© 2005 by BMJ Publishing Group Ltd & British Society of Gastroenterology
RECENT ADVANCES IN CLINICAL PRACTICE
Genotypes and phenotypes in Crohns disease: do they help in clinical management?
Medical University Vienna, Department of Medicine 4, Division of Gastroenterology and Hepatology, Austria
Correspondence to:
Correspondence to:
Professor C Gasche
Neues AKH, KIM 4, Wahringer Gurtel 18-20, A-1090 Vienna, Austria; christoph.gasche@meduniwien.ac.at
Keywords: Crohns disease; CARD15; Nod2; phenotype; genotype; Vienna classification
| The first 150 words of the full text of this article appear below. |
Rather than a unique disorder, Crohns disease is regarded as a common denominator for various immune mediated inflammatory diseases of the gastrointestinal tract. These various subforms of Crohns disease are characterised by T cell mediated tissue destruction in the gut. In contrast with autoimmune diseases where autoantibodies react with self antigens, inflammation in Crohns disease is directed against antigens that are mainly derived from the environment.1 Although it may sound trivial, this adjustment in the understanding of the pathogenetic mechanisms has a vast number of consequences for the search of the disease causing factors and identification of therapeutic targets.
The various subforms of Crohns disease have not been recognised until recently. Historically, colonic Crohns disease was not distinguished from ulcerative colitis. Approximately 30 years ago, the first studies highlighted the diverse natural history of colonic and ileal Crohns disease.2 Inherent differences in disease behaviour (obstructing versus perforating) were later recognised
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