Nakagome Shigeki, Takeyama Yasuaki, Mano Shuhei, Sakisaka Shotaro, Matsui Toshiyuki, Kawamura Shoji, Oota Hiroki
Department of Integrated Biosciences, Graduate School of Frontier Sciences, University of Tokyo, Chiba, Japan.
Ann Hum Genet. 2010 Mar;74(2):126-36. doi: 10.1111/j.1469-1809.2010.00567.x.
Crohn's disease (CD), a type of chronic inflammatory bowel disease (IBD), is commonly found in European and East Asian countries. The calculated heritability of CD appears to be higher than that of ulcerative colitis (UC), another type of IBD. Recent genome-wide association studies (GWAS) have identified more than thirty CD-associated genes/regions in the European population. In the East Asian population, however, a clear association between CD and an associated gene has only been detected with TNFSF15. In order to determine if CD susceptibility differs geographically, nine SNPs from seven of the European CD-associated genomic regions were selected for analysis. The genotype frequencies for these SNPs were compared among the 380 collected Japanese samples, which consisted of 212 IBD cases and 168 controls. We detected a significant association of both CD and UC with only the TNFSF15 gene. Analysis by the modified genotype relative risk test (mGRR) indicated that the risk allele of TNFSF15 is dominant for CD, but is recessive for UC. These results suggest that CD and UC susceptibility differs between the Japanese and European populations. Furthermore, it is also likely that CD and UC share a causative factor which exhibits a different dominant/recessive relative risk in the Japanese population.
克罗恩病(CD)是一种慢性炎症性肠病(IBD),在欧洲和东亚国家较为常见。CD的计算遗传度似乎高于另一种IBD——溃疡性结肠炎(UC)。最近的全基因组关联研究(GWAS)在欧洲人群中已鉴定出30多个与CD相关的基因/区域。然而,在东亚人群中,仅检测到CD与关联基因TNFSF15之间存在明确关联。为了确定CD易感性是否存在地域差异,从7个欧洲CD相关基因组区域中选择了9个单核苷酸多态性(SNP)进行分析。在收集的380份日本样本(包括212例IBD病例和168例对照)中比较了这些SNP的基因型频率。我们仅检测到CD和UC均与TNFSF15基因存在显著关联。通过改良基因型相对风险检验(mGRR)分析表明,TNFSF15的风险等位基因对CD呈显性,但对UC呈隐性。这些结果表明,日本人群和欧洲人群在CD和UC易感性方面存在差异。此外,CD和UC也可能共有一个致病因素,该因素在日本人群中表现出不同的显性/隐性相对风险。