Skip to main content
Log in

Prenatal Diet as a Modifier of Environmental Risk Factors for Autism and Related Neurodevelopmental Outcomes

  • Early Life Environmental Health (H Volk and J Buckley, Section Editors)
  • Published:
Current Environmental Health Reports Aims and scope Submit manuscript

A Correction to this article was published on 02 June 2022

This article has been updated

Abstract

Purpose of Review

Environmental chemicals and toxins have been associated with increased risk of impaired neurodevelopment and specific conditions like autism spectrum disorder (ASD). Prenatal diet is an individually modifiable factor that may alter associations with such environmental factors. The purpose of this review is to summarize studies examining prenatal dietary factors as potential modifiers of the relationship between environmental exposures and ASD or related neurodevelopmental outcomes.

Recent Findings

Twelve studies were identified; five examined ASD diagnosis or ASD-related traits as the outcome (age at assessment range: 2–5 years) while the remainder addressed associations with neurodevelopmental scores (age at assessment range: 6 months to 6 years). Most studies focused on folic acid, prenatal vitamins, or omega-3 fatty acids as potentially beneficial effect modifiers. Environmental risk factors examined included air pollutants, endocrine disrupting chemicals, pesticides, and heavy metals. Most studies took place in North America. In 10/12 studies, the prenatal dietary factor under study was identified as a significant modifier, generally attenuating the association between the environmental exposure and ASD or neurodevelopment.

Summary

Prenatal diet may be a promising target to mitigate adverse effects of environmental exposures on neurodevelopmental outcomes. Further research focused on joint effects is needed that encompasses a broader variety of dietary factors, guided by our understanding of mechanisms linking environmental exposures with neurodevelopment. Future studies should also aim to include diverse populations, utilize advanced methods to optimize detection of novel joint effects, incorporate consideration of timing, and consider both synergistic and antagonistic potential of diet.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

Change history

References

Papers of particular interest, published recently, have been highlighted as: •• Of major importance

  1. American Psychiatric Association. Diagnostic and statistical manual of mental disorders: DSM-5. 5th ed ed. Washington, D.C.2013.

  2. Maenner MJ, Shaw KA, Bakian AV, et al. Prevalence and characteristics of autism spectrum disorder among children aged 8 years — autism and developmental disabilities monitoring network, 11 sites, United States, 2018. Morb Mortal Wkly Rep MMWR. 2021;70:1–15.

    Google Scholar 

  3. Boyle CA, Boulet S, Schieve LA, et al. Trends in the prevalence of developmental disabilities in US children, 1997–2008. Pediatrics. 2011;127:1034–42.

    Article  PubMed  Google Scholar 

  4. Lyall K, Croen L, Daniels J, et al. The changing epidemiology of autism spectrum disorders. Annu Rev Public Health. 2017;38:81–102.

    Article  PubMed  Google Scholar 

  5. Hallmayer J, Cleveland S, Torres A, et al. Genetic heritability and shared environmental factors among twin pairs with autism. Arch Gen Psychiatry. 2011;68:1095–102.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Bölte S, Girdler S, Marschik PB. The contribution of environmental exposure to the etiology of autism spectrum disorder. Cell Mol Life Sci. 2019;76:1275–97.

    Article  PubMed  CAS  Google Scholar 

  7. Lyall K, Schmidt RJ, Hertz-Picciotto I. Maternal lifestyle and environmental risk factors for autism spectrum disorders. Int J Epidemiol. 2014;43:443–64.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Chun HK, Leung C, Wen SW, McDonald J, Shin HH. Maternal exposure to air pollution and risk of autism in children: a systematic review and meta-analysis. Environ Pollut. 2020;256:113307.

    Article  CAS  PubMed  Google Scholar 

  9. Imbriani G, Panico A, Grassi T, et al. Early-life exposure to environmental air pollution and autism spectrum disorder: a review of available evidence. Int J Environ Res. 2021;18:1–24.

    Google Scholar 

  10. Yu X, Rahman MM, Wang Z, et al. Evidence of susceptibility to autism risks associated with early life ambient air pollution: a systematic review. Environ Res. 2021;208:112590.

