
==== Front
BMC Public Health
BMC Public Health
BMC Public Health
1471-2458
BioMed Central London

39223561
19742
10.1186/s12889-024-19742-w
Systematic Review
Environmental pollutants as risk factors for autism spectrum disorders: a systematic review and meta-analysis of cohort studies
Duque-Cartagena Tatiana 12
Dalla Marcello Dala Bernardina 345
Mundstock Eduardo 67
Neto Felipe Kalil 8
Espinoza Sergio Angelo Rojas 2
de Moura Sara Kvitko 9
Zanirati Gabriele 110
Padoin Alexandre Vontobel 1
Jimenez Juan Gabriel Piñeros 11
Stein Airton Tetelbom 12
Cañon-Montañez Wilson 13
Mattiello Rita rita.mattiello@ufrgs.br

2
1 https://ror.org/025vmq686 grid.412519.a 0000 0001 2166 9094 School of Medicine, Postgraduate Program in Medicine and Health Sciences, Pontifical Catholic University of Rio Grande do Sul (PUCRS), Porto Alegre, RS Brazil
2 https://ror.org/041yk2d64 grid.8532.c 0000 0001 2200 7498 Universidade Federal do Rio Grande do Sul, Porto Alegre, RS Brazil
3 https://ror.org/05sxf4h28 grid.412371.2 0000 0001 2167 4168 Cassiano Antônio de Moraes University Hospital, Universidade Federal do Espírito Santo (HUCAM/UFES), Vitória, ES Brazil
4 Capixaba Institute for Teaching Research and Innovation of the State Health Department of Espirito Santo (ICEPI-SESA), Vitória, ES Brazil
5 Espirito Santense College – FAESA, Cariacica, ES Brazil
6 Universidade Leonardo da Vinci, Polo Canela, RS Brazil
7 Secretaria da Educação Esporte e Lazer de Canela-Escola Zeferino José Lopes, Canela, RS Brazil
8 https://ror.org/025vmq686 grid.412519.a 0000 0001 2166 9094 School of Medicine, Pontifical Catholic University of Rio Grande Do Sul (PUCRS), Porto Alegre, RS Brazil
9 Presidente Vargas Maternal and Child Hospital, Porto Alegre, RS Brazil
10 https://ror.org/007j2dm88 grid.493339.7 Brain Institute of Rio Grande do Sul (BraIns), Porto Alegre, RS Brazil
11 https://ror.org/03bp5hc83 grid.412881.6 0000 0000 8882 5269 National Faculty of Public Health, Universidad de Antioquia, Medellín, Colombia
12 grid.412344.4 0000 0004 0444 6202 Departamento de Saúde Pública, Universidade Federal de Ciências da Saúde de Porto Alegre, and Hospital Conceição, Porto Alegre, RS Brazil
13 https://ror.org/03bp5hc83 grid.412881.6 0000 0000 8882 5269 Faculty of Nursing, Universidad de Antioquia, Medellín, Colombia
3 9 2024
3 9 2024
2024
24 238828 11 2023
9 8 2024
© The Author(s) 2024
2024
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Background

Autism Spectrum Disorder (ASD) is a lifelong neurodevelopmental condition affecting communication, social interaction, and behavior. Evidence suggests that environmental pollutants are associated with ASD incidence. This review aimed to analyze the effect of environmental pollutants on ASD.

Methods

Systematic review and meta-analysis of cohort studies evaluated the association between exposure to environmental pollutants and ASD. We searched COCHRANE CENTRAL, MEDLINE, CINAHL, LILACS, EMBASE, PsycINFO, Web of Science, SciELO, and gray literature from inception to January 2023. The model used for meta-analysis was inverse variance heterogeneity (IVhet). The effect measures were the beta coefficient (β) and the relative risk (RR) with their 95% confidence intervals (95% CI). Sensitivity analyses were carried out using an instrument to screen or diagnose autism.

Results

A total of 5,780 studies were identified; 27 were included in the systematic review, and 22 were included in the meta-analysis. These studies included 1,289,183 participants and 129 environmental pollutants. Individual meta-analyses found a significant association between nitrogen dioxide RR = 1.20 (95% CI: 1.03 to 1.38; I2: 91%), copper RR = 1.08 (95% CI: 1.03 to 1.13; I2: 0%), mono-3-carboxy propyl phthalate β = 0.45 (95% CI: 0.20 to 0.70; I2: 0%), monobutyl phthalate β = 0.43 (95% CI: 0.13 to 0.73; I2: 0%) and polychlorinated biphenyl (PCB) 138 RR = 1.84 (95% CI: 1.14 to 2.96; I2:0%) with ASD. Subgroup meta-analyses found a significant association with carbon monoxide RR = 1.57 (95% CI: 1.25 to 1.97; I2: 0%), nitrogen oxides RR = 1.09 (95% CI: 1.04 to 1.15; I2: 34%) and metals RR = 1.13 (95% CI: 1.01 to 1.27; I2:24%).

Conclusion

This study found positive associations nitrogen dioxide, copper, mono-3-carboxypropyl phthalate, monobutyl phthalate, and PCB 138, and the development of ASD, likewise, with subgroups of pollutants carbon monoxide, nitrogen oxides, and metals. Therefore, it is important to identify these risk factors in children and adolescents to contribute to ASD and identify prevention strategies effectively.

Supplementary Information

The online version contains supplementary material available at 10.1186/s12889-024-19742-w.

Keywords

Autism
Environmental pollutants
Systematic review
Cohort studies
issue-copyright-statement© BioMed Central Ltd., part of Springer Nature 2024
==== Body
pmcBackground

Autism spectrum disorder (ASD) is a lifelong neurodevelopmental condition that impacts communication, social interaction, and behavior. Its prevalence has been on the rise globally. In a recent systematic review, it was estimated that 1 in 100 children worldwide are affected by ASD [1]. The Centers for Disease Control and Prevention (CDC), 1 in 36 children aged eight years will be diagnosed with ASD [2]. In the United States, the economic burden of ASD was estimated to be $11.5 billion in 2011 [3]. A complex interplay of biological and environmental factors has been linked to autism spectrum disorder.

