炎症性肠病
全基因组关联研究
疾病
基因
基因组
遗传关联
单核苷酸多态性
遗传学
医学
生物
内科学
基因型
作者
Richard H. Duerr,Kent D. Taylor,Steven R. Brant,John D. Rioux,Mark S. Silverberg,Mark J. Daly,A. Hillary Steinhart,Clara Abraham,Miguel Regueiro,Anne M. Griffiths,Themistocles Dassopoulos,Alain Bitton,Huiying Yang,Stephan R. Targan,Lisa W. Datta,Emily O. Kistner,L. Philip Schumm,Annette T. Lee,Peter K. Gregersen,M. Michael Barmada
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2006-10-27
卷期号:314 (5804): 1461-1463
被引量:2949
标识
DOI:10.1126/science.1135245
摘要
The inflammatory bowel diseases Crohn's disease and ulcerative colitis are common, chronic disorders that cause abdominal pain, diarrhea, and gastrointestinal bleeding. To identify genetic factors that might contribute to these disorders, we performed a genome-wide association study. We found a highly significant association between Crohn's disease and the IL23R gene on chromosome 1p31, which encodes a subunit of the receptor for the proinflammatory cytokine interleukin-23. An uncommon coding variant (rs11209026, c.1142G>A, p.Arg381Gln) confers strong protection against Crohn's disease, and additional noncoding IL23R variants are independently associated. Replication studies confirmed IL23R associations in independent cohorts of patients with Crohn's disease or ulcerative colitis. These results and previous studies on the proinflammatory role of IL-23 prioritize this signaling pathway as a therapeutic target in inflammatory bowel disease.
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