Abstract
Autism Spectrum Disorder (ASD) is a complex neurodevelopmental condition characterized by challenges in social communication and repetitive behavior. While the exact etiology of ASD remains elusive, researchers have increasingly turned their attention to the role of environmental factors in its development. Among these factors, environmental pollution has emerged as a potential contributor to the rising prevalence of ASD cases worldwide. This review delves into the growing body of scientific evidence suggesting a significant association between environmental pollution and the risk of ASD. It explores the environmental pollution that have been implicated, including air pollution, water contaminants, heavy metals, pesticides, and endocrine-disrupting chemicals. The detrimental impact of these pollutants on the developing brain, particularly during critical periods of gestation and early childhood has been discussed. This will provide insights into the possible mechanisms by which the various pollutants may influence the neurodevelopmental pathways underlying ASD. Additionally, the potential interplay between genetic susceptibility and environmental exposure is explored to better understand the multifactorial nature of ASD causation. Considering the alarming increase in ASD prevalence and the ubiquity of environmental pollutants, this review emphasizes the urgent need for further investigation and the adoption of comprehensive preventive measures.
-
Research ethics: Not applicable.
-
Informed consent: Not applicable.
-
Author contributions: All the authors have accepted responsibility for the entire content of this manuscript and approved its submission.
-
Use of Large Language Models, AI and Machine Learning Tools: None declared.
-
Conflict of interest: The authors state no conflict of interest.
-
Research funding: None declared.
-
Data availability: Not applicable.
References
1. GBD 2019 Mental Disorders Collaborators. Global, regional, and national burden of 12 mental disorders in 204 countries and territories, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019. Lancet Psychiatry 2022;9:137–50. https://doi.org/10.1016/S2215-0366(21)00395-3.Suche in Google Scholar PubMed PubMed Central
2. Meimand, SE, Amiri, Z, Shobeiri, P, Malekpour, M-R, Moghaddam, SS, Ghanbari, A, et al.. Burden of autism spectrum disorders in North Africa and Middle East from 1990 to 2019: a systematic analysis for the global burden of disease study 2019. Brain Behav 2023;13:e3067. https://doi.org/10.1002/brb3.3067.Suche in Google Scholar PubMed PubMed Central
3. Cruz, S, Zubizarreta, SCP, Costa, AD, Araújo, R, Martinho, J, Tubío-Fungueiriño, M, et al.. Is there a bias towards males in the diagnosis of autism? A systematic review and meta-analysis. Neuropsychol Rev 2024;35:153–76.10.1007/s11065-023-09630-2Suche in Google Scholar PubMed PubMed Central
4. Almandil, NB, Alkuroud, DN, Abdulazeez, S, Alsulaiman, A, Elaissari, A, Borgio, JF. Environmental and genetic factors in autism spectrum disorders: Special emphasis on data from arabian studies. Int J Environ Res Publ Health 2019;16. https://doi.org/10.3390/ijerph16040658.Suche in Google Scholar PubMed PubMed Central
5. Belcher, HL, Uglik-Marucha, N, Vitoratou, S, Ford, RM, Morein-Zamir, S. Gender bias in autism screening: measurement invariance of different model frameworks of the Autism Spectrum Quotient. BJPsych Open 2023;9:1–11. https://doi.org/10.1192/bjo.2023.562.Suche in Google Scholar PubMed PubMed Central
6. Grabrucker, AM. Environmental factors in autism. Front Psychiatr 2013;3:1–13. https://doi.org/10.3389/fpsyt.2012.00118.Suche in Google Scholar PubMed PubMed Central
7. Keil-Stietz, K, Lein, PJ. Gene × environment interactions in autism spectrum disorders. Curr Top Dev Biol 2023;152:221–84. https://doi.org/10.1016/bs.ctdb.2022.11.001.Suche in Google Scholar PubMed PubMed Central
8. State of Global Air. Special report (online); 2024. Available from: https://www.stateofglobalair.org/sites/default/files/documents/2024-06/soga-2024-report_0.pdf [Accessed 26 Mar 2025].Suche in Google Scholar
9. Air quality Index (AQI) Basics (online). Available from: https://www.airnow.gov/aqi/aqi-basics/ Suche in Google Scholar
10. The latest data on air quality (Online). Available from: https://www.stateofglobalair.org/[Accessed 26 Mar 2025]Suche in Google Scholar
11. Lin, CK, Chang, YT, Lee, FS, Chen, ST, Christiani, D. Association between exposure to ambient particulate matters and risks of autism spectrum disorder in children: a systematic review and exposure-response meta-analysis. Environ Res Lett 2021;16. https://doi.org/10.1088/1748-9326/abfcf7.Suche in Google Scholar
12. Volk, HE, Lurmann, F, Penfold, B, Hertz-Picciotto, I, McConnell, R. Traffic-related air pollution, particulate matter, and autism. JAMA Psychiatry 2013;70:71–7. https://doi.org/10.1001/jamapsychiatry.2013.266.Suche in Google Scholar PubMed PubMed Central
