Native liver survival in bile salt export pump deficiency: results of a retrospective cohort study

Hepatol Commun. 2023 Mar 30;7(4):e0092. doi: 10.1097/HC9.0000000000000092. eCollection 2023 Apr 1.

Abstract

Background: Bile salt export pump (ABCB11) deficiency [Progressive familial intrahepatic cholestasis (PFIC2)] is the most common genetic cause of PFIC and is associated with pruritus and progressive liver disease. Surgical biliary diversion or pharmacological [ileal bile acid transporter inhibitor (IBATi)] approaches can be used to block the recirculation of bile acids to the liver. There is a paucity of detailed data on the natural history and, in particular, the longitudinal evolution of bile acid levels to predict treatment response. Cross-sectional data from large international consortia suggested a maximum cutoff value of bile acids after the intervention to predict a successful outcome.

Methods: This retrospective, single-center, cohort study included all patients with confirmed biallelic pathogenic ABCB11 genotype PFIC2 treated at our institution with ≥2 years follow-up. The outcomes of interventions and predictors of long-term health were analyzed.

Results: Forty-eight cases were identified with PFIC2. Eighteen received partial external biliary diversion (PEBD) surgery, and 22 patients underwent liver transplantation. Two patients developed HCC and 2 died. Improved survival with native liver was closely associated with genotype, complete normalization of serum bile acids following PEBD, and alleviation of pruritus. Persistence of mild-to-moderate elevation of bile acids or a secondary rise following normalization was associated with liver disease progression and led to transplantation, suggesting that any prolonged elevation of bile acids worsens the chance of native liver survival. Higher-grade fibrosis at the time of PEBD was not associated with reduced long-term native liver survival. Patients with PFIC2 benefit from PEBD even at a stage of advanced fibrosis.

Conclusion: Serum bile acid levels are an early predictor of treatment response and might serve as the gold standard in the evaluation of novel therapies including IBATi.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 11 / genetics
  • Bile Acids and Salts
  • Carcinoma, Hepatocellular* / complications
  • Cholestasis* / complications
  • Cohort Studies
  • Cross-Sectional Studies
  • Humans
  • Liver Cirrhosis / pathology
  • Liver Neoplasms* / complications
  • Pruritus / complications
  • Pruritus / genetics
  • Retrospective Studies
  • Treatment Outcome

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 11
  • Bile Acids and Salts

Supplementary concepts

  • Cholestasis, progressive familial intrahepatic 1