The Lautenberg Center for Immunology, Hebrew University Hadassah Medical School, Jerusalem, Israel.
Genes Immun. 2010 Jul;11(5):423-31. doi: 10.1038/gene.2010.20. Epub 2010 May 13.
Different multiple sclerosis (MS) prevalence rates were reported for Muslim and Christian Arabs in Israel. In this study, we evaluated whether associations of human leukocyte antigen (HLA) genes with MS may contribute to this prevalence difference. DNA samples from Israeli Arab MS patients (n=109) and controls (n=132) were typed for HLA class I (HLA-A, -B and -C) and II (HLA-DRB1 and -DQB1) genes. Global comparisons of HLA allele frequencies revealed significant differences between Christians and Muslims; therefore, case-control analyses were stratified by religious affiliation. Disease characteristics of Muslim and Christian Arab MS patients were similar to those reported for European populations. Opposing association signals with MS were observed for alleles composing the DRB10301-DQB10201 haplotype: positive association of the HLA-DRB10301 allele in Muslims (P(Bonferroni)=0.004, odds ratio (OR)=3.07), and negative association in Christian Arabs (P(Bonferroni)=0.01, OR=0.12), with similar results obtained for HLA-DQB10201. HLA-B52 was negatively associated with MS only in Muslims (P(Bonferroni)=0.01, OR=0.03). The study presents for the first time a high-resolution HLA gene analysis in clinically well-characterized Arab populations with MS, and shows the population-specific contribution of the DRB10301-DQB1*0201 haplotype to disease susceptibility.
在以色列,不同的多发性硬化症(MS)患病率在穆斯林和基督教阿拉伯人之间有所报道。在这项研究中,我们评估了人类白细胞抗原(HLA)基因与 MS 的关联是否有助于解释这种患病率差异。对来自以色列阿拉伯裔 MS 患者(n=109)和对照(n=132)的 DNA 样本进行了 HLA Ⅰ类(HLA-A、-B 和 -C)和Ⅱ类(HLA-DRB1 和 -DQB1)基因分型。HLA 等位基因频率的全球比较显示了基督教徒和穆斯林之间的显著差异;因此,根据宗教信仰对病例对照分析进行了分层。穆斯林和基督教阿拉伯裔 MS 患者的疾病特征与欧洲人群报告的相似。与 MS 相关的等位基因组成的 DRB10301-DQB10201 单体型表现出相反的关联信号:在穆斯林中,HLA-DRB10301 等位基因呈正关联(Bonferroni 校正后 P 值=0.004,优势比(OR)=3.07),而在基督教阿拉伯人中呈负关联(Bonferroni 校正后 P 值=0.01,OR=0.12),HLA-DQB10201 也得到了类似的结果。HLA-B52 仅在穆斯林中与 MS 呈负相关(Bonferroni 校正后 P 值=0.01,OR=0.03)。本研究首次在具有 MS 的临床特征良好的阿拉伯人群中进行了高分辨率 HLA 基因分析,并显示了 DRB10301-DQB1*0201 单体型对疾病易感性的特定人群贡献。