Genetics of inflammatory bowel disease: implications for disease pathogenesis and natural history

Expert Rev Gastroenterol Hepatol. 2009 Oct;3(5):513-34. doi: 10.1586/egh.09.45.


Epidemiological data, detailed molecular studies and recent genome-wide association studies strongly suggest that ulcerative colitis (UC) and Crohn's disease (CD) are related polygenic diseases that share some susceptibility loci, but differ at others. To date, there are more than 50 confirmed inflammatory bowel disease genes/loci, a number that is widely anticipated to at least double in the next 2 years. Germline variation in IL23R, IL12B, JAK2 and STAT3 is associated with inflammatory bowel disease susceptibility, consistent with the newly described role for IL23 signaling and Th17 cells in disease pathogenesis. Several genes involved in different aspects of bacterial handling are defective only in CD, including NOD2 and the autophagy genes ATG16L1 and IRGM. IL10 and ECM1 are associated with UC, while inherited variation at the HLA region is related to an inflammatory colonic phenotype. The application of genome-wide association studies to inflammatory bowel disease has been successful in defining the genetic architecture of CD and UC and in delivering genuinely novel and important insights into disease pathogenesis. This has unearthed a plethora of attractive targets for the development of future therapeutics. Insights into the natural history of these complex diseases will follow and may enable appropriate patient selection for early aggressive therapy with the view to modifying the disease course.

Publication types

  • Review

MeSH terms

  • Autophagy / genetics*
  • Colitis, Ulcerative / genetics*
  • Colitis, Ulcerative / immunology
  • Colitis, Ulcerative / microbiology
  • Colitis, Ulcerative / pathology
  • Crohn Disease / genetics*
  • Crohn Disease / immunology
  • Crohn Disease / microbiology
  • Crohn Disease / pathology
  • Disease Progression
  • Environment
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Humans
  • Immunity, Innate / genetics*
  • Phenotype
  • Racial Groups / genetics
  • Risk Factors
  • Signal Transduction / genetics*