13. Volk, HE, Hertz-Picciotto, I, Delwiche, L, Lurmann, F, McConnell, R. Residential proximity to freeways and autism in the CHARGE study. Environ Health Perspect 2011;119:873–7. https://doi.org/10.1289/ehp.1002835.Suche in Google Scholar PubMed PubMed Central
14. Wang, SY, Cheng, YY, Guo, HR, Tseng, YC. Air pollution during pregnancy and childhood autism spectrum disorder in taiwan. Int J Environ Res Publ Health 2021;18. https://doi.org/10.3390/ijerph18189784.Suche in Google Scholar PubMed PubMed Central
15. Li, Y, Xie, T, Melo, RDC, Vries, M, Lakerveld, J, Zijlema, W, Hartman, CA. Longitudinal effects of environmental noise and air pollution exposure on autism spectrum disorder and attention-deficit/hyperactivity disorder during adolescence and early adulthood: the TRAILS study. Environ Res 2023;227:115704. https://doi.org/10.1016/j.envres.2023.115704.Suche in Google Scholar PubMed
16. Flanagan, E, Malmqvist, E, Rittner, R, Gustafsson, P, Källén, K, Oudin, A. Exposure to local, source-specific ambient air pollution during pregnancy and autism in children: a cohort study from southern Sweden. Sci Rep 2023;13:1–13. https://doi.org/10.1038/s41598-023-30877-5.Suche in Google Scholar PubMed PubMed Central
17. Moschetti, A, Giangreco, M, Ronfani, L, Cervellera, S, Ruffilli, MP, Nume, C, et al.. An ecological study shows increased prevalence of autism spectrum disorder in children living in a heavily polluted area. Sci Rep 2024;14:1–8. https://doi.org/10.1038/s41598-024-67980-0.Suche in Google Scholar PubMed PubMed Central
18. Climate action Fast facts (online). Available from: https://www.un.org/en/climatechange/science/key-findings [Accessed 26 Mar 2025].Suche in Google Scholar
19. Walker, DB, Baumgartner, DJ, Gerba, CP, Fitzsimmons, K. Surface water pollution. In: Brusseau, ML, Pepper, IL, Gerba, CP, editors. Environmental and Pollution Science, 3rd ed. San Diego, CA, USA: Academic Press; 2019:261–92 pp.10.1016/B978-0-12-814719-1.00016-1Suche in Google Scholar
20. Panda, BP, Majhi, BK, Parida, SP. Occurrence and fate of micropollutants in water bodies. In: Hashmi, MZ, Wang, S, Ahmed, Z, editors. Environmental Micropollutants Advances in Pollution Research. San Diego, CA, USA: Elsevier; 2022:271–93 pp.10.1016/B978-0-323-90555-8.00005-2Suche in Google Scholar
21. Dickerson, AS, Rahbar, MH, Bakian, AV, Bilder, DA, Harrington, RA, Pettygrove, S, et al.. Autism spectrum disorder prevalence and associations with air concentrations of lead, mercury, and arsenic. Environ Monit Assess 2016;188:407. https://doi.org/10.1007/s10661-016-5405-1.Suche in Google Scholar PubMed
22. Sealey, LA, Hughes, BW, Sriskanda, AN, Guest, JR, Gibson, AD, Johnson-Williams, L, et al.. Environmental factors in the development of autism spectrum disorders. Environ Int 2016;88:288–98. https://doi.org/10.1016/j.envint.2015.12.021.Suche in Google Scholar PubMed
23. Shaw, CA, Li, Y, Tomljenovic, L. Administration of aluminium to neonatal mice in vaccine-relevant amounts is associated with adverse long term neurological outcomes. J Inorg Biochem 2013;128:237–44. https://doi.org/10.1016/j.jinorgbio.2013.07.022.Suche in Google Scholar PubMed
24. Al-Ayadhi, LY. Heavy metals and trace elements in hair samples of autistic children in central Saudi Arabia. Neurosciences 2005;10:213–18.Suche in Google Scholar
25. Albizzati, A, More, L, Di Candia, D, Saccani, M, Lenti, C. Normal concentrations of heavy metals in autistic spectrum disorders. Minerva Pediatr 2012;64:27–31.Suche in Google Scholar
26. Duque-Cartagena, T, Dalla, MDB, Mundstock, E , Neto, FK, Espinoza, SAR, de Moura, SK, et al.. Environmental pollutants as risk factors for autism spectrum disorders: a systematic review and meta-analysis of cohort studies. BMC Public Health 2024; 24, 2388 https://doi.org/10.1186/s12889-024-19742-w.Suche in Google Scholar PubMed PubMed Central
27. Fido, A, Al-Saad, S. Toxic trace elements in the hair of children with autism. Autism 2005;9:290–8. https://doi.org/10.1177/1362361305053255.Suche in Google Scholar PubMed
28. Levy, RJ. Carbon monoxide pollution and neurodevelopment: a public health concern. Neurotoxicol Teratol 2015;49:31–40. https://doi.org/10.1016/j.ntt.2015.03.001.Suche in Google Scholar PubMed PubMed Central
29. Jung, CR, Lin, YT, Hwang, BF. Air pollution and newly diagnostic autism spectrum disorders: a population-based cohort study in Taiwan. PLoS One 2013;8:e75510. https://doi.org/10.1371/journal.pone.0075510.Suche in Google Scholar PubMed PubMed Central
30. Kim, JH, Yan, Q, Uppal, K, Cui, X, Ling, C, Walker, DI, et al.. Metabolomics analysis of maternal serum exposed to high air pollution during pregnancy and risk of autism spectrum disorder in offspring. Environ Res 2021;196:110823. https://doi.org/10.1016/j.envres.2021.110823.Suche in Google Scholar PubMed PubMed Central
