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日本克罗恩病患者的Hla - B基因型

Hla-B genotype in Japanese patients with Crohn's disease.

作者信息

Kinouchi Yoshitaka, Matsumoto Keisuke, Negoro Kenichi, Takagi Sho, Takahashi Seiichi, Hiwatashi Nobuo, Shimosegawa Tooru

机构信息

Division of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.

出版信息

Dis Colon Rectum. 2003 Oct;46(10 Suppl):S10-4. doi: 10.1097/01.DCR.0000083386.69865.76.

Abstract

PURPOSE

The HLA-B gene is one of the susceptibility genes for inflammatory bowel disease. Previous association studies of HLA-B showed several associated alleles and haplotypes of HLA-B in patients with ulcerative colitis, and among the associated alleles HLA-B52 is well known to be strongly associated with ulcerative colitis in Japanese patients. However, there are no convincing reports about HLA-B including the B52 allele in patients with Crohn's disease. The purpose of this study was to determine if HLA-B, especially the B*52 allele, confers susceptibility to Crohn's disease or determines the disease phenotype of Crohn's disease.

METHODS

A total of 195 patients with Crohn's disease (49 ileitis, 106 ileocolitis, 34 colitis, 6 uncertain) and 185 healthy controls were studied in this case-controlled study. All patients and healthy controls were Japanese. Genotyping of the HLA-B gene was performed by a polymerase chain reaction, sequence-specific primer that can classify the gene into 23 allele groups. Allele frequencies were compared between patients with Crohn's disease and healthy controls with chi-squared test using a 2 x 2 contingency table. P value was corrected by the number of allele groups (n = 23) observed in the Japanese population or the number of clinical subgroups. Corrected P values of <0.05 were considered to be statistically significant.

RESULTS

Before the correction for multiple testing, B4001 and B44 were associated with patients with Crohn's disease, positively and negatively, respectively. However, after the correction there were no significant differences in any HLA-B alleles between patients with Crohn's disease and healthy controls. In the subgroup analysis according to clinical phenotypes (disease location, anal lesion, age at diagnosis, need for surgery), none of the HLA-B alleles except B52 showed any disease phenotype-genotype associations. The allele frequency of B52 in the colitis type (16.2 percent; corrected P = 0.011) was significantly higher than that in the combined group of the ileitis (7.1 percent) and ileocolitis (5.2 percent) types.

CONCLUSIONS

These results demonstrated that HLA-B did not confer overall susceptibility to Crohn's disease in Japan, but the B*52 allele may affect the location of the disease.

摘要

目的

HLA - B基因是炎症性肠病的易感基因之一。先前关于HLA - B的关联研究显示,溃疡性结肠炎患者中有几种HLA - B的相关等位基因和单倍型,在相关等位基因中,HLA - B52在日本溃疡性结肠炎患者中与疾病强相关已为人熟知。然而,关于克罗恩病患者中包括B52等位基因在内的HLA - B,尚无令人信服的报道。本研究旨在确定HLA - B,尤其是B*52等位基因是否赋予克罗恩病易感性或决定克罗恩病的疾病表型。

方法

在这项病例对照研究中,共纳入了195例克罗恩病患者(49例回肠炎、106例回结肠型、34例结肠炎型、6例不确定型)和185名健康对照。所有患者和健康对照均为日本人。采用聚合酶链反应 - 序列特异性引物对HLA - B基因进行基因分型,该方法可将基因分为23个等位基因组。使用2×2列联表,通过卡方检验比较克罗恩病患者与健康对照之间的等位基因频率。P值通过在日本人群中观察到的等位基因组数量(n = 23)或临床亚组数量进行校正。校正后P值<0.05被认为具有统计学意义。

结果

在进行多重检验校正之前,B4001和B44分别与克罗恩病患者呈正相关和负相关。然而,校正后,克罗恩病患者与健康对照之间的任何HLA - B等位基因均无显著差异。在根据临床表型(疾病部位、肛门病变、诊断年龄、手术需求)进行的亚组分析中,除B52外,没有任何HLA - B等位基因显示出疾病表型 - 基因型关联。结肠炎型中B52的等位基因频率(16.2%;校正后P = 0.011)显著高于回肠炎型(7.1%)和回结肠型(5.2%)的合并组。

结论

这些结果表明,在日本,HLA - B不会赋予克罗恩病总体易感性,但B*52等位基因可能影响疾病部位。

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