Nomura E, Kinouchi Y, Negoro K, Kojima Y, Oomori S, Sugimura M, Hiroki M, Takagi S, Aihara H, Takahashi S, Hiwatashi N, Shimosegawa T
Division of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Genes Immun. 2004 Sep;5(6):477-83. doi: 10.1038/sj.gene.6364114.
Ulcerative colitis (UC) is a multifactorial disorder with both genetic and environmental factors. HLA-B52 and DRB11502 are reported to be strongly associated with UC in Japan. However, the actual susceptible gene has not been identified yet. In this study, to map precisely the susceptible locus for UC, we performed association mapping in the chromosome 6p using 24 microsatellite markers distributed over 16 Mb. A total of 183 patients with UC and 186 healthy controls (HC) were included in this study. In all, 15 markers around the human leukocyte antigen (HLA) region showed statistical significance in the genotypic differentiation test concerned with the allelic distribution between the UC and HC. Especially, the markers between the centromeric region of HLA class I and the telomeric region of class III showed remarkably low P-values and the allele239 of C2-4-4 in class I marker showed the strongest association (Pc=2.9 x 10(-9): OR=3.74, 95% CI=2.50-5.60). Furthermore, we found strong linkage disequilibrium (LD) between the allele239 of C2-4-4 and HLA-B52 in haplotype analysis. These results provide evidence that, in Japanese, important determinants of disease susceptibility to UC may exist in HLA, especially between the centromeric region of class I and the telomeric region of class III, under the strong LD with HLA-B52.
溃疡性结肠炎(UC)是一种由遗传和环境因素共同导致的多因素疾病。在日本,据报道HLA - B52和DRB11502与UC密切相关。然而,实际的易感基因尚未确定。在本研究中,为了精确绘制UC的易感位点,我们使用分布在16 Mb区域的24个微卫星标记,在6号染色体p上进行了关联图谱分析。本研究共纳入了183例UC患者和186例健康对照(HC)。总体而言,在人类白细胞抗原(HLA)区域周围的15个标记物在关于UC和HC之间等位基因分布的基因型分化测试中显示出统计学意义。特别是,HLA I类着丝粒区域和III类端粒区域之间的标记物显示出极低的P值,I类标记物C2 - 4 - 4的等位基因239显示出最强的关联性(Pc = 2.9×10^(-9):OR = 3.74,95% CI = 2.50 - 5.60)。此外,在单倍型分析中,我们发现C2 - 4 - 4的等位基因239与HLA - B52之间存在强连锁不平衡(LD)。这些结果提供了证据,表明在日本人中,UC疾病易感性的重要决定因素可能存在于HLA中,特别是在I类着丝粒区域和III类端粒区域之间,与HLA - B52存在强LD。