31. Fluegge, K. Does environmental exposure to the greenhouse gas, N2O, contribute to etiological factors in neurodevelopmental disorders? A mini-review of the evidence. Environ Toxicol Pharmacol 2016;47:6–18. https://doi.org/10.1016/j.etap.2016.08.013.Suche in Google Scholar PubMed
32. Gandal, MJ, Anderson, RL, Billingslea, EN, Carlson, GC, Roberts, TP, Siegel, SJ. Mice with reduced NMDA receptor expression: more consistent with autism than schizophrenia? Gene Brain Behav 2012;11:740–50. https://doi.org/10.1111/j.1601-183x.2012.00816.x.Suche in Google Scholar
33. Lee, EJ, Choi, SY, Kim, E. NMDA receptor dysfunction in autism spectrum disorders. Curr Opin Pharmacol 2015;20:8–13. https://doi.org/10.1016/j.coph.2014.10.007.Suche in Google Scholar PubMed
34. Reiprich, P, Kilb, W, Luhmann, HJ. Neonatal NMDA receptor blockade disturbs neuronal migration in rat somatosensory cortex in vivo. Cereb Cortex 2005;15:349–58. https://doi.org/10.1093/cercor/bhh137.Suche in Google Scholar PubMed
35. Wegiel, J, Kuchna, I, Nowicki, K, Imaki, H, Marchi, E, Ma, SY, et al.. The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes. Acta Neuropathol 2010;119:755–70. https://doi.org/10.1007/s00401-010-0655-4.Suche in Google Scholar PubMed PubMed Central
36. Jevtovic-Todorovic, V, Todorovic, SM, Mennerick, S, Powell, S, Dikranian, K, Benshoff, N, et al.. Nitrous oxide (laughing gas) is an NMDA antagonist, neuroprotectant and neurotoxin. Nat Med 1998;4:460–3. https://doi.org/10.1038/nm0498-460.Suche in Google Scholar PubMed
37. Kuhlmann, L, Foster, BL, Liley, DT. Modulation of functional EEG networks by the NMDA antagonist nitrous oxide. PLoS One 2013;8:e56434. https://doi.org/10.1371/journal.pone.0056434.Suche in Google Scholar PubMed PubMed Central
38. Mennerick, S, Jevtovic-Todorovic, V, Todorovic, SM, Shen, W, Olney, JW, Zorumski, CF. Effect of nitrous oxide on excitatory and inhibitory synaptic transmission in hippocampal cultures. J Neurosci 1998;18:9716–26. https://doi.org/10.1523/jneurosci.18-23-09716.1998.Suche in Google Scholar PubMed PubMed Central
39. Cahill, FJ, Ellenberger, EA, Mueller, JL, Tseng, LF, Quock, RM. Antagonism of nitrous oxide antinociception in mice by intrathecally administered antisera to endogenous opioid peptides. J Biomed Sci 2000;7:299–303. https://doi.org/10.1159/000025463.Suche in Google Scholar
40. Fukagawa, H, Koyama, T, Fukuda, K. kappa-Opioid receptor mediates the antinociceptive effect of nitrous oxide in mice. Br J Anaesth 2014;113:1032–8. https://doi.org/10.1093/bja/aeu254.Suche in Google Scholar PubMed
41. Koyama, T, Fukuda, K. Involvement of the kappa-opioid receptor in nitrous oxide-induced analgesia in mice. J Anesth 2010;24:297–9. https://doi.org/10.1007/s00540-010-0886-5.Suche in Google Scholar PubMed
42. Branda, EM, Ramza, JT, Cahill, FJ, Tseng, LF, Quock, RM. Role of brain dynorphin in nitrous oxide antinociception in mice. Pharmacol Biochem Behav 2000;65:217–21. https://doi.org/10.1016/s0091-3057(99)00202-6.Suche in Google Scholar PubMed
43. Mague, SD, Pliakas, AM, Todtenkopf, MS, Tomasiewicz, HC, Zhang, Y, Stevens, WCJr., et al.. Antidepressant-like effects of kappa-opioid receptor antagonists in the forced swim test in rats. J Pharmacol Exp Therapeut 2003;305:323–30. https://doi.org/10.1124/jpet.102.046433.Suche in Google Scholar PubMed
44. Panju, S, Brian, J, Dupuis, A, Anagnostou, E, Kushki, A. Atypical sympathetic arousal in children with autism spectrum disorder and its association with anxiety symptomatology. Mol Autism 2015;6:64. https://doi.org/10.1186/s13229-015-0057-5.Suche in Google Scholar PubMed PubMed Central
45. Moore, DJ. Acute pain experience in individuals with autism spectrum disorders: a review. Autism 2015;19:387–99. https://doi.org/10.1177/1362361314527839.Suche in Google Scholar PubMed
46. Rahman, MM, Shu, YH, Chow, T, Lurmann, FW, Yu, X, Martinez, MP, et al.. Prenatal exposure to air pollution and autism spectrum disorder: sensitive windows of exposure and sex differences. Environ Health Perspect 2022;130:17008. https://doi.org/10.1289/ehp9509.Suche in Google Scholar PubMed PubMed Central
47. Girirajan, S, Johnson, RL, Tassone, F, Balciuniene, J, Katiyar, N, Fox, K, et al.. Global increases in both common and rare copy number load associated with autism. Hum Mol Genet 2013;22:2870–80. https://doi.org/10.1093/hmg/ddt136.Suche in Google Scholar PubMed PubMed Central
48. Kim, D, Volk, H, Girirajan, S, Pendergrass, S, Hall, MA, Verma, SS, et al.. The joint effect of air pollution exposure and copy number variation on risk for autism. Autism Res 2017;10:1470–80. https://doi.org/10.1002/aur.1799.Suche in Google Scholar PubMed PubMed Central
