Department of Medicine, School of Medicine, Emory University, Atlanta, GA 30303, USA.
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.
Reprod Toxicol. 2019 Aug;87:70-78. doi: 10.1016/j.reprotox.2019.05.058. Epub 2019 May 20.
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.
高分辨率代谢组学(HRM)分析代谢指纹图谱可以帮助我们更好地理解多氟和全氟烷基物质(PFAS)如何改变宫内环境并影响胎儿健康。本研究对 1959 年至 1967 年期间在儿童健康与发展研究(CHDS)中收集的 397 例孕产妇围生期血清样本进行了 HRM 分析和 PFASs 定量分析。我们采用代谢组学全基因组关联研究(MWAS)和通路富集分析,研究了 PFOS、其前体 EtFOSAA 和 EtFOSAA 与 PFOS 比值与代谢物的相关性。结果发现 EtFOSAA 和 PFOS 与不同的代谢物谱相关。精氨酸、赖氨酸和肌酸等尿素循环代谢物与 EtFOSAA(负相关)和 PFOS(正相关)呈相反关联;而肉碱穿梭代谢物则与 PFOS 呈显著正相关,表明脂肪酸代谢受到干扰。这些前体和终产物的差异代谢关联代表了识别 PFASs 如何改变宫内环境并可能导致疾病风险的重要第一步。