Obeticholic acid for severe bile acid diarrhea with intestinal failure: A case report and review of the literature

World J Gastroenterol. 2018 Jun 7;24(21):2320-2326. doi: 10.3748/wjg.v24.i21.2320.

Abstract

Bile acid diarrhea results from excessive amounts of bile acids entering the colon due to hepatic overexcretion of bile acids or bile acid malabsorption in the terminal ileum. The main therapies include bile acid sequestrants, such as colestyramine and colesevelam, which may be given in combination with the opioid receptor agonist loperamide. Some patients are refractory to conventional treatments. We report the use of the farnesoid X receptor agonist obeticholic acid in a patient with refractory bile acid diarrhea and subsequent intestinal failure. A 32-year-old woman with quiescent colonic Crohn's disease and a normal terminal ileum had been diagnosed with severe bile acid malabsorption and complained of watery diarrhea and fatigue. The diarrhea resulted in hypokalemia and sodium depletion that made her dependent on twice weekly intravenous fluid and electrolyte infusions. Conventional therapies with colestyramine, colesevelam, and loperamide had no effect. Second-line antisecretory therapies with pantoprazole, liraglutide, and octreotide also failed. Third-line treatment with obeticholic acid reduced the number of stools from an average of 13 to an average of 7 per 24 h and improved the patient's quality of life. The fluid and electrolyte balances normalized. The effect was sustained during follow-up for 6 mo with treatment at a daily dosage of 25 mg. The diarrhea worsened shortly after cessation of obeticholic acid. This case report supports the initial report that obeticholic acid may reduce bile acid production and improve symptoms in patients with bile acid diarrhea.

Keywords: Bile acid malabsorption; Crohn’s disease; Diarrhea; Farnesoid X-activated receptor.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Bile Acids and Salts / metabolism*
  • Chenodeoxycholic Acid / analogs & derivatives*
  • Chenodeoxycholic Acid / pharmacology
  • Chenodeoxycholic Acid / therapeutic use
  • Crohn Disease / complications*
  • Crohn Disease / physiopathology
  • Diarrhea / drug therapy*
  • Diarrhea / etiology
  • Diarrhea / physiopathology
  • Feedback, Physiological / drug effects
  • Female
  • Fibroblast Growth Factors / metabolism
  • Gastrointestinal Agents / therapeutic use*
  • Humans
  • Ileum / drug effects
  • Ileum / metabolism
  • Ileum / physiopathology
  • Intestinal Absorption / drug effects
  • Liver / drug effects
  • Liver / metabolism
  • Malabsorption Syndromes / drug therapy
  • Malabsorption Syndromes / etiology
  • Malabsorption Syndromes / physiopathology
  • Receptors, Cytoplasmic and Nuclear / metabolism

Substances

  • Bile Acids and Salts
  • FGF19 protein, human
  • Gastrointestinal Agents
  • Receptors, Cytoplasmic and Nuclear
  • obeticholic acid
  • farnesoid X-activated receptor
  • Chenodeoxycholic Acid
  • Fibroblast Growth Factors