    Article  PubMed  CAS  Google Scholar 

  11. Rahman MM, Shu YH, Chow T, et al. Prenatal exposure to air pollution and autism spectrum disorder: sensitive windows of exposure and sex differences. Environ Health Perspect. 2022;130:17008.

    Article  CAS  PubMed  Google Scholar 

  12. Nesan D, Kurrasch DM. Gestational exposure to common endocrine disrupting chemicals and their impact on neurodevelopment and behavior. Annu Rev Physiol. 2020;82:177–202.

    Article  CAS  PubMed  Google Scholar 

  13. Radke EG, Braun JM, Nachman RM, Cooper GS. Phthalate exposure and neurodevelopment: a systematic review and meta-analysis of human epidemiological evidence. Environ Int. 2020;137.

  14. He X, Tu Y, Song Y, Yang G, You M. The relationship between pesticide exposure during critical neurodevelopment and autism spectrum disorder: a narrative review. Environ Res. 2021;203:111902.

    Article  PubMed  CAS  Google Scholar 

  15. Riederer AM, Bartell SM, Barr DB, Ryan PB. Diet and nondiet predictors of urinary 3-phenoxybenzoic acid in NHANES 1999–2002. Environ Health Perspect. 2008;116:1015–22.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Merced-Nieves FM, Arora M, Wright RO, Curtin P. Metal mixtures and neurodevelopment: recent findings and emerging principles. Curr Opin Toxicol. 2021;26:28–32.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Wei H, Feng Y, Liang F, et al. Role of oxidative stress and DNA hydroxymethylation in the neurotoxicity of fine particulate matter. Toxicology. 2017;380:94–103.

    Article  CAS  PubMed  Google Scholar 

  18. Ghassabian A and Trasande L. Disruption in thyroid signaling pathway: a mechanism for the effect of endocrine-disrupting chemicals on child neurodevelopment. Front Endocrinol. 2018;9.

  19. Keil KP, Lein PJ. DNA methylation: a mechanism linking environmental chemical exposures to risk of autism spectrum disorders? Environ Epigenet. 2016;2:1–15.

    Article  CAS  Google Scholar 

  20. Zhong C, Tessing J, Lee BK, Lyall K. Maternal dietary factors and the risk of autism spectrum disorders: a systematic review of existing evidence. Autism Res. 2020;13:1634–58. Scoping review of maternal prenatal dietary factors associated with ASD. Found strongest evidence for an inverse association between maternal folic acid supplementation and ASD; results were suggestive for vitamin D and less consistent for polyunsaturated fatty acids, and insufficient work conducted for other nutrients.

  21. Kannan S, Misra DP, Dvonch JT, Krishnakumar A. Exposures to airborne particulate matter and adverse perinatal outcomes: a biologically plausible mechanistic framework for exploring potential effect modification by nutrition. Environ Health Perspect. 2006;114:1636–42.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Barthelemy J, Sanchez K, Miller MR, Khreis H. New opportunities to mitigate the burden of disease caused by traffic related air pollution: antioxidant-rich diets and supplements. Int J Environ Res Public Health. 2020;17.

  23. Lyall K, Munger KL, O’Reilly ÉJ, Santangelo SL, Ascherio A. Maternal dietary fat intake in association with autism spectrum disorders. Am J Epidemiol. 2013;178:209–20.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Schmidt RJ, Tancredi DJ, Krakowiak P, Hansen RL, Ozonoff S. Maternal intake of supplemental iron and risk of autism spectrum disorder. Am J Epidemiol. 2014;180:890–900.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Bailey RL, Pac SG, Fulgoni VL III, Reidy KC, Catalano PM. Estimation of total usual dietary intakes of pregnant women in the United States. JAMA Netw Open. 2019;2:e195967.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Pacyga DC, Sathyanarayana S, Strakovsky RS. Dietary predictors of phthalate and bisphenol exposures in pregnant women. Adv Nutr. 2019;10:803–15.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Bailey RL, Pac SG, Fulgoni VL 3rd, Reidy KC, Catalano PM. Estimation of total usual dietary intakes of pregnant women in the United States. JAMA network open. 2019;2:e195967.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Schmidt RJ, Kogan V, Shelton JF, et al. Combined prenatal pesticide exposure and folic acid intake in relation to autism spectrum disorder. Environ Health Perspect. 2017;125:1–12. First study to examine joint effects of folic acid and an environmental exposure in association with ASD. Found evidence for modification of the association between pesticide exposure and ASD by folate.