Gene-environment interactions are critical factors in ASD development. Environmental pollutants, including toxic metals, are linked to epigenetic modifications and de novo mutations, potentially contributing to ASD onset [4]. These pollutants, particularly during gestation and postnatal periods, pose health risks and are associated with ASD [5]. Toxic heavy metals can disrupt enzymatic functions, interfere with cell signaling, and trigger oxidative stress, potentially leading to cell death pathways. Elevated levels of cadmium and mercury are frequently found in children with ASD [6]. However, more research is needed to fully understand how metal-induced neurotoxicity might play a role in ASD.

Recent systematic reviews and meta-analyses have evaluated the link between environmental pollutants and the development of ASD, but these reviews exhibit notable limitations. Among the 21 identified studies, 18 relied on four or fewer databases [5, 7–23], 11 imposed language restrictions (English, French, or Chinese)) [7, 8, 12, 13, 15, 18–20, 22–24], and six confined their searches to brief periods [9, 13, 15, 19, 20, 22]. This approach potentially overlooks some available evidence. Additionally, most reviews concentrated on air pollutants [7, 8, 10, 12, 13, 15, 18, 20, 23–26], with fewer addressing metals [5, 8, 14, 15, 22, 27], pesticides [9, 11, 16, 17, 27], polychlorinated biphenyls [19], or perfluoroalkyl substances [21]. The evidence primarily stems from cross-sectional, case–control, ecological, and cohort studies, and some reviews failed to stratify results by study type, blending cohort and case–control data [5, 8, 10, 12, 14]. Only one review exclusively considered cohort studies [13], However, it was limited to children under five and focused solely on-air pollution, not accounting for prolonged exposures or older children. This study aims to analyze the association between various environmental pollutants and ASD incidence through cohort studies, evaluating different pollutants and their effects on subgroups.

Methods

Protocol and registration

This study was performed according to the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses – PRISMA [28] and registered in the International Prospective Register of Systematic Reviews (PROSPERO) under the number CRD42018093510.

Eligibility criteria

The PECOS strategy was defined as follows: Population: children and adolescents from 0 to 18 years old; Exposure: higher levels of environmental pollutants during the prenatal and postnatal period; Comparison: lower levels of environmental pollutants; Outcome: incidence of ASD, Studies: cohort studies.

The exclusion criteria were as follows: (a) studies that only included participants older than 19 years; (b) tobacco exposure; and (c) response letters, reviews, editorials, animal, and duplicate studies. Duplicate studies were considered when they had the same author, title and year. Additionally, when the studies were updating previous versions, the most current version with the largest sample size was chosen.

Environmental pollutant exposure included air pollution; PM; inorganic carbon compounds; lead; sulfur oxides; nitrogen oxides; soot; polychlorinated biphenyls (PCBs), inorganic chemicals; pesticides; volatile organic compounds (VOC); hydrocarbons; endocrine disruptors; plasticizers, and plastics.

The air pollutants were classified according to American international guidelines [29]. The groups were ground-level ozone, PM, carbon monoxide (CO), sulfur oxides (SOx), and nitrogen oxides (NOx). The toxic substances included in this study were classified according to the International Guidelines on Toxic Substances [30]. The categories of these pollutants were coal ash; dioxins, furans, PCBs; benzidines/aromatic amines; inorganic substances; nitrosamines/ethers/alcohols; pesticides; phenols/phenoxy acids; organophosphates and carbamates; phthalates; halogenated pesticides and related compounds; volatile organic compounds; radionuclides (radioactive materials) and warfare and terrorism agents.

Sources of information and search strategy

We searched the Cochrane Central Register of Controlled Trials (COCHRANE CENTRAL), MEDLINE (via PUBMED), Cumulative Index to Nursing and Allied Health Literature (CINAHL), Scientific Electronic Library Online (SciELO), Latin American Caribbean Health Sciences Literature (LILACS), Excerpta Medica Database (EMBASE), American Psychological Association database (PsycINFO), Web of Science (WoS), and gray literature from inception to January 2023. We checked the references of the included studies and reviews (Additional file 1: Supplementary Chart 1. Databases search strategy). Searches were not limited by date or language.

Study selection

Three independent review authors independently (GZ and SK; MDBD and SE; FKN and EM) inspected all titles and abstracts identified. The second review stage consisted of reading the articles selected in the previous step in full text.

When a difference in opinion was found at each stage, the article selection was decided independently by the other two review authors (MDBD and EM).

Data extraction

Two authors (TDC and MDBD) extracted the following study characteristics: a) first author's name, b) publication year, c) population, d) the number of subjects in the studye) study location, f) pollution measurement method, g) types of contaminants, h) ASD diagnostic assessment, i) control group, j) participant age, k) follow-up time and l) results.

Summary measures and data analysis

Table 1 qualitatively summarizes the main characteristics of the included studies. Effect sizes using the beta coefficient (β) or relative risk (RR). The relative risk consolidates various metrics from individual studies, including the incidence rate ratio, odds ratio, hazard ratio, adjusted hazard ratio, cumulative hazard ratio, and Bayesian predictive odds ratio, each accompanied by its corresponding 95% confidence intervals (95% CI). If both the beta coefficient and relative risk were accessible for a specific outcome, both measures were described for comprehensive reporting. The meta-analyses were calculated with MetaXL 5.3 [31] software. The "ContCI" type for studies that report a β value and the "RRCI" type for studies that report an RR value were used for the meta-analysis. The method selected was inverse variance heterogeneity (IVhet) [32]. The meta-analyses were conducted exclusively with studies of high methodological quality (Additional file 1: Table S1). Furthermore, a sensitivity analysis was performed, considering the type of instrument used for ASD detection (either diagnosis or screening).

