## Background: Although many genetic variants are identified in association with crohn's disease (cd), card15, il23r, and atg16l1 association with cd have been firmly confirmed in caucasians of european ancestry. the prevalence of cd is rapidly rising in brazil, where european ancestry is firmly ad
IL23R haplotypes provide a large population attributable risk for Crohn's disease
β Scribed by Kent D. Taylor; Stephan R. Targan; Ling Mei; Andrew F. Ippoliti; Dermot McGovern; Emebet Mengesha; Lily King; Jerome I. Rotter
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 292 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1078-0998
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β¦ Synopsis
Background:
The IL-23 pathway plays a pivotal role in the development of chronic mucosal inflammation seen in the inflammatory bowel diseases. Multiple studies have now established the contribution of the interleukin 23 receptor gene (IL23R) to Crohn's disease (CD) risk in general and of the IL23R R381Q variant in particular. The aim of this work was to estimate the total contribution of this gene to CD risk test using a haplotype approach.
Methods: In all, 763 CD subjects and 254 controls were genotyped for single nucleotide polymorphisms in the IL23R gene using Illumina and ABI methods. Haplotypes were assigned using PHASEv2 and tested for association with CD by chi-square and permutation.
Results:
Haplotypes with both increased and decreased risk for CD were observed in 2 of the 4 observed blocks (Block 2 H1: 55.4% control, 64% CD, P Ο 0.019; H2: 64.5% control, 54.4% CD, P Ο 0.006; Block 3 H1: 55.8% control, 64.4% CD, P Ο 0.013; H2: 47.0% control, 36.6% CD, P Ο 0.001). The population attributable risk for these haplotypes was substantially larger than that estimated for the IL23R R381Q variant (Block 2 H1 and block 3 H1 Ο·20%, compared with Ο·4% for Block 3 H6, containing the variant).
Conclusions:
These observations suggest that IL23R makes a substantial contribution to CD susceptibility, larger than that estimated from the population frequency of the R381Q variant. These observations also support the expectation that finding "hits" from genomewide association studies will be but an important chapter in the story of unraveling the genetic contribution to CD, rather than the final chapter that brings clarity to all the plot twists of a complicated story.
π SIMILAR VOLUMES
Background: IBD5, IL23R, and ATG16L1 genetic variations are established Crohn's disease (CD) risks alleles. We evaluated these in a population-based case-control study within a cohort to determine their penetrance, population attributable risk, independence, and relationship to other established CD