  29. Goodrich AJ, Volk HE, Tancredi DJ, et al. Joint effects of prenatal air pollutant exposure and maternal folic acid supplementation on risk of autism spectrum disorder. Autism Res. 2018;11: 69–80. First study to examine joint effects of folic acid and air pollution in association with ASD. Found evidence for attenuation of the association between prenatal air pollution exposure and ASD by folic acid supplementation.

  30. Oulhote Y, Lanphear B, Braun JM, et al. Gestational exposures to phthalates and folic acid, and autistic traits in Canadian children. Environ Health Perspect. 2020;128:27004. First study to examine joint effects of folic acid and prenatal phthalate exposure in association with ASD-related traits. Found evidence for attenuation of the association between prenatal phthalate exposure and ASD-related traits by folic acid.

  31. Shin H-M, Schmidt RJ, Tancredi D, et al. Prenatal exposure to phthalates and autism spectrum disorder in the MARBLES study. Environ Health. 2018;17:85.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Shin H-M, Bennett DH, Calafat AM, Tancredi D, Hertz-Picciotto I. Modeled prenatal exposure to per- and polyfluoroalkyl substances in association with child autism spectrum disorder: a case control study. Environ Res. 2020;186:109514.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. Kim B, Shah S, Park HS, et al. Adverse effects of prenatal mercury exposure on neurodevelopment during the first 3 years of life modified by early growth velocity and prenatal maternal folate level. Environ Res. 2020;191:109909.

    Article  CAS  PubMed  Google Scholar 

  34. Loftus CT, Hazlehurst MF, Szpiro AA, et al. Prenatal air pollution and childhood IQ: preliminary evidence of effect modification by folate. Environ Res. 2019;176:108505. Examined modification of association between air pollution exposure and child intelligence scores by maternal 2nd trimester plasma folate and by reported fruit and vegetable intake. Evidence of attenuation of effects by folate; decreases in IQ scores with higher PM10 exposure were seen for those with low prenatal folate but not for those with higher folate.

  35. Guxens M, Aguilera I, Ballester F, et al. Prenatal exposure to residential air pollution and infant mental development: modulation by antioxidants and detoxification factors. Environ Health Perspect. 2012;120:144–9. First study to examine joint effects of prenatal dietary factors and air pollution on child neurodevelopment. Found evidence for stronger adverse effects of air pollution exposure on cognitive scores among those with low fruit and vegetable and vitamin D intake.

  36. Mérida-Ortega Á, Rothenberg SJ, Torres-Sánchez L, et al. Polyunsaturated fatty acids and child neurodevelopment among a population exposed to DDT: a cohort study. Environ Health: Glob Access Sci Source. 2019;18:1–7. Examined modification of pesticide exposure and neurodevelopment by PUFAs. Did not find evidence of interactions.

  37. Ogaz-González R, Mérida-Ortega Á, Torres-Sánchez L, et al. Maternal dietary intake of polyunsaturated fatty acids modifies association between prenatal DDT exposure and child neurodevelopment: a cohort study. Environ Pollut. 2018;238:698–705. First study to examine modification of prenatal pesticide exposure-neurodevelopment association by PUFAs. Found evidence for attenuation of effects of prenatal exposure to the pesticide DDE by the PUFAs DHA and ARA; inverse association between prenatal DDE exposure and cognitive scores found only among those with <median intake of these PUFAs.

