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Exposure to environmental contaminants is associated with altered hepatic lipid metabolism in non-alcoholic fatty liver disease

Arola Johanna; Sen Partho; Luukkonen Panu K; Hyötyläinen Tuulia; Schlezinger Jennifer J; McGlincheyAidan; Webster Thomas F; Ragnarsdottir Oddny; Orešič Matej; Juuti Anne; Qadri Sami; Jäntti Sirkku; Yki-Järvinen Hannele

Exposure to environmental contaminants is associated with altered hepatic lipid metabolism in non-alcoholic fatty liver disease

Arola Johanna
Sen Partho
Luukkonen Panu K
Hyötyläinen Tuulia
Schlezinger Jennifer J
McGlincheyAidan
Webster Thomas F
Ragnarsdottir Oddny
Orešič Matej
Juuti Anne
Qadri Sami
Jäntti Sirkku
Yki-Järvinen Hannele
Katso/Avaa
Publisher's PDF (1.083Mb)
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Elsevier
doi:10.1016/j.jhep.2021.09.039
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2022021519249
Tiivistelmä

Background & aims

Recent experimental models and epidemiological studies suggest that specific environmental contaminants (ECs) contribute to the initiation and pathology of NAFLD. However, the underlying mechanisms linking EC exposure with NAFLD remain poorly understood and there is no data on their impact on the human liver metabolome. Herein, we hypothesized that exposure to ECs, particularly perfluorinated alkyl substances (PFAS), impacts liver metabolism, specifically bile acid metabolism.

Methods

In a well-characterized human NAFLD cohort of 105 individuals, we investigated the effects of EC exposure on liver metabolism. We characterized the liver (via biopsy) and circulating metabolomes using four mass spectrometry-based analytical platforms, and measured PFAS and other ECs in serum. We subsequently compared these results with an exposure study in a PPARα-humanized mouse model.

Results

PFAS exposure appears associated with perturbation of key hepatic metabolic pathways previously found altered in NAFLD, particularly as regards bile acid and lipid metabolism. We identified stronger associations between the liver metabolome, chemical exposure and NAFLD-associated clinical variables (liver fat content, HOMA-IR), in female subjects versus males. Specifically, we observed PFAS-associated up-regulation of bile acids, triacylglycerols and ceramides, and association between chemical exposure and dysregulated glucose metabolism in females. The murine exposure study further corroborated our findings, vis-à-vis a sex-specific association between PFAS exposure and NAFLD-associated lipid changes.

Conclusions

Females may be more sensitive to the harmful impacts of PFAS. Lipid-related changes subsequent to PFAS exposure may be secondary to the interplay between PFAS and bile acid metabolism.

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  • Rinnakkaistallenteet [19207]

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