49. Devlin, RB, McDonnell, WF, Mann, R, Becker, S, House, DE, Schreinemachers, D, et al.. Exposure of humans to ambient levels of ozone for 6.6 hours causes cellular and biochemical changes in the lung. Am J Respir Cell Mol Biol 1991;4:72–81. https://doi.org/10.1165/ajrcmb/4.1.72.Suche in Google Scholar PubMed
50. Rossignol, DA, Frye, RE. Evidence linking oxidative stress, mitochondrial dysfunction, and inflammation in the brain of individuals with autism. Front Physiol 2014;5:150. https://doi.org/10.3389/fphys.2014.00150.Suche in Google Scholar PubMed PubMed Central
51. Morales-Suarez-Varela, M, Peraita-Costa, I, Llopis-Gonzalez, A. Systematic review of the association between particulate matter exposure and autism spectrum disorders. Environ Res 2017;153:150–60. https://doi.org/10.1016/j.envres.2016.11.022.Suche in Google Scholar PubMed
52. Guxens, M, Ghassabian, A, Gong, T, Garcia-Esteban, R, Porta, D, Giorgis-Allemand, L, et al.. Air pollution exposure during pregnancy and childhood autistic traits in four European population-based cohort studies: the ESCAPE project. Environ Health Perspect 2016;124:133–40. https://doi.org/10.1289/ehp.1408483.Suche in Google Scholar PubMed PubMed Central
53. Becerra, TA, Wilhelm, M, Olsen, J, Cockburn, M, Ritz, B. Ambient air pollution and autism in Los Angeles county, California. Environ Health Perspect 2013;121:380–6. https://doi.org/10.1289/ehp.1205827.Suche in Google Scholar PubMed PubMed Central
54. Raz, R, Roberts, AL, Lyall, K, Hart, JE, Just, AC, Laden, F, et al.. Autism spectrum disorder and particulate matter air pollution before, during, and after pregnancy: a nested case-control analysis within the Nurses’ Health Study II Cohort. Environ Health Perspect 2015;123:264–70. https://doi.org/10.1289/ehp.1408133.Suche in Google Scholar PubMed PubMed Central
55. Geng, R, Fang, S, Li, G. The association between particulate matter 2.5 exposure and children with autism spectrum disorder. Int J Dev Neurosci 2019;75:59–63. https://doi.org/10.1016/j.ijdevneu.2019.05.003.Suche in Google Scholar PubMed
56. McGuinn, LA, Windham, GC, Kalkbrenner, AE, Bradley, C, Croen, LA, Fallin, MD, et al.. Early life exposure to air pollution and autism spectrum disorder: findings from a multisite case-control study. Epidemiology 2020;31:103–14. https://doi.org/10.1097/EDE.0000000000001109.Suche in Google Scholar PubMed PubMed Central
57. Murphy, MS, Abdulaziz, KE, Erwin, E, Guo, Y, Dingwall-Harvey, AL, Walker, MC, et al.. Association between prenatal air pollutant exposure and autism spectrum disorders in young children: a matched case-control study in Canada. Environ Res 2024;261. https://doi.org/10.1016/j.envres.2024.119706.Suche in Google Scholar PubMed
58. Kalkbrenner, AE, Windham, GC, Serre, ML, Akita, Y, Wang, X, Hoffman, K, et al.. Particulate matter exposure, prenatal and postnatal windows of susceptibility, and autism spectrum disorders. Epidemiology 2015;26:30–42. https://doi.org/10.1097/ede.0000000000000173.Suche in Google Scholar PubMed
59. Magen-Molho, H, Weisskopf, MG, Nevo, D, Shtein, A, Chen, S, Broday, D, et al.. Air pollution and autism spectrum disorder in Israel: a negative control analysis. Epidemiology 2021;32:773–80. https://doi.org/10.1097/ede.0000000000001407.Suche in Google Scholar
60. Dutheil, F, Comptour, A, Morlon, R, Mermillod, M, Pereira, B, Baker, JS, et al.. Autism spectrum disorder and air pollution: a systematic review and meta-analysis. Environ Pollut 2021;278:116856. https://doi.org/10.1016/j.envpol.2021.116856.Suche in Google Scholar PubMed
61. Allen, JL, Oberdorster, G, Morris-Schaffer, K, Wong, C, Klocke, C, Sobolewski, M, et al.. Developmental neurotoxicity of inhaled ambient ultrafine particle air pollution: parallels with neuropathological and behavioral features of autism and other neurodevelopmental disorders. Neurotoxicology 2017;59:140–54. https://doi.org/10.1016/j.neuro.2015.12.014.Suche in Google Scholar PubMed PubMed Central
62. Bjørklund, G, Skalny, AV, Rahman, MM, Dadar, M, Yassa, HA, Aaseth, J, et al.. Toxic metal(loid)-based pollutants and their possible role in autism spectrum disorder. Environ Res 2018;166:234–50. https://doi.org/10.1016/j.envres.2018.05.020.Suche in Google Scholar PubMed
63. Zhou, N, Huang, Y, Li, M, Zhou, L, Jin, H. Trends in global burden of diseases attributable to lead exposure in 204 countries and territories from 1990 to 2019. Front Public Health 2022;10. https://doi.org/10.3389/fpubh.2022.1036398.Suche in Google Scholar PubMed PubMed Central
64. Goel, A, Aschner, M. The effect of lead exposure on autism development. Int J Mol Sci 2021;22. https://doi.org/10.3390/ijms22041637.Suche in Google Scholar PubMed PubMed Central
