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对日本1型自身免疫性肝炎患者进行的全基因组DNA微卫星关联研究。

A genomewide DNA microsatellite association study of Japanese patients with autoimmune hepatitis type 1.

作者信息

Yokosawa Shuichi, Yoshizawa Kaname, Ota Masao, Katsuyama Yoshihiko, Kawa Shigeyuki, Ichijo Tetsuya, Umemura Takeji, Tanaka Eiji, Kiyosawa Kendo

机构信息

Department of Medicine, Shinshu University School of Medicine, Matsumoto, Japan.

出版信息

Hepatology. 2007 Feb;45(2):384-90. doi: 10.1002/hep.21518.

Abstract

UNLABELLED

Genetic predisposition to type 1 autoimmune hepatitis (AIH) is linked mainly to HLA class II genes. We previously searched the whole HLA region for AIH susceptibility genes using microsatellite markers and found only HLA-DR/DQ to be a candidate region for this suspected multifactorial disease. As such, the aim of this study was to broaden our search and screen the whole genome for additional genes that might contribute to type 1 AIH susceptibility. Eighty-one patients with type 1 AIH (15 men, 66 women, average age 55.9) and 80 healthy sex- and age-matched Japanese controls were enrolled in this study. We performed a case-control association study using 400 polymorphic microsatellite markers with an average spacing of 10.8 cM distributed throughout the whole genome. Two markers, one on chromosome 11 (D11S902, Pc = 0.013) and one on chromosome 18 (D18S464, Pc = 0.008), were revealed to have statistically significant associations with AIH. An additional 7 markers (D2S367, D6S309, D9S273, D11S1320, D16S423, D17S938, and D18S68) were also found to be candidate susceptibility regions. In addition, our results showed there were 17 regions that may contain genes of resistance to AIH. No specific markers were detected in HLA-DR4-negative patients, and no differences were seen in the clinical courses of patients (severe versus mild to moderate).

CONCLUSION

This first genomewide scan of Japanese AIH patients revealed at least 26 candidate AIH susceptibility or resistance regions other than HLA class II loci. These results also suggested that the products of several genes interact to determine heritable susceptibility to AIH.

摘要

未标注

1型自身免疫性肝炎(AIH)的遗传易感性主要与人类白细胞抗原(HLA)Ⅱ类基因相关。我们之前使用微卫星标记在整个HLA区域搜索AIH易感基因,发现只有HLA - DR/DQ是这种疑似多因素疾病的候选区域。因此,本研究的目的是扩大搜索范围,在全基因组中筛选可能导致1型AIH易感性的其他基因。本研究纳入了81例1型AIH患者(15名男性,66名女性,平均年龄55.9岁)和80名年龄及性别匹配的日本健康对照者。我们使用平均间距为10.8厘摩(cM)且分布于整个基因组的400个多态性微卫星标记进行病例对照关联研究。结果显示,位于11号染色体上的一个标记(D11S902,Pc = 0.013)和位于18号染色体上的一个标记(D18S464,Pc = 0.008)与AIH存在统计学显著关联。另外7个标记(D2S367、D6S309、D9S273、D11S1320、D16S423、D17S938和D18S68)也被发现是候选易感区域。此外,我们的结果表明有17个区域可能包含对AIH的抗性基因。在HLA - DR4阴性患者中未检测到特异性标记,患者的临床病程(重度与轻度至中度)也未见差异。

结论

对日本AIH患者进行的首次全基因组扫描显示,除了HLAⅡ类基因座外,至少还有26个候选AIH易感或抗性区域。这些结果还提示,多个基因的产物相互作用以决定AIH的遗传易感性。

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