Crohn disease: a current perspective on genetics, autophagy and immunity

Autophagy. 2011 Apr;7(4):355-74. doi: 10.4161/auto.7.2.13074. Epub 2011 Apr 1.

Abstract

Crohn disease (CD) is a chronic and debilitating inflammatory condition of the gastrointestinal tract. Prevalence in Western populations is 100-150/100,000 and somewhat higher in Ashkenazi Jews. Peak incidence is in early adult life, although any age can be affected and a majority of affected individuals progress to relapsing and chronic disease. Medical treatments rely significantly on empirical corticosteroid therapy and immunosuppression, and intestinal resectional surgery is frequently required. Thus, 80% of patients with CD come to surgery for refractory disease or complications. It is hoped that an improved understanding of pathogenic mechanisms, for example by studying the genetic basis of CD and other forms of inflammatory bowel diseases (IBD), will lead to improved therapies and possibly preventative strategies in individuals identified as being at risk.

Publication types

  • Review

MeSH terms

  • Adrenal Cortex Hormones / therapeutic use
  • Autophagy
  • Autophagy-Related Proteins
  • Carrier Proteins / genetics
  • Chronic Disease
  • Colitis, Ulcerative / physiopathology
  • Crohn Disease / genetics*
  • Crohn Disease / immunology*
  • Crohn Disease / physiopathology*
  • Dendritic Cells / metabolism
  • Genome-Wide Association Study
  • Genotype
  • Humans
  • Inflammatory Bowel Diseases / physiopathology
  • Intestines / microbiology
  • Paneth Cells / metabolism
  • Recurrence
  • Th17 Cells / metabolism

Substances

  • ATG16L1 protein, human
  • Adrenal Cortex Hormones
  • Autophagy-Related Proteins
  • Carrier Proteins