65. Alabdali, A, Al-Ayadhi, L, El-Ansary, A. A key role for an impaired detoxification mechanism in the etiology and severity of autism spectrum disorders. Behav Brain Funct 2014;10:14. https://doi.org/10.1186/1744-9081-10-14.Suche in Google Scholar PubMed PubMed Central
66. Fuentes-Albero, M, Puig-Alcaraz, C, Cauli, O. Lead excretion in Spanish children with autism spectrum disorder. Brain Sci 2015;5:58–68. https://doi.org/10.3390/brainsci5010058.Suche in Google Scholar PubMed PubMed Central
67. Shilpa, O, Anupama, KP, Antony, A, Gurushankara, HP. Lead (Pb)-induced oxidative stress mediates sex-specific autistic-like behaviour in Drosophila melanogaster. Mol Neurobiol 2021;58:6378–93. https://doi.org/10.1007/s12035-021-02546-z.Suche in Google Scholar PubMed
68. Mostafa, GA, Bjorklund, G, Urbina, MA, Al-Ayadhi, LY. The positive association between elevated blood lead levels and brain-specific autoantibodies in autistic children from low lead-polluted areas. Metab Brain Dis 2016;31:1047–54. https://doi.org/10.1007/s11011-016-9836-8.Suche in Google Scholar PubMed
69. Shin, K, Lim, G, Hong, YS, Kim, S, Hwang, S, Lee, J, et al.. Exposure to lead on expression levels of brain immunoglobulins, inflammatory cytokines, and brain-derived neurotropic factor in fetal and postnatal mice with autism-like characteristics. J Toxicol Environ Health A Curr Issues 2021;84:891–900. https://doi.org/10.1080/15287394.2021.1945985.Suche in Google Scholar PubMed
70. Kasten-Jolly, J, Heo, Y, Lawrence, DA. Central nervous system cytokine gene expression: modulation by lead. J Biochem Mol Toxicol 2011;25:41–54. https://doi.org/10.1002/jbt.20358.Suche in Google Scholar PubMed PubMed Central
71. Li, N, Liu, F, Song, L, Zhang, P, Qiao, M, Zhao, Q, et al.. The effects of early life Pb exposure on the expression of IL1-beta, TNF-alpha and Abeta in cerebral cortex of mouse pups. J Trace Elem Med Biol 2014;28:100–4. https://doi.org/10.1016/j.jtemb.2013.07.003.Suche in Google Scholar PubMed
72. Saghazadeh, A, Rezaei, N. Systematic review and meta-analysis links autism and toxic metals and highlights the impact of country development status: higher blood and erythrocyte levels for mercury and lead, and higher hair antimony, cadmium, lead, and mercury. Prog Neuropsychopharmacol Biol Psychiatry 2017;79:340–68. https://doi.org/10.1016/j.pnpbp.2017.07.011.Suche in Google Scholar PubMed
73. McCaulley, ME. Autism spectrum disorder and mercury toxicity: use of genomic and epigenetic methods to solve the etiologic puzzle. Acta Neurobiol Exp 2019;79:113–25. https://doi.org/10.21307/ane-2019-010.Suche in Google Scholar
74. Dack, K, Fell, M, Taylor, CM, Havdahl, A, Lewis, SJ. Prenatal mercury exposure and neurodevelopment up to the age of 5 Years: a systematic review. Int J Environ Res Publ Health 2022;19. https://doi.org/10.3390/ijerph19041976.Suche in Google Scholar PubMed PubMed Central
75. Khaled, EM, Meguid, NA, Bjorklund, G, Gouda, A, Bahary, MH, Hashish, A, et al.. Altered urinary porphyrins and mercury exposure as biomarkers for autism severity in Egyptian children with autism spectrum disorder. Metab Brain Dis 2016;31:1419–26. https://doi.org/10.1007/s11011-016-9870-6.Suche in Google Scholar PubMed
76. Ryu, J, Ha, EH, Kim, BN, Ha, M, Kim, Y, Park, H, et al.. Associations of prenatal and early childhood mercury exposure with autistic behaviors at 5years of age: the Mothers and Children’s Environmental Health (MOCEH) study. Sci Total Environ 2017;605-606:251–7. https://doi.org/10.1016/j.scitotenv.2017.06.227.Suche in Google Scholar PubMed
77. Adams, JB, Romdalvik, J, Ramanujam, VM, Legator, MS. Mercury, lead, and zinc in baby teeth of children with autism versus controls. J Toxicol Environ Health A Curr Issues 2007;70:1046–51. https://doi.org/10.1080/15287390601172080.Suche in Google Scholar PubMed
78. Mostafa, GA, Al-Ayadhi, LY. The relationship between the increased frequency of serum antineuronal antibodies and the severity of autism in children. Eur J Paediatr Neurol 2012;16:464–8. https://doi.org/10.1016/j.ejpn.2011.12.010.Suche in Google Scholar PubMed
79. Boretti, A. Reviewing the association between aluminum adjuvants in the vaccines and autism spectrum disorder. J Trace Elem Med Biol 2021;66:126764. https://doi.org/10.1016/j.jtemb.2021.126764.Suche in Google Scholar PubMed
80. Mold, M, Umar, D, King, A, Exley, C. Aluminium in brain tissue in autism. J Trace Elem Med Biol 2018;46:76–82. https://doi.org/10.1016/j.jtemb.2017.11.012.Suche in Google Scholar PubMed
81. Morris, G, Puri, BK, Frye, RE. The putative role of environmental aluminium in the development of chronic neuropathology in adults and children. How strong is the evidence and what could be the mechanisms involved? Metab Brain Dis 2017;32:1335–55. https://doi.org/10.1007/s11011-017-0077-2.Suche in Google Scholar PubMed PubMed Central
82. Prakash, D, Gopinath, K, Sudhandiran, G. Fisetin enhances behavioral performances and attenuates reactive gliosis and inflammation during aluminum chloride-induced neurotoxicity. NeuroMolecular Med 2013;15:192–208. https://doi.org/10.1007/s12017-012-8210-1.Suche in Google Scholar PubMed
83. Kumar, V, Gill, KD. Oxidative stress and mitochondrial dysfunction in aluminium neurotoxicity and its amelioration: a review. Neurotoxicology 2014;41:154–66. https://doi.org/10.1016/j.neuro.2014.02.004.Suche in Google Scholar PubMed
84. Akinrinade, ID, Memudu, AE, Ogundele, OM, Ajetunmobi, OI. Interplay of glia activation and oxidative stress formation in fluoride and aluminium exposure. Pathophysiology 2015;22:39–48. https://doi.org/10.1016/j.pathophys.2014.12.001.Suche in Google Scholar PubMed
85. Johnson, VJ, Sharma, RP. Aluminum disrupts the pro-inflammatory cytokine/neurotrophin balance in primary brain rotation-mediated aggregate cultures: possible role in neurodegeneration. Neurotoxicology 2003;24:261–8. https://doi.org/10.1016/s0161-813x(02)00194-8.Suche in Google Scholar
86. Jeddi, MZ, Janani, L, Memari, AH, Akhondzadeh, S, Yunesian, M. The role of phthalate esters in autism development: a systematic review. Environ Res 2016;151:493–504. https://doi.org/10.1016/j.envres.2016.08.021.Suche in Google Scholar PubMed
87. Miodovnik, A. Environmental neurotoxicants and developing brain. Mt Sinai J Med 2011;78:58–77. https://doi.org/10.1002/msj.20237.Suche in Google Scholar PubMed
88. Patti, MA, Newschaffer, C, Eliot, M, Hamra, GB, Chen, A, Croen, LA, et al.. Gestational exposure to phthalates and social responsiveness scores in children using quantile regression: the EARLI and HOME studies. Int J Environ Res Publ Health 2021;18. https://doi.org/10.3390/ijerph18031254.Suche in Google Scholar PubMed PubMed Central
89. Bennett, DH, Busgang, SA, Kannan, K, Parsons, PJ, Takazawa, M, Palmer, CD, et al.. Environmental exposures to pesticides, phthalates, phenols and trace elements are associated with neurodevelopment in the CHARGE study. Environ Int 2022;161:107075. https://doi.org/10.1016/j.envint.2021.107075.Suche in Google Scholar PubMed PubMed Central
90. Haggerty, DK, Strakovsky, RS, Talge, NM, Carignan, CC, Glazier-Essalmi, AN, Ingersoll, BR, et al.. Prenatal phthalate exposures and autism spectrum disorder symptoms in low-risk children. Neurotoxicol Teratol 2021;83:106947. https://doi.org/10.1016/j.ntt.2021.106947.Suche in Google Scholar PubMed PubMed Central
91. Stein, TP, Schluter, MD, Steer, RA, Ming, X. Autism and phthalate metabolite glucuronidation. J Autism Dev Disord 2013;43:2677–85. https://doi.org/10.1007/s10803-013-1822-y.Suche in Google Scholar PubMed PubMed Central
92. Ghisari, M, Bonefeld-Jorgensen, EC. Effects of plasticizers and their mixtures on estrogen receptor and thyroid hormone functions. Toxicol Lett 2009;189:67–77. https://doi.org/10.1016/j.toxlet.2009.05.004.Suche in Google Scholar PubMed
93. Hartoft-Nielsen, ML, Boas, M, Bliddal, S, Rasmussen, AK, Main, K, Feldt-Rasmussen, U. Do thyroid disrupting chemicals influence foetal development during pregnancy? J Thyroid Res 2011;2011:342189. https://doi.org/10.4061/2011/342189.Suche in Google Scholar PubMed PubMed Central
94. Nadeem, A, Al-Harbi, NO, Ahmad, SF, Alhazzani, K, Attia, SM, Alsanea, S, et al.. Exposure to the plasticizer, Di-(2-ethylhexyl) phthalate during juvenile period exacerbates autism-like behavior in adult BTBR T + tf/J mice due to DNA hypomethylation and enhanced inflammation in brain and systemic immune cells. Prog Neuropsychopharmacol Biol Psychiatry 2021;109:110249. https://doi.org/10.1016/j.pnpbp.2021.110249.Suche in Google Scholar PubMed
95. Nadeem, A, Ahmad, SF, Al-Harbi, NO, Attia, SM, Bakheet, SA, Alsanea, S, et al.. Aggravation of autism-like behavior in BTBR T+tf/J mice by environmental pollutant, di-(2-ethylhexyl) phthalate: role of nuclear factor erythroid 2-related factor 2 and oxidative enzymes in innate immune cells and cerebellum. Int Immunopharmacol 2021;91:107323. https://doi.org/10.1016/j.intimp.2020.107323.Suche in Google Scholar PubMed
96. Miodovnik, A, Edwards, A, Bellinger, DC, Hauser, R. Developmental neurotoxicity of ortho-phthalate diesters: review of human and experimental evidence. Neurotoxicology 2014;41:112–22. https://doi.org/10.1016/j.neuro.2014.01.007.Suche in Google Scholar PubMed
97. Stein, TP, Schluter, MD, Steer, RA, Guo, L, Ming, X. Bisphenol A exposure in children with autism spectrum disorders. Autism Res 2015;8:272–83. https://doi.org/10.1002/aur.1444.Suche in Google Scholar PubMed PubMed Central
98. Hansen, JB, Bilenberg, N, Timmermann, CAG, Jensen, RC, Frederiksen, H, Andersson, AM, et al.. Prenatal exposure to bisphenol A and autistic- and ADHD-related symptoms in children aged 2 and5 years from the Odense Child Cohort. Environ Health 2021;20:24. https://doi.org/10.1186/s12940-021-00709-y.Suche in Google Scholar PubMed PubMed Central
99. Stein, TP, Schluter, MD, Steer, RA, Ming, X. Bisphenol-A and phthalate metabolism in children with neurodevelopmental disorders. PLoS One 2023;18:e0289841. https://doi.org/10.1371/journal.pone.0289841.Suche in Google Scholar PubMed PubMed Central
100. Kaur, K, Chauhan, V, Gu, F, Chauhan, A. Bisphenol A induces oxidative stress and mitochondrial dysfunction in lymphoblasts from children with autism and unaffected siblings. Free Radic Biol Med 2014;76:25–33. https://doi.org/10.1016/j.freeradbiomed.2014.07.030.Suche in Google Scholar PubMed
101. Metwally, FM, Rashad, H, Zeidan, HM, Kilany, A, Abdol Raouf, ER. Study of the effect of bisphenol A on oxidative stress in children with autism spectrum disorders. Indian J Clin Biochem 2018;33:196–201. https://doi.org/10.1007/s12291-017-0667-0.Suche in Google Scholar PubMed PubMed Central
102. Hallmayer, J, Cleveland, S, Torres, A, Phillips, J, Cohen, B, Torigoe, T, et al.. Genetic heritability and shared environmental factors among twin pairs with autism. Arch Gen Psychiatry 2011;68:1095–102. https://doi.org/10.1001/archgenpsychiatry.2011.76.Suche in Google Scholar PubMed PubMed Central
103. Kanlayaprasit, S, Thongkorn, S, Panjabud, P, Jindatip, D, Hu, VW, Kikkawa, T, et al.. Autism-related transcription factors underlying the sex-specific effects of prenatal bisphenol A exposure on transcriptome-interactome profiles in the offspring prefrontal cortex. Int J Mol Sci 2021;22. https://doi.org/10.3390/ijms222413201.Suche in Google Scholar PubMed PubMed Central
104. Thongkorn, S, Kanlayaprasit, S, Panjabud, P, Saeliw, T, Jantheang, T, Kasitipradit, K, et al.. Sex differences in the effects of prenatal bisphenol A exposure on autism-related genes and their relationships with the hippocampus functions. Sci Rep 2021;11:1241. https://doi.org/10.1038/s41598-020-80390-2.Suche in Google Scholar PubMed PubMed Central
105. Xi, T, Wu, J. A review on the mechanism between different factors and the occurrence of autism and ADHD. Psychol Res Behav Manag 2021;14:393–403. https://doi.org/10.2147/prbm.s304450.Suche in Google Scholar PubMed PubMed Central
106. Sjodin, A, Jones, RS, Caudill, SP, Wong, LY, Turner, WE, Calafat, AM. Polybrominated diphenyl ethers, polychlorinated biphenyls, and persistent pesticides in serum from the national health and nutrition examination survey: 2003-2008. Environ Sci Technol 2014;48:753–60. https://doi.org/10.1021/es4037836.Suche in Google Scholar PubMed PubMed Central
107. Woodruff, TJ, Zota, AR, Schwartz, JM. Environmental chemicals in pregnant women in the United States: nhanes 2003-2004. Environ Health Perspect 2011;119:878–85. https://doi.org/10.1289/ehp.1002727.Suche in Google Scholar PubMed PubMed Central
108. Lyall, K, Croen, LA, Sjodin, A, Yoshida, CK, Zerbo, O, Kharrazi, M, et al.. Polychlorinated biphenyl and organochlorine pesticide concentrations in maternal mid-pregnancy serum samples: association with autism spectrum disorder and intellectual disability. Environ Health Perspect 2017;125:474–80. https://doi.org/10.1289/ehp277.Suche in Google Scholar
109. Mehri, F, Bashirian, S, Khazaei, S, Jenabi, E. Association between pesticide and polychlorinated biphenyl exposure during pregnancy and autism spectrum disorder among children: a meta-analysis. Clin Exp Pediatr 2021;64:286–92. https://doi.org/10.3345/cep.2020.00864.Suche in Google Scholar PubMed PubMed Central
110. Kimura-Kuroda, J, Nagata, I, Kuroda, Y. Disrupting effects of hydroxy-polychlorinated biphenyl (PCB) congeners on neuronal development of cerebellar Purkinje cells: a possible causal factor for developmental brain disorders? Chemosphere 2007;67:S412–420. https://doi.org/10.1016/j.chemosphere.2006.05.137.Suche in Google Scholar PubMed
111. Liu, C, Wang, C, Yan, M, Quan, C, Zhou, J, Yang, K. PCB153 disrupts thyroid hormone homeostasis by affecting its biosynthesis, biotransformation, feedback regulation, and metabolism. Horm Metab Res 2012;44:662–9. https://doi.org/10.1055/s-0032-1311569.Suche in Google Scholar PubMed
112. Pruitt, DL, Meserve, LA, Bingman, VP. Reduced growth of intra- and infra-pyramidal mossy fibers is produced by continuous exposure to polychlorinated biphenyl. Toxicology 1999;138:11–17. https://doi.org/10.1016/s0300-483x(99)00073-6.Suche in Google Scholar PubMed
113. Panesar, HK, Kennedy, CL, Keil Stietz, KP, Lein, PJ. Polychlorinated biphenyls (PCBs): risk factors for autism spectrum disorder? Toxics 2020;8. https://doi.org/10.3390/toxics8030070.Suche in Google Scholar PubMed PubMed Central
114. Pu, Y, Yang, J, Chang, L, Qu, Y, Wang, S, Zhang, K, et al.. Maternal glyphosate exposure causes autism-like behaviors in offspring through increased expression of soluble epoxide hydrolase. Proc Natl Acad Sci U S A 2020;117:11753–9. https://doi.org/10.1073/pnas.1922287117.Suche in Google Scholar PubMed PubMed Central
