4.7 Article

Bile acids profile, histopathological indices and genetic variants for non-alcoholic fatty liver disease progression

Journal

METABOLISM-CLINICAL AND EXPERIMENTAL
Volume 116, Issue -, Pages -

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.metabol.2020.154457

Keywords

Bile acids; Fibrosis; Metabolomics; NAFLD; NASH

Funding

  1. Office of Dietary Supplements [P01 HL147823, ROl HL103866, ROl HL126827, ROl DK120679, P50 AA024333, RO1 HL133169, RO1 HL148110, U01 DK061732, R01 GM119174, Dial DK113598]
  2. Leducq Foundation [17CVD01]
  3. Shimadzu Center of Excellence award
  4. NIH

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Metabolomic studies have shown that plasma levels of bile acids are elevated in subjects with NAFLD compared to healthy controls. Specific bile acids are associated with the transition from simple hepatic steatosis to NASH, as well as genetic determinants. This suggests a potential role for bile acid metabolism in the development and progression of NASH.
Objective: Metabolomic studies suggest plasma levels of bile acids (BAs) are elevated amongst subjects with nonalcoholic fatty liver disease (NAFLD) compared to healthy controls. However, it remains unclear whether or not specific BAs are associated with the clinically relevant transition from nonalcoholic fatty liver (i.e. simple steatosis) to non-alcoholic steatohepatitis (NASH), or enhanced progression of hepatic fibrosis, or genetic determinants of NAFLD/NASH. Methods: Among sequential subjects (n=102) undergoing diagnostic liver biopsy, we examined the associations of a broad panel of BAs with distinct histopathological features of NAFLD, the presence of NASH, and their associations with genetic variants linked to NAFLD and NASH. Results: Plasma BA alterations were observed through the entire spectrum of NAFLD, with several glycine conjugated forms of the BAs demonstrating significant associations with higher grades of inflammation and fibrosis. Plasma 7-Keto-DCA levels showed the strongest associations with advanced stages of hepatic fibrosis [odds ratio(95% confidence interval)], 4.2(1.2-16.4), NASH 24.5(4.1-473), and ballooning 18.7(4.8-91.9). Plasma 7-Keto-LCA levels were associated with NASH 9.4(1.5-185) and ballooning 5.9(1.4-28.8). Genetic variants at several NAFLD/NASH loci were nominally associated with increased levels of 7-Ketoand glycine-conjugated forms of BAs, and the NAFLD risk allele at the TRIB1 locus showed strong tendency toward increased plasma levels of GCA (p=0.02) and GUDCA (p=0.009). Conclusions: Circulating bile acid levels are associated with histopathological and genetic determinants of the transition from simple hepatic steatosis into NASH. Further studies exploring the potential involvement of bile acid metabolism in the development and/or progression of distinct histopathological features of NASH are warranted. (C) 2020 Elsevier Inc. All rights reserved.

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