AI Article Synopsis

  • The study investigates the differences in serum bile acid profiles between individuals with nonalcoholic fatty liver disease (NAFLD) and those without, revealing distinct patterns based on the severity of liver fibrosis.
  • In a sample of 312 participants, the presence of higher levels of certain bile acids was noted in NAFLD cases compared to non-NAFLD controls, while differences in total bile acids were minimal between nonalcoholic fatty liver and nonalcoholic steatohepatitis.
  • As fibrosis stage increases, total serum bile acids rise, and specific types of bile acids show significant changes, indicating that bile acid profiles may serve as important indicators of liver disease progression.

Article Abstract

Background: The fasting-state serum bile acid profile in nonalcoholic fatty liver disease (NAFLD) has been reported to differ when nonalcoholic steatohepatitis is compared to nonalcoholic fatty liver. However, there are few data comparing changes in NAFLD vs non-NAFLD, or whether the bile acid profile differs according to the degree of fibrosis.

Aim: To examine the serum bile acid profile across the entire spectrum of NAFLD.

Methods: We performed a cross-sectional analysis of two complementary cohorts: a Twin and Family cohort of 156 participants, and a biopsy-proven-NAFLD cohort of 156 participants with fasting bile acid profiling using liquid chromatography/mass spectrometry.

Results: In the Twin and Family cohort (mean age 46.3 years and body mass index (BMI) 26.6 kg/m ), 36 (23%) participants had NAFLD (magnetic resonance imaging proton density fat fraction ≥ 5%). Higher chenodeoxycholyl conjugates (9.0% vs 6.5%, P = 0.019) and lower glycohyocholate (1.2% vs 3.6%, P < 0.001) were observed in NAFLD compared to non-NAFLD-controls. In the biopsy-proven-NAFLD cohort (mean age 49.8 years, BMI 32.0 kg/m ), no differences in total bile acid were seen between nonalcoholic fatty liver vs nonalcoholic steatohepatitis. The total unconjugated bile acid significantly decreased across nonalcoholic steatohepatitis categories (P = 0.044). The distribution of stage of fibrosis was F0: 42.3%, F1: 32.7%, F2: 10.3%, F3: 8.3% and F4: 6.4%. The total serum bile acid increased with increase in fibrosis stage (P < 0.001). The primary conjugated bile acid proportion increased (P < 0.001) whereas unconjugated bile acid (P = 0.006), unconjugated cholyl (P < 0.001) and chenodeoxycholyl conjugates (P < 0.002) significantly decreased with increase in liver fibrosis stage.

Conclusions: Fasting-state serum bile acid profile alterations are seen across the entire spectrum of NAFLD. The total serum bile acids did not differ significantly between NAFLD vs non-NAFLD and nonalcoholic fatty liver vs nonalcoholic steatohepatitis, but were significantly perturbed progressively as liver fibrosis increases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6319963PMC
http://dx.doi.org/10.1111/apt.15035DOI Listing

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