PFAS Exposures and the Human Metabolome: A Systematic Review of Epidemiological Studies

代谢组学 代谢组 流行病学 生物 系统回顾 生物信息学 环境卫生 生物化学 医学 梅德林 病理
作者
Sandra India Aldana,Meizhen Yao,Vishal Midya,Elena Colicino,Leda Chatzi,Jaime Chu,Chris Gennings,Dean P. Jones,Ruth J. F. Loos,Veronica Wendy Setiawan,Matthew Ryan Smith,Ryan W. Walker,Dinesh Kumar Barupal,Douglas Ian Walker,Damaskini Valvi
出处
期刊:Current pollution reports [Springer Science+Business Media]
卷期号:9 (3): 510-568 被引量:118
标识
DOI:10.1007/s40726-023-00269-4
摘要

There is a growing interest in understanding the health effects of exposure to per- and polyfluoroalkyl substances (PFAS) through the study of the human metabolome. In this systematic review, we aimed to identify consistent findings between PFAS and metabolomic signatures. We conducted a search matching specific keywords that was independently reviewed by two authors on two databases (EMBASE and PubMed) from their inception through July 19, 2022 following PRISMA guidelines.We identified a total of 28 eligible observational studies that evaluated the associations between 31 different PFAS exposures and metabolomics in humans. The most common exposure evaluated was legacy long-chain PFAS. Population sample sizes ranged from 40 to 1,105 participants at different stages across the lifespan. A total of 19 studies used a non-targeted metabolomics approach, 7 used targeted approaches, and 2 included both. The majority of studies were cross-sectional (n = 25), including four with prospective analyses of PFAS measured prior to metabolomics.Most frequently reported associations across studies were observed between PFAS and amino acids, fatty acids, glycerophospholipids, glycerolipids, phosphosphingolipids, bile acids, ceramides, purines, and acylcarnitines. Corresponding metabolic pathways were also altered, including lipid, amino acid, carbohydrate, nucleotide, energy metabolism, glycan biosynthesis and metabolism, and metabolism of cofactors and vitamins. We found consistent evidence across studies indicating PFAS-induced alterations in lipid and amino acid metabolites, which may be involved in energy and cell membrane disruption.
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