4.7 Article

Ratio of Conjugated Chenodeoxycholic to Muricholic Acids is Associated with Severity of Nonalcoholic Steatohepatitis

Journal

OBESITY
Volume 27, Issue 12, Pages 2055-2066

Publisher

WILEY
DOI: 10.1002/oby.22627

Keywords

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Funding

  1. Natural Science Foundation of China [81570524, 81700510, 81500665]
  2. design initiative for agricultural and social development of Hangzhou Municipal Science and Technology Bureau [20172016A02, 2016MHZ13]
  3. Scientific Research Foundation of Wenzhou [Y20160223]
  4. Natural Science Foundation of Minhang District of Shanghai [2018MHZ027]

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Objective Bile acids (BAs) are important molecules in the progression of nonalcoholic fatty liver disease. This study aimed to investigate BA profile alterations in Chinese nonalcoholic steatohepatitis (NASH) patients. Methods BA profiles in serum and liver tissues were determined by ultraperformance liquid chromatography coupled to tandem mass spectrometry in patients from two different clinical centers. Results A total of 134 participants were enrolled in this study to serve as the training (n = 87) and validation (n = 47) cohorts. The ratio of circulating conjugated chenodeoxycholic acids to muricholic acids (P = 0.001) was elevated from healthy controls to non-NASH individuals to NASH individuals in a stepwise manner in the training cohort and was positively associated with the histological severity of NASH: steatosis (R-2 = 0.12), lobular inflammation (R-2 = 0.12), ballooning (R-2 = 0.11), and fibrosis stage (R-2 = 0.18). The ratio was elevated in the validation cohort of NASH patients (P < 0.001), and it was able to predict NASH (area under the receiver operating characteristic curve: 75%) and significant fibrosis (area under the receiver operating characteristic curve: 71%) in these two cohorts. Moreover, this elevated ratio and impaired farnesoid X receptor signaling were found in the NASH liver. Conclusions Altered BA profile in NASH is closely associated with the severity of liver lesions, and it has the potential for predicting NASH development.

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