No evidence for involvement of IL-4R and CD11B from the IBD1 region and STAT6 in the IBD2 region in Crohn's disease

被引:11
作者
de Jong, DJ
Franke, B
Naber, AHJ
Willemen, JJHT
Heister, AJGAM
Brunner, HG
de Kovel, CGF
Hol, FA
机构
[1] Univ Med Ctr Nijmegen, Dept Gastroenterol & Hepatol, NL-6500 HB Nijmegen, Netherlands
[2] Univ Med Ctr Nijmegen, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
关键词
Crohn's disease; IBD; IL-4R; CD11B; STAT6; ITGAM;
D O I
10.1038/sj.ejhg.5201058
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Linkage studies have identified the inflammatory bowel disease (IBD) 1 locus on chromosome 16 and the IBD2 locus on chromosome 12 to be involved in Crohn's disease. NOD2/CARD15 was identified as the gene of interest within the IBD1 region. However, linkage to this region could not be explained by NOD2/ CARD15 alone. Here we set out to assess the association of additional candidate genes from the IBD1 and IBD2 loci with Crohn's disease using transmission disequilibrium testing in patient - parent triads. No significant association was observed with genetic variants in the genes coding for interleukin-4 receptor gene (IL-4R), CD11B and signal transducer and activator of transcription type 6 (STAT6). Results for IL-4R were not affected by exclusion of all families carrying one of three risk alleles in NOD2. From this we conclude that IL-4R and CD11B in the IBD1 region and STAT6 in the IBD2 region are not involved in Crohn's disease in this Dutch cohort.
引用
收藏
页码:884 / 887
页数:4
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