MICA gene polymorphism in Takayasu's arteritis and Buerger's disease

被引:40
作者
Kimura, A
Kobayashi, Y
Takahashi, M
Ohbuchi, N
Kitamura, H
Nakamura, T
Satoh, M
Sasaoka, T
Hiroi, S
Arimura, T
Akai, J
Aerbajinai, W
Yasukochi, Y
Numano, F
机构
[1] Tokyo Med & Dent Univ, Dept Mol Pathogenesis, Div Adult Dis, Med Res Inst,Chiyoda Ku, Tokyo 1010062, Japan
[2] Tokyo Med & Dent Univ, Med Res Inst, Etiol & Pathogenesis Res Unit, Tokyo 1010062, Japan
[3] Tokyo Med & Dent Univ, Fac Med, Dept Internal Med 3, Tokyo 1138519, Japan
[4] Kurume Univ, Sch Med, Dept Internal Med 3, Kurume, Fukuoka 830, Japan
[5] Tokyo Med & Dent Univ, Med Res Inst, Div Genet, Dept Mol Genet, Tokyo 1138591, Japan
关键词
D O I
10.1016/S0167-5273(98)00157-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To further clarify the HLA-linked genes susceptible to arterio-vasculitis of unknown etiology, Takayasu's arteritis and Buerger's disease, polymorphism in the MICA gene, a newly identified gene near the HLA-B gene and expressed in epithelial cell lineage, was investigated. Polymerase chain reaction (PCR)-DNA conformation polymorphism (DCP) analysis and subsequent sequencing of the MICA gene have revealed that there are 5 MICA alleles which are different in the number of a GCT repeat in exon 5: MICA alleles MICA-1.1, -1.2, -1.3 and -1.4 have 9, 6, 5 and 4 GCT repeats, respectively, and MICA-1.5 has 5 GCT repeats with a 1 bp frameshift insertion in the repeat. MICA genotyping data in 81 Japanese patients with Takayasu's arteritis, 38 Japanese patients with Buerger's disease, and 160 healthy Japanese controls showed that MICA-1.2 and -1.4 were significantly associated with Takayasu's arteritis and Buerger's disease, respectively. Because MICA-1.2 and -1.4 were in strong linkage disequilibria with HLA-B52 and -B54 in the Japanese populations, respectively, we have compared the odds ratio (OR) of the risk to the diseases for individuals having both or each of the disease-associated MICA and HLA-B alleles. It was found that MICA-1.2 gave a significantly high OR of risk to Takayasu's arteritis in the absence of HLA-B52, suggesting that the HLA-linked gene susceptible to Takayasu's arteritis is mapped near the MICA gene. In contrast, MICA-1.4 gave a significantly high OR of risk to Buerger's disease only in the presence of HLA-B54, suggesting that the HLA-linked gene susceptible to Buerger's disease is linked to the HLA-B54-MICA-1.4 haplotype, and may be differently mapped from that to Takayasu's arteritis. (C) 1998 Elsevier Science B.V. All rights reserved.
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收藏
页码:S107 / S113
页数:7
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