In utero pyrethroid pesticide exposure in relation to autism spectrum disorder (ASD) and other neurodevelopmental outcomes at 3 years in the MARBLES longitudinal cohort.


Journal

Environmental research
ISSN: 1096-0953
Titre abrégé: Environ Res
Pays: Netherlands
ID NLM: 0147621

Informations de publication

Date de publication:
03 2021
Historique:
received: 29 05 2020
revised: 12 11 2020
accepted: 13 11 2020
pubmed: 22 11 2020
medline: 22 4 2021
entrez: 21 11 2020
Statut: ppublish

Résumé

We assessed the relationships between prenatal pyrethroid pesticide exposure and autism spectrum disorders (ASD) or non-typical development (non-TD) at 3 years. Participants were mother-child pairs (n = 201) in the MARBLES (Markers of Autism Risk in Babies-Learning Early Signs) cohort. Because familial recurrence risk is high, MARBLES enrolls pregnant women with a family history of ASD. Children from these pregnancies were clinically assessed at 3 years of age and classified into 3 outcome categories: ASD, typically developing (TD), or non-TD (neither TD or ASD). Repeated maternal second and third trimester urine samples were analyzed for pyrethroid metabolite 3-phenoxybenzoic acid (3-PBA). Multinomial logistic regression was used to obtain relative risk ratios (RRR) linking 3-PBA concentrations averaged across each trimester and over pregnancy with child's outcome: ASD or non-TD vs. TD. Models were adjusted for specific gravity, maternal pre-pregnancy BMI, prenatal vitamin use, birth year, home-ownership, and pregnancy concentrations of TCPy (3,5,6-trichloro-2-pyridinol, a metabolite of chlorpyrifos). The median specific gravity corrected 3-PBA concentration of all samples was 1.46 ng/mL. Greater second trimester 3-PBA concentrations were associated with a relative risk ratio (RRR) for ASD of (RRR: 1.50 (95% CI 0.89 to 2.51), p = 0.12). There were no differences between non-TD and TD. This study found no evidence for differences in 3-PBA comparing non-TD with TD. A modestly elevated RRR was found comparing second trimester urinary 3-PBA concentrations for ASD versus TD; however, the confidence interval was wide and hence, these findings cannot be considered definitive.

Sections du résumé

BACKGROUND
We assessed the relationships between prenatal pyrethroid pesticide exposure and autism spectrum disorders (ASD) or non-typical development (non-TD) at 3 years.
METHODS
Participants were mother-child pairs (n = 201) in the MARBLES (Markers of Autism Risk in Babies-Learning Early Signs) cohort. Because familial recurrence risk is high, MARBLES enrolls pregnant women with a family history of ASD. Children from these pregnancies were clinically assessed at 3 years of age and classified into 3 outcome categories: ASD, typically developing (TD), or non-TD (neither TD or ASD). Repeated maternal second and third trimester urine samples were analyzed for pyrethroid metabolite 3-phenoxybenzoic acid (3-PBA). Multinomial logistic regression was used to obtain relative risk ratios (RRR) linking 3-PBA concentrations averaged across each trimester and over pregnancy with child's outcome: ASD or non-TD vs. TD. Models were adjusted for specific gravity, maternal pre-pregnancy BMI, prenatal vitamin use, birth year, home-ownership, and pregnancy concentrations of TCPy (3,5,6-trichloro-2-pyridinol, a metabolite of chlorpyrifos).
RESULTS
The median specific gravity corrected 3-PBA concentration of all samples was 1.46 ng/mL. Greater second trimester 3-PBA concentrations were associated with a relative risk ratio (RRR) for ASD of (RRR: 1.50 (95% CI 0.89 to 2.51), p = 0.12). There were no differences between non-TD and TD.
CONCLUSIONS
This study found no evidence for differences in 3-PBA comparing non-TD with TD. A modestly elevated RRR was found comparing second trimester urinary 3-PBA concentrations for ASD versus TD; however, the confidence interval was wide and hence, these findings cannot be considered definitive.

Identifiants

pubmed: 33220244
pii: S0013-9351(20)31392-X
doi: 10.1016/j.envres.2020.110495
pmc: PMC7946720
mid: NIHMS1658966
pii:
doi:

Substances chimiques

Pesticides 0
Pyrethrins 0
Calcium Carbonate H0G9379FGK

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

110495

Subventions

Organisme : NIEHS NIH HHS
ID : P01 ES011269
Pays : United States
Organisme : NIEHS NIH HHS
ID : R01 ES020392
Pays : United States
Organisme : NICHD NIH HHS
ID : U54 HD079125
Pays : United States
Organisme : NIEHS NIH HHS
ID : P30 ES023513
Pays : United States
Organisme : NICHD NIH HHS
ID : P50 HD103526
Pays : United States
Organisme : NIEHS NIH HHS
ID : P30 ES019776
Pays : United States
Organisme : NIEHS NIH HHS
ID : R24 ES028533
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Références

