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Gut 2007;56:149-150; doi:10.1136/gut.2006.102723
Copyright © 2007 BMJ Publishing Group Ltd & British Society of Gastroenterology.

LETTER

Letters

IBD5 is associated with an extensive complicated Crohn’s disease feature: implications from genotype–phenotype analysis

S Brescianini1,*, T Trinh2,*, M Stoll3, S Schreiber4, J D Rioux5 and M J Daly6

1 Istituto Superiore di Sanita’, Rome, Italy
2 University of Virginia Health System, Charlottesville, Virginia, USA
3 Leibniz-Institute for Arteriosclerosis Research, Muenster, Germany
4 Christian-Albrechts-University, Kiel, Germany
5 Universite de Montreal, Montreal Heart Institute, Montreal, Quebec, Canada
6 The Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA

Correspondence to:
Correspondence to:
Dr S Brescianini
Reparto di Epidemiologica Genetica, Centro Nazionale di Epidemiologia, Sorveglianza e Promozione della Salute, Istituto Superiore di Sanità, V.le Regina Elena, 299, 00161 Roma, Italy; sonia.brescianini@iss.it

The first 150 words of the full text of this article appear below.

Currently, decisions regarding patient care in Crohn’s disease are largely dictated by clinical phenotypes, incorporating disease localisation and behaviour. In this context, a molecular classification based on genetic susceptibility can provide a far more meaningful stratification for biologically relevant genotype–phenotype associations, and ultimately, the individualisation of patient treatment.1

The IBD5 risk haplotype (IBD5risk) located within the 5q31 cytokine gene cluster has been unequivocally associated with Crohn’s disease.2 Specific clinical phenotypes have not been firmly established for IBD5risk, although an association with perianal and with fistulising Crohn’s disease has been proposed.3–8 We performed genotype–phenotype correlations for IBD5risk and Crohn’s disease in a cohort of 325 German patients, described elsewhere,3 to determine whether IBD5risk is associated with specific localisation phenotypic features and, in particular, with an extensive disease feature. Disease characteristics and age of onset were also analysed. Phenotyping procedures have been tested for interobserver and intraobserver stability, and . . . [Full text of this article]


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