Table 1 Characteristics of included studies

Study, Year	Country	Population	Total cohort	Number of eligible participants	Age of ASD diagnosis (Years), mean  ±  SD	Follow-up period	Time of exposure	Pollution Detection Method	Subgroup of pollutant	Diagnostic or screening method	Inclusion criteria	Exclusion criteria	Exposure group	Control Group	
Alampi JD, 2021 [33]	Canada	Children	8.716	478	3–4 (median, 40 months old)	4 years	The first trimester of pregnancy	Cord blood	Inorganic substances

Metals

Pesticides

Phthalates

Hydrocarbons

Plastics

Dioxins, Furans, PCBs

Phenols/phenoxy acids

	Social Responsiveness Scale- 2 (SRS-2) questionnaire. Preschool-aged version	Pregnant being at least 18 years old, being able to communicate in French or English, and consenting to cord blood collection	Women who carried a fetus with a known abnormality had a primary chronic disease, used illicit drugs, or threatened abortion	Not described	Not described	
Barkoski JM, 2021 [34]	USA	Children	Not described	201	Not described	3 years	Second and third trimester of pregnancy	Urine	Pesticides	Autism

Diagnostic Observation Scale (ADOS)

	Mother or father had one or more children with ASD and or the gestating younger child had an older half-sibling or an equivalent or closer blood relative with ASD; Mother was at least 18 years of age or older; Mother was already pregnant or planning a pregnancy and biologically able to become pregnant; and Mother lived within 2 h of the Davis/Sacramento region at time of enrollment	Not described	 > LOD

(> 0,1 ng/mL)

Unit: natural log-transformed

	 < LOD

(< 0,1 ng/mL)

Unit: natural log-transformed

	
Bernardo BA, 2019 [35]	Canada	Children	Not described	546	3.4 ± 0.16	4 years	The first trimester of pregnancy	Plasma	Dioxins, Furans, PCBs	Social Responsiveness Scale-2 (SRS-2)	Mothers who had sociodemographic and child neurodevelopment information, plasma PCB concentrations, and total lipid concentrations measured during the first trimester of the pregnancy	Breastfeeding and pregnancy outcomes from our models and biomarkers of other prenatal contaminant exposures, including lead	Fourth quartile exposure (> 3.6 ng/g)

Unit: log 2 transformed

	First quartile exposure (< 1.4 ng/g)

Unit: log 2 transformed

	
Braun JM, 2014 [36]	USA	Children	389	175	4–5 (mean ± SD Not described)	5 years	Second trimester of pregnancy and after childbirth	Serum or urine	Phthalates

Dioxins, Furans, PCBs

Polyfluoroalkyl substances

Pesticides

Hydrocarbons

	Social Responsiveness Scale (SRS)	a) 16 ± 3 weeks of pregnancy,

b) age ≥ 18 years, c) residence in a home built

before 1978, d) no history of HIV infection, and e) no medications taken for seizures or thyroid disorders

	Not described	Pollutant unit

Unit:

log10-transformed

	Pollutant unit

Unit:

log10-transformed

	
Carter SA, 2022 [37]	USA	Children	Not described	314.391	Not described	1 year	Throughout pregnancy	Freeway traffic load with California line-source dispersion model (CALINE4)	Particular matter	International Classification of Diseases (ICD)-9 codes and, after October 1, 2015, from ICD-10 codes	Mother–child pairs of singleton deliveries at Kaiser Permanente Southern California (KPSC) hospitals between

January 1, 2001, and December 31, 2014. Only geocodes with accuracy scores ≥ 98 and point or street address types were considered sufficiently accurate for traffic exposure assignments

	Missing or errors in birth weight, gender, maternal race/ethnicity and age at delivery, maternal age at delivery < 15 or > 55 years, and incomplete maternal residential address history in pregnancy, or due to geocodes not suitable for exposure assignment	Five quintile exposure

(> 3.80 ppb)

	First quintile exposure

(≤ 0.89 ppb)

	
Gong T, 2014 [38]	Sweden	Children	17.22	3.426	10.3 ± 1.5	9 years	Throughout pregnancy and the postnatal period	Air pollution concentrations at residential addresses during the mother's pregnancy, the child's first year of life, and the a year before the neurodevelopmental assessment was established mated by dispersion models,	Nitrogen oxides

Particular matter

	Autism-Tics, ADHD, and other Comorbidities inventory (A-TAC)	Twins born during 1992–2000	Not described	High exposure (95th percentile)	Low exposure (5th percentile)	
Granillo L, 2019 [39]	USA	Children	Not described	104	Not described	3 years	Throughout pregnancy	Plasma	Dioxins, Furans, PCBs	Autism Diagnostic Observation Schedule (ADOS) and Mullen Scales of Early Learning

(MSEL)

	Families must reside within 2.5 h driving distance from the MIND Institute. Confirmed diagnosis of ASD in an older sibling of the child and active status in the MARBLES cohort, meaning participants had no loss to follow-up. They had not declined further participation in the study	The child of interest was a twin or had no final diagnosis	50% highest concentration of PCB	50% lowest concentration of PCB	
Guxens M, 2016 [40]	Italy; the Netherlands; Sweden; Spain	Children	Not described	8.079	4–10 (mean ± SD Not described)	10 years	Throughout pregnancy	Were estimated for birth addresses by land-use regression models based on monitoring campaigns performed between 2008 and 2011	Nitrogen oxides

Particular matter

	Swedish cohort: Autism-Tics, Attention deficit and hyperactivity disorders, and other Comorbidities (A-TAC) inventory; Dutch and Italian cohorts: Pervasive Developmental Problems (PDP) subscale of the Child Behavior Checklist for Toddlers (CBCL11⁄2–5); Dutch cohorts: Adapted 18-item version of the Social Responsiveness Scale (SRS); Spanish cohort: Childhood Autism Spectrum Test (CAST);	Mother–child pairs were recruited from 1992 through 2008	Not described	 > cutoff limit	 < cutoff limit	
Haggerty DK, 2021 [41]	USA	Children	Not described	77	3–6 (mean ± SD Not described)	6 years	The first trimester of pregnancy	Urine	Phthalates	Social Responsiveness Scale (SRS)	Women had to be 18 years of age or older and be able to communicate in English	Not described	Pollutant unit (ng/mL)

Unit:

ln-transformed

	Pollutant unit (ng/mL)

Unit:

ln-transformed

	
Hansen J, 2021 [42]	Denmark	Children	2.874	427	2 – 5 (mean ± SD Not described)	5 years	End of the second trimester or beginning of the third trimester of pregnancy	Urine	Plastics	Child Behavior Checklist; 11⁄2–5 (CBCL/11⁄2–5)	2010 to 2012, women residing in the municipality of Odense with a newly diagnosed pregnancy before 16 weeks of gestation	Twins and mothers of nonwestern origin	Third tertile exposure

(≥ 1.97 ng/mL)

	First tertile exposure

(< 0.87 ng/mL)

