The Functional -765G arrow right C Polymorphism of the COX-2 Gene May Reduce the Risk of Developing Crohn's Disease

Cyclooxygenase-2 (COX-2) is a key enzyme involved in the conversion of arachidonic acid into prostaglandins. COX-2 is mainly induced at sites of inflammation in response to proinflammatory cytokines such as interleukin-1 alpha / beta , interferon- gamma and tumor necrosis factor- alpha produced by i...

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Published inPloS one Vol. 5; no. 1
Main Authors de Vries, Hilbert S, te Morsche, Rene HM, van Oijen, Martijn GH, Nagtegaal, Iris D, Peters, Wilbert HM, de Jong, Dirk J
Format Journal Article
LanguageEnglish
Published 24.11.2010
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Summary:Cyclooxygenase-2 (COX-2) is a key enzyme involved in the conversion of arachidonic acid into prostaglandins. COX-2 is mainly induced at sites of inflammation in response to proinflammatory cytokines such as interleukin-1 alpha / beta , interferon- gamma and tumor necrosis factor- alpha produced by inflammatory cells. The aim of this study was to investigate the possible modulating effect of the functional COX-2 polymorphisms -1195 A arrow right G and -765G arrow right C on the risk for development of inflammatory bowel disease (IBD) in a Dutch population. Genomic DNA of 525 patients with Crohn's disease (CD), 211 patients with ulcerative colitis (UC) and 973 healthy controls was genotyped for the -1195 A arrow right G (rs689466) and -765G arrow right C (rs20417) polymorphisms. Distribution of genotypes in patients and controls were compared and genotype-phenotype interactions were investigated. The genotype distribution of the -1195A arrow right G polymorphism was not different between the patients with CD or UC and the control group. The -765GG genotype was more prevalent in CD patients compared to controls with an OR of 1.33 (95%CI 1.04-1.69, p&0.05). The -765GC and -765CC genotype carriers showed a tendency to be less frequent in patients with CD compared to controls, with ORs of 0.78 (95%CI: 0.61-1.00) and 0.49 (95%CI 0.22-1.08), respectively. Combining homozygous and heterozygous patients with the -765C allele showed a reduced risk for developing CD, with an OR of 0.75 (95%CI: 0.59-0.96). In the context of this, the G-1195G-765/A-1195C-765 diplotype was significantly less common in patients with CD compared to controls, with an OR of 0.62 (95%CI: 0.39-0.98). For UC however, such an effect was not observed. No correlation was found between COX-2 diplotypes and clinical characteristics of IBD. The -765G arrow right C polymorphism was associated with a reduced risk for developing Crohn's disease in a Dutch population.
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ISSN:1932-6203
DOI:10.1371/journal.pone.0015011