Metabolome Wide Association Study of Serum Poly and Perfluoroalkyl Substances (PFASs) in Pregnancy and Early Postpartum.

Reprod Toxicol

The Center for Research on Women and Children's Health, Child Health and Development Studies, Public Health Institute, 1683 Shattuck Avenue, Suite B, Berkeley, CA 94709, USA. Electronic address:

Published: August 2019

AI Article Synopsis

  • High-resolution metabolomics profiling of maternal serum samples helps to understand how poly and perfluoroalkyl substances (PFASs) affect fetal health by altering their metabolic environment.
  • Metabolome-Wide Association Studies (MWAS) revealed distinct metabolic profiles related to PFAS compounds, specifically highlighting differences between the precursor EtFOSAA and the end product PFOS.
  • Key findings include opposing associations of urea cycle metabolites with these substances and unique links between PFOS and fatty acid metabolism, suggesting how PFAS exposure might contribute to health risks during pregnancy.

Article Abstract

High-resolution metabolomics (HRM) profiling of metabolic fingerprints can improve understanding of how poly and perfluoroalkyl substances (PFASs) induce metabolic alterations of in utero environment and impact fetal health. HRM profiling and quantification of PFASs were performed for 397 maternal perinatal serum samples collected from 1959-1967 in the Child Health and Development Studies (CHDS). We used Metabolome-Wide Association Studies (MWAS) and pathway enrichment analysis for metabolic associations with PFOS, its precursor EtFOSAA, and EtFOSAA-to-PFOS ratio. Distinct metabolic profiles were found with EtFOSAA and PFOS. Urea cycle metabolites such as arginine, lysine and creatine had opposite associations with EtFOSAA (negative) and PFOS (positive); whereas, carnitine shuttle metabolites were found to be exclusively and positively associated with PFOS indicating perturbation in fatty acid metabolism. These differential metabolic associations for precursor and end-product represent an important first step in identifying how PFASs alter the in utero environment and potentially leads to disease risk.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7117788PMC
http://dx.doi.org/10.1016/j.reprotox.2019.05.058DOI Listing

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