Abstract

BackgroundOrganophosphate esters (OPEs) are synthetic chemicals used as flame retardants and plasticizers in a variety of goods. Despite ubiquitous human exposures and laboratory evidence that prenatal OPE exposures may disrupt offspring metabolism, perinatal studies of OPE health effects are limited. The objectives of this study were to: 1) Determine predictors and reproducibility of urinary OPE biomarker concentrations during pregnancy, and 2) Estimate the relation of prenatal OPE exposures with birth outcomes and cord blood adipokine and insulin concentrations.MethodsWe analyzed five OPE metabolites in urine samples collected at up to three visits during pregnancy from 90 women enrolled in the ORigins of Child Health And Resilience in Development (ORCHARD) pregnancy cohort in Baltimore, MD from 2017 to 2019. To quantify the variability of metabolite concentrations during pregnancy, we calculated intraclass correlation coefficients (ICCs) for each metabolite using mixed effects regression models. Using self-reported questionnaire data collected during gestation, we assessed possible sociodemographic and environmental/behavioral predictors of each OPE metabolite using generalized estimating equations to account for repeated exposure measures. We ascertained birth outcomes of 76 offspring from medical records, including weight-for-gestational age, length, ponderal index, and gestational age. In a subset of 37 infants, we measured cord blood concentrations of leptin, adiponectin, and insulin. To account for repeated exposure measures, we used linear structural equation models to assess the relations of standard deviation (SD) increases in prenatal OPE metabolite factor scores with continuous birth outcomes and cord blood biomarker concentrations.ResultsICCs ranged from 0.09 for isopropylphenyl-phenyl phosphate (ip-PPP) to 0.59 for bis(1,3-dichloro-2-propyl) phosphate (BDCIPP). We observed little consistency in environmental or behavioral predictors of OPE exposures, although concentrations were generally lower for samples collected in the afternoon compared to morning and winter compared to other seasons. In adjusted analyses, a SD increase in BDCIPP concentration was associated with a 0.06 g/cm3 (95% CI: 0.00, 0.12) greater ponderal index. A SD increase in BDCIPP was associated with a 0.37 (95% CI: − 0.62, − 0.13) SD lower insulin concentration and 0.24 (95% CI: − 0.39, − 0.08) SD lower leptin concentration. Other OPEs were not associated with infant outcomes.ConclusionsThese findings suggest some OPEs may be metabolic disruptors warranting investigation in larger studies.

Highlights

  • Organophosphate esters (OPEs) are a class of synthetic chemicals primarily used as additive flame retardants that are found in a variety of products including clothing, furniture, electronics, and baby products [1,2,3]

  • We observed little consistency in environmental or behavioral predictors of OPE exposures, concentrations were generally lower for samples collected in the afternoon compared to morning and winter compared to other seasons

  • A standard deviation (SD) increase in BDCIPP concentration was associated with a 0.06 g/cm3 greater ponderal index

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Summary

Introduction

Organophosphate esters (OPEs) are a class of synthetic chemicals primarily used as additive flame retardants that are found in a variety of products including clothing, furniture (i.e., polyurethane foam), electronics, and baby products [1,2,3]. Studies report widespread exposure to pregnant women and toddlers as measured using urinary biomarkers of exposure [2, 11,12,13,14]. Short half-lives of OPEs may lead to exposure misclassification when a single measure is used for exposure characterization [21]. Organophosphate esters (OPEs) are synthetic chemicals used as flame retardants and plasticizers in a variety of goods. The objectives of this study were to: 1) Determine predictors and reproducibility of urinary OPE biomarker concentrations during pregnancy, and 2) Estimate the relation of prenatal OPE exposures with birth outcomes and cord blood adipokine and insulin concentrations

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