(1): 132-138. [ii] Serrano, S.E., Braun, J., Trasande, L., Dills, R., and Sathyanarayana, S. 2014. Phthalates and diet: a review of the food monitoring and epidemiology data. Environmental Health 13: 43. [iii] Guart, A., Bono-Blay, F., Borrell, A., and Lacorte, S. 2011. Migration of plasticizers phthalates, bisphenol A and alkylphenols from plastic containers and evaluation of risk. Food Additives & Contaminants Part A: Chemistry, Analysis, Control, Exposure & Risk Assessment 25(5): 676-685. [iv] Bhunia, K., Sablani, S.S., Tang, J., and Rasco, B. 2013. Migration of chemical compounds from packaging polymers during microwave, conventional heat treatment, and storage. Comprehensive Reviews in Food Science and Food Safety 12(5): 523-545. [v] Bang, D.Y., Kyung, M., Kim, M.J., Jung, B.Y., Cho, M.C., Choi, S.M., Kim, Y.W., Lim, S.K., Lim, D.S., Won, A.J., Kwack, S.J., Lee, Y., Kim, H.S., and Lee, B.M. 2012. Human risk assessment of endocrine-disrupting chemicals derived from plastic food containers. Comprehensive Reviews in Food Science and Food Safety 11(5): 453-470. [vi] Groh, K.J., Geuke, B., and Muncke, J. 2017. Food contact materials and gut health: Implications for toxicity assessment and relevance of high molecular weight migrants. Food and Chemical Toxicology 109(1): 1-18. [vii] Bittner, G.D., Denison, M.S., Yang, C.Z., Stoner, M.A., and He, G. 2014. Chemicals having estrogenic activity can be released from some bisphenol a-free hard and clear, thermoplastic resins. Environmental Health 13: 103. [viii] Schecter, A., Lorber, M., Guo, Y., Wu, Q., Yun, S.H., Kannan, K., Hommel, M., Imran, N., Hynan, L.S., Cheng, D., […]
Indexing in Progress and Regularly Updated
Please be patient. A massive amount of information and photos on apparatus, food sourcing, preparation and other protocol-related data are being uploaded as swifty as possible given limited resources. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Basic scientific principles designed to establish causality. Scientific standards and food-related laboratory best practices Black Box meals Controlling non-food exposures, Co-confounding factors and micro-nutrients. The problem with animal models. How food processing adds plastic-derived chemical contamination Best practices — Herbs and Spices: Powerful in small amounts, precise measurement needed Best Practices Backgrounder: Micro- and Nanoplastics Best practices: Herbs and Spices – avoiding contamination Best practices – Spices: Make your own baking powder Best practices: Scale calibration Prepping bacon and lunch meat ham to minimize plastic packaging contamination. Avoiding plastic contamination when storing food. Best practices: De-waxing apples Best practices — Sourcing Dairy: Milk, Cheese, Yogurt, Butter methods and barriers Best practices: Sourcing cheese & butter and minimizing plastic contamination from packaging.
Replicability: Additional sourcing, preparation, and best practices
This page has been replaced by: Best Practices Index This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. This is an ongoing index links illustrating techniques and actions developed and taken to increase the changes of successful replication. Our ultimate course of action often vary from those anticipated in our original protocol. You can find those original protocols listed in The Study – Deconstructed which is found in the right hand column of the main web site. We will eventually match up all our specific actions and protocols to each of the links in the “Deconstructed” section. We will have multiple links for each of those sections. When finished, each link will contain appropriate citations and expanded explanations. This is a sampling: Sourcing Dairy: Milk, Cheese, Yogurt, Butter methods and barriers The cheese/butter dilemma Avoiding plastic contamination when storing food. Prepping bacon to minimize plastic packaging contamination. De-waxing apples

Supplemental Information – Apparatus, Formulae (Recipes), Reagents (Food)

