Authors
Sijia Gu, Ji Ma, Xiangying Sun, Keyi Li, Mingzhu Wu, Yumeng Shi, Miao Xu, Hongkai Zhu, Hongwen Sun
Published in
Environmental pollution (Barking, Essex : 1987). Pages 128980. Aug 17, 2026. Epub Aug 17, 2026.
Abstract
Per- and polyfluoroalkyl substances (PFAS) are persistent environmental contaminants associated with cancer risk, but their relevance to multiple myeloma remains poorly understood. In an unmatched case-control study of 173 participants, we integrated PFAS biomonitoring, immunoglobulin profiling, and untargeted metabolomics to characterize PFAS-associated immune and metabolic alterations. Higher circulating concentrations of perfluorodecanoic acid and perfluoroheptane sulfonate were associated with increased odds of multiple myeloma and lower polyclonal immunoglobulin G (IgG). Metabolomic analyses identified candidate alterations involving glycolysis, pentose phosphate pathway-related metabolism, redox homeostasis, lipid peroxidation, and arachidonic acid-derived mediators. Several PFAS-IgG and PFAS-metabolic associations were also observed among controls, suggesting that these patterns were not solely attributable to diagnosed multiple myeloma. Complementary PFAS mixture experiments showed lower circulating IgG, reduced bone marrow plasma-cell frequency, and increased serum lactate dehydrogenase activity in mice; experiments in human bone marrow-derived mesenchymal stromal cells showed disrupted redox homeostasis and enhanced oxidative stress. Exploratory mediation analysis further prioritized metabolites potentially mediating the associations between PFAS exposure and multiple myeloma. Together, these findings identify the bone marrow immunometabolic environment as a biologically relevant interface for PFAS-associated effects and support further prospective and targeted experimental investigation.
PMID:
42607791
Bibliographic data and abstract were imported from PubMed on 18 Aug 2026.
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