Ileal bile acid transporter inhibition as an anticholestatic therapeutic target in biliary atresia and other cholestatic disorders

Hepatol Int. 2020 Sep;14(5):677-689. doi: 10.1007/s12072-020-10070-w. Epub 2020 Jul 11.


Biliary atresia is a rare cholestatic liver disease that presents in infants and rapidly advances to death in the absence of intervention. As a result of blockage or destruction of the biliary tract, bile acids accumulate and drive inflammation, fibrosis, and disease progression. The standard of care, Kasai portoenterostomy (KPE), is typically performed shortly after diagnosis (currently at ~ 2 months of age) and aims to restore bile flow and relieve cholestasis. Nevertheless, most patients continue to experience liver injury from accumulation of bile acids after KPE, since there are no known effective therapeutics that may enhance survival after KPE. Improving cholestasis via interruption of the enterohepatic circulation of bile acids may directly attenuate hepatic bile acid retention and reduce the risk of early organ failure. Directly addressing intrahepatic accretion of bile acids to avoid inherent bile acid toxicities provides an attractive and plausible therapeutic target for biliary atresia. This review explores the novel therapeutic concept of inhibiting the sole ileal bile acid transporter (IBAT), also known as ASBT (apical sodium-bile acid transporter, encoded by SLC10A2), as a means to reduce hepatic bile acid concentration after KPE. By reducing return of bile acids to the cholestatic liver, IBAT inhibitors may potentially lessen or delay liver damage associated with the hepatotoxicity and cholangiopathy of bile acid accumulation. The clinical programs of 2 IBAT inhibitors in development for the treatment of pediatric cholestatic liver diseases, maralixibat and odevixibat, are highlighted.

Keywords: Apical sodium-bile acid transporter; Bile acids; Biliary atresia; Cholestasis; Cholestatic liver disease; Enterohepatic circulation; Ileal bile acid transporter; Kasai portoenterostomy; Maralixibat; Odevixibat; Pediatrics.

Publication types

  • Review

MeSH terms

  • Benzodiazepines / pharmacology*
  • Biliary Atresia* / diagnosis
  • Biliary Atresia* / metabolism
  • Biliary Atresia* / physiopathology
  • Biliary Atresia* / therapy
  • Butyrates / pharmacology*
  • Disease Progression
  • Gastrointestinal Agents / pharmacology
  • Humans
  • Infant
  • Organic Anion Transporters, Sodium-Dependent* / antagonists & inhibitors
  • Organic Anion Transporters, Sodium-Dependent* / metabolism
  • Portoenterostomy, Hepatic* / adverse effects
  • Portoenterostomy, Hepatic* / methods
  • Prognosis
  • Protective Agents / pharmacology
  • Symporters* / antagonists & inhibitors
  • Symporters* / metabolism


  • Butyrates
  • Gastrointestinal Agents
  • Organic Anion Transporters, Sodium-Dependent
  • Protective Agents
  • Symporters
  • Benzodiazepines
  • sodium-bile acid cotransporter
  • odevixibat