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单核苷酸多态性在 MMP-9 基因与易感性发展多发性硬化症的意大利病例对照研究。

Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study.

机构信息

Institute of Neurological Sciences, National Research Council, Cosenza, Italy.

出版信息

J Neuroimmunol. 2010 Aug 25;225(1-2):175-9. doi: 10.1016/j.jneuroim.2010.04.016. Epub 2010 May 14.

Abstract

To investigate the role of the matrix metalloproteinase-9 gene (MMP-9) in multiple sclerosis (MS), we analyzed the functional -1562C/T and -90 (CA)(n) repeat polymorphisms in 243 Italian patients with MS and 173 healthy controls. A significant increase of the -1562T allele carriers was found in patients with MS compared to controls. Moreover, haplotype analysis showed that the haplotype formed by the -1562T allele and the L allele ((CA)(<or=20)) was over-represented in patients with MS versus controls. These results suggest that a genetic polymorphism of the MMP-9 promoter region may influence the susceptibility to MS.

摘要

为了研究基质金属蛋白酶-9 基因(MMP-9)在多发性硬化症(MS)中的作用,我们分析了 243 名意大利 MS 患者和 173 名健康对照者的功能性-1562C/T 和-90(CA)(n)重复多态性。与对照组相比,MS 患者中-1562T 等位基因携带者明显增加。此外,单体型分析表明,MS 患者中由-1562T 等位基因和 L 等位基因组成的单体型((CA)(<或=20))明显多于对照组。这些结果表明 MMP-9 启动子区域的遗传多态性可能影响 MS 的易感性。

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