Bile acid disease: the emerging epidemic

Curr Opin Gastroenterol. 2017 May;33(3):189-195. doi: 10.1097/MOG.0000000000000344.

Abstract

Purpose of review: Our objective was to review advances in bile acids in health and disease published in the last 2 years. Bile acid diarrhea (BAD) is recognized as a common cause of chronic diarrhea, and its recognition has been facilitated by development of new screening tests.

Recent findings: Primary BAD can account for 30% of cases of chronic diarrhea. The mechanisms leading to BAD include inadequate feedback regulation by fibroblast growth factor 19 (FGF-19) from ileal enterocytes, abnormalities in synthesis or degradation of proteins involved in FGF-19 regulation in hepatocytes and variations as a function of the bile acid receptor, TGR5 (GPBAR1). SeHCAT is the most widely used test for diagnosis of BAD. There has been significant validation of fasting serum FGF-19 and 7 α-hydroxy-cholesten-3-one (C4), a surrogate measure of bile acid synthesis. Bile acid sequestrants are the primary treatments for BAD; the farnesoid X-receptor-FGF-19 pathway provides alternative therapeutic targets for BAD. Bile acid-stimulated intestinal mechanisms contribute to the beneficial effects of bariatric surgery on obesity, glycemic control and the treatment of recurrent Clostridium difficile infection.

Summary: Renewed interest in the role of bile acids is leading to novel management of diverse diseases besides BAD.

Publication types

  • Review

MeSH terms

  • Antidiarrheals / therapeutic use
  • Bile Acids and Salts / physiology*
  • Chronic Disease
  • Diarrhea / diagnosis
  • Diarrhea / epidemiology
  • Diarrhea / metabolism*
  • Diarrhea / therapy
  • Enterohepatic Circulation / physiology
  • Fibroblast Growth Factors / metabolism
  • Gastric Bypass
  • Humans
  • Obesity, Morbid / metabolism
  • Obesity, Morbid / surgery

Substances

  • Antidiarrheals
  • Bile Acids and Salts
  • FGF19 protein, human
  • Fibroblast Growth Factors