	
Jo H, 2019 [43]	USA	Children	246.42	2.471	0—5 (mean ± SD Not described)	5 years	Preconception, each trimester, the entire pregnancy, and the first year of life	Birth certificate residential addresses were geocoded using MapMarker USA Version

28.0.0.11. Exposure metrics at each geocoded address included regional O3, PM2.5, PM ≤ 10 μm in diameter (PM10), and nitrogen dioxide (NO2)

	Ozone

Particular matter

Nitrogen oxides

	Autism in Toddlers (CHAT)	Mother–child pairs with singleton deliveries in

KPSC hospitals between January 1, 1999, and December 31, 2009, in 14 service areas

located across Southern California

	Children with birth certificate addresses outside Southern California or addresses that could not be accurately geocoded because of an address missing or not matchable to a U.S. postal service address	 > to the scaled average

(PM 2.5 > 6.5 µg/m3; PM 10 > 16.1 µg/m3; NO2 > 10.4 ppb and O3 > 15.7 ppb)

	 < to scaled average

(PM 2.5 < 6.5 µg/m3; PM 10 < 16.1 µg/m3; NO2 < 10.4 ppb and O3 < 15.7 ppb)

	
Joyce EE, 2022 [44]	USA	Children	256	154	Not described	3 years	First and second trimester of pregnancy	Dietary information was collected through a modified version of the National Cancer Institute's Dietary History Questionnaire (DHQ), which included additional questions from the validated version to capture contaminant exposure	Pesticides	Social Responsiveness Scale (SRS)	Women had to be 18 years or older, less than 29 weeks pregnant, English or Spanish-speaking, and living no farther than 2 h from recruitment sites	Not have outcome information available (either Social Responsiveness Scale (SRS) or diagnostic evaluation, both conducted at the 36-month visit and if they did not have information on prenatal diet. Twins were excluded due to the small number and correlation in exposures, following these exclusions	Fourth quartile exposure	First quartile exposure	
Jung CR, 2013 [45]	China	Children	49.833	535	6.26 ± 2.91	4 years	Early childhood ( up to 6 years)	Taiwan Environmental Protection Agency (EPA) monitoring station on Taiwan's main island. These air pollutants are measured hourly—CO by nondispersive infrared absorption, NO2 by chemiluminescence, O3 by ultraviolet absorption, SO2 by ultraviolet fluorescence, and PM10 by beta-gauge—and continuously	Carbon monoxide

Nitrogen oxides

Sulfur oxides

Ozone

Particular matter

	International Classification of Diseases, Ninth Revision, Clinical Modification

(ICD-9-CM)

	Individual's first date of enrollment until the first diagnosis of ASD	Children who had experienced ASD at the baseline and those who had missing information on air pollution	 > 75th percentile	 < 25th percentile	
Kim JI, 2021 [46]*	South Korea	Children	13.484	547	95.1 ± 1.4 months	8 years	The second trimester of pregnancy and the postnatal period	Urine	Phthalates	Social Communication Questionnaire (SCQ)	Pregnant women in the second trimester (between 14 and 27 weeks of gestation) were enrolled in the Congenital Anomaly Study from 2008 to 2010	Children who did not visit at least once between the ages of 4 and 8 years and children who did not see due to missing information on the social communication questionnaire (SCQ) scores	 > LOD	 < LOD	
Lizé M, 2022 [47]*	France	Children	3.421	185	4–11 (mean ± SD Not described)	11 years	First and second trimester of pregnancy	Urine samples	Organophosphates and carbamates

Pesticides

	The Childhood Autism Spectrum Test (CAST)	Women with less than 19 weeks of gestation	Not described	Third tertile, > LOD or detectable exposure	First tertile, < LOD or not detectable exposure	
Nowack N, 2015 [48]	Germany	Children	234	116	10.23 ± 0.59	12 years	The third trimester of pregnancy and the postnatal period	Blood samples	Dioxins, Furans, PCBs	Social Responsiveness Scale (SRS)	Babies from German- or Turkish-speaking families are born at term (weeks 38–42 of pregnancy) with an APGAR score of at least 8

Parity 1–3

	Serious complications or illness during pregnancy or at parturition, and without congenital anomalies	Pollutant unit (pg/g lipid base)	Pollutant unit (pg/g lipid base)	
Oudin A, 2019 [49]	Sweden	Adolescents	48.571	768	8 ± 1.9	17 years	Throughout pregnancy	Geocoding	Nitrogen oxides	International Statistical Classification of Diseases and Related Health Problems (ICD-10)	Being born between 1999 and 2009	Not described	Fourth quartile exposure	First quartile exposure	
Oulhote Y, 2020 [50]	Canada	Children	2.001	556	3.4 ± 0.74	4 years	The first trimester of pregnancy	Urine samples	Phthalates	Social Responsiveness Scale (SRS-2)	Pregnant woman older than 18 years	Have a chronic disease

Threatened abortion

Consumption of psychoactive substances

	Pollutant unit (µg/L)

Unit:

Log 2-transformed

	Pollutant unit (µg/L)

Unit:

Log 2-transformed

	
Pagalan L, 2019 [51]	Canada	Children	132.256	129.439	4.2 ± 1.4	5 years	Throughout pregnancy and the postnatal period	Land use regression model	Particular matter

Nitrogen oxides

	Autism Diagnostic Observation Schedule (ADOS)

Autism Diagnostic Interview–Revised (ADI-R)

	Be registered in the provincial health insurance plan for 275 days or more

Reside in the Vancouver metropolitan area during the calendar year of your pregnancy

	Unknown gestational age	Per interquartile range

(PM 2.5 > 1.5 µg/m3; NOX > 10.5 ppb and NO2 > 4.8 ppb)

	Per interquartile range

(PM 2.5 < 1.5 µg/m3; NOX < 10.5 ppb and NO2 < 4.8 ppb)

	
Pham C, 2022 [52]	Australia	Children	1.047	676	2–4 (mean ± SD Not described)	4 years	Throughout pregnancy and the postnatal period	Geocoding	Particular matter

Nitrogen oxides

	Child Behavior Checklist for ages 1½–5 (CBCL 1½–5)	Not described	Pregnant women under 18 years of age

Require an interpreter to answer the questionnaires

Baby with severe disease before 32 weeks

	Pollutant unit

PM 2.5 (µg/m3)

NO2 (ppb)

	Pollutant unit

PM 2.5 (µg/m3)

NO2 (ppb)

	
Philippat C, 2018 [53]	United States	Children	203	101	Not described	3 years	Throughout pregnancy	Urine samples	Phthalates	Autism Diagnostic Observation Schedule (ADOS)	Be at least 18 years of age

Be the biological mother of a child with autism spectrum disorder

Live within a 2-h drive of Davis/Sacramento

	Not taking the follow-up questionnaire	Not described	Not described	
Rahman MM, 2022 [54]	United States	Children	343.813	294.937	3.5(IQR 2.6 ± 5.3)	9 years	Throughout pregnancy	Air Quality System (AQS)

Moderate Resolution Imaging Spectroradiometer

	Particular matter

Nitrogen oxides

Ozone

	International Statistical Classification of Diseases and Related Health Problems (ICD-10)	Mothers with singleton deliveries at Kaiser Permanente Southern California	Maternal age at delivery < 15 or > 55 years of age

Maternal residential address history in pregnancy

	Per interquartile range

(PM2.5 > 7.4 μg/m3

NO2 > 17.4 ppb

O3 > 19.3 ppb)

	Per interquartile range

(PM2.5 < 7.4 μg/m3

NO2 < 17.4 ppb

O3 < 19.3 ppb)

	
Rahman MM, 2023 [55]	United States	Children	370.723	318.750	3.0 (IQR 2.3 ± 3.7)	5 years	Throughout pregnancy	Geocoding	Elemental carbon

Organic carbon

Metals

Inorganic substances

	International Statistical Classification of Diseases and Related Health Problems (ICD-9)	Mothers with singleton deliveries at Kaiser Permanente Southern California	Maternal age at delivery < 15 or > 55 years of age

Maternal residential address history in pregnancy

	Per interquartile range (ng/m3)

EC > 329.10

OC > 1249.74

Cu > 11.06

Fe > 169.56

Mn > 2.75

	Per interquartile range (ng/m3)

EC < 329.10

OC < 1249.74

Cu < 11.06

Fe < 169.56

Mn < 2.75

	
Sagiv SK, 2018 [56]	United States	Adolescents	601	534	14.06 ± 0.23	14 years	First and third trimester of pregnancy	Urine samples

Geocoding

	Dialkyl phosphates

Diethyl phosphates

Dimethyl phosphates

Chlorpyrifos

Diazinon

Malathion

Oxydemeton-methyl

	Social Responsiveness Scale (SRS-2)	 ≥ 18 years old

 < 20 weeks gestation

Spanish or English-speaking

Qualifying for low-income health insurance

Planning to deliver at the public hospital

	Not described	Pollutant unit (nmol/L)

Unit:

Log-normal distribution

	Pollutant unit (nmol/L)

Unit:

Log-normal distribution

	
Van den Dries MA, 2019 [57]	Netherlands	Children	9.778	622	Not described	6 years	Throughout pregnancy and postnatal period	Urine samples	Organophosphates and carbamates	Social Responsiveness Scale (SRS)	Resided in the study area in Rotterdam, the Netherlands	Not described	Pollutant unit (nmol/g)

Unit:

log10 transformed

	Pollutant unit (nmol/g)

Unit:

log10 transformed

	
Von Ehrenstein OS, 2014 [58]	United States	Children	1′745.754	148.722	Not described	5 years	Throughout pregnancy	Geocoding	Volatile organic compounds

Inorganic substances

Hydrocarbons

	Diagnostic and Statistical Manual of Mental Disorders (DSM IV-R) (code 299.00)	Not described	Not described	 > Interquartile range and km Buffers	 < Interquartile range and km Buffers	
Wang SY, 2021 [59]*	China	Adolescents	1′000.000	62.919	15.30 ± 2.20	17 years	Throughout pregnancy	Automatic monitoring stations	Particular matter 10

Carbon monoxide

Nitrogen Dioxide

Sulfur dioxide

Ozone

	Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM)	Not described	Those who had missing data on the insurance enrollment date

Lived outside the Taiwan main island

	Higher than the average exposure level in each trimester	Less than the average exposure level in each trimester	
LOD Lower Detection Limit, PM Particular matter, NO2 Nitrogen dioxide, NOX Nitrogen oxides, O3 Ozone, EC Elemental carbon, OC Organic carbon, Cu Copper/ Fe Iron, Mn Manganese

* Only studies included in the systematic review

Cochran's Q, tau-squared (tau2) tests and I2 statistics were used to test heterogeneity. The I2 statistic interpretation was 0% to 40% might not be significant; 30% to 60% may represent moderate heterogeneity; 50% to 90% may represent substantial heterogeneity; 75% to 100% means considerable heterogeneity [60].

For studies that did not outline the mean and standard deviation, these values were computed using the Hozo et al. method specified in the research conducted by Wan X [61] and colleague.

Risk of bias in studies and certainty of evidence

Two reviewers independently judged the methodological quality of the individual studies (S.K. and E.M.) following the Quality Assessment Tool for Observational Cohort Studies from the National Institute of Health [62]. The studies were classified as good, fair, or poor (Additional file 1: Table S1). The GradePro tool was used to conduct the certainty analysis. The degree of evidence uncertainty was rated as high, moderate, low, and very low.

Results

A total of 5,780 studies were identified, of which 2,723 were duplicates. The remaining 3,057 studies of these 3,019 articles were excluded: 2,501 did not evaluate the association between environmental pollutants and ASD; 513 were studies with another type of design (cross-sectional, case studies, case series, experimental models, reviews, response letters or editorials); and five included participants older than 19 years. Thirty-eight articles were selected to read the full text, of which 11 were excluded: eight did not evaluate the association between air pollutants and ASD, and three had another design. Finally, 27 articles were included in the systematic review, and 22 were included in the meta-analysis (Fig. 1).Fig. 1 Flowchart of the study selection process

The 27 articles included 1,289,183 individuals aged ranging from childhood to adolescence. Twenty-four studies were conducted on children [33–44, 46–48, 50–55, 57, 58] (n = 1,225,715), and three studies were conducted in adolescents [49, 56, 59] (n = 63,468). The average exposure duration was 6,9 years, with follow-up times ranging from 2 years [52] to 17 years [49, 59] across the studies (Table 1).