115. von Ehrenstein, OS, Ling, C, Cui, X, Cockburn, M, Park, AS, Yu, F, et al.. Prenatal and infant exposure to ambient pesticides and autism spectrum disorder in children: population based case-control study. Br Med J 2019;364:l962. https://doi.org/10.1136/bmj.l962.Suche in Google Scholar PubMed PubMed Central
116. Pu, Y, Ma, L, Shan, J, Wan, X, Hammock, BD, Hashimoto, K. Autism-like behaviors in male juvenile offspring after maternal glyphosate exposure. Clin Psychopharmacol Neurosci 2021;19:554–8. https://doi.org/10.9758/cpn.2021.19.3.554.Suche in Google Scholar PubMed PubMed Central
117. 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 2022;203:111902. https://doi.org/10.1016/j.envres.2021.111902.Suche in Google Scholar PubMed
118. Alexandrov, PN, Pogue, AI, Lukiw, WJ. Synergism in aluminum and mercury neurotoxicity. Integr Food Nutr Metab 2018;5. https://doi.org/10.15761/IFNM.1000214.Suche in Google Scholar PubMed PubMed Central
119. El-Ansary, A, Bjørklund, G, Tinkov, AA, Skalny, AV, Al Dera, H. Relationship between selenium, lead, and mercury in red blood cells of Saudi autistic children. Metab Brain Dis 2017;32:1073–80. https://doi.org/10.1007/s11011-017-9996-1.Suche in Google Scholar PubMed
120. Yang, J, Liao, A, Hu, S, Zheng, Y, Liang, S, Han, S, et al.. Acute and chronic toxicity of binary mixtures of bisphenol A and heavy metals. Toxics 2022;10:2551–14. https://doi.org/10.3390/toxics10050255.Suche in Google Scholar PubMed PubMed Central
121. Li, X, Yin, P, Zhao, L. Effects of individual and combined toxicity of bisphenol A, dibutyl phthalate and cadmium on oxidative stress and genotoxicity in HepG 2 cells. Food Chem Toxicol 2017;105:73–81. https://doi.org/10.1016/j.fct.2017.03.054.Suche in Google Scholar PubMed
122. Fu, J, Guo, Y, Yang, L, Han, J, Zhou, B. Nano-TiO2 enhanced bioaccumulation and developmental neurotoxicity of bisphenol a in zebrafish larvae. Environ Res 2020;187. https://doi.org/10.1016/j.envres.2020.109682 February 2020].Suche in Google Scholar PubMed
© 2025 Walter de Gruyter GmbH, Berlin/Boston
Artikel in diesem Heft
- Frontmatter
- Reviews
- The association of particulate matter PM2.5 and nitrogen oxides from ambient air pollution and mental health of children and young adults- a systematic review
- Plant endophytic bacteria reduce phthalates accumulation in soil-crop-body system: a review
- A review in analytical progress for house dust mite allergens
- Global research trends and emerging hotspots in acute high altitude illness: a bibliometric analysis and review (1937–2024)
- Sustainable materials and energy from pine needle waste – a review
- Interrelation between prenatal mercury-selenium exposure and glutathione gene polymorphism: impact on growth and development in children
- Connecting the dots: environmental pollution and Autism Spectrum Disorder
- Phthalates, bisphenols and per-and polyfluoroalkyl substances migration from food packaging into food: a systematic review
- Dietary intake of dioxins and cancer – where do we stand?
- Unfinished business: formaldehyde exposure from uniforms and the case for U.S. textile regulation
- A mini-review on the health risks associated with sodium p-perfluorous nonenoxybenzene sulfonate exposure
- Maternal exposure to particulate matter and nitrogen oxides during pregnancy and attention deficit hyperactivity disorder in offspring: a systematic review and meta-analysis
Artikel in diesem Heft
- Frontmatter
- Reviews
- The association of particulate matter PM2.5 and nitrogen oxides from ambient air pollution and mental health of children and young adults- a systematic review
- Plant endophytic bacteria reduce phthalates accumulation in soil-crop-body system: a review
- A review in analytical progress for house dust mite allergens
- Global research trends and emerging hotspots in acute high altitude illness: a bibliometric analysis and review (1937–2024)
- Sustainable materials and energy from pine needle waste – a review
- Interrelation between prenatal mercury-selenium exposure and glutathione gene polymorphism: impact on growth and development in children
- Connecting the dots: environmental pollution and Autism Spectrum Disorder
- Phthalates, bisphenols and per-and polyfluoroalkyl substances migration from food packaging into food: a systematic review
- Dietary intake of dioxins and cancer – where do we stand?
- Unfinished business: formaldehyde exposure from uniforms and the case for U.S. textile regulation
- A mini-review on the health risks associated with sodium p-perfluorous nonenoxybenzene sulfonate exposure
- Maternal exposure to particulate matter and nitrogen oxides during pregnancy and attention deficit hyperactivity disorder in offspring: a systematic review and meta-analysis