Journal
INTERNATIONAL JOURNAL OF HYGIENE AND ENVIRONMENTAL HEALTH
Volume 251, Issue -, Pages -Publisher
ELSEVIER GMBH
DOI: 10.1016/j.ijheh.2023.114189
Keywords
Perfluoroalkyl substances; Mixture; Liver function; Thyroid function; Sex-specific effect
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Although previous studies have investigated the individual effects of PFASs on liver and thyroid function, little is known about their combined and sex-specific effects. This study found that increased PFASs concentrations were associated with elevated ALT and GGT levels, and these associations were only significant in males. These findings provide epidemiological evidence for the combined and sex-specific effects of PFASs on liver function.
Although studies have investigated the effects of perfluoroalkyl substances (PFASs) on liver and thyroid function, little is known about its combined and sex-specific effect. A total of 688 participants were interviewed and serum PFASs concentration was measured using liquid chromatography/mass spectrometry. Five biomarkers of liver and thyroid function (ALT, GGT, TSH, FT3 and FT4) were chosen as outcomes. A restriction cubic spline function was applied to capture the dose-response relationship between PFASs and liver enzymes and thyroid hormones. Multivariable regression and Bayesian kernel machine regression (BKMR) models were performed to assess the single and overall associations of PFASs with targeted biomarkers. Single-pollutant analyses indicated that increased PFASs concentrations were associated with elevated ALT and GGT levels. BKMR models suggested positive dose-response relationships between PFASs mixtures and ALT and GGT levels. Significant associations were only detected between several PFASs and thyroid hormones, and joint effect of PFASs mixtures on FT3 levels was found at higher concentrations. Meanwhile, sex differences were found in the associations of PFASs with ALT and GGT levels, with significant results only in males. Our findings provide epidemiological evidence for combined and sex-specific effects of PFASs on ALT and GGT levels.
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