Open AccessGenetic predictors of medically refractory ulcerative colitis
Author(s) -
Haritunians Talin,
Taylor Kent D.,
Targan Stephan R.,
Dubinsky Marla,
Ippoliti Andrew,
Kwon Soonil,
Guo Xiuqing,
Melmed Gil Y.,
Berel Dror,
Mengesha Emebet,
Psaty Bruce M.,
Glazer Nicole L.,
Vasiliauskas Eric A.,
Rotter Jerome I.,
Fleshner Phillip R.,
McGovern Dermot P.B.
Publication year - 2010
Publication title -
inflammatory bowel diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.932
H-Index - 146
eISSN - 1536-4844
pISSN - 1078-0998
DOI - 10.1002/ibd.21293
Subject(s) - ulcerative colitis , genome wide association study , colectomy , medicine , refractory (planetary science) , cohort , single nucleotide polymorphism , disease , genotype , biology , genetics , gene , astrobiology
Background: Acute severe ulcerative colitis (UC) remains a significant clinical challenge and the ability to predict, at an early stage, those individuals at risk of colectomy for medically refractory UC (MR‐UC) would be a major clinical advance. The aim of this study was to use a genome‐wide association study (GWAS) in a well‐characterized cohort of UC patients to identify genetic variation that contributes to MR‐UC. Methods: A GWAS comparing 324 MR‐UC patients with 537 non‐MR‐UC patients was analyzed using logistic regression and Cox proportional hazards methods. In addition, the MR‐UC patients were compared with 2601 healthy controls. Results: MR‐UC was associated with more extensive disease ( P = 2.7 × 10 −6 ) and a positive family history of UC ( P = 0.004). A risk score based on the combination of 46 single nucleotide polymorphisms (SNPs) associated with MR‐UC explained 48% of the variance for colectomy risk in our cohort. Risk scores divided into quarters showed the risk of colectomy to be 0%, 17%, 74%, and 100% in the four groups. Comparison of the MR‐UC subjects with healthy controls confirmed the contribution of the major histocompatibility complex to severe UC (peak association: rs17207986, P = 1.4 × 10 −16 ) and provided genome‐wide suggestive association at the TNFSF15 (TL1A) locus (peak association: rs11554257, P = 1.4 × 10 −6 ). Conclusions: A SNP‐based risk scoring system, identified here by GWAS analyses, may provide a useful adjunct to clinical parameters for predicting the natural history of UC. Furthermore, discovery of genetic processes underlying disease severity may help to identify pathways for novel therapeutic intervention in severe UC. (Inflamm Bowel Dis 2010)