  38. Strain JJ, Yeates AJ, Van Wijngaarden E, et al. Prenatal exposure to methyl mercury from fish consumption and polyunsaturated fatty acids: associations with child development at 20 mo of age in an observational study in the Republic of Seychelles. Am J Clin Nutr. 2015;101:530–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Liu J, Martin LJ, Dinu I, Field CJ, Dewey D and Martin JW. Interaction of prenatal bisphenols, maternal nutrients, and toxic metal exposures on neurodevelopment of 2-year-olds in the APrON cohort. Environ Int. 2021;155:106601. First study to examine the relationships between cognitive scores and levels of prenatal bisphenols, maternal nutrients, and metals, measured in maternal biosamples, considering interactions of these factors. Found evidence for modification of effects of BPA and BPS exposure by selenium on cognitive scores, with protective effects of selenium.

  40. Institute of Medicine. Dietary reference intakes for thiamin, riboflavin, niacin, vitamin B6, folate, vitamin B12, pantothenic acid, biotin, and choline. Washington, D.C. 1998.

  41. Dolinoy DC, Huang D, Jirtle RL. Maternal nutrient supplementation counteracts bisphenol A-induced DNA hypomethylation in early development. Proc Natl Acad Sci U S A. 2007;104:13056–61.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Joshi R, Adhikari S, Patro BS, Chattopadhyay S, Mukherjee T. Free radical scavenging behavior of folic acid: evidence for possible antioxidant activity. Free Radic Biol Med. 2001;30:1390–9.

    Article  CAS  PubMed  Google Scholar 

  43. Wang T, Zhang T, Sun L, et al. Gestational B-vitamin supplementation alleviates PM2.5-induced autism-like behavior and hippocampal neurodevelopmental impairment in mice offspring. Ecotoxicol Environ Saf. 2019;185.

  44. Wiens D, DeSoto MC. Is high folic acid intake a risk factor for autism? A review. Brain Sci. 2017;7.

  45. Cao D, Kevala K, Kim J, et al. Docosahexaenoic acid promotes hippocampal neuronal development and synaptic function. J Neurochem. 2009;111:510–21.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Calder PC. Very long-chain n-3 fatty acids and human health: Fact, fiction and the future. Proc Nutr Soc. 2018;77:52–72.

    Article  CAS  PubMed  Google Scholar 

  47. Food and Agriculture Organization of the United Nations. Fats and fatty acids in human nutrition: report of an expert consultation. Rome: Italy; 2010. p. 1–166.

    Google Scholar 

  48. Kitajka K, Sinclair AJ, Weisinger RS, et al. Effects of dietary omega-3 polyunsaturated fatty acids on brain gene expression. PNAS. 2004;101:10931–6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Lee H-S, Barraza-Villarreal A, Hernandez-Vargas H, et al. Modulation of DNA methylation states and infant immune system by dietary supplementation with omega-3 PUFA during pregnancy in an intervention study. Am J Clin Nutr. 2013;98:480–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  50. Lee H-S, Barraza-Villarreal A, Biessy C, et al. Dietary supplementation with polyunsaturated fatty acid during pregnancy modulates DNA methylation at IGF2/H19 imprinted genes and growth of infants. Physiol Genomics. 2014;46:851–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Kajarabille N, Hurtado JA, Pena-Quintana L, et al. Omega-3 LCPUFA supplement: a nutritional strategy to prevent maternal and neonatal oxidative stress. Matern Child Nutr. 2017;13.

  52. Colombo J, Shaddy DJ, Kerling EH, Gustafson KM, Carlson SE. Docosahexaenoic acid (DHA) and arachidonic acid (ARA) balance in developmental outcomes. Prostaglandins Leukot Essent Fatty Acids. 2017;121:52–6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  53. Xue J, Schoenrock SA, Valdar W, Tarantino LM, Ideraabdullah FY. Maternal vitamin D depletion alters DNA methylation at imprinted loci in multiple generations. Clin Epigenetics. 2016;8:107.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  54. Vinkhuyzen AAE, Eyles DW, Burne THJ, et al. Gestational vitamin D deficiency and autism spectrum disorder. BJPsych Open. 2017;3:85–90.