What Does Peer Review Mean?-old draft
When a study is peer-reviewed, it means that it has undergone a critical evaluation by one or more experts in the same field (peers) before it is published in a scientific journal or presented at a conference. The peer review process is a fundamental aspect of scholarly research and is intended to ensure the quality, validity, and significance of the research. Here’s how it works and what it means: Submission: After researchers conduct a study and write a paper detailing their methods, results, and conclusions, they submit the paper to a scientific journal or conference. Editorial Assessment: Initially, an editor at the journal reviews the submission to ensure it meets basic journal criteria and is within the scope of the journal. Peer Review Process: If it passes the initial check, the editor sends the manuscript to several experts in the field. These peers are usually researchers or academics with expertise in the subject area of the paper. Evaluation: The peer reviewers evaluate the manuscript on several aspects: Methodology: Is the study’s design and methodology sound and appropriate? Originality: Does the study contribute new knowledge or insights to the field? Significance: Are the results significant enough to warrant publication? Clarity and Presentation: Is the manuscript well-written and clearly presented? Ethical Standards: Does the study meet ethical guidelines, particularly in medical or psychological research? Feedback: Reviewers provide feedback, critique, and recommendations. This can include suggestions for improvement, requests for clarification, or identification of potential errors. Revision: Based on the feedback, authors may be asked to revise their manuscript. This could involve conducting additional experiments, reanalyzing data, or rewriting parts of the paper. Final Decision: After revisions, the paper is either accepted, rejected, or sent back for further revisions. An accepted paper is then prepared for publication. Confidentiality and Objectivity: The peer review process is typically anonymous and confidential to encourage objectivity and honest feedback. The peer-review process is crucial for maintaining scientific quality and integrity. It acts as a filter to ensure that only high-quality research is published, providing a form of quality control by preventing flawed or unsubstantiated studies from entering the public domain. However, it’s important to note that peer review is not infallible and does not guarantee the validity of a study, but it significantly increases the likelihood that the research is sound, reliable, and valuable to the field.
Food and beverage sourcing and selections: background
Food selections for both legs of the study were patterned after a “typical American diet”as defined by the United States Department of Agriculture (USDA). In addition, identical (or extremely similar) foods chosen for each leg needed to be widely available in the United States in a practical manner convenient to other investigators. Absent an unrealistically massive budget that would allow LC/MS testing on every food component in both legs of this study, certain assumptions needed to be made regarding food sourcing and the effects on replicability. Investigators based those assumptions on (among many considerations) on how food processing adds plastic-derived chemical (PDC) contamination and the ways that PDCs infiltrate the food chain. Baseline leg For the “typical” plastic-contaminated baseline leg, food was sourced from national brands available at a large chain store, Safeway. While there are no truly national food chains[x], large regional chains such as Kroger, Safeway and others offer many of the same national brands. Because national brands are processed according to consistent corporate manufacturing standards [x] investigators gave them preference. This is preference based on an unverifiable assumption that, for example, Oreo cookies purchased at a California Safeway are likely to have the identical (or close to) nutritional composition and plastic-derived chemical contamination as Oreo cookies purchased in Ohio, New York or Florida. In addition, processed foods provide nutrition information that is likely to be relatively accurate and probably consistent regardless of the purchase location. Further, these foods experience a higher degree of processing than fresh foods which exposes them to numerous additives and polymer surfaces[x]. lastly, these national brands are frozen, canned, and packaged in other extended-shelf life materials which are substantially plastic-based[x]. That set of assumptions also postulates that these foods are likely to provide sufficient plastic-based contamination levels to contrast with levels in the intervention leg. It’s important to acknowledge that many items in chain stores — such as fresh fruit, vegetables and milk — are obtained from local or regional sources whose contamination levels likely vary widely. Investigators in this study, therefore, relied upon frozen fruit and vegetables for the contamination leg. Because milk is sourced locally or regionally even by large chains we had milk samples analyzed via LC-MS/MS which offers future investigators the advantage of choosing milk with the same or similar BPA quantification. This testing was also performed because our original protocol called for using the least contaminated milk to produce our own cheese. Time constraints and other issues of practicality make that unfeasible. We elected to select cheese from a nationally available dairy brand whose milk scored below LOQ in the LC-MS/MS tests. Food Sourcing: Intervention leg For the intervention leg, food was sourced as close as possible in the food chain to its actual production from a vendor capable of shipping nationally. Investigators developed detailed standards for intervention food selections based on literature searches detailing detected or projected contamination sources. Special attention was devoted to the health effects of micro- and nanoplastics and to minimizing exposure to those particles. Key for these considerations were that the producer: Either dry-farmed or used well water for irrigation No irrigation with recycled wastewater or biosolids (sewage plant sludge) Adhered — as a minimum — to USDA organic standards Food was sourced by the ability to trace items to the source of production, and vetting of the source for complying with standards according to food type. The exhaustively detailed standards used are described in Appendix 2 of the Revised Stealth Syndromes Human Study Protocol, If the absence of contamination could not be determined, then specific foods were considered contaminated and eliminated from the intervention diet. Some entire classes of food — such as fish and seafood –were excluded because the constant environmental pollution variability makes it impossible to assess contamination potential (fish).
Possibilities for Further Investigation
This n=1 trial points out two further factors to make a larger trial better able to more accurately determine causality between human clinical health indicators and BPA and other plastic-derived chemicals. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. The reasons for those flaws are multiple and include: Markers for ultra-processed food additives The first factor would be to determine a blood marker associated with one or more of the most common additives found in ultra-processed foods. The second would be to include hsCRP along with other indicators in an expanded diagnostic blood panel. Expanded blood profiling Because high inflammation is associated with many metabolic health problems, this expanded blood panel would include additional indicators such as ghrelin, adiponectin, and insulin resistance. Because hsCRP is non-specific to the sources of inflammation, further accuracy in human causality determinations may also be enhanced by the employment of select cytokines and chemokines to determine direct BPA influences on inflammation sources such as immune system disorders and tumorigenesis. Moving BPA causality forward will probably require another proof-of-concept investigation: Controlled dosing If the above alternatives are not satisfactory — or are likely to prove inadequate in determining human health effects specifically as relates to BPA — a third method would be to conduct a dietary intervention with exactly the same menu in the typical diet and BPA dosing in the intervention diet. All ingredients would be pre-tested for BPA levels at the sourcing stage and alternatives selected if levels are determined to be above an acceptable threshold. Subsequent BPA levels would be established after meal preparation and a total daily BPA dosage calculated. Then, prepared (and tested) meals would be divided into two segments: one for the meals as prepared and a second — intervention menu –to be dosed with BPA at the federally acceptable “safe” level. This regime would isolate BPA as the only contributor to the inflammation and other clinically relevant manifestations. With a sufficient number of markers measured — similar or identical to those in the NIH/Hall study — it may be possible to develop a profile of markers that is specific to BPA. This study protocol would be — by far — the most expensive alternative. That means that a proof-of-concept investigation will probably be wise to determine any further confounding factors.
Reducing Non-Food Exposures in Dietary Intervention
Attempts can be made to reduce non-food exposures (NFEs) in dietary intervention studies. However, it is impractical (and probably impossible) to eliminate them. Plastic micro- and nanoparticles, as well as the chemical compounds used to produce, are ubiquitous in the environment and present formidable confounding factors that make it impossible to establish causal relationships between a single chemical and measured human health outcomes. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. That reality ranks among the top reasons that dormitory conditions offer the optimum solution for study results that can be both reproducible and clinically significant. Reducing non-food exposures (NFEs) Sathyanarayana et al. (2013) posited that substantial non-food exposures such as those with personal care products could mask BPA and phthalate reductions from dietary intervention.[xxxvii] A quick picture of the complexity of NFEs can be illustrated by this diagram from Endocrine Disruptors and Asthma-Associated Chemicals in Consumer Products[xxxviii]: An extensive discussion of NFE contamination sources may be accessed in Appendix 4. Triaging NFE elimination Given the impossibility of avoiding BPA, phthalates, and other harmful chemicals in the environment, reproducibility of studies must focus on the practical reduction of known exposures reducing those exposures that are: Most easily identified and, Practical to control, Likely to produce maximum reduction via minimum study subject effort, and Can be adequately documented and replicated. An ideal scenario would be to conduct trials in a well-defined residential/dormitory setting where all study subjects experience near-identical environmental conditions for the entire term of the study. However, expense and practicality dictate that many studies must engage subjects who will modify their diets while living in their own homes as well as engaged in multiple additional sites for work, school, shopping, and recreation. Because of those practical limitations, investigators should — to the best of their ability — thoroughly document the environmental circumstances under which a dietary intervention is conducted. This should include questionnaires about known exposure sources for their: External environment (home, work, school, recreation including floor surfaces) and, Personal environment (pharmaceuticals, personal care products, appliances, fabrics for clothing and bedding, presence of plastic dental and other implants and prosthetics, etc.). Participants with excessive and/or uncontrollable external environmental exposures should be excluded. Study subjects should then be counseled on contamination sources and given a checklist of specific controllable sources to avoid during the trial. Investigators should schedule frequent reminders and follow-ups with each participant to assess and assure the best possible compliance. As a potential starting point for assessing personal environmental exposures, investigators should consider the EDC Footprint Calculator developed by the Pennsylvania State University Extension Service. While this Excel version was designed to offer an indication of contamination products found in municipal wastewater and is not all-inclusive, it could be modified and updated to better serve the purposes of this study or future efforts. Personal environment controls As the above chart from “Endocrine Disruptors and Asthma-Associated Chemicals in Consumer Products” illustrates, most personal care products contain relevant chemical contaminants that can potentially confound this study’s chosen health effects markers. Select three-day reduction actions for the personal environment: NOTE: To make these reductions possible and assure the greatest possibilities for reproducibility, study subjects must be healthy, non-smoking adults without recent dental work or invasive medical procedures. Subjects should not have body fat of more than 32% for women and 25% for men. Subjects should not be taking any medicines or dietary supplements other than low-dose or 325 mg aspirin. Additional requirements should include: Use recommended toothpaste without Triclosan and reduced or zero levels of contaminants. No mouthwash. Uncoated nylon fiber dental floss (no plastic strips). No hand creams or lotions. No perfumes or any other products containing fragrances. Use recommended shampoo with reduced or zero-levels of contaminants. Use recommended hand soap with reduced or zero-levels of contaminants. No cosmetics. No hair color treatment. No teeth whitener. No hand sanitizers. Use recommended deodorant. No contact lenses. Use of eyeglasses only. No contact with cash register receipts. No hair spray, gel, or other treatment. No body wash. No sunscreen. No nail polish. No Tshirts, sweatshirts, or other clothing with printed designs. In addition, subjects must note the synthetic composition of clothing and bedding items. That data may be valuable for investigating possible confounding factors. External environment controls In addition to food contamination issues, home, workplace, and public spaces also provide significant — but widely variable — exposure to humans to endocrine disruptors, CECs and, other environmental chemicals[xxxix]. Thus, additional requirements should include: Do not use inkjet printers, gel rollerball pens, or ballpoint pens. No use of volatile adhesives such as rubber cement or spray cans. Use no household cleaners. No reusable, non-paper grocery/shopping bags with printed designs. No plastic wallets/purses/backpacks. Inform investigators if beds or pillows have plastic covers. No air fresheners. Avoid areas irrigated with recycled wastewater. Do not get into a vehicle until the interior has been thoroughly ventilated with outside air. Ride in vehicles with all windows open. Do not use an air freshener. Avoid new vehicles and those whose interiors have been recently cleaned commercially. Wear only those clothes that have been washed with phthalate-free laundry detergents. Unless a phthalate-free laundry detergent has been used previously, run two loads of towels, then dry. If fabric softeners have been used in the dryer, run two additional loads of towels after decontaminating the washer and dry them in the dryer to reduce accumulated phthalate levels. Avoid bathing in homes whose water supply is delivered with plastic plumbing: PVC, Pex, etc. Dust particles Household dust presents a significant confounding factor because it is the residual detritus from many environmental sources shown to contain BPA, phthalates, and other chemicals relevant to this study: Phthalates in Indoor Dust and Their Association with Building Characteristics[xl]. That study contains a home materials inventory that will be adapted for the study subject questionnaire. See also PM 2.5[xli]. Reduction actions for dust particles: […]
SSHS-Supplemental Material – Mass Spectrometry
Serum BPA and Conjugate Analysis Report_OSU 2021 Updated-LinusPauling-serumdata_10212021-1 This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research.
Stealth Syndrome Study – Typical and Intervention Diets
StealthSyndromeStudy-TrialMenu-InterventionDiet-Recipes StealthSyndromeStudy-Trial-Menu-TypicalDiet For food and menu selection, please see the full revised protocol and appendices at this PDF document This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research.
Professional-Grade Kitchen – Wood, Glass & Stainless Steel
We removed the flowers and other non-investigation materials. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research.
How Dairy Products Complicated Our 2022 Study – And What We Had To Do To Solve The Issue
When we conducted the investigation for our 2022published paper, the goal was to create a menu that was a “typical” American diet as defined by the U.S. Department of Agriculture. That “typical” diet demanded that we include cow’s milk. And that was a problem. Dairy has many opportunities for plastic contamination For dairy products, we created an ultra-strict sourcing protocol that assumed that the introduction of plastic chemicals into the dairy food chain begins with the milking process. That strict protocol had to be drastically altered will be described below. To consumers, the most obvious connection between plastic and dairy products comes in packaging — shrink wrap, plastic bottles (“paper” bottles have plastic coatings), plastic yogurt containers, butter in plastic tubs or wrapped in paper impregnated with chemicals. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Additionally, previous studies — including dietary interventions — have focused primarily on packaging materials as sources of contamination. H0wever, the dairy chain’s many contamination sources from plastic-derived chemicals (BPA and phthalates involves numerouds additional contacts with plastic and other chemicals before it reaches the consumer. Some of those contacts include: include “teat washes” to clean and disinfect cow udders, as well: polymer filters to screen out dairy and other foreign matter, hoses to transfer raw milk from the milking machine to holding tanks, hoses to transfer milk from holding tanks to transport tankers whose stainless steel tanks may have polymer liners and potentially traces of chemicals used for disinfection. More hoses are used to transfer milk from tanker trucks to the creamery which uses a variety of plastic and stainless steel components to process the milk and get it ready for sale to tee consumer. In addition, once at the creamery, there are polymer-based components used for the movement of milk through filtering, pasteurization, cream separation, homogenization, and finished packaging. Dairy contamination begins with what the cow eats While there are few studies studying the presence of plastic chemicals in milk produced by American dairy cows, work in Europe <citations to be added here and elsewhere in final version> indicates that milk produced in warmer weather when cows are eating in pastures seems to have fewer contaminants than when they are fed manufactured (processed) feed in colder weather. Because of the extensive contamination from feed to consumption our original approved protocol for sourcing milk demanded that we start as low as possible on the processing chain. That approved protocol required us to obtain certified organic raw milk from cows raised in pastures that were not irrigated. Especially, not irrigated with recycled municipal wastewater which contains scores of pharmaceutical byproducts, illegal drug metabolites, and toxic chemicals. Our plan for the raw milk was to obtain the milk directly from the milking machine. While milking machines use many plastic components, we were prepared to pay for replacing the most common plastic parts with ones that were known not to leach BPA and phthalates. Processing, transparency, source traceability and reproducibility The most reproducible results for our study meant we had to start with the least-contaminated dairy products.The logic dictated that, if we knew where the raw milk came from, we could trace the source for the cheese (for cheeseburgers and sandwiches), the butter (to be used as the only oil for cooking), and the milk products for consumption. That also meant that we would rely on those resulting dairy products were to use in preparing other foods. Because of that, dairy became a foundational role for the study’s entire menu. For more on that, see Menu: Dairy – Milk, Cheese, Yogurt, Butter. In addition, the wide variety of possible materials and used by individual dairies and creameries, plastic contamination levels are likely to vary significantly from one operation to the next. That, we reasoned, would mean that other investigators wishing to replicate our study might could might up with substantially different conclusions unless they obtained raw milk from our source and used the same methods and materials we did to process raw milk. That requirement meant that processing our own raw milk and resulting foods could make our study more reproducible. Because reproducibility is a key foundation of a well-conducted investigation, we were ready to exert the extra effort. Based on this set of assumptions, we hypothesized that the minimum contamination and the best chances of replicability of the study protocol demanded a “back to the future” effort that required us to acquire raw milk — milked by hand (with conditions). Once we had obtained the raw milk, the protocol required that we: Filter the raw milk to remove physical contaminants such as hair. Pasteurize the milk. Separate the cream from the milk. Use the cream to make butter which we would use as our basic fat/oil for cooking. Make yogurt Use the lower-butterfat (approximately 4%) milk from the separation for cooking and direct consumption. Make cheese. By taking on so many basic processing steps, we could minimize plastic contamination by making sure that only glass and stainless steel came in contact with the milk once we had obtained it from the milking machine. Based on our study protocol revision approved by the Committee on Human Research at the University of California San Francisco Medical School, in latye 2018, we began to contact Sonoma and Marin County dairies, creameries, farm organizations, and agriculture-related educational institutions. Unexpectedly, we ran into a stonewall of silence and lack of cooperation from the dairy industry. Over a period of eight months least 43 phone calls and emails to dairies, creameries, went un-returned. We failed to get even a reply from dairies, creameries, farm organizations, ag-oriented educational institutions — even — cheese and yogurt makers — anyone who might know a dairy farm who would cooperate. When that produced no results, we resorted to personal visits and “milk driving” around Sonoma and Marin County looking for any dairy or […]
The Cream Separator From Hell = No Cheese & Butter As Originally Planned. (And Reflected Flawed Logic and Impossible Logistics)
Cream separator, as sold.Even if we had solved the reproducibility conflicts with our “close to source, minimum contamination” plans for milk, the final problem was the fact that the only small-production cream separator we could find was full of plastic parts and “stainless steel” that was actually aluminum. That despite the fact that the seller said it contained all food grade stainless steel and contained no plastic So after spending far too much time and effort — eight months — trying to source raw milk, there we were in July 2019 with four major problems to solve for a study that was way behind on time: This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. It was proving to be impossible to obtain raw milk to pasteurize and use in the study <<link>> The cream separator was vital to producing all our dairy products: milk, cheese & butter. More importantly, obtaining raw milk from with the same precise composition as we had secured from the single small producer we had located in Sonoma County would have been practically impossible for another lab to obtain and replicate. Furthermore, that milk was dependent on the plant composition of its specific pasture location — something that would change day to day and season to season. The metal parts — supposedly stainless steel — were highly attracted to magnets. That indicated inferior “stainless” construction.
Oil for Cutting Boards
For treating wooden cutting boards, in our dietary intervention lab/kitchen, we used olive oil packaged in glass from a local supplier who has minimal plastic components in their oil-making mill. While some food sources suggest that vegetable-based oils will somehow turn rancid in contact with water, we found no evidence of this. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. We washed and scrubbed the boards frequently — and in hot water when meat was in contact — let them dry thoroughly and applied a modest coating of olive oil. No flavor transfer to food was observed. Avoiding mineral oil We avoided food-grade mineral oil for several reasons: First because many plastic-based chemicals contaminate liquids of all sorts when they leach out into the contents. Plastic contact occurs in both the production and packaging stages. Second, because mineral oils are a products of crude oil production, the origin of the oil is undetermined as it its precise chemical composition given unknown and variable production and packaging. Both of those reasons violate our protocol to eliminate both known and unknown sources of contamination.
Milk Samples: Making Aluminum Foil Barriers to Avoid Contamination by Migration of Plastic Bottle Caps
To avoid possible plastic contamination in the milk samples we sent for Mass Spec testing, we used glass bottles and aluminum foil to prevent sample contact with the plastic cap. This technique also works well in the kitchen when glass storage containers have plastic lids. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research.
Home-Made Pasta — As UNprocessed as Possible
This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research.
Choose a Healthy Grinder/Mill for Pepper & Spices to Avoid Microplastics and Harmful Chemicals
This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Like most ground spices, pepper experiences significant plastic contact during processing and packaging. Use whole spices and grind your own.

