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Prenatal exposures to organophosphate ester metabolites and early motor development in the MADRES cohort.

Authors :
Hernandez-Castro I
Eckel SP
Chen X
Yang T
Vigil MJ
Foley HB
Kannan K
Robinson M
Grubbs B
Lerner D
Lurvey N
Al-Marayati L
Habre R
Dunton GF
Farzan SF
Aung MT
Breton CV
Bastain TM
Source :
Environmental pollution (Barking, Essex : 1987) [Environ Pollut] 2024 Feb 01; Vol. 342, pp. 123131. Date of Electronic Publication: 2023 Dec 11.
Publication Year :
2024

Abstract

Organophosphate esters (OPEs) are increasingly considered neurotoxicants which may impact gross and fine motor development. We evaluated associations between prenatal OPE exposures and infant motor development. Third trimester urinary concentrations of nine OPE metabolites were measured in 329 mother-infant dyads participating in the Maternal And Developmental Risks from Environmental and Social Stressors (MADRES) cohort. Child gross and fine motor development at 6, 9, 12, and 18-months were assessed with the Ages and Stages Questionnaire-3 (ASQ-3) and operationalized in models using dichotomous instrument-specific cutoffs for typical motor development. Five OPE metabolites with >60% detection were specific-gravity-adjusted, natural log-transformed, and modeled continuously, while four metabolites with <60% detection were modeled dichotomously (detected/not-detected). We fit mixed effects logistic regression between OPE metabolites and fine/gross motor development and assessed sex-specific effects using a statistical interaction term and sex-stratified models. Among children, 31% and 23% had gross and fine motor scores, respectively, below the ASQ-3 at-risk cutoffs at least once across infancy. A doubling in prenatal diphenyl phosphate (DPHP) exposure was associated with 26% increased odds of potential fine motor delays (OR <subscript>fine</subscript>  = 1.26, 95% CI: 1.02, 1.57, p = 0.04). We also observed significant interactions by infant sex for associations of detected dipropyl phosphate (DPRP) with gross motor development (p <subscript>interaction</subscript>  = 0.048) and detected bis(1-chloro-2-propyl) phosphate (BCIPP) with fine motor development (p <subscript>interaction</subscript>  = 0.02). Females had greater odds of potential motor delays for both detected DPRP (females vs males OR <subscript>gross</subscript> (95% CI) = 1.48 (0.71, 3.09), p = 0.30 vs 0.27 (0.06, 1.29), p = 0.10) and detected BCIPP (females vs males OR <subscript>fine</subscript> (95% CI) = 2.72 (1.27, 5.85), p = 0.01 vs 0.76 (0.31, 1.90), p = 0.56). There were no other significant associations between other metabolites and motor development, despite similar patterns. We found evidence of adverse effects of prenatal OPE exposures on infant motor development with greater adverse effects among female infants with some OPE metabolites.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1873-6424
Volume :
342
Database :
MEDLINE
Journal :
Environmental pollution (Barking, Essex : 1987)
Publication Type :
Academic Journal
Accession number :
38092343
Full Text :
https://doi.org/10.1016/j.envpol.2023.123131