The studies reported one hundred twenty-nine pollutants, which are air pollutants and toxic substances. Seven studies reported nitrogen dioxide [40, 43, 45, 51, 52, 54, 59]; six studies reported PM 2.5 [37, 40, 43, 51, 52, 54]; five studies reported PM 10 [38, 40, 43, 45, 59]; four studies reported ozone [43, 45, 54, 59] and mono-n-butyl phthalate [33, 36, 41, 46, 50]. diethyl phosphite [33, 47, 53, 56], mono-ethyl phthalate [33, 36, 41, 50], PCB 118 [33, 35, 36, 39], and PCB 153 [33, 35, 36, 39]. Three studies reported bisphenol A [33, 36, 42], dialkyl phosphates [47, 56, 57], dimethyl phosphate [33, 47, 56], manganese [33, 55, 58], mono-(2-ethyl-5-hydroxyhexyl) phthalate [33, 36, 46], mono-3-carboxy propyl phthalate, mono-benzyl phthalate [33, 36, 50], nitrogen oxides [38, 40, 49], PCB 138 and PCB 180 [33, 35, 39]. 3,5,6-Trichloro-2-pyridinol [47, 53], carbon monoxide [45, 59], copper [55, 58], diazinon [47, 56], dimethylthiophosphate [33, 53], lead [33, 58], mono-(2-ethyl-5-oxohexyl) phthalate [33, 46], mono-2-ethyl-hexyl phthalate, trans-nonachlor, β-hexachlorocyclohexane [33, 36], mono-isobutyl phthalate [36, 41], oxychlordane, p,p-dichlorodiphenyldichloroethylene [33, 36], PCB 101 [36, 39], PCB 187 [35, 36] and sulfur dioxide [45, 59] were described in 2 studies each (Additional file 1: Table S2).

And finally, the following pollutants were described in a single study: 1,3-butadiene, acetaldehyde, benzene, chloroform, chromium, ethyl benzene, formaldehyde, hexavalent chromium, meta/para-xylen, methylene chloride, molybdenum, nickel, ortho-dichlorobenzene, ortho-xylene, paradichlorobenzene, perchloroethylene, polycyclic aromatic hydrocarbon, selenium, toluene, trichloroethylene, vanadium [58], 3-phenoxybenzoic acid [34], arsenic, cadmium, mercury, triclosan [33], brominated biphenyl 153, hexachlorobenzene, mono-2-ethyl-5-carboxypentyl phthalate, p,p-dichlorodiphenyltrichloroethane, perfluorohexane sulfonate, perfluorononanoate, perfluorooctane sulfate, perfluorooctanoate, polybrominated diphenyl ether (PBDE) 100, PBDE 153, PBDE 154, PBDE 183, PBDE 28, PBDE 47, PBDE 85, PBDE 99, PCB 172, PCB 105, PCB 138/158, PCB 146, PCB 156, PCB 157, PCB 167, PCB 170, PCB 177, PCB 178, PCB 183, PCB 194, PCB 195, PCB 196/203, PCB 199, PCB 206, PCB 209, PCB 28, PCB 66, PCB 74, PCB 99 [36], chlorpyrifos, malathion, oxydemeton-methyl [56], chlropyrifos-oxon, terbufos, [47], di-(2-ethylhexyl) phthalate [41], diethyl alkyl phosphates, dimethyl alkyl phosphates [57], elemental carbon, iron, organic carbon [55], nitric oxide [51], organochlorine, organophosphate [44], PM 2.5 absorbance, PM coarse [40], PCB 11, PCB 132, PCB 136, PCB 174, PCB 175, PCB 176, PCB 196, PCB 52, PCB 77, PCB 84, PCB 91, PCB 95 [39], polychlorinated biphenyls, polychlorinated dibenzo-p-dioxins and dibenzofurans [48] and three metabolites of di-(2-ethylhexyl) phthalate [50] (Additional file 1: Table S2).

Results of the association between environmental pollutants and ASD from individual studies

Individual studies reported a significant association with the following contaminants: cadmium, bisphenol A [33], PCB 138 [35], PBDE 28, PBDE 47, PBDE 99, PBDE 100, PBDE 154 [36], PM 2.5 [37, 43, 51, 52, 54], PCB 101 [39], mono-i-butyl phthalate [41], nitrogen dioxide [43, 45, 51, 59], carbon monoxide [45, 59], sulfur dioxide [45], chlropyrifos-oxon [47], nitrogen oxides [49], mono-n-butyl phthalate, mono-3-carboxypropyl phthalate [33, 50], nitric oxide [51], elemental carbon, organic carbon, iron, manganese [55], dialkylphosphates, dimethylphosphate [56], benzene, perchloroethylene, 1,3-butadiene, toluene, ortho-xylene, meta/para-xylen, ethyl benzene, lead, acetaldehyde, formaldehyde, trichloroethylene [58] and copper [55, 58] (Additional file 1: Table S3).

A significant association was also reported with PCB 74, PCB 146, PCB 153, PCB 156, PCB 157, PCB 170, PCB 172, PCB 177, PCB 178, PCB 183, PCB 187, PCB 194, PCB 195, PCB 196/203, PCB 199, PCB 209, β-hexachlorocyclohexane [36], brominated biphenyl 153, PCB 136, PCB 175, PCB 176 [39], ozone [45], polychlorinated dibenzo-p-dioxins and dibenzofurans [48], diethyl alkyl phosphates [57], vanadium [58] and PM 10 [59] (Additional file 1: Table S3). No significant associations were reported with the remaining pollutants.

Quality of studies

The evaluation of the quality of the studies is presented in Additional file 1: Table S1 and Figure S2. When carrying out this analysis, it was found that the majority of the included studies (n = 22) showed high quality [33–35, 37–40, 42, 43, 45, 46, 48–55, 57–59], a smaller proportion (n = 5) presented fair quality [36, 41, 44, 47, 56], and none presented poor quality.

Meta-analysis

The results of the individual and subgroup meta-analyses are presented below. It should be noted that, on some occasions, meta-analyses included the same study because they provide results for different environmental pollutants.