Reagents: Consumables and Food

How Dairy Products Complicated Our 2022 Study – And What We Had To Do To Solve The Issue
When we conducted the investigation for our 2022published paper, the goal was to create a menu that was a “typical” American diet as defined by the U.S. Department of Agriculture. That “typical” diet demanded that we include cow’s milk. And that was a problem. Dairy has many opportunities for plastic contamination For dairy products, we created an ultra-strict sourcing protocol that assumed that the introduction of plastic chemicals into the dairy food chain begins with the milking process. That strict protocol had to be drastically altered will be described below. To consumers, the most obvious connection between plastic and dairy products comes in packaging — shrink wrap, plastic bottles (“paper” bottles have plastic coatings), plastic yogurt containers, butter in plastic tubs or wrapped in paper impregnated with chemicals. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Additionally, previous studies — including dietary interventions — have focused primarily on packaging materials as sources of contamination. H0wever, the dairy chain’s many contamination sources from plastic-derived chemicals (BPA and phthalates involves numerouds additional contacts with plastic and other chemicals before it reaches the consumer. Some of those contacts include: include “teat washes” to clean and disinfect cow udders, as well: polymer filters to screen out dairy and other foreign matter, hoses to transfer raw milk from the milking machine to holding tanks, hoses to transfer milk from holding tanks to transport tankers whose stainless steel tanks may have polymer liners and potentially traces of chemicals used for disinfection. More hoses are used to transfer milk from tanker trucks to the creamery which uses a variety of plastic and stainless steel components to process the milk and get it ready for sale to tee consumer. In addition, once at the creamery, there are polymer-based components used for the movement of milk through filtering, pasteurization, cream separation, homogenization, and finished packaging. Dairy contamination begins with what the cow eats While there are few studies studying the presence of plastic chemicals in milk produced by American dairy cows, work in Europe <citations to be added here and elsewhere in final version> indicates that milk produced in warmer weather when cows are eating in pastures seems to have fewer contaminants than when they are fed manufactured (processed) feed in colder weather. Because of the extensive contamination from feed to consumption our original approved protocol for sourcing milk demanded that we start as low as possible on the processing chain. That approved protocol required us to obtain certified organic raw milk from cows raised in pastures that were not irrigated. Especially, not irrigated with recycled municipal wastewater which contains scores of pharmaceutical byproducts, illegal drug metabolites, and toxic chemicals. Our plan for the raw milk was to obtain the milk directly from the milking machine. While milking machines use many plastic components, we were prepared to pay for replacing the most common plastic parts with ones that were known not to leach BPA and phthalates. Processing, transparency, source traceability and reproducibility The most reproducible results for our study meant we had to start with the least-contaminated dairy products.The logic dictated that, if we knew where the raw milk came from, we could trace the source for the cheese (for cheeseburgers and sandwiches), the butter (to be used as the only oil for cooking), and the milk products for consumption. That also meant that we would rely on those resulting dairy products were to use in preparing other foods. Because of that, dairy became a foundational role for the study’s entire menu. For more on that, see Menu: Dairy – Milk, Cheese, Yogurt, Butter. In addition, the wide variety of possible materials and used by individual dairies and creameries, plastic contamination levels are likely to vary significantly from one operation to the next. That, we reasoned, would mean that other investigators wishing to replicate our study might could might up with substantially different conclusions unless they obtained raw milk from our source and used the same methods and materials we did to process raw milk. That requirement meant that processing our own raw milk and resulting foods could make our study more reproducible. Because reproducibility is a key foundation of a well-conducted investigation, we were ready to exert the extra effort. Based on this set of assumptions, we hypothesized that the minimum contamination and the best chances of replicability of the study protocol demanded a “back to the future” effort that required us to acquire raw milk — milked by hand (with conditions). Once we had obtained the raw milk, the protocol required that we: Filter the raw milk to remove physical contaminants such as hair. Pasteurize the milk. Separate the cream from the milk. Use the cream to make butter which we would use as our basic fat/oil for cooking. Make yogurt Use the lower-butterfat (approximately 4%) milk from the separation for cooking and direct consumption. Make cheese. By taking on so many basic processing steps, we could minimize plastic contamination by making sure that only glass and stainless steel came in contact with the milk once we had obtained it from the milking machine. Based on our study protocol revision approved by the Committee on Human Research at the University of California San Francisco Medical School, in latye 2018, we began to contact Sonoma and Marin County dairies, creameries, farm organizations, and agriculture-related educational institutions. Unexpectedly, we ran into a stonewall of silence and lack of cooperation from the dairy industry. Over a period of eight months least 43 phone calls and emails to dairies, creameries, went un-returned. We failed to get even a reply from dairies, creameries, farm organizations, ag-oriented educational institutions — even — cheese and yogurt makers — anyone who might know a dairy farm who would cooperate. When that produced no results, we resorted to personal visits and “milk driving” around Sonoma and Marin County looking for any dairy or […]
Oil for Cutting Boards
For treating wooden cutting boards, in our dietary intervention lab/kitchen, we used olive oil packaged in glass from a local supplier who has minimal plastic components in their oil-making mill. While some food sources suggest that vegetable-based oils will somehow turn rancid in contact with water, we found no evidence of this. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. We washed and scrubbed the boards frequently — and in hot water when meat was in contact — let them dry thoroughly and applied a modest coating of olive oil. No flavor transfer to food was observed. Avoiding mineral oil We avoided food-grade mineral oil for several reasons: First because many plastic-based chemicals contaminate liquids of all sorts when they leach out into the contents. Plastic contact occurs in both the production and packaging stages. Second, because mineral oils are a products of crude oil production, the origin of the oil is undetermined as it its precise chemical composition given unknown and variable production and packaging. Both of those reasons violate our protocol to eliminate both known and unknown sources of contamination.
Study Recipes & Trial Menus
Stealth Syndrome Study-Trial-Menu-Typical Diet (Excel) Stealth Syndrome Study-Trial Menu – Intervention Diet + Recipes (Excel) This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Intervention Study Recipes 2019 Kate’s Pasta Dough Ingredients: 280g 00 flour 25g for dusting surfaces 168g whole eggs 32g egg yolks 1.45g salt 7g Baking Olive Oil Directions: Measure ingredients. Make a well on a clean workspace with the flour Make sure the sides are high enough to accommodate liquid ingredients Mix eggs, olive oil, and salt in a separate mixing bowl Pour eggs into well and slowly incorporate flour until it becomes a thick dough Knead dough for 3-5 minutes until elastic Dough should spring back when poked Dust with extra flour if dough remains sticky Let rest at room temperature for 45 minutes Roll out dough into desired shape Cook for 3-4 minutes or until pasta floats Classic Maple Waffles Ingredients: 263g flour 42g honey 6.51g baking powder 3.31g salt 220g whole milk 106g eggs 26g oil Directions: Mix flour, sugar, baking powder and salt in a large bowl Whisk eggs, milk and oil in a separate bowl Gradually incorporate wet mixture into dry ingredients until fully incorporated Let batter sit for 25 minutes at room temperature Pre-heat waffle iron Pour batter on to waffle iron at the center Cook 2 minutes per side Homemade Mayonnaise Ingredients: 50 whole egg 32g lemon juice 154g canola oil 8.37g salt Directions: In bowl of blender or food processor add egg, salt, and lemon juice Turn on to medium-high speed and slowly incorporate oil until combined Continue to beat mixture until it thickens in texture and holds shape Yeastless Focaccia Ingredients: 238g water (room temperature) 250g flour 7g baking powder 5g salt 13g olive oil 2g black peppers 5g crushed garlic 1g dried basil 34g grated Reggiano parmesan cheese Directions: Preheat oven to 425F (220C) Pour water and garlic into bowl of an electric mixer fitted with a dough hook Soft together flour, baking powder, and salt to previous bowl Mix on medium speed until dough forms into a ball Put dough into baking pan Using oiled fingers, spread dough to ½ inch thickness. Make sure there are no holes in the dough Rub top and sides of dough with olive oil. Season with black pepper and basil Bake in preheated oven for 20 minutes Remove from oven and sprinkle with cheese and return to oven Bake for an additional 8 minutes or until golden brown Oven Fries Ingredients: 311g potatoes 22g olive oil Additional 11g to brush baking tray 6g salt 1.25g pepper Directions: Preheat oven to 375F Wash potatoes leaving skin on and cut into desired size Soak potatoes in cold water in sink or bowl for 30 minutes then remove and dry well Toss in oil and seasonings Place on greased tray and bake for 20 minutes, then turn the oven up to 425F and cook 15 minutes or until fries are golden. “Boring” Baked Chicken Ingredients: 662g boneless chicken breasts w/ skin 22g olive oil Directions: Preheat oven to 450F Brush making sheet with 11g olive oil Baste chicken with 11g olive oil Cook for 10 minutes and flip Baste with oil already in pan Cook another 15-20 minutes or until internal temperature is at least 165F at the thickest part Put on platter and cover loosely with tin foil to cool Olive Oil Roasted Almonds Ingredients: 469g whole raw almonds 26g olive oil 12g salt Directions: Preheat oven to 350F In a medium bowl toss all ingredients together until evenly coated Spread onto a single layer in baking tray Roast for 10 minutes, stir, and continue to roast for 5-8 minutes or until lightly browned Watch carefully as they can burn easily Cool completely on baking sheet until storing in an airtight container Basic Quick Bread Ingredients: 286g flour 15g baking powder 2g salt 160g eggs, room temperature 373g whole milk 77g canola oil Directions: Preheat oven to 350F (177C) and prepare a 9” x 5” (23cm x 13cm) loaf pan with light butter In a large mixing bowl whisk together flour, baking powder and salt. In a separate mixing bowl combine eggs, milk and oil. Pour liquid ingredients into dry ingredients and using a spoon stir the two together until combined Do not over mix the dough. The more you mix the tougher the bread becomes Pour batter into loaf pan and bake for 40-45 minutes or until a toothpick inserted in the center comes out with moist crumb Baked Macaroni and Cheese Ingredients: 105g pasta 15g butter 14g bread crumbs 70g minced onion 5g flour 1.75g salt 1g pepper 355g whole milk 227g shredded cheddar cheese Directions: Prepare pasta in boiling water (about 2 minutes) Preheat oven to 350F and grease 2 quart casserole dish with 3g butter In a saucepan, melt 12g butter, add onion until tender (aprox 3 min) Stir in flour, salt and pepper until blended gradually stir in milk and cheese until smooth Place pasta in casserole dish and pour cheese sauce over pasta, mixing lightly. Sprinkle breadcrumbs over top Bake 18-20 minutes or until bubbly and golden brown Greek Olive Oil Cinnamon Cookies Ingredients: 100g canola oil 100g honey 6.5g butter 66g maple syrup 77g orange juice 278g flour 5.46g baking powder 2.55g baking soda 1g cinnamon Directions: Preheat oven to 350F (180C) In a large bowl mix oil, honey, syrup and orange juice In a smaller bowl mix together flour, baking powder, baking soda, and. Cinnamon Gradually add dry mixture to wet mixture until a soft dough is formed Cover dough and let it sit for 10 minutes Grease a pan with 6.5g of butter Bake […]
Best Practices: Spices/Black Pepper
Best practices for spices and pepper mills.

Appendices to the study

Revised Stealth Syndromes Human Study Protocol: APPENDIX 1 – Reproducibility
REPRODUCIBILITY – THE SCIENTIFIC PROBLEM THAT DEMANDED ENHANCED SOURCING OF THE STUDY DIET Reproducibility + Confounding factors drive changes, increase complexity, & costs Reproducibility is the acid test of properly done studies that produce valid data. In the past couple of years, the “reproducibility crisis” has been the subject of numerous scholarly articles and comments. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. The most data-based is this one from Nature (1,500 scientists lift the lid on reproducibility Survey sheds light on the ‘crisis’ rocking research.). That article found that: “More than 70% of researchers have tried and failed to reproduce another scientist’s experiments, and more than half have failed to reproduce their own experiments.” While data do not indicate a substantial rise in irreproducible results, the persistence of non-replicable studies is unacceptable. We should not add to that phenomenon. See also: When Quality Beats Quantity: Decision Theory, Drug Discovery, and the Reproducibility Crisis Opinion: Is science really facing a reproducibility crisis, and do we need it to?
Revised Stealth Syndromes Human Study Protocol: APPENDIX 2 – Detailed Parameters of Intervention Diet Selections
PLEASE NOTE: Extensive photographs and study documenting the following items will be added as time allows after the main study text is finished. Those photos to be added are of apparatus, supplies, utensils, and will demonstrate methods used to further decrease plastic contamination in intervention foods whose surfaces were potentially contaminated by contact with plastic packaging. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Water All water consumed and/or used for cooking, washing, drinking or used to irrigate self-grown plants will be obtained from a commercial device using a solid-block carbon filter and certified by NSF for reduction of BPA and phthalates. One such device is the Aquaversa filter from Multipure which uses a carbon block filter that lists BPA among its contaminant reduction list. The list does not mention phthalates. However, the list does cover many chemical with similar phenolic structures. If study funds are available, it would be valuable to determine BPA and phthalate levels in the water water before the filter and afterwards. In addition, independently published research indicates that other types of carbon filters are effective in reducing many harmful compounds including organic chemicals. Effects of activated carbon types and service life on removal of endocrine disrupting chemicals: amitrol, nonylphenol, and bisphenol-A. Adsorption characteristics of selected pharmaceuticals and an endocrine disrupting compound—Naproxen, carbamazepine and nonylphenol—on activated carbon Bisphenol A Removal from Water by Activated Carbon. Effects of Carbon Characteristics and Solution Chemistry, Environmental Science and Technology, 39 (16) (2005), pp. 6246-6250 Beverages Coffee Only locally roasted and ground beans will be used. Provider will be selected on the smallest amount of plastic involved. Beans and grounds will be handled with metal or glass only and packed in glass jars. Beans will be ground in a mill with no plastic components. The beans will be prepared using either an all glass and stainless steel French press or a stainless steel percolator with all metal parts. Also acceptable is the Moka pot-style espresso maker or a pour-over, glass and metal coffee maker with water from an all metal tea kettle. All metal wire basket for grounds must be used, no filter paper. If an automatic drip system can be located with no plastic ever touching the water or coffee stream, that will be obtained and used. The weakest links in drip coffee makers that appear to be all glass and/or metal usually lies in plastic tubing that connects the heating element to the water reservoir, the hot water application tube, and the filter basket. Tea No tea will be allowed. Like spices, the extensive harvest, curing, processing, and packaging offers many contamination routes. Also like spices, the tiny fragments that compose tea increase the surface area capable of acquiring chemical contamination. Soft drinks Highly processed. Not allowed in the study diet. Fruit juice No commercial juices allowed. Highly processed. Not allowed in the study diet. Freshly prepares using no plastic contact. In general, whole fruits are a healthier alternative to juices. Beer and wine No commercial products allowed. All are extensively processed using plastic. Sourcing ingredients All food items will be sourced from the provider. All provider locations will be personally visited and inspections made of their premises, equipment and processes. Beef, lamb, chicken, pork, fish Minimum standards: Organic certification, no plastic in growing, harvesting, handling, or packaging. All animals must be free-range. Even if allowed by exceptions to organic regulations: No commercial fertilizers, pesticides, or recycled wastewater irrigation are allowed in this study. No irrigation of pasture and feeding areas is preferred. Drinking water from well or municipal water only. No PVC or other plastics. Beef and lamb must be grass-fed and comply with AGA Statement of Best Practices. Preference given to non-irrigated pasturing. For welfare of animals, supplemental hay is allowed but must come from non-irrigated pasture. Possible source: Crowd Cow Slaughter standards Must be humane. Solid cuts of meat only. No sausage or ground meat. Slaughter to avoid all plastic contact unless absolutely vital for health and hygiene. Nitrile gloves. Finished cuts to be placed in glass containers covered with aluminum foil (not in contact with meat) and finally sealed with a plastic lid. Beef, lamb & goat Lean cuts (minimum marbling) on beef and lamb. Lower fat content helps minimize lipophilic content. Visible fat to be removed before cooking to minimize lipophilic concentration. Chicken Skin to remain on chicken, to be removed before cooking to minimize lipophilic concentration. Breasts only for chicken. Pork, fish Not included in the study diet. Diet and subsequent flesh contamination are extremely hard to control or monitor. Study note: An exception was made for organic, un-smoked bacon because the intervention diet needed to include a version of the all-American bacon cheeseburger. An exception was also made to use organic sliced ham (minimal water, no preservatives) in a ham and cheese sandwich. Dairy Same water, feed, and pasturing requirements as beef, lamb, and goat. Udder and teat cleaning and treatments for animal welfare and human hygiene must be examined for plastic exposures and contamination minimized. Milking must be done preferably by hand or using milk machines certified as BPA and phthalate-free. Nitrile gloves to be used. All collected milk must be in stainless steel vessels. Filtering stages cannot use polymer filters. Separation, homogenization (if any) and pasteurization must be plastic free. Glass containers must be used for bottling of milk. Cream gathered during the separation process will either be used for cheese or discarded to minimize lipophilic contaminate concentration. Cheese will be made using milk prepared as described above. Preference will be given to low- or moderate-butterfat cheeses. The cheese process will use stainless steel in the initial heating processes. Curds will be gathered and drained in stainless-steel wire baskets. The whey will be discarded. Drained curds will be pressed in stainless steel molds. Finished cheese will be packed in aluminum foil then placed in Ziploc-type airtight […]
Revised Stealth Syndromes Human Study Protocol: APPENDIX 4 – Additional References: Non-food Contamination Sources
This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Xenobiotic Organic Compounds in Greywater and Environmental Health Impacts Phthalates in Indoor Dust and Their Association with Building Characteristics Green Chemistry and the Search for New Plasticizers Overview of air pollution and endocrine disorders Neurotoxicity of fragrance compounds: A review Poly(Vinyl Chloride) Green Chemistry in Textiles Formaldehyde in your fabrics Toxic Free Supply Chain for Textiles and Clothing Bisphenols, Benzophenones, and Bisphenol A Diglycidyl Ethers in Textiles and Infant Clothing Eco-testing of textiles By K. Amutha, K. Saranya Phthalates in cosmetic and personal care products: Concentrations and possible dermal exposure Hazardous substances in plastics: – ways to increase recycling Green Chemistry and the Search for New Plasticizers Characterization of phthalates exposure and risk for cosmetics and perfume sales clerks Risk assessment to human health: Consumer exposure to ingredients in air fresheners Xenobiotic Organic Compounds in Greywater and Environmental Health Impacts Overview of air pollution and endocrine disorders Personal care product use as a predictor of urinary concentrations of certain phthalates, parabens, and phenols in the HERMOSA study Possible endocrine disrupting effects of parabens and their metabolites Phthalates in Indoor Dust and Their Association with Building Characteristics Fragrance compounds: The wolves in sheep’s clothings Development of an Endocrine Disrupting Compounds Footprint Calculator Determination of phthalate esters in cleaning and personal care products by dispersive liquid–liquid microextraction and liquid chromatography–tandem mass spectrometry Characterization of phthalates exposure and risk for cosmetics and perfume sales clerks Risk assessment to human health: Consumer exposure to ingredients in air fresheners *PDF: FINAL REPORT — Study on the Link Between Allergic Reactions and Chemicals in Textile Products Principal European Commission, DG Enterprise and Industry *PDF: Phthalates and Their Alternatives: Health and Environmental Concerns – VALUABLE FOR LIST Can That New Car Smell Harm You? Or Someone Else? Reprinted by permission from the Feb. 9, 2014 issue of Nano Active By Lewis Perdue Driving with the windows down when you are tired may keep you awake in more ways than just the sounds and tactile effects of air currents. It could also keep you from being poisoned and, perhaps, prevent you from killing someone. Take, for instance, Navindra Kumar Jain, a 63-year-old retired Silicon Valley tech executive who told police that the intense new car smell of his Tesla S made him drowsy enough to fall asleep at the wheel. When Jain lost control of the Tesla on Nov. 2, 2013, he killed 40-year-old librarian Joshua Alper who had been riding a bicycle in a wide shoulder lane on Highway 1 north of Santa Cruz. Most public reactions to Jain’s claim have been met with derision and disbelief. But scientific evidence, including a major one by Australia’s CSIRO14, indicate that many of the chemicals given off by automotive dashboards, upholstery, wiring, adhesives and interior trim can offer the same consciousness-impairing and mind-altering effects as sniffing glue. The CSIRO study and others have found that — in addition to toluene, xylene, benzene and other Volatile Organic Counpounds (VOCs)(1-4) , there are phthalates (5-7), flame-retardants(11,12) and other Endocrine Disrupting Compounds that are outgassed from car interior materials and form the scummy film on windshields and windows.(5-7). And, in a contra-Darwinian sense, people love the fragrance of these VOCs so much that they support an entire industry of sprays and air fresheners containing many of the same petrochemicals and EDCs. (See: shop on Google for new car smell) The National Highway Traffic Safety Administration considers toluene (a key compound in “sniffing glue”) to be a Central Nervous System depressant(8) with symptoms that include: “Dizziness, euphoria, grandiosity, floating sensation, drowsiness, reduced ability to concentrate, slowed reaction time, distorted perception of time and distance, confusion, weakness, fatigue, memory loss, delusions, and hallucinations.” The California Department of Public Health says in an official statement that, “Toluene, like most organic solvents, can affect your brain the same way drinking alcohol does.” Significantly, in addition to VOCs like toluene, xylene, and benzene — all of which can cause leukemia(10) — we found studies that detected more than 100 compounds — many of which are petrochemicals and fit into the California Department of Public Health’s definition of “organic solvents.” The CSIRO study stated that, “Controlled exposures of human subjects to a 22-compound mixture at TVOC [Total VOC] concentrations of 7,000–33,000 µg/m3 have observed effects within minutes, such as subjective reactions (odour, discomfort, drowsiness, fatigue/confusion), eye/nose/throat irritation, headache, and (in symptomatic subjects) neurobehavioural impairment” Further, the CSIRO study noted conditions which suggest that it is altogether possible that Tesla driver Jain had been impaired, as he has stated, by the sedan’s new car smell. “Investigation into VOCs in new cars has been limited. Bauhof and Wensing (1999) described a standardised test procedure used in Germany in which VOC concentrations were measured at car interior temperatures of 23–65°C and an unspecified ventilation rate. “TVOC concentrations of 35,000–120,000 µg/m3 were reported for six new cars (test temperature not specified), these concentrations decreasing exponentially over a 40-day period to about 10,000–30,000 µg/m3. VOCs consisted of aromatics, glycol ethers and esters, aldehydes, ketones and amines. “Grabbs et al. (1999) screened four new cars in the USA, all after being closed for one hour and without temperature control. Three exhibited initial TVOC concentrations of 300–600 µg/m3 and the fourth 7500 µg/m3. The latter decreased exponentially by about 90% within three weeks.” Click here for a chart of chemicals from Grabbs, et. al. Click here for a chart of chemicals from Faber, et. al. A sampling of the top 10 petrochemicals found were: Methylcyclohexane is also used in perfumes for its minty fragrance. This compound is closely related to 4-Methylcyclohexanemethanol, MCHM, spilled in the vast West Virginia chemical spill in January 2014. Ironically, MCHM has been patented for use in air fresheners. (13) Undecane, the National Toxicological Program says, is an organic solvent and Central Nervous System depressant. Ethylbenzene, is classified by the […]

