Mixture effects of prenatal exposure to polybrominated diphenyl ethers on urinary oxidative stress biomarkers in the Chemicals in Our Bodies Cohort

Author:

Sehgal Neha1,Morello-Frosch Rachel23,Padula Amy M3,DeMicco Erin3,Wang Yunzhu4,Smith Sabrina4,Park June-Soo34,Milne Ginger L5,Woodruff Tracey J3,Eick Stephanie M1

Affiliation:

1. Emory University Gangarosa Department of Environmental Health, Rollins School of Public Health, , Atlanta, GA, USA

2. University of California Department of Environmental Science, Policy and Management and School of Public Health, , Berkeley

3. University of California Program on Reproductive Health and the Environment, Department of Obstetrics, Gynecology and Reproductive Sciences, , San Francisco

4. Environmental Chemistry Laboratory , Department of Toxic Substances Control, California Environmental Protection Agency

5. Vanderbilt University Medical Center Division of Clinical Pharmacology, Department of Medicine,

Abstract

Abstract Polybrominated diphenyl ethers (PBDEs) exposure is associated with preterm birth. Laboratory studies suggest that PBDEs lead to elevated oxidative stress, a known contributor to preterm birth in epidemiologic studies. We hypothesized that elevated levels of PBDEs would be associated with increased oxidative stress during human pregnancy. Participants in this analysis were enrolled in the Chemicals in Our Bodies cohort and resided in the San Francisco Bay Area (N=201). Four PBDEs (BDE-47, -99, -100, -153) were measured in second trimester serum. Urinary oxidative stress biomarkers were measured at two timepoints (second and third trimester) and included 8-isoprostane-prostaglandin-F2α [8-iso-PGF2α], 2,3-dinor-5,6-dihydro-8-iso-PGF2α, 2,3-dinor-8-iso-PGF2α, and prostaglandin-F2α [PGF2α]. Associations between individual PBDEs and oxidative stress biomarkers (averaged and trimester specific) were examined using linear regression. Quantile g-computation and Bayesian kernel machine regression (BKMR) were used to assess cumulative effects of PBDEs. Quantile g-computation showed that higher concentrations of PBDEs were associated with increasing 8-iso-PGF2α, 2,3-dinor-8-iso-PGF2α, and PGF2α. Associations were greatest in magnitude for second trimester levels of 2,3-dinor-8-iso-PGF2α (mean change per quartile increase=0.25, 95% confidence interval=0.09, 0.41). Associations were similar using BKMR and linear regression. Our findings suggest that oxidative stress may be a plausible biological pathway by which PBDE exposure might lead to preterm birth.

Publisher

Oxford University Press (OUP)

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