| Literature DB >> 20561984 |
Nieves Perdigones1, Ezequiel Martín, Gema Robledo, José Ramón Lamas, Carlos Taxonera, Manuel Díaz-Rubio, Emilio G de la Concha, Miguel Angel López-Nevot, Antonio García, María Gómez-García, Benjamín Fernández-Gutiérrez, Javier Martín, Elena Urcelay.
Abstract
Chromosomal region 5p13 includes regulatory elements of the prostaglandin receptor EP4 (PTGER4) gene and is associated with inflammatory bowel disease (IBD) susceptibility. We aimed at corroborating the association of the PTGER4 risk variant in IBD. Given the proinflammatory activity of prostaglandin E(2) in rheumatoid arthritis (RA), the reduction in incidence and severity of collagen-induced arthritis observed in mice deficient in the prostaglandin receptor EP4, and a modest signal of association found in an RA genome-wide scan, we proposed to extend the investigation of this locus to RA patients. A total of 709 Crohn's disease (CD) patients, 662 ulcerative colitis (UC) patients, and 1369 control subjects were genotyped for rs17234657. This polymorphism was also analyzed in 605 RA patients, and rs6871834 was studied in the RA patient group. Replication of the previous finding in CD was achieved in our independent collections, although with a milder effect (odds ratios = 1.23) than that originally described. No further association of the previously mentioned polymorphisms was detected with either UC or RA patients. We validated this 5p13 signal as a genuine susceptibility factor for CD in Caucasian populations. Our data seem to rule out a major influence of these polymorphisms on UC or RA predisposition. Copyright 2010 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20561984 DOI: 10.1016/j.humimm.2010.05.010
Source DB: PubMed Journal: Hum Immunol ISSN: 0198-8859 Impact factor: 2.850