Meta-analysis of each pollutant and its association with ASD

The first meta-analysis was performed separately for each pollutant, and a significant association was found with nitrogen dioxide, copper, mono-3-carboxypropyl phthalate, monobutyl phthalate and PCB 138 (Additional file 1: Figure S2). Additionally, these meta-analyses suggest a potential association with PM 10 (Additional file 1: Figure S3). No associations were found with the other pollutants.

The association between nitrogen dioxide and ASD was significant RR 1.20 (95% CI: 1.03 to 1.38). However, this association showed high heterogeneity among studies (I2 = 91%) (Fig. 2). Conversely, copper exposure displayed a significant association with ASD, with an RR of 1.08 (95% CI: 1.03 to 1.13) and low heterogeneity (I2 = 0%) (Fig. 3A).Fig. 2 Meta-analysis association between nitrogen dioxide and ASD

Fig. 3 Meta-analysis association (A) copper; B mono-3-carboxypropyl phthalate; C monobutyl phthalate; D PCB 138 with ASD

Similarly, exposure to mono-3-carboxy propyl phthalate was associated with ASD (β = 0.45, 95% CI: 0.20 to 0.70), with low heterogeneity (I2 = 0%) (Fig. 3B). Monobutyl phthalate also exhibited a positive coefficient (β = 0.43, 95% CI: 0.13 to 0.73) with low heterogeneity (I2 = 0%) (Fig. 3C). Lastly, PCB 138 showed an association with ASD, reflected in an RR of 1.84 (95% CI: 1.14 to 2.96) and low heterogeneity (I2 = 0%) (Fig. 3D).

Meta-analysis by subgroups of pollutants and their association with ASD

The pollutants were classified into 16 subgroups: ground-level ozone; PM; carbon monoxide; sulfur oxides; nitrogen oxides; volatile organic compounds; dioxins, furans, PCBs; hydrocarbons; inorganic substances; metals; organophosphates and carbamates; pesticides; phthalates; phenols/phenoxy acids; polyfluoroalkyl substances and plastics. Positive associations were found with carbon monoxide, nitrogen oxides, and metals (Fig. 4) (Additional file 1: Figure S2). A negative association with organophosphates and carbamates was observed (Fig. 5). Finally, potential associations with ozone (Additional file 1: Figure S4), PM (Additional file 1: Figure S5), inorganic substances (Additional file 1: Figure S6), pesticides (Additional file 1: Figure S7), dioxins, furans, and PCBs (Additional file 1: Figure S8).Fig. 4 Meta-analysis association of (A) carbon monoxide, B nitrogen oxides, and (C) metals with ASD

Fig. 5 Meta-analysis association between organophosphates and carbamates and ASD

Also, the association between carbon monoxide and ASD was found to be significant, with an RR of 1.57 (95% CI: 1.25 to 1.97) and low heterogeneity (I2 = 0%), (Fig. 4A). Nitrogen oxides, including nitrogen dioxide and nitric oxides, were also associated with ASD, with an RR of 1.09 (95% CI: 1.04 to 1.15) and moderate heterogeneity (I2 = 34%) (Fig. 4B).

Metal elements such as iron and molybdenum were linked to ASD with an RR of 1.13 (95% CI: 1.01 to 1.27) and low heterogeneity (I2 = 24%) (Fig. 4C). Conversely, exposure to organophosphates and carbamates, which include compounds such as diethyl phosphate, dimethyl phosphate, dimethyl thiophosphate, dialkyl phosphates, diethyl alkyl phosphates, and dimethyl alkyl phosphates, showed a negative association with ASD (β = -0.49, 95% CI: -0.85 to -0.13) and high heterogeneity (I2 = 85%) (Fig. 5).

Sensitivity analysis

For the sensitivity analysis, we pooled the studies by pollutant and according to the instrument applied to determine autism, either diagnosis or screening. Once the meta-analyses were carried out, the results remained constant for nitrogen dioxide with diagnostic tools (Additional file 1: Figure S9), copper (Additional file 1: Figure S10), mono-3-carboxy propyl phthalate (Additional file 1: Figure S11), and mono-n-butyl phthalate (Additional file 1: Figure S12) with screening instruments. PCB 138 could not be meta-analyzed because there were not enough studies with either of the two types of tools.

In the case of the subgroups, the association between pollutants and ASD was maintained in carbon monoxide with diagnostic instruments (Additional file 1: Figure S13), nitrogen oxides with diagnostic and monitoring tools (Additional file 1: Figure S14-15), metals with diagnostic instruments (Additional file 1: Figure S16), and organophosphates and carbamates with monitoring instruments (Additional file 1: Figure S17). Finally, when meta-analyzed only with tracking instruments, the PM found as a possible association reported a significant association (Additional file 1: Figure S18).

Certainty of evidence

The analysis of evidence certainty using the GradePro tool consistently reveals a landscape characterized by low or very low certainty across all conducted analyses. The main factors contributing to this were heterogeneity between studies and the risk of publication bias (Additional file 1: Table S4-S7).

Discussion

This systematic review and meta-analysis investigated the association between environmental pollutants and the incidence ASD in children and adolescents. The results indicated that exposure to individual pollutants such nitrogen dioxide, copper, mono-3-carboxy propyl phthalate, monobutyl phthalate, and PCB 138 increases the risk of developing ASD. Subgroup analyses further linked carbon monoxide, nitrogen oxides, and metals to higher ASD risk. Additionally, trends suggested associations between ASD and exposure to particulate matter, inorganic substances, and pesticides. The associations found in this study can be explained according to the pollutant type, individually or by subgroup.

The associations with PCB 138 [19, 63], carbon monoxide [7], nitrogen oxides [10], and metals [64, 65] and risk of ASD were consistent with findings from other systematic reviews. However, there were discrepancies between those with nitrogen dioxide [10, 15], copper [66], mono-3-carboxypropyl phthalate and monobutyl phthalate [67, 68] and other reviews.

Differences can justify the possible differences between our findings from other reviews can be justified that some studies carried out subgroup analyses by exposure time [10, 15], did not only include a cohort study [15], considering the exposure window [15], the differences between pollutant concentrations and other methodologies for estimating associations [67, 68].