Collaborator Biographies

Lewis Perdue, Project Co-Founder, Study Designer and Principal Investigator
William Lewis Perdue IIIChairman, Center for Research on Environmental Chemicals in HumansInvestigator, Study Designer Stealth Syndromes Human StudyCo-Founder, Stealth Syndromes Project Education B.S., Communications & Biology (Ecology, Evolution & Systematics), With Distinction, Cornell University, 1972 A.S., Math & Science, (First in class, first-ever to graduate with perfect 4.0 GPA), State University of New York (SUNY)/Corning, 1970. Commencement speaker, 2009 for Fiftieth Anniversary of college founding. Fellowship, Aerospace Engineering, Mississippi State University, summer 1966 Internship, Westinghouse Electric (Nuclear Reactor and Special Purpose Tube Divisions), summer 1967 Independent Study, Multiple collaborators & mentors including: Dr. Arthur C. Guyton, Dean of the University of Mississippi Medical School, NASA, Oak Ridge National Laboratory, 1960-1967 Publications Perdue, W. L., Reus, V. I., van Breemen, R. B., Muchiri, R. N., & Yeamans-Irwin, R. L. (2022). Stricter protocols combined with a clinical serum biomarker can increase replicability and causality for dietary intervention studies. Plus empirical data on BPA regrettable substitutions. medRxiv, 2022-08 Perdue, L., The Mendelian Randomization by Millwood et al.: Observations and Expressions of Concern, 2019 Perdue, L., “Precision evaluation of environmental chemical risk assessment: Using existing pharmaceutical evaluation results as a more accurate paradigm,” 2016 Perdue, L., “Heat Shock Protein Hsp27 points to causal link between BPA and cancer & chemotherapy resistance.”2016 Perdue, L., & Yeamans-Irwin, R.L. “Low-Dose BPA Paper in Toxicological Sciences is Contaminated by Massive Errors & Should Be Retracted.”, 2014 Strongest Evidence Yet Between BPA and Thyroid Cancer, 2014 Many more articles and research at two web sites founded by Perdue: Stealth Syndromes Human Study, and The Stealth Syndromes Project. Research & Teaching Experience Cornell University – 1970-72 Received the only A+ awarded in an organic chemistry class of 150. Also only student to accurately answer final exam extra credit question to diagram the quantum resonance bonding orbitals of ozone. As a first semester junior, offered a scholarship to change biology major to chemistry after I alerted the department to 27 errors (many in quantum bonding orbital diagrams) in the new text book for organic chemistry. Added communications as an unsanctioned double major. Cornell did not formally support double majors at the time. Because of that, I changed my major to communications at the end of my junior year during which I completed all required courses in just two semesters. Financially self-supporting since age 18: paid for college and living expenses by working as a journalist and photographer. Financial considerations — which included substantial student loan debt — mandated that I interrupt my lifelong passion for science and technology to follow a temporary vocational path in communications instead. Honors program: allowed to take courses at Cornell Law School. Teaching Assistant, Mass Communications Law. State University of New York (SUNY)/Corning Community College – 1968-1970 Independent research: Conducted abiogenesis experiments including complete replication of Miller-Urey experiment confirming that complex organic compounds including vital amino acids, could have been created from simple inorganic compounds during the by postulated primitive environmental conditions which mat have been present on Earth more than 4 billion years ago. Teaching Assistant & Faculty-Appointed Tutor, Calculus, Physics, & Biology Westinghouse Nuclear & Space Technology Internship — Summer 1967 Course work in the theory, instrumentation and practice of nuclear fission, reactor design, and mechanics of neutron cross sections, capture, fission moderation. Responsible for calibrating neutron sensors used in civilian and military reactors. Created custom calibration curves unique for each neutron counter. Responsible for construction of, and suggesting design changes for, solar flux measurement sensor tubes for NASA’s 1969 Mariner 6 Mars flyby. Course work in theory of electron guns used in color cathode ray tubes. Hands on experience with efforts to reduce corner landing misplacement of electron beams in color picture tubes. Course work in the theory of quantum-based spectral output of specific pure elements, primarily metals. Hands on work in the utilization and calibration of the Westinghouse Hollow Cathode spectral output tubes. Independent Study — 1966-67 Research focus: Magnetohydrodynamics, plasma physics, ultra-high-vacuum physics. Designed and built a magnetohydrodynamic thrust accelerator for space propulsion. The ionized particle stream was provided by a plasma jet. The thruster used sequential electromagnetic field compression to provide thrust. A variation of this is currently used in NASA’s deep space probes such as dawn. Enabling technologies required the design and construction of a plasma jet, functioning proton accelerator, and a six-cubic-foot ultra-high (10-12 Torr) vacuum chamber and associated electronic and high-voltage electrical systems. Mississippi State University – Summer 1966 Coursework and lab experience in plasma physics, fluid flow instrumentation, mechanical resonance. Collaborated with faculty in further exploring ion thruster linear accelerator. Independent Study, 1965-66 Mentors: Werner Von Braun, NASA scientists at Redstone Arsenal (George C. Marshall Space Flight Center) and the Oak Ridge National Laboratory. Research focus: high-energy particle physics, plasma physics, ultra-high-vacuum physics, interplanetary and interstellar particle flux density, ultra-high-vacuum technology With a suggestion from NASA that they would welcome a way to increase the relatively small thrust of the ion engine as it currently existed, I designed and built a two-stage thruster. And a vacuum chamber capable of 10-12 Torr to simulate the vacuum of outer space. The first stage was an improved version of my previous ion engine design coupled with a linear particle accelerator for the second stage. This thruster was designed to use the interplanetary particle flux as fuel. This required an electromagnetic collector to attract and compress a simulated solar plasma (He and H ions). The particles from the collector were then separated using mass spectrometer principles to provide a uniform He+ stream to the particle accelerator. Dubbed “The Cosmic Engine” by the media, the entire system won a number of awards at the International Science and Engineering Fair. Independent Study — 1964-65 Research focus: plasma physics, fluidics of ionized gases Completed design and construction of electromagnetic ion space thruster and vacuum chamber required for operation. Exhibited and demonstrated ion space thruster and modulated laser combined under the title, “Space Communications and Propulsion.” Won First Class overall Bay State science fair along with numerous awards from NASA, AAAS and other […]
Victor Reus, Co-Principal Investigator
Victor Reus biography can be found at this link This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research.

The Study

The Stealth Syndromes MedRxiv Study, Revisited and Thoughts for the Future
The chart on the left was published October 27, 2020 in MedRxiv: as Investigating hsCRP as a clinical inflammation marker for human Bisphenol A food contamination offers protocol suggestions for conducting replicable, causal dietary intervention studies (doi: https://doi.org/10.1101/2020.10.25.20212282). By contrast, the chart on the right, from September 2021 mass spec data, revealed scant evidence of BPA and substantial presence of BPA chemical structure analogues BPF and BPS. These issues confirm the original study’s recommendations including the need for dosing, and dormitory environment to improve dietary intervention study replicability, and determination of causality. A brief summary of how we got here (And why it has taken so long ) After The Nov. 25, 2015 approval of the study by the University of California San Francisco School of Medicine (UCSF) IRB/Committee on Human Research, the Parnassus campus pathology lab at UCSF Medical Center agreed to analyze blood samples of hsCRP. Following that, a qualified UCSF research lab agreed to perform serum analysis. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. The time to conduct the trial was extended on Oct. 27, 2019 because of delays caused by a fundamental re-examination of food sourcing requirements in order to facilitate replicability. The head of the UCSF research lab provided blood draw “vacutainer kits” which the lab had validated as being free of leaching BPA and other plastic-derived chemicals. While it would be less expensive to use urinalysis. that method measures the glucuronide metabolized form of BPA, I was hoping to compare ratios of free BPA (serum) with BPA-glucuronide. While measuring free BPA in human serum was difficult in the early 2000-teens, reliable LC/MS methods have been developed to surmount early obstacles The ratio of free/metabolized BPA levels compared with hsCRP inflammation indicators would have been further instructional given recent research that indicate that BPA-glucuronide may be more harmful in the human body than free BPA. Selected citations for this and other sections are included in (Citations, Appendix 2)at the end of this document. In the run-up to the trial, I exchanged multiple emails with the Silent Spring Institute who had a program — Detox Me Action Kit that accepted urine samples from the public and researchers. Those discussions dragged on and in early October 2019 — just weeks before the trial was to begin — the SSI responded that they were too busy and would not accept our samples. The trial began in late October 2019 but had to be interrupted by continuing intermittent power outages from the Kincade Fire which was the largest of that year’s California wildfire season. The trial was restarted in early December. Accordingly, test subject blood was drawn by the pathology lab of a UCSF affiliate hospital — Sonoma Valley Hospital —and delivered to the UCSF research lab and to the Parnassus campus hospital lab within an hour of draw as specified by the head of the UCSF research for BPA analysis. In January 2020, investigators inquired about the UCSF research lab’s progress on analyzing the blood samples. The head of the lab then said he would not be processing the samples as previously agreed. The lab agreed to preserve the samples at -80C and hold them for our removal. With significant information from the hsCRP data, but lacking BPA data, investigators decided to begin working on a paper based on the incomplete data which had been captured. What have we learned? As noted in the MedRxiv study, even without BPA data, the results approximately replicated a larger, NIH-sponsored published trial. That trial did not measure any specific chemical biomarker compounds suspected of influencing biological processes, but used the NOVA system that provides a broad, generic distinction between processed and ultra-processed foods Unfortunately, the lack of serum analysis was a major omission in the paper, so after the MedRxiv digital publication on October 27, 2020, a search was launched for a new lab to process the serum BPA samples with the goal of editing that publication or creating a follow-up paper.. The search dragged on because there are not many labs qualified to perform mass spectrometry analysis on BPA/human serum. However, in mid-May 2021 the Linus Pauling Institute at Oregon State University agreed to perform mass spec analysis on the samples . Elaborate preparations were made to maintain the sample cold chain from UCSF to Corvallis and where they were delivered on May 13, 2021. Another delay followed because BPA analysis of human blood requires an extreme degree of precision, the Linus Pauling Institute required its mass spec devices to be cleaned by manufacturer representatives followed by re-calibration. The Director of the Linus Pauling lab analyzed the blood samples using ultrahigh pressure liquid chromatography-tandem mass spectrometry using a triple quadrupole Shimadzu mass spectrometer which allows the study of the presence of other chemical compounds. Puzzling results The results, delivered on September 24, 2012 unexpectedly revealed BPA concentrations that were beneath the LOQ (Limit of Quantification). The lab also analyzed the serum extracts using a high resolution quadrupole time-of-flight mass spectrometer using untargeted scanning for BPA, BPF and BPS which may be studied for the presence of other compounds. As evidenced by comparing initial results with those from the Linus Pauling Institute (below), the comparison with NIH/Hall are consistent while, the mass spectrometry results contain multiple anomalies. By contrast, the chart on the right revealed scant evidence of BPA and substantial presence of BPA chemical structure analogues BPF and BPS. Multiple Anomalies in Mass Spec results The anomalous Mass Spec concentration ratios among indicate that product manufacturers have substituted analogues for BPA. This may be an effort for manufacturers to make marketing claims that items are “BPA free.” Evidence, however, exists to indicate that the analogues are not less harmful than BPA, and may actually be more harmful. (see citations) While not a chronological study, this paper: “Determination of trace levels of eleven bisphenol A analogues […]
UCSF IRB/CHR Approves Study Extension
2019-UCSF-CHR-IRB-study-Extension-to-102720 This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Human Research Protection Program Institutional Review Board (IRB) Expedited Review Approval Principal Investigator Victor I. Reus, MD Co-Principal Investigator Lewis Perdue Type of Submission: Continuing Review Submission Form Study Title: Clinical blood profile assays as biomarkers to directly assess potential health effects resulting from the controlled elimination of suspected dietary and environmental chemical toxins. IRB #: 15-17703 Reference #: 265715 Committee of Record: San Francisco General Hospital Panel Study Risk Assignment: Minimal Approval Date: 10/27/2019 Expiration Date: 10/26/2020
SSHS – Early Study Results, Thoughts, and Anomalies
Note: There is an inconsistency in the literature on reporting high sensitivity C-Reactive Protein levels. The actual protein is properly abbreviated CRP. The test procedure for measuring quantities below 10 mg/L is hsCRP. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. However, published papers most often refer to the protein as hsCRP which is, technically, incorrect because that is the test, not the protein. Because most papers use hsCRP consistently to refer to the protein, Investigators have followed the inaccurate terminology and done that as well even though it seems like a foolish consistency. Stealth Syndromes Human Study – Follow-up thoughts and questions The hsCRP readings at the end of the trial were not what was expected. On the other hand, real science often starts when the results are not as anticipated. The following is a quick summary of findings and possible considerations and roots of the unexpected results. Citations are available. Note that the analysis of concentrations of BPA and other chemicals in the panel are not yet available. Initial expectations Investigators expected hsCRP to increase over baseline after the “typical diet” leg of the trial. Investigators also expected hsCRP to decrease substantially after the “minimum plastic/processing” intervention leg. Investigator expectations were that final hsCRP mg/L concentration would be substantially lower than baseline. EXPECTED FOR STEALTH SYNDROMES HUMAN STUDY (SSHS) SSHS AS MEASURED UNEXPECTED RESULTS ALSO IN NIH/HALL DIETARY INTERVENTION STUDY Interestingly, a major NIH funded study (Hall et al., 2019, Cell Metabolism 30, 67–77, July 2, 2019 (https://doi.org/10.1016/j.cmet.2019.05.008) also showed a similar anomaly after the ultra-processed menu phase, but then showed a further decrease after intervention. NIH/HALL vs SSHS – CONCENTRATIONS, DELTAS Both studies showed a net decrease in hsCRP at the end of the trial, with the NIH/Hall study showing a decrease almost double that of the SSHS. The NIH/Hall study began with a baseline almost twice that of the SSHS. In addition, investigators expected that SSHS would show a larger decrease in hsCRP following the intervention. This is because the SSHS study protocol was stricter than NIH/Hall because it eliminated commercial food processing contamination and, in addition, employed the most extreme measures to reduce BPA and plastic chemical exposure in sourcing and food storage and preparation. One unknown data point in the comparison is the margin or error on the hsCRP measurements conducted by UCSF labs. The NIH/Hal study cited a +/- 0.3 mg/L margin of error. Assuming UCSF labs have a similar margin of error, that is more relevant given the low concentrations involved. However, doesn’t change the overall relative behavior of the amounts in either study. The difference might possibly be explained by the length of the studies. Our study ran for a week. The NIH/Hall study ran for four weeks which may have offered more time for hsCRP to reach equilibrium. The NIH/Hall study The NIH/Hall study was designed to investigate a possible connection between ultra-processed foods and excess intake of calories. As such, it was an ad libitum trial which allowed subjects to eat as much (or little) of the foods in each leg. The 28-day trial included 20 adults (10 male, 10 females) and was conducted at the NIH Metabolic Clinical Research Unit. The NIH study is noted not only because of the apparent anomaly in the first leg results, but also because it is the only dietary intervention in my literature searches with an extensive blood panel for the subjects and the only one in which hsCRP was measured. Accordingly, the hsCRP level decrease after the ultra-processed leg in the Hall study — like that in the SSHS — would seem to run counter to expectations. The Hall study is also significant because it measured so-called “appetite” compounds: leptin, ghrelin, and adiponectin as well as insulin. This is important because: BPA and phthalates exercise effects on those proteins in a similar manner as illustrated in the Hall study. Ultra-processed foods are also higher in BPA and phthalates due to the extensive use of plastics in processing and packaging. An expanded discussion of this study as related to ours is in order, given that the investigators of that study made numerous protocol errors that render the study incapable of being replicated. Some of those fundamental errors include: Failure to provide recipes (formula), sourcing of materials, preparation, description of equipment, materials including relevant food contact materials. Failure to note whether food preferences of test subjects were taken into account. Failure to take into account that ad libitum food consumption will depend on food preferences (or aversions) as well as seasoning, preparation method or time. What’s going on? A look at the baseline versus “unhealthy” trial leg hsCRP anomaly Unhealthy pre-baseline diet? The anomalous results in both the NIH/Hall study and the SSHS could indicate that the processed/plastic contaminated legs were actually healthier than baseline. In my case, the initial efforts to begin the actual study were urgent and rushed in order to try to complete the trial before the CHR expiration date. As a result, my baseline diet relied heavily on pre-prepared supermarket meals and fast food. Thus, my baseline could have been less healthy than the plastic contamination leg of the trial. The same “unhealthier baseline” diet, may have influenced the NIH/Hall anomaly with hsCRP levels dropping after the end of the ultra-processed leg of the study. Air pollution confounding factors The Kincade Fire in northern Sonoma County started on October 23, 2019, was contained on Nov. 6 but continued to burn and affect the test location during and after the SSHS study was finished. Because PM 2.5 is a potent inflammatory agent, a monitoring device was purchased to track indoor air quality and activated the day before the first (baseline) blood draw. In retrospect, activities probably should have been restricted before the baseline draw. However, a literature search has not found a reference dealing with the pharmacokinetics […]
UCSF IRB/CHR Approves Revised Study Protocol
This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Right-click images to view a much larger version. The full revised protocol and appendices are at this PDF document Summary Revised Protocol: UCSF IRB/CHR Number: 15-17703 Approved by IRB/CHR Co-Principal Investigators: W. Lewis Perdue, Dr. Victor I. Reus MD Study Title: Clinical blood profile assays as biomarkers to directly assess potential health effects resulting from the controlled elimination of suspected dietary and environmental chemical toxins. This study is the first of its kind to go beyond simply measuring serum and urine concentrations of the subject chemicals. Instead, this study will measure clinically useful outcomes using widely accepted diagnostic tests available at most medical facilities. The investigators of this study recommend a revised protocol to increase reproducibility and decrease costs. This revision is based on 2-1/2 years of intensive research that has determined that the original protocol would be impractical, too expensive for allocated resources, and could not be replicated by other investigators. These revisions did not result from a single incident of sudden enlightenment. Instead, they are the result of a steady accumulation of insight built upon the closer scrutiny of previously published diet intervention studies. Underpinning that was the accumulated discovery of confounding basic science factors never before considered in these previous studies. which rendered them irreproducible. Chief among the non-replicability of is the fact that the food supply chain is ubiquitously contaminated with widely varying and uncontrolled levels of Bisphenol A, phthalates and other environmental chemicals. The investigators believe they have developed a reliable method of preparing and sourcing foods that will allow consistent results across other investigations. The full revised protocol and appendices are at this PDF document

This study supported by the Center for Research on Environmental Chemicals in Humans

The Center for Research on Environmental Chemicals in Humans, is a 501(c)(3), Tax-Exempt Nonprofit Organization
Please visit the Center for Research on Environmental Chemicals in Humans to learn more about our tax-exempt research. Our Mission: The Center’s mission is to enable individuals and health professionals to take medically valid actions to avoid the risks of Endocrine and Epigenetic Disrupting Chemicals (EEDCs). The CDC says that EEDCs are found in most Americans. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. To do this, our first-ever human research is designed to establish a scientific cause-and-effect connection between EEDCs and their effects on clinically proven health indicators such as standard hospital blood tests. Read more

Why Is This Study Important?

The Importance of Addressing the Previously Unaddressable
The outcome of this study may make a substantial contribution by definitively and credibly evaluating the human effects of endocrine disruptors and other environmental chemicals. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Regardless of whether the thesis of this study is proven or not, it will add vital data that can help scientists, health professionals, and the general public to understand risks that may be caused by the small levels of chemicals that federal regulators have decided are “safe” to consume but which hundreds of university studies say are harmful. If the study does provide support for its thesis, it will help resolve the current regulatory and scientific stalemate caused by: (a) arguments about correlation and causation, (b) flaws with animal models, and (c) the dismissal of low-dose, non-monotonic effects by many traditional toxicologists. Missing Links There are missing links in environmental chemical risk assessment including: Moving beyond “associated with” to “causes.” (Correlation does not equal causation). The absence of controlled trials on humans. (Unethical to deliberately expose humans to harmful substances). Research conducted on rats, mice and other lab animals is no guarantee the same effects will be seen in humans. How does this study address the missing links? Epidemiology is the science of using data to find correlations — connections or links — between substances, behaviors or environmental factors and diseases or other harms. But while links, associations, and connections can save lives, such statistical correlations are not scientific conclusions or proofs of cause. This study moves conclusions about cause and effect closer than epidemiology can by past “associated with.” If the results provide support for the thesis, this study will advance knowledge that the chemicals in question cause changes in clinical blood tests, double-stranded DNA breaks and epigenetic profiles already established as valid markers of health and illness by the medical and scientific community. The ethical considerations are resolved by this study by using a controlled protocol to systematically remove specific environmental chemicals from the test population rather than adding them. This is possible because very, very few people are without measurable levels of environmental chemicals in their bodies. For example, Bisphenol A, which this study focuses on, is already ubiquitous in the environment and, according to the Centers for Disease Control, is present in 95 % of Americans. Removing potentially harmful chemicals already present in test subjects from environmental exposure is not unethical. It is worth noting hat deliberate exposure of an unwitting population to potentially harmful chemicals is an ethical quandary that neither governments, nor companies, nor universities has addressed. What are the benefits to society? Society can benefit because: This study can offer new, outcomes-based diagnostic and recommendation tools for doctors and other health professionals. This study can give individuals additional of clear, credible, fact-based, steps that are actionable and convenient to adapt to everyday lives. Food, beverage, chemical manufacturers and government agencies will — for the first time — have credible, cause-and-effect data for solid, evidence-based decision making. Cause-and-effect data for solid, evidence-based decision making can allow members of the general public and their health professionals to leapfrog regulatory inertia and special interests in order to take direct healthy personal actions.

