Oksenberg Jorge R, Barcellos Lisa F, Cree Bruce A C, Baranzini Sergio E, Bugawan Teodorica L, Khan Omar, Lincoln Robin R, Swerdlin Amy, Mignot Emmanuel, Lin Ling, Goodin Douglas, Erlich Henry A, Schmidt Silke, Thomson Glenys, Reich David E, Pericak-Vance Margaret A, Haines Jonathan L, Hauser Stephen L
Department of Neurology, University of California at San Francisco, San Francisco, CA 94143-0435, USA.
Am J Hum Genet. 2004 Jan;74(1):160-7. doi: 10.1086/380997. Epub 2003 Dec 10.
An underlying complex genetic susceptibility exists in multiple sclerosis (MS), and an association with the HLA-DRB11501-DQB10602 haplotype has been repeatedly demonstrated in high-risk (northern European) populations. It is unknown whether the effect is explained by the HLA-DRB1 or the HLA-DQB1 gene within the susceptibility haplotype, which are in strong linkage disequilibrium (LD). African populations are characterized by greater haplotypic diversity and distinct patterns of LD compared with northern Europeans. To better localize the HLA gene responsible for MS susceptibility, case-control and family-based association studies were performed for DRB1 and DQB1 loci in a large and well-characterized African American data set. A selective association with HLA-DRB115 was revealed, indicating a primary role for the DRB1 locus in MS independent of DQB10602. This finding is unlikely to be solely explained by admixture, since a substantial proportion of the susceptibility chromosomes from African American patients with MS displayed haplotypes consistent with an African origin.
多发性硬化症(MS)存在潜在的复杂遗传易感性,并且在高危(北欧)人群中已反复证明与HLA - DRB11501 - DQB10602单倍型相关。尚不清楚这种效应是由易感单倍型中的HLA - DRB1基因还是HLA - DQB1基因所解释,这两个基因处于强连锁不平衡(LD)状态。与北欧人相比,非洲人群的特点是单倍型多样性更高且连锁不平衡模式不同。为了更好地定位导致MS易感性的HLA基因,在一个大型且特征明确的非裔美国人数据集中对DRB1和DQB1基因座进行了病例对照和基于家系的关联研究。结果显示与HLA - DRB115存在选择性关联,表明DRB1基因座在MS中独立于DQB10602发挥主要作用。这一发现不太可能完全由基因混合来解释,因为相当一部分患有MS的非裔美国患者的易感染色体显示出与非洲起源一致的单倍型。