It is recognized that environmental pollutants disrupt cellular metabolism through mechanisms like breaching cell membranes, intracellular accumulation, and inhibition of critical metabolic pathways [69]. For instance, heavy metals can trigger oxidative stress by generating reactive oxygen species, which can harm lipids, proteins, and DNA and compromise mitochondrial function, potentially leading to cell death, tissue damage, or neurological disorders [70]. Particulate matter and polycyclic aromatic hydrocarbons can breach the blood–brain barrier, initiating brain inflammation that may disrupt neurotransmitter systems and synaptic function [69]. Persistent immune system activation by pollutants can induce chronic neuroinflammation, disrupting brain architecture connectivity and impeding normal brain development [71].

Moreover, pollutants can cause DNA damage, leading to epigenetic alterations like DNA methylation and histone modifications that influence gene expression tied to brain development and function [72, 73]. This, in turn, could potentially contribute to the pathophysiology of ASD. Compelling evidence suggests that environmental contaminants significantly impact cellular metabolism and neurological well-being, connecting these molecular changes to broader neurodevelopmental consequences [55, 74].

Exposure routes to environmental pollutants are crucial in ASD pathogenesis. Alterations in neuronal connectivity, occurring from prenatal to early adulthood, can result from genetic and epigenetic factors [76]. The ENVIRONAGE cohort study found that increased PM 2.5 exposure during pregnancy was associated with relationship and prosocial behavior problems in preschoolers [76]. These effects may be due to higher mutation rates and DNA repair alterations during fetal and neonatal stages [72]. Conversely, low-pollution maternal environments are associated with beneficial DNA methylation in neurodevelopmental genes, highlighting the importance of pollution levels and particulate matter composition in understanding ASD risk [73].

The characteristics of the population may impact the associations identified in this meta-analysis study and the timing of exposure. ASD symptoms typically manifest early in life, exerting significant developmental effects during the prenatal and early postnatal periods [76]. Both acute and chronic exposure to environmental pollutants during these critical phases can influence neurogenesis and neuronal maturation [76]. Evidence suggests that prenatal and postnatal exposure to contaminants can bring about developmental alterations in children, with the developing nervous system being especially vulnerable to environmental toxins, even at low exposure levels [76]. Accurate assessment of the timing of contaminant exposure is crucial for comprehending the underlying mechanisms and crafting effective interventions.

Recognizing that the absence of significant associations with specific contaminants, individually or in combination, or inconclusive findings does not imply their non-existence is crucial. Further research is imperative to pinpoint the risk factors contributing to our understanding of ASD and to inform the development of enhanced preventive measures.

Strengths and limitations of the systematic review

Our systematic review stands out for several key reasons. Firstly, it adopts a broad approach, incorporating a wide array of databases and gray literature sources. Unlike other reviews, our search was not constrained by time or language, ensuring inclusivity and breadth of scope. Additionally, we excluded observational studies, which often present limitations for causal inference, thereby enhancing the robustness of our findings.

Furthermore, our review maintained a stringent focus on studies of high methodological quality, ensuring the reliability of our results. Unlike comparable reviews, our analysis encompassed a broad range of contaminants, facilitating a deeper understanding of their impact on ASD incidence. Moreover, our study evaluated the effects of both individual and grouped contaminants, offering a novel perspective on the issue.

This study also has some limitations. First, the studies included a variability of exposure time, pollutant detection method, and the instrument used to determine ASD. However, to avoid overestimating the effect, sensitivity analyses were performed that supported the validity of the association with ASD. In addition, the instruments, although diverse, are all approved by the scientific community for the screening or diagnosis of ASD. Second, some meta-analyses had high heterogeneity.

In summary, our systematic review represents an original contribution to the field, distinguished by its meticulous methodology, broad inclusion, and comprehensive analysis of the effects of pollutants on the incidence of autism.

Conclusion and future directions

This systematic review and meta-analysis suggest that children and adolescents exposed to higher contamination levels by pollutants such as nitrogen dioxide, copper, mono-3-carboxy propyl phthalate, mono butyl phthalate, and PCB 138 have a higher risk of developing ASD. Likewise, those exposed to subgroups of environmental pollutants such as carbon monoxide, nitrogen oxides, and metals were associated with ASD. Therefore, it is important to identify the factors that underlie the susceptibility of children and adolescents to contribute effectively to ASD and identify prevention strategies. Future studies should standardize the exposure time to pollutants and the detection methods, allowing for more precise comparisons and better interpretation of the results.

Supplementary Information

Supplementary Material 1

Abbreviations

ASD Autism Spectrum Disorder

CDC Centers for Disease Control and Prevention

PM Particulate matter

PRISMA Preferred Reporting Items for Systematic Reviews and Meta-Analyses

PCBs Polychlorinated biphenyls

VOC Volatile organic compounds

CO Carbon monoxide

SOx Sulfur oxides

NOx Nitrogen oxides

COCHRANE CENTRAL Cochrane Central Register of Controlled Trials

CINAHL Cumulative Index to Nursing and Allied Health Literature

SciELO Scientific Electronic Library Online

EMBASE Excerpta Medica Database

PsycINFO American Psychological Association database

WoS Web of Science

RR Relative risk

β Beta coefficient

95% CI 95% confidence intervals

IVhet Inverse variance heterogeneity

ES Estimate

Acknowledgements

Not applicable.

Authors' contributions

TDC: methodology, formal analysis, investigation, data curation, writing—original draft, writing—revision and editing. MDBD: conceptualization methodology, validation, investigation, writing—review, and editing. EM: investigation, validation and writing – review and editing. FKN: investigation and writing – review and editing. SE: investigation and writing – review and editing. SKM: investigation and writing – review and editing. GZ: investigation and writing – review and editing. AVP: writing – review and editing. JGP: writing – review and editing. ATS: writing – review and editing. WCM: methodology, formal analysis, writing – review and editing. RM: conceptualization, methodology, validation, investigation, data curation, writing—original draft, writing—revision and editing, supervision, project administration. All authors read and approved the final manuscript.

Funding

Rio Grande do Sul Research Support Foundation (FAPERGS), the National Research Council of Brazil (CNPq), the Coordination for the Improvement of Higher Education Personnel (CAPES—Financial Code 001) and Ministry of Science, Technology and Innovation of Colombia grant No. 751–2018.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Data availability

No datasets were generated or analysed during the current study.

Declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Publisher's Note

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