The Science

Mice Are Not People: Why The Most Important Studies Done With Them Ultimately Fail In Humans
Pharmaceutical studies are among the most demanding scientific investigations because the results can be a matter of life or death. Astonishingly, 92% of drugs deemed safe and effective in animals, fail when tested in humans. The murine model — mostly mice and sometimes rats — is invaluable in the preliminary stages of investigating pharmaceuticals and toxic chemicals. However, when the ultimate decision needs to be made — such as approving a drug for use — only human experimental subjects will suffice. In many other types of studies, human tests are vital, but cannot be performed for ethical reasons. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. But when ethical and practical concerns can be accommodated, humans are the gold standard. And when that gold standard is used, it surpasses murine test results about 90% of the time. Here is some background on how rats became star test subjects: Rats are Not Little People — But Science Assumes That They Are. More Referencess Clinical development success rates for investigational drugs BIO-Biomed Tracker study: overall likelihood of approval (LOA) by FDA from Phase I was 9.6% Reconsidering Drug Discovery & Development in the Face of Another Failed Clinical Trial The High Price Of Failed Clinical Trials: Time To Rethink The Model
Bisphenol A and Analogues – NHANES
Fourth National Report on Human Exposure to Environmental Chemicals Updated Tables, March 2021 Geometric mean and selected percentiles of urine concentrations (in μg/L) for the U.S. population from the National Health and Nutrition Examination Survey. Excerpted data. Selected full data tables follow Volume One: NHANES 1999-2010 Bisphenol A Bisaphenol F and S not monitored Volume Two: NHANES 2011-2016 Bisphenol A Bisphenol F * Not calculated: proportion of results below limit of detection was too high to provide a valid result. Bisphenol S This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Selected full data tables Volume One: NHANES 1999-2010 Biomonitoring Summary: https://www.cdc.gov/biomonitoring/BisphenolA_BiomonitoringSummary.htmlFactsheet: https://www.cdc.gov/biomonitoring/BisphenolA_FactSheet.html No monitoring data for Bisphenol F or Bisphenol S Volume Two: NHANES 2011-2016 https://www.cdc.gov/exposurereport/pdf/FourthReport_UpdatedTables_Volume2_Mar2021-508.pdf Biomonitoring Summary: https://www.cdc.gov/biomonitoring/BisphenolA_BiomonitoringSummary.htmlFactsheet: https://www.cdc.gov/biomonitoring/BisphenolA_FactSheet.html
Hall Flaws
A high-profile 2019 nutritional study headed NIH research section head Kevin Hall is coming under increasing fire for data and protocol shortcomings. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. In addition, the presence of avoidable confounding factors addressed in this post indicate more serious shortcomings than those already disclosed. The issue was raised widely when research watchdog, Retraction Watch, noted that the open source paper published in Cell Metabolism– “Ultra-Processed Diets Cause Excess Calorie Intake and Weight Gain” — was accompanied by an editorial which urged caution in interpreting the results. In addition to broad attention in general media outlets, Retraction Watch on January 22, noted that the study “[H]as been cited 164 times, according to Clarivate Analytics’ Web of Science, giving it ‘highly cited paper’ and hot paper’ designations. (The paper has also been subject to a correction in October of last year.)” The first detailed expression of concern for the Hall paper came more than two years ago from Edward Archer in PubPeer in which he detailed four methodological errors. More recently, on January 21, two posts — one from by Nick Brown and another by Brown in collaboration with Ethan and Sarah Ludwin-Peery — raised numerous questions about data integrity and experimental protocols. Fundamental Errors in Hall Study Are Common in Most (If not all) Dietary Intervention Studies Like most (if not all) dietary intervention studies, the Hall study is non-replicable and its results inconclusive because it fails to use standard and long-accepted laboratory practices that are basic bench-science standards. (NOTE: Citations and other details on this and the following statements and assertions can be found as part of this study and at this site.) First of all, in a proper scientific experiment, the consumed substances must be treated as reagents with sources and other provenance details fully disclosed to investigators who may attempt to replicate the results. It is especially crucial to avoid food-chain contaminants which exhibit physiological effects similar to those being measured by the investigation — (such as plastic-derived chemicals like Bisphenol A and phthalates whose metabolic effects are the same or similar to those measured by Ultra-Processed Foods — UPF’s). See detail and chart farther down. In addition, basic experimental science demands that a recipe be treated as an experimental procedure including the conditions, apparatus, timing, temperature, measurement accuracy. Further, the food preparation facility must be treated as a laboratory including environmental conditions (PM2.5, ventilation, temperature etc.), the number and qualifications of the food preparers, measures to detect and prevent contamination by substances (such as plastic-derived chemicals like Bisphenol A and phthalates) Intensive efforts to reduce confounding factors need to be undertaken, and documented. This post will enumerate these and other errors in basic science practice in the Hall study that render it non-replicable and its results unreliable. A look at a single meal in the Hall study menu presented in the Supplemental Materials offers a vivid glimpse to many of these variations from valid scientific practices and offers a quick look at the issues facing current practice in dietary intervention investigations. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. First of all, the yogurt will have undergone substantially more processing than whole milk. A look at the meal “Unprocessed Menu, Day 2: Lunch” in which “skim milk” is presented as “unprocessed” indicates a lack of understanding about dairy products in general and that skim and reduced-fat milk undergo more processing steps, many of which involve plastic contact. While it is true that many Plastic Derived Chemicals (PDCs) are lipophilic and may be more prevalent in higher-fat foods, this is yet another ignored unknown in this menu presentation. Second, the Hall material does not indicate which milk-fat content of the the Fage brand yogurt served. Third, the yogurt was packaged in a plastic container from which polymer-based chemicals (PBCs) such as BPA and phthalates can leach . Fourth, while not specified, the Blue Diamond walnuts most likely came packaged in as plastic container which can leach PDCs.. In addition, shelled nuts undergo processing steps that expose them to plastic surfaces. Fifth, no washing or preparation measures are available for the fresh fruit. Was the rinse tap water or carbon-filtered. Were they in contact with plastic bowls, cutting boards or other items. Was an attempt made to reduce the quantity of polymer/wax-based materials used to help- preserve the fresh apple’s moisture level? Were the fresh fruits certified organic which reduces potential pesticide contamination? Where were fresh fruit and vegetables acquired? Sixth, how were the preparation and eating utensils and dishes washed and handled? Were they rinsed in carbon filtered water to remove any cleaning residues from detergents, ethoxylates and other contaminants? Eighth, commercial table salt contains unknown additives including iodine supplements and anti-caking agents of undisclosed identity or quantity. In addition, common table salt is contaminated in widely varying amounts by microplastics, either from processing or environmental contamination. A preferred substitute for a dietary intervention would be NaCl from a reputable laboratory supply company. Ninth, was the olive oil first cold press (no chemical extraction), processed with plastic-free apparatus and packaged in glass? Finally, NONE of the meals presented in the supplemental, materials documents procedures, sources of materials, preparation details. In addition, no data on the weight or volume of the foods served and the error tolerance. It’s also worth noting that all quantities — include liquids — should be recorded in grams to avoid meniscus errors for liquids as well as packing errors for granulated substances such as sugar, flour, spices etc. Black Box Meals and Non-Replicability All of the meals in the Hall study are “Black Box Meals” which are standard in dietary intervention investigations. Black Box means that the investigators in the study have […]
Air Pollution: Confounding Factors for Study
Air pollution confounding factors The Kincade Fire in northern Sonoma County started on October 23, 2019, was contained on Nov. 6 but continued to burn and affect the test location during and after the SSHS study was finished. Because PM 2.5 is a potent inflammatory agent, a monitoring device was purchased to track indoor air quality and activated the day before the first (baseline) blood draw. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. PM2.5 is used to make health recommendations AIR QUALITY INDEX (AQI)The following text and Figure 3, from the California Department of Public Health (PDF) “The US EPA created the Air Quality Index (AQI) to communicate information about air quality to the public.10 The AQI communicates the health impacts of air pollutant concentration using a 6-level color system (Green, Yellow, Orange, Red, Purple and Maroon). “Each color-coded level has an associated descriptive term, progressing from “Good” to “Hazardous.” For each pollutant, the AQI scale value of 100 corresponds to the 24-hour primary health standard. The AQI is most often displayed for two pollutants, PM2.5 and ozone. For PM2.5, the 24-hour health standard of 35 μg/m3 corresponds to the AQI value of 100; AQI values greater than 100 indicate increasing levels of health risk, beginning with “Sensitive Groups” in the Orange category and progressing to “Everyone” in the Red, Purple, and Maroon categories. See Table 3 below.” In retrospect, activities probably should have been restricted before the baseline draw. However, a literature search has not found a reference dealing with the pharmacokinetics of PM 2.5. It is, at this point, unknown how long a pre-baseline isolation period would need to be for an un-confounded valid baseline. Accordingly, outdoor activity was limited during the trial because of wildfire smoke pollution. In addition, a new HVAC filter was installed and two stand-alone HEPA air purifiers employed at the trial location to keep indoor air in the range of healthy as defined by Because outdoor activities were not restricted before the trial, the baseline hsCRP was probably affected, contributing to an unhealthy baseline measurement. Indoor air quality at the test site was constantly monitored. Multiple HEPA air purifiers assured that indoor quality was maintained at a healthy level which was most often below 5 ppb. In addition, the air was extremely unhealthy on the North coast on Nov. 8: the date of the first blood draw and the first day of the “Typical” diet. Significant to the PM 2.5 exposure is that the blood sample for BPA and other toxics testing needed to be delivered to the lab at UCSF Mt. Zion within four hours of the draw. Because the test subject and investigator were the same person, that means that the scientist/lab rat had to be exposed to extremely unhealthy PM 2.5 for at least 3 hours including the commute into San Francisco and the deliveries of blood samples to the lab and the hsCRP sample to the lab at the Parnassus campus. More air quality snapshots are available at: Air quality exposure may have confounded results. Restriction of outdoor exercise meant forgoing regular exercise such as jogging. The lack of that exercise and the effect of being “trapped” had a noticeable effect on SSHS subject psychological stress. Unhealthy environmental pre-baseline stress? Many environmental factors affect hsCRP levels and inflammation via psychological and physical factors including: Noise — traffic, neighbors, housemates, barking dogs. Psychological stress (increases in cortisol production) — work, co-workers, work and domestic interpersonal interactions, commuting, driving in traffic. Air quality (especially PM2.5) Home, & Office — cooking, vinyl flooring, wall coverings, upholstery, and other plastic-based products, pet dander, printer toner. External – Smog, wildfires. Adequate regular exercise Physical exercise has been shown to decrease cortisol levels and reduce inflammation.