    Article  PubMed  PubMed Central  Google Scholar 

  55. Becker KG. Autism, immune dysfunction and Vitamin D. Acta Psychiatr Scand. 2011;124:74.

    Article  PubMed  Google Scholar 

  56. Speckmann B, Grune T. Epigenetic effects of selenium and their implications for health. Epigenetics. 2015;10:179–90.

    Article  PubMed  PubMed Central  Google Scholar 

  57. Black MM, Walker SP, Fernald LCH, et al. Early childhood development coming of age: science through the life course. Lancet. 2017;389:77–90.

    Article  PubMed  Google Scholar 

  58. Walker SP, Wachs TD, Grantham-McGregor S, et al. Inequality in early childhood: risk and protective factors for early child development. Lancet. 2011;378:1325–38.

    Article  PubMed  Google Scholar 

  59. Thompson LM. Household air pollution from cooking fires is a global problem. Am J Nurs. 2019;119:61–4.

    Article  PubMed  Google Scholar 

  60. Ritz BR, Chatterjee N, Garcia-Closas M, et al. Lessons learned from past gene-environment interaction successes. Am J Epidemiol. 2017;186:778–86.

    Article  PubMed  PubMed Central  Google Scholar 

  61. Volk HE, Kerin T, Lurmann F, Hertz-Picciotto I, McConnell R, Campbell DB. Autism spectrum disorder: interaction of air pollution with the MET receptor tyrosine kinase gene. Epidemiology. 2014;25:44–7.

    Article  PubMed  PubMed Central  Google Scholar 

  62. Schmidt RJ, Hansen RL, Hartiala J, et al. Prenatal vitamins, one-carbon metabolism gene variants, and risk for autism. Epidemiology. 2011;22:476–85.

    Article  PubMed  PubMed Central  Google Scholar 

  63. Jo H, Eckel SP, Chen J-C, et al. Gestational diabetes mellitus, prenatal air pollution exposure, and autism spectrum disorder. Environ Int. 2019;133:105110.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. Wang R, Sun DG, Song G, et al. Choline, not folate, can attenuate the teratogenic effects ofdibutyl phthalate (DBP) during early chick embryo development. Environ Sci Pollut Res. 2019;26:29763–79.

    Article  CAS  Google Scholar 

  65. Langley EA, Krykbaeva M, Blusztajn JK, Mellott TJ. High maternal choline consumption during pregnancy and nursing alleviates deficits in social interaction and improves anxiety-like behaviors in the BTBR T+Itpr3tf/J mouse model of autism. Behav Brain Res. 2015;278:210–20.

    Article  CAS  PubMed  Google Scholar 

  66. Tang J, Yuan Y, Wei C, et al. Neurobehavioral changes induced by di(2-ethylhexyl) phthalate and the protective effects of vitamin E in Kunming mice. Toxicol Res. 2015;4:1006–15.

    Article  CAS  Google Scholar 

  67. Lombardi VC, De Meirleir KL, Subramanian K, et al. Nutritional modulation of the intestinal microbiota; future opportunities for the prevention and treatment of neuroimmune and neuroinflammatory disease. J Nutr Biochem. 2018;61:1–16.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Spencer JP. Flavonoids and brain health: multiple effects underpinned by common mechanisms. Genes Nutr. 2009;4:243–50.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  69. Nuttall JR. The plausibility of maternal toxicant exposure and nutritional status as contributing factors to the risk of autism spectrum disorders. Nutr Neurosci. 2017;20:209–18.

    Article  CAS  PubMed  Google Scholar 

  70. Oken E, Rifas-Shiman SL, Amarasiriwardena C, et al. Maternal prenatal fish consumption and cognition in mid childhood: mercury, fatty acids, and selenium. Neurotoxicol Teratol. 2016;57:71–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  71. Vecchione R, Vigna C, Whitman C, et al. The association between maternal prenatal fish intake and child autism-related traits in the EARLI and HOME studies. J Autism Dev Disord. 2021;51:487–500.