Environ Health Perspect. 2017 May 25;125(5):057002
pubmed: 28557711
Nat Genet. 2014 Aug;46(8):881-5
pubmed: 25038753
JAMA. 2013 Feb 13;309(6):570-7
pubmed: 23403681
JAMA Psychiatry. 2019 Apr 1;76(4):391-398
pubmed: 30810722
J Am Acad Child Adolesc Psychiatry. 2014 Apr;53(4):398-407.e2
pubmed: 24655649
Environ Sci Pollut Res Int. 2017 Jul;24(19):15949-15958
pubmed: 28540549
Environ Res. 2018 Aug;165:400-409
pubmed: 29860212
Arch Toxicol. 2012 Feb;86(2):165-81
pubmed: 21710279
J Am Acad Child Adolesc Psychiatry. 2014 Dec;53(12):1317-1327.e1
pubmed: 25457930
Occup Environ Med. 2017 Mar;74(4):275-281
pubmed: 28250046
Neurotoxicology. 2017 Sep;62:231-238
pubmed: 28811173
Sci Rep. 2019 Mar 14;9(1):4529
pubmed: 30872602
Int J Environ Res Public Health. 2017 May 09;14(5):
pubmed: 28486423
Mol Pharmacol. 2014 Apr;85(4):630-9
pubmed: 24482397
Pediatrics. 2012 May;129(5):e1121-8
pubmed: 22492772
Environ Health Perspect. 2006 Sep;114(9):1419-23
pubmed: 16966099
Indoor Air. 2014 Aug;24(4):390-402
pubmed: 24387593
Environ Res. 2016 May;147:307-13
pubmed: 26922411
Environ Health Perspect. 2014 Oct;122(10):1103-9
pubmed: 24954055
Arch Gen Psychiatry. 2011 Nov;68(11):1095-102
pubmed: 21727249
Toxicol In Vitro. 2010 Oct;24(7):2053-7
pubmed: 20800091
PLoS Med. 2018 Oct 24;15(10):e1002671
pubmed: 30356230
Anal Chem. 2004 May 1;76(9):2453-61
pubmed: 15117183
Toxicol Lett. 2015 Jan 22;232(2):369-75
pubmed: 25498136
Pediatrics. 2006 Dec;118(6):e1845-59
pubmed: 17116700
Environ Health Perspect. 2010 Jun;118(6):742-8
pubmed: 20129874
Neurosci Lett. 2001 Mar 16;300(3):161-5
pubmed: 11226636
Vet Hum Toxicol. 1993 Apr;35(2):119-22
pubmed: 8385837
Am J Clin Nutr. 2012 Jul;96(1):80-9
pubmed: 22648721
Nutr Res. 2019 May;65:4-16
pubmed: 30952506
Environ Health. 2018 Dec 5;17(1):85
pubmed: 30518373
J Child Psychol Psychiatry. 1977 Sep;18(4):297-321
pubmed: 562353
Environ Health Perspect. 2007 May;115(5):792-8
pubmed: 17520070
Environ Sci Technol. 2014;48(3):1931-9
pubmed: 24422434
Mol Psychiatry. 2013 Feb;18(2):137-8
pubmed: 22371046
MMWR Surveill Summ. 2020 Mar 27;69(4):1-12
pubmed: 32214087
JAMA Psychiatry. 2018 Feb 1;75(2):176-184
pubmed: 29299606
JAMA Psychiatry. 2019 Oct 1;76(10):1035-1043
pubmed: 31314057
Pediatrics. 2016 Feb;137(2):e20152206
pubmed: 26826214
BMJ. 2019 Mar 20;364:l962
pubmed: 30894343
Pediatrics. 2011 Mar;127(3):e699-706
pubmed: 21300677
Environ Health Perspect. 2006 Feb;114(2):260-3
pubmed: 16451864
Environ Health Perspect. 2005 Feb;113(2):123-36
pubmed: 15687048
Int J Hyg Environ Health. 2018 Apr;221(3):548-555
pubmed: 29478806
Environ Health Perspect. 2007 Oct;115(10):1482-9
pubmed: 17938740
Epidemiology. 2011 Jul;22(4):476-85
pubmed: 21610500
Environ Int. 2015 Sep;82:69-75
pubmed: 26057254
Environ Health Perspect. 2018 Nov;126(11):117004
pubmed: 30465702
JAMA. 2014 May 7;311(17):1770-7
pubmed: 24794370
Environ Health Perspect. 2004 Dec;112(17):1734-40
pubmed: 15579421
Psychol Med. 1995 Jan;25(1):63-77
pubmed: 7792363

Auteurs

Jacqueline M Barkoski (JM)

Department of Public Health Sciences, School of Medicine, University of California, Davis, CA, USA. Electronic address: jmbarkoski@ucdavis.edu.

Claire Philippat (C)

University Grenoble Alpes, Inserm, CNRS, Team of Environmental Epidemiology applied to Reproduction and Respiratory Health, Institute for Advanced Biosciences (IAB), Grenoble, France.

Daniel Tancredi (D)

Department of Pediatrics, School of Medicine, University of California, Davis, CA, USA.

Rebecca J Schmidt (RJ)

Department of Public Health Sciences, School of Medicine, University of California, Davis, CA, USA; MIND (Medical Investigations of Neurodevelopmental Disorders) Institute, University of California, Davis, CA, USA.

Sally Ozonoff (S)

MIND (Medical Investigations of Neurodevelopmental Disorders) Institute, University of California, Davis, CA, USA; Department of Psychiatry and Behavioral Sciences, School of Medicine, University of California, Davis, CA, USA.

Dana Boyd Barr (DB)

Rollins School of Public Health, Emory University, Atlanta, GA, USA.

William Elms (W)

Department of Public Health Sciences, School of Medicine, University of California, Davis, CA, USA.

Deborah H Bennett (DH)

Department of Public Health Sciences, School of Medicine, University of California, Davis, CA, USA.

Irva Hertz-Picciotto (I)

Department of Public Health Sciences, School of Medicine, University of California, Davis, CA, USA; MIND (Medical Investigations of Neurodevelopmental Disorders) Institute, University of California, Davis, CA, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH