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基于 SNP 的日本多发性硬化症患者 HLA 基因座分析。

SNP-based analysis of the HLA locus in Japanese multiple sclerosis patients.

机构信息

Department of Neurology, University of California, San Francisco (UCSF), San Francisco, CA 94143, USA.

出版信息

Genes Immun. 2011 Oct;12(7):523-30. doi: 10.1038/gene.2011.25. Epub 2011 Jun 9.

Abstract

Although several major histocompatibility complex (MHC)-wide single-nucleotide polymorphism (SNP) studies have been performed in populations of European descent, none have been performed in Asian populations. The objective of this study was to identify human leukocyte antigen (HLA) loci associated with multiple sclerosis (MS) in a Japanese population genotyped for 3534 MHC region SNPs. Using a logistic regression model, two SNPs (MHC Class III SNP rs422951 in the NOTCH4 gene and MHC Class II SNP rs3997849, susceptible alleles A and G, respectively) were independently associated with MS susceptibility (204 patients; 280 controls), two (MHC Class II SNP rs660895 and MHC Class I SNP rs2269704 in the NRM gene, susceptible alleles G and G, respectively) with aquaporin-4- (AQP4-) MS susceptibility (149 patients; 280 controls) and a single SNP (MHC Class II SNP rs1694112, susceptible allele G) was significant when contrasting AQP4+ against AQP4- patients. Haplotype analysis revealed a large susceptible association, likely DRB104 or a locus included in the DRB104 haplotype, with AQP4- MS, which excluded DRB1*15:01. This study is the largest study of the HLA's contribution to MS in Japanese individuals.

摘要

尽管已经在欧洲血统的人群中进行了几项主要组织相容性复合体 (MHC) 全基因组单核苷酸多态性 (SNP) 研究,但在亚洲人群中尚未进行此类研究。本研究的目的是鉴定在日本人群中进行的 3534 个 MHC 区域 SNP 基因分型中与多发性硬化症 (MS) 相关的人类白细胞抗原 (HLA) 基因座。使用逻辑回归模型,两个 SNP(NOTCH4 基因中的 MHC 类 III SNP rs422951 和 MHC 类 II SNP rs3997849,分别为易感等位基因 A 和 G)与 MS 易感性(204 例患者;280 例对照)独立相关,两个 SNP(NRM 基因中的 MHC 类 II SNP rs660895 和 MHC 类 I SNP rs2269704,分别为易感等位基因 G 和 G)与水通道蛋白 4-(AQP4-)MS 易感性(149 例患者;280 例对照)相关,当对比 AQP4+与 AQP4-患者时,单个 SNP(MHC 类 II SNP rs1694112,易感等位基因 G)也具有显著意义。单体型分析显示,AQP4-MS 存在一个大的易感关联,可能是 DRB104 或包含在 DRB104 单体型中的一个基因座,该单体型排除了 DRB1*15:01。本研究是针对日本人群中 HLA 对 MS 贡献的最大研究。

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