Discipline of Nutrition, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.
Hum Immunol. 2010 Jun;71(6):602-9. doi: 10.1016/j.humimm.2010.03.003. Epub 2010 Apr 8.
Recent genome-wide association studies have provided evidence for the involvement of 3p21 in the pathogenesis of Crohn's disease (CD). Here we attempted to validate the 3p21 region in a well characterized CD case-control New Zealand dataset of 329 CD patients and 521 controls by genotyping tagging single nucleotide polymorphisms (SNPs) across this region. Analysis revealed significant differences between patients and controls for six of 14 SNPs: rs9874472, rs1800668, rs11716445, rs4283605, rs2131109, and rs6446298. Five of these demonstrated strong interaction with CARD15 and phenotypic analysis demonstrated association of these SNPs with age at first diagnosis, CD location, CD behavior and requirement of bowel resection. The results from this study support the accumulating evidence that suggests the 3p21 region is a CD-associated locus, although it remains unclear which is the causative SNP and/or gene.
最近的全基因组关联研究为 3p21 在克罗恩病(CD)发病机制中的作用提供了证据。在这里,我们通过对该区域的标签单核苷酸多态性(SNP)进行基因分型,试图在一个具有良好特征的新西兰 329 例 CD 病例对照数据集(521 名对照)中验证 3p21 区域。分析显示,在 14 个 SNP 中,有 6 个 SNP 在患者和对照组之间存在显著差异:rs9874472、rs1800668、rs11716445、rs4283605、rs2131109 和 rs6446298。其中 5 个与 CARD15 具有强烈的相互作用,表型分析表明这些 SNP 与首次诊断的年龄、CD 位置、CD 行为和肠切除术的需求有关。这项研究的结果支持了越来越多的证据,表明 3p21 区域是一个与 CD 相关的基因座,尽管尚不清楚哪个是致病 SNP 和/或基因。