    Article  PubMed  PubMed Central  Google Scholar 

  72. Julvez J, Mendez M, Fernandez-Barres S, et al. Maternal consumption of seafood in pregnancy and child neuropsychological development: a longitudinal study based on a population with high consumption levels. Am J Epidemiol. 2016;183:169–82.

    Article  PubMed  Google Scholar 

  73. Liu SH, Bobb JF, Claus Henn B, et al. Bayesian varying coefficient kernel machine regression to assess neurodevelopmental trajectories associated with exposure to complex mixtures. Stat Med. 2018;37:4680–94.

    Article  PubMed  PubMed Central  Google Scholar 

  74. Bobb JF, Claus Henn B, Valeri L, Coull BA. Statistical software for analyzing the health effects of multiple concurrent exposures via Bayesian kernel machine regression. Environ Health. 2018;17:67.

    Article  PubMed  PubMed Central  Google Scholar 

  75. Bello GA, Arora M, Austin C, Horton MK, Wright RO, Gennings C. Extending the distributed lag model framework to handle chemical mixtures. Environ Res. 2017;156:253–64.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  76. Buckley JP, Hamra GB, Braun JM. Statistical approaches for investigating periods of susceptibility in children’s environmental health research. Curr Environ Health Rep. 2019;6:1–7.

    Article  PubMed  PubMed Central  Google Scholar 

  77. Zhang M, Liu C, Li WD, et al. Individual and mixtures of metal exposures in associations with biomarkers of oxidative stress and global DNA methylation among pregnant women. Chemosphere. 2022;293:133662.

    Article  CAS  PubMed  Google Scholar 

  78. Cowell W, Colicino E, Levin-Schwartz Y, et al. Prenatal metal mixtures and sex-specific infant negative affectivity. Environ Epidemiol. 2021;5:e147.

    Article  PubMed  PubMed Central  Google Scholar 

  79. Valeri L, Mazumdar MM, Bobb JF, et al. The joint effect of prenatal exposure to metal mixtures on neurodevelopmental outcomes at 20–40 months of age: evidence from rural Bangladesh. Environ Health Perspect. 2017;125:067015.

    Article  PubMed  PubMed Central  Google Scholar 

  80. Bauer JA, Devick KL, Bobb JF, et al. Associations of a metal mixture measured in multiple biomarkers with IQ: evidence from italian adolescents living near ferroalloy industry. Environ Health Perspect. 2020;128:97002.

    Article  PubMed  Google Scholar 

  81. Vilahur N, Bustamante M, Byun HM, et al. Prenatal exposure to mixtures of xenoestrogens and repetitive element DNA methylation changes in human placenta. Environ Int. 2014;71:81–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  82. Doherty BT, Romano ME, Gui J, et al. Periconceptional and prenatal exposure to metal mixtures in relation to behavioral development at 3 years of age. Environ Epidemiol. 2020;4.

Download references

Funding

This work was supported by funding from the NIEHS under grant #R01 ES032469-01A1 (Lyall, Volk) and P30 ES000002 (Hart).

Author information

Authors and Affiliations

Authors

Contributions

Conceptualization, design, and initial literature review were performed by Kristen Lyall. The formal literature review was completed and the manuscript was drafted by Megan Bragg. Additional drafting and manuscript revision were completed by all authors. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Kristen Lyall.

Ethics declarations

Conflict of Interest

The authors declare no competing interests.

Human and Animal Rights and Informed Consent

All reported studies/experiments with human or animal subjects performed by the authors have been previously published and complied with all applicable ethical standards (including the Helsinki declaration and its amendments, institutional/national research committee standards, and international/national/institutional guidelines).

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

This article is part of the Topical Collection on Early Life Environmental Health

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 19 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Bragg, M., Chavarro, J.E., Hamra, G.B. et al. Prenatal Diet as a Modifier of Environmental Risk Factors for Autism and Related Neurodevelopmental Outcomes. Curr Envir Health Rpt 9, 324–338 (2022). https://doi.org/10.1007/s40572-022-00347-7

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40572-022-00347-7

Keywords

Navigation