The Study – Deconstructed

Methods: Food Preparation and Serving
Note: The complete set of exhaustively detailed standards developed for this trial, can be accessed at this link: Basic scientific lab standards — Best practices for a replicable dietary intervention. That link is an ongoing work. See also: Stealth Syndrome Study – Typical and Intervention Diets To facilitate replicability the kitchen was operated in much the same manner as a bench lab. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Food preparation took place in a 400-square-foot professional kitchen with stainless steel countertops and carbon-filtered water. A 1,200 cubic-feet/minute, four-centrifugal-fan exhaust hood was used over an eight-burner natural gas stove. Central air with HEPA filters ventilated the kitchen which was also equipped with two auxiliary standalone HEPA filter machines. Two electric ovens were used for baking. Additional efforts were also made to reduce other non-food exposures and confounding factors. PM2.5 levels were monitored via sensors from PurpleAir.Com, one which monitored the kitchen air quality, as wel as numerous other outdoor sensors in a roughly five-mile radius. All unacceptable materials were removed from the kitchen, including plastic and polymer items utensils, containers, and cookware with non-stick coatings. Only glass, stainless steel, aluminum foil, and tight grain maple cutting boards were allowed. Vinyl gloves were used in food preparation for sanitary control in both legs of the trial, but actual food contact with the gloves was minimal and incidental. 100% cotton dish towels were allowed, but paper towels could only be used for cleanup. All measurements were by metric weight, and none by volume. This facilitated the kitchen’s staff’s accommodation from English to metric measurement because they could dispense with volumetric measurements which are problematic because of packing and granular particle size in solid items, and meniscus errors for liquid. In converting recipes with English measurements, initial measurements for liquids was done in measuring cups with dual English/Metric gradations. Then, with a glass mixing bowl with dry ingredients already on a metric measuring scale, the liquid was added to the bowl and the metric weight recorded for the investigation data. All main ingredients were measured to the nearest gram, but small-weight items such as spices, herbs and other seasonings and other items were measured to the nearest tenth of a gram. This is vital because those ingredients often have metabolic and other health effects in amounts out of proportion to their weight. For the same reasons, Investigators used spices they had grown for the purpose. Black pepper was obtained from an organic source. Peppercorns were rinsed, dried and ground with a grinder without plastic components. These measures were necessary because store-bought spices are among the most contaminated. Items with known plastic contamination (such as micro-plastic contamination of table salt) were replaced where possible with reagents from Sigma-Aldrich. Small kitchen-ready scales were obtained and calibrated using brass gram weights. Culinary assistants were briefed on the measurement procedures and adapted very quickly. All recipes and menus and a calendar of their serving dates and times were posted on a kitchen whiteboard directly above a dedicated counter surface on which recipes were places, and data recorded. Hand-written data was transferred to two master Excel spreadsheets for the Baseline and Intervention legs.
Moving Toward the Trial: Some Final Thoughts on Procedures, Methods, Food Acquisition, and Best Practices
Developing a scientifically sound set of methods for a dietary intervention that could result in replicable, causally valid results took investigators five years of intensive effort. That was a necessary first step because no such standards, protocols, methods or best practices existed. That absence required investigators to develop those standards and protocols de novo in order to move dietary intervention studies closer to replicability and credible conclusions of causality. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. Establishing principles for replicability The University of California, San Francisco IRB/Commitee on Human Research approved the n=20 study & on Nov. 14, 2014. Once approved, the investigators began an intense effort to scrutinize every aspect of the study. That resulted in the recognition that no such effort at using basic laboratory practices and data recording had ever been made. This realization came from an examination of five dietary intervention studies. A sixth study, which was published in 2019, should be add to that list: At that point, investigators determined the following principle: A kitchen must be subject to the same established practices as a laboratory. Consequently, the following three implementation strategies were created: Food, water, spices and all consumables must be treated as reagents whose sources, provenance, treatment, handling, measurement, and usage must be fully disclosed. Cookware, dishes, appliances, utensils and all other items involved in the preparation, cooking, serving and consumption must be treated as laboratory devices and apparatus. Recipes must be treated as protocols with scientifically accurate and complete conditions, materials, procedures, and timing recorded. Researching and developing specific implementations of the revised protocols took four years, As a result, the UCSF-IRB/CHR Approved a revised study protocol and a one-year extension on Nov. 14 2018. A further extension was granted due to delays — including planned and actual power outages — caused by wildfires in the San Francisco Bay area. The PM2.5 particles in wildfire smoke can cause many adverse health effects including inflammation. (See also). This situation was a serious concern because our study’s primary indicator was hsCRP — a potent measure of inflammation. Sourcing the Menu – Sources & Provenance The primary goal of this strategy was to define Plastic-Derived Chemical contamination sources for specific menu items. This work — described in a lengthy appendix to the revised protocol — determined the principles of which foods could be used for the uncontaminated intervention leg and which PDC-contaminated analogs would be used for the initial leg. The following guiding principles would later cause numerous difficult decisions as investigators applied the principles to the acquisition and treatment of specific foods from specific sources. Decisions were made on the basis of whether the foods were typical of An American diet (according to the USDA) and which could be readily obtained in the United States by investigators who wished to replicate the study. Sourcing the Menu: Water & Beverages Sourcing the Menu: Dairy – Milk, Cheese, Yogurt, Butter Sourcing the Menu: Fish Sourcing the menu: Sugar and sweeteners Sourcing the Menu: Background on GMO Sourcing the Menu: Background on Lipophilia – Prime contamination problem for cooking and food processing. Sourcing the Menu: Snacks Sourcing the Menu: The spice lipo-paradox Sourcing the Menu: Water & fertilizers: Ubiquitous contamination sources. Sourcing the Menu: Avoiding Microplastics, biosolids and nano particles Sourcing the Menu: Oils Sourcing the Menu: Going against the grain: Bread and cereal Sourcing the Menu: Fruit & veggies Sourcing the Menu: Dairy – Milk, Cheese, Yogurt, Butter Sourcing the Menu: Meat & Poultry Sourcing the menu: Pork Accommodating the ideal with the realistic As the trial grew near in 2019, investigators refined and tightened strategies 2 and 3/ They also reconciled their ideal measures of menu item purity with the practical need need to execute of a trial which could be conducted without going to hysterical lengths which were proving to be un-necessary, expensive and time-consuming. Items in progress Actual selection choices, their rationale, and concordance with the revised protocol will be noted as an update at the top each of the sourcing links, above. Choices will also be described in a detailed list of final ingredients that is analogous to a list of reagents and their sources. A separate methods section will detail preparation and all recipes. Best Practices Following the UCSF/CHR approval of the revised study protocol, investigators also began developing a set of best laboratory practices to implement the study. Note that the following is a partial presentation of a much larger number of links. Basic scientific lab standards — Best practices for a replicable dietary intervention Best practices — Herbs and Spices: Powerful in small amounts, precise measurement needed Best Practices Backgrounder: Micro- and Nanoplastics Best practices: Herbs and Spices – avoiding contamination Best practices – Spices: Make your own baking powder Best practices: Scale calibration Prepping bacon and lunch meat ham to minimize plastic packaging contamination. Avoiding plastic contamination when storing food. Best practices: De-waxing apples Best practices — Sourcing Dairy: Milk, Cheese, Yogurt, Butter methods and barriers Best practices: Sourcing cheese & butter and minimizing plastic contamination from packaging. Best practices – Precise measurements NOTE: there are approximately 30 more food specific “Best practices” yet to be written Reducing Non-Food Exposures in dietary intervention Micro- and Nanoplastics: Health Implications How Food Processing Adds Plastic-Derived Chemical Contamination
Examining Co-existing Factors that Confounded Causality Conclusions in Two Human Dietary Studies
Dietary interventions as now conducted are incapable of rendering valid causal conclusions about specific substances, compounds, or chemicals. This is because the near-infinite variations in foods produce unknown and unknowable co-contamination errors that are further confounded by preparation inconsistencies. This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. This can be illustrated by comparing two recent dietary intervention studies — one studying Plastic-Derived Chemicals (Reus, Perdue) and the second of Ultra-Processed Foods (NIH/Hall). While the two studies were quite different in scope, size, and duration, they arrived at very similar results in the behavior of the high-sensitivity C-Reactive Protein (hsCRP) test as a clinical measure of intervention inflammation changes. The NIH/Hall study, “Ultra-Processed Diets Cause Excess Calorie Intake and Weight Gain,” was a 28-day trial published in the May 16, 2019 issue of Cell Metabolism and represented the most thoroughly documented dietary intervention published so far. In addition to documenting the association between Ultra-Processed Foods (UPFs) and weight gain from over-eating, the study was conducted in a dormitory setting to compensate for non-food environmental exposures, test subject compliance and differences in exercise, and metabolism. In addition, the study conducted an expensive battery of clinical tests (op. cit. Table 3) including hsCRP, insulin, and the appetite peptides leptin, ghrelin, and adiponectin. The Reus, Perdue six-day trial was far more limited in scope and sought primarily to determine whether hsCRP levels could be affected by Bisphenol A and other commonly associated Plastic-Derived Chemicals (PDCs). Extensive efforts conducted by investigators over a period of more than three years to determine which foods, sources, packaging, and preparation methods were least — and most — contaminated by PDCs. That work included efforts to: develop a set of protocols and best practices to avoid PDC contamination in sourcing and preparation, determine how the food chain gets contaminated with PFCs, and ascertain how food processing adds PDC contamination. Among the data and methods developed by the Reus, Perdue investigators in that pre-trial effort was the determination that fast, convenient, ready-to eat, and pre-prepared — Ultra-Processed — foods were the most contaminated by PDCs. For that reason, UPFs were often chosen for the “contamination” leg of the study. Intervention leg meals were “reverse engineered” to match the composition of the UPFs in order to make the”before and after” legs as identical as possible save for PDC contamination. Within days of the publication of the NIH/Hall study, Reus, Perdue investigators initially considered replicating the “before and after” selections of that extensive study and requested recipes. No response was ever made. A thorough examination of supplemental material from NIH/Hall failed to find recipes or any food sourcing and preparation details. In the interim, a closer examination by the Reus, Perdue investigators revealed that the NIH/Hall intervention meals included foods that the Reus, Perdue investigators had previously determined had been processed more than minimally and likely contained higher PDC levels than desired. Similar results and an anomaly indicate unavoidable mutual co-contaminants that confounded both dietary interventions and negated causal conclusions Levels of hsCRP decreased 21.4% from baseline to end of the minimally contaminated leg: 1.1 mg/L from 1.4 mg/L. In addition, our study results demonstrated a final reduction in hsCRP that was approximately half of that reposted by a major NIH-funded dietary intervention by Hall, et. al. published in 2019 approximately four months prior to our trial. The lower overall decrease in hsCRP in the Reus, Perdue study was reasonably attributable to: The shorter duration of our trial (six days rather than 28), and The Northern California wildfires of November/December 2019, whose smoke pollution dramatically increased PM2.5 particulate which is a notorious promoter of inflammation. Further discussion is available in the Reus, Perdue study. Investigating An Unexpected Anomaly of the Intervention Legs Despite expectations that inflammation would increase with foods projected to contain higher levels of BPA, hsCRP actually declined at the end of the “typical/contaminated” diet leg. Significantly, NIH/Hall independently exhibited this same anomaly. Efforts to explain this anomaly led investigators to consider possible causes. NIH/Hall’s primary outcome focused on obesity and investigated weight gain from the ad libitum consumption of UPFs versus less processed foods. The results confirmed weight gain from the contaminated UPF leg of the study. In looking for a possible cause of the anomaly of how BPA, hsCRP counterintuitively declined at the end of the “typical/contaminated” diet, Reus, Perdue study investigators had long recognized that Bisphenol A has been widely accepted as an “obesegen<Google Scholar cite>” and associated with obesity, diabetes, insulin dependence, as well as cancer and cardiovascular disease. Further, chronic inflammation is associated with all of those syndromes and non-communicable diseases. That was a primary reason Reus, Perdue study investigators had chosen hsCRP as a marker for PDC concentrations. The NIH/Hall study included the “appetite peptides” ghrelin, leptin, and adiponectin which we previously knew were associated with eating behavior. Because of that, the Reus, Perdue investigators searched the literature for relevant BPA clinical markers of health outcome associations. Data revealed that Bisphenol A affected ghrelin, leptin, and adiponectin affected in the ways as the NIH/Hall study recorded for Ultra-Processed Foods. In addition, the metabolic peptide behavior in the NIH/Hall study is the same as those caused by BPA exposure A further search for disease/syndromes and clinical indicator similarities between Plastic-Derived Chemicals and Ultra-Processed Foods (table below) further confirms that both show nearly identical activity. From this, the only conclusion that can be reached is that neither trial can delineate a specific causal action of PDC’s or UPFs because both are present in study foods, exert almost identical effects and are, therefore, mutually confounding factors. Click this link to download Excel spreadsheet with full-sized text The path to a revised protocol: Confounding factors lead to greater complexity and expense This study’s investigators, from the beginning, recognized that basic nutritional levels — protein, fat, and sugar/carbohydrates would need to be the same at each […]
Summary: What’s the Stealth Syndromes Human Study About?
NOTE: This is a summary of the current amended menu selection, rationale, and other information. The full study, including revised scientific protocol and the expanded nutritional and food selection process as approved by the University of San Francisco Medical School Committee on Human Research can be accessed at this link (pdf). This ad-free article is made possible by the financial support of the Center for Research on Environmental Chemicals in Humans: a 501(c)(3) non-profit. Please consider making a tax-deductible donation for continued biomedical research. A previously approved (UCSF-IRB/CHR) version that includes numerous footnoted references describing the scientific and health needs for the study can be found at this link. Internal web footnotes do not work as well in this web summary version. They can be found in the full 66-page pdf. PHASE 1: Exposure, Typical American Diet During this three-day period, study subjects will consume a diet designed to emulate a “typical” American diet. To create that diet, investigators will rely, in part, upon the U.S. Department of Agriculture’s 2016 study: Americans’ Eating Patterns and Time Spent on Food: The 2014 Eating & Health Module Data[xv]. A more recent edition will be relied upon if available. The search will begin in the frozen foods section of a supermarket. Ultimately, the retailer may be Walmart because they are located in all American states making specific brands easily accessible to other investigators. Our assumption for this strategy is that a branded frozen food is likely to be consistent in content, nutrition and contaminant exposure regardless of the location of purchase. This is not a certainty because processing may have taken place at different facilities depending upon distribution and location of sale. We will make an effort to determine the processing facility for all goods. Because data from numerous sources indicate that chicken, beef and pork are the most popular meats, we will reflect this by using each for one of the evening dinner menus during the 3-day exposure phase. In cases where a suitable complete meal is not available, we will select multiple items and combine as a meal. Items will be prepared as indicated on their labels. This will, inevitably mean microwaving frozen foods in plastic containers or in paper containers with plastic liners. To best reflect “typical American” meal and to assure widespread availability and reproducibility, we will select best-selling brands. PHASE 2 – Reduced contamination, commercial Once a menu has been established for the typical exposure phase, the components of this diet phase will be structured to emulate the typical exposure phase meals as closely as possible using less-contaminated food choices. This phase, which has been missing from all other diet intervention studies of BPA and phthalates, offers study participants a “standard dose” of BPA and phthalates. This phase is intended not only to assess the effects of a typical American diet, but also to “standardize” food-exposure levels for each participant. Standardized food exposure levels, combined with the final phase (minimum non-food exposure – NFE) may be useful in establishing estimates of overall individual NFE. Foods and beverages will be obtained from Organic Certified sources, selected for minimum processing and plastic food contact materials. Currently, Whole Foods is the only national chain that prohibits biosolid use in its foods and may be a primary source because its availability facilitates reproducibility by other investigators. Other widely available sources will be sought, especially from among direct-shipping vendors who adhere to the enhanced organic rules developed by this study’s investigators. No plastic contact. Exceptions are not preferred, but may include BPA and phthalate-free nitrile gloves and tubing such as Tygon S3 B-44-3 Beverage Tubing or other manufacturer’s equivalent. Any plastic product used must be tested to assure manufacturer claims because studies have shown that some manufacturer claims are false.[xvi],[xvii],[xviii] Preparation & cooking The following are forbidden: Sous vide non-stick pans most cooking oils plastic utensils plastic prep bowls synthetic gloves plastic bags plastic wrap drip coffee makers Sodastream Keurig and other “pod” beverage makers Beverages in cans, plastic bottles or glass. PHASE 3: Enhanced organic This diet will work to provide identical menu items served in previous phases but will follow a set of guidelines developed by this study’s investigators for sourcing local food and beverage products. Those guidelines eliminate many sources of endocrine disruptors — such as recycled wastewater irrigation — that are allowable under USDA organic regulations. Adherence to these rules should facilitate reproducibility. The guiding principals are summarized below. More details are available in Appendix 2 of this document. Commercially processed foods are unacceptable. All food will be obtained directly from local Certified USDA Organic sources whose premises have been voluntarily inspected for compliance with those and the following enhanced requirements. Do not consume any ingredient whose composition cannot be traced to, and inspected at its origin. No recycled wastewater is allowed in irrigation or other on-premises uses. No biosolids are allowed in irrigation or other on-premises uses. No food contact with plastics or recycled paper or cardboard. Minimum or incidental contact may be approved depending upon the plastic composition. Irrigation water must not be transported via plastic pipes. Drip irrigation is discouraged, but if used must not contact edible surfaces. Harvest and food transport must be in metal containers. PHASE 4 – Enhanced, local sourced, reduced contamination diet, minimum Non-Food Exposure The unknown — and possibly unknowable — variabilities in this class of exposures offers the greatest set of hazards to reproducibility. Numerous non-food sources of BPA are present in the environment and likely pose significant “background” contamination which will vary depending upon the test subjects’ lifestyles and environments. This is particularly critical because the major health effects being measured in this study; estrogen/testosterone disruptions, inflammation, and metabolic events such as insulin resistance and lipid imbalance, can also be affected by a wide variety of chemicals other than BPA and phthalates. This is why this final phase of the protocol has been added to reduce non-food exposures of all harmful chemicals as much as possible. In addition, the personal environments […]