The Gut-Liver Axis in Primary Sclerosing Cholangitis

Clin Liver Dis. 2016 Feb;20(1):1-14. doi: 10.1016/j.cld.2015.08.012. Epub 2015 Sep 26.

Abstract

Dysregulation of the key genetic, immunologic, and microbiome compounds of the gut-liver axis is the basis for inflammatory bowel disease (IBD) and primary sclerosing cholangitis (PSC). This creates opportunities to accelerate therapies that have been traditionally developed for IBD to be used in PSC to the benefit of both diseases. Shared genetic susceptibility loci has yielded important clues into the pathogenesis of PSC-IBD. Understanding of the critical links between PSC and IBD are essential in designing clinical care pathways for these complex patients.

Keywords: Cholangiocarcinoma; Genetics; Inflammatory bowel disease; Microbiome; Pouchitis; Primary sclerosing cholangitis; Vedolizumab.

Publication types

  • Review

MeSH terms

  • Cholangitis, Sclerosing / drug therapy*
  • Cholangitis, Sclerosing / epidemiology
  • Cholangitis, Sclerosing / etiology*
  • Cytokines / metabolism*
  • Fucosyltransferases / genetics
  • Galactoside 2-alpha-L-fucosyltransferase
  • Gastrointestinal Microbiome / drug effects
  • Genetic Predisposition to Disease*
  • Hepatocyte Growth Factor / genetics
  • Humans
  • Inflammatory Bowel Diseases / drug therapy*
  • Inflammatory Bowel Diseases / epidemiology
  • Inflammatory Bowel Diseases / etiology*
  • Inflammatory Bowel Diseases / pathology
  • Interleukin-2 / genetics
  • Interleukin-2 Receptor alpha Subunit / genetics
  • Molecular Targeted Therapy
  • Pouchitis / etiology
  • Protein Serine-Threonine Kinases / genetics
  • Proto-Oncogene Proteins / genetics
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors

Substances

  • Cytokines
  • Interleukin-2
  • Interleukin-2 Receptor alpha Subunit
  • Proto-Oncogene Proteins
  • Tumor Necrosis Factor-alpha
  • macrophage stimulating protein
  • Hepatocyte Growth Factor
  • Fucosyltransferases
  • salt-inducible kinase-2, human
  • Protein Serine-Threonine Kinases