O'Doherty Catherine, Roos Izaura M, Antiguedad Alfredo, Aransay Ana M, Hillert Jan, Vandenbroeck Koen
Applied Genomics Research Group, Queen's University of Belfast, UK.
J Neuroimmunol. 2007 Sep;189(1-2):151-7. doi: 10.1016/j.jneuroim.2007.07.006. Epub 2007 Aug 8.
In multiple sclerosis (MS), alpha(4)beta(1) integrin, also known as Very Late Antigen 4 (VLA4), facilitates migration of leukocytes across the blood brain barrier. Several studies suggest that expression of alpha(4) integrin may be increased in MS patients compared to controls, and down-regulation or antagonism of alpha(4) integrin may be associated with immunomodulatory treatment success. We analysed association of 13 single nucleotide polymorphisms (SNPs) in the gene encoding alpha(4) integrin (ITGA4) with susceptibility to MS in two distinct populations comprising cases and controls from the Basque Country in northern Spain (352 patients; 235 controls) and Nordic countries (1119 patients; 1235 controls). Carriage of the C allele of the ITGA4 promoter SNP rs1449263 was independently and weakly increased in MS patients from each population compared to respective controls (P = 0.037 in Basque; and P = 0.042 in Nordic cohorts), though these associations were lost upon application of permutation correction. Meta-analysis of rs1449263*C carriage revealed a Mantel-Haenszel common OR of 1.26 (95% CI 1.06-1.49; P = 0.0069). Though our data only modestly argue for a role of ITGA4 in determining susceptibility to MS, we suggest that further examination of this gene, particularly the promoter region, is warranted.
在多发性硬化症(MS)中,α(4)β(1)整合素,也称为极迟抗原4(VLA4),促进白细胞穿过血脑屏障的迁移。多项研究表明,与对照组相比,MS患者中α(4)整合素的表达可能会增加,并且α(4)整合素的下调或拮抗作用可能与免疫调节治疗的成功有关。我们分析了编码α(4)整合素(ITGA4)的基因中的13个单核苷酸多态性(SNP)与MS易感性之间的关联,研究对象为两个不同的人群,包括来自西班牙北部巴斯克地区的病例和对照(352例患者;235例对照)以及北欧国家的病例和对照(1119例患者;1235例对照)。与各自的对照组相比,ITGA4启动子SNP rs1449263的C等位基因携带者在每个群体的MS患者中独立且微弱增加(巴斯克地区P = 0.037;北欧队列中P = 0.042),尽管在应用置换校正后这些关联消失了。对rs1449263*C携带者的荟萃分析显示Mantel-Haenszel共同比值比为1.26(95%可信区间1.06-1.49;P = 0.0069)。尽管我们的数据仅适度支持ITGA4在决定MS易感性中的作用,但我们建议对该基因,特别是启动子区域进行进一步研究。