Abstract summary 

The contribution of rare coding sequence variants to genetic susceptibility in complex disorders is an important but unresolved question. Most studies thus far have investigated a limited number of genes from regions which contain common disease associated variants. Here we investigate this in inflammatory bowel disease by sequencing the exons and proximal promoters of 531 genes selected from both genome-wide association studies and pathway analysis in pooled DNA panels from 474 cases of Crohn's disease and 480 controls. 80 variants with evidence of association in the sequencing experiment or with potential functional significance were selected for follow up genotyping in 6,507 IBD cases and 3,064 population controls. The top 5 disease associated variants were genotyped in an extension panel of 3,662 IBD cases and 3,639 controls, and tested for association in a combined analysis of 10,147 IBD cases and 7,008 controls. A rare coding variant p.G454C in the BTNL2 gene within the major histocompatibility complex was significantly associated with increased risk for IBD (p = 9.65x10-10, OR = 2.3[95% CI = 1.75-3.04]), but was independent of the known common associated CD and UC variants at this locus. Rare (<1%) and low frequency (1-5%) variants in 3 additional genes showed suggestive association (p<0.005) with either an increased risk (ARIH2 c.338-6C>T) or decreased risk (IL12B p.V298F, and NICN p.H191R) of IBD. These results provide additional insights into the involvement of the inhibition of T cell activation in the development of both sub-phenotypes of inflammatory bowel disease. We suggest that although rare coding variants may make a modest overall contribution to complex disease susceptibility, they can inform our understanding of the molecular pathways that contribute to pathogenesis.

Authors & Co-authors:  Prescott Natalie J NJ Lehne Benjamin B Stone Kristina K Lee James C JC Taylor Kirstin K Knight Jo J Papouli Efterpi E Mirza Muddassar M MM Simpson Michael A MA Spain Sarah L SL Lu Grace G Fraternali Franca F Bumpstead Suzannah J SJ Gray Emma E Amar Ariella A Bye Hannah H Green Peter P Chung-Faye Guy G Hayee Bu'Hussain B Pollok Richard R Satsangi Jack J Parkes Miles M Barrett Jeffrey C JC Mansfield John C JC Sanderson Jeremy J Lewis Cathryn M CM Weale Michael E ME Schlitt Thomas T Mathew Christopher G CG

Study Outcome 

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