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基质金属蛋白酶-3 基因功能性多态性与中国汉族人群烟雾病的相关性研究。

Association of a functional polymorphism in the MMP-3 gene with Moyamoya Disease in the Chinese Han population.

机构信息

Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing, PR China.

出版信息

Cerebrovasc Dis. 2010;30(6):618-25. doi: 10.1159/000319893. Epub 2010 Oct 15.

Abstract

BACKGROUND

Moyamoya disease (MMD) is an uncommon cerebrovascular disease characterized by progressive stenosis of the intracranial internal carotid arteries and their proximal branches. The important role of genetic factors in the etiology and pathogenesis of MMD is being increasingly recognized. The study was designed to examine the association of single nucleotide polymorphisms in matrix metalloproteinase (MMP) and tissue inhibitors of metalloproteinase (TIMP) genes with MMD occurrence.

METHODS

A case-control study was performed. Five functional promoter polymorphisms in the MMP-2, MMP-3, MMP-9 and MMP-13 genes and a potentially functional promoter polymorphism in the TIMP-2 gene were determined by polymerase chain reaction-restriction fragment length polymorphism. Their associations with MMD were analyzed by multivariate logistic regression.

RESULTS

In total, 208 definite patients with MMD (including 31 familial MMD, FMMD, patients) and 224 healthy subjects were recruited. The frequency of the MMP-3 5A/6A and 5A/5A genotypes was significantly lower in MMD patients (OR = 0.57, 95% CI 0.38-0.86, p(corr) = 0.042) compared with healthy controls in a dominant genetic model. Significant differences of the MMP-3 5A/6A polymorphism were also detected between FMMD patients and controls both in the dominant genetic model (OR = 0.23, 95% CI 0.08-0.68, p(corr) = 0.048) and the additive genetic model (OR = 0.24, 95% CI 0.08-0.69, p(corr) = 0.048).

CONCLUSION

The functional polymorphism in the MMP-3 promoter might be associated with susceptibility to both MMD and FMMD in the Chinese Han population. The findings need to be validated in further studies including more subjects from different populations.

摘要

背景

烟雾病(MMD)是一种罕见的脑血管疾病,其特征是颅内颈内动脉及其近端分支进行性狭窄。遗传因素在 MMD 的病因和发病机制中起着重要作用,这一点正日益得到认可。本研究旨在探讨基质金属蛋白酶(MMP)和金属蛋白酶组织抑制剂(TIMP)基因的单核苷酸多态性与 MMD 发病的相关性。

方法

采用病例对照研究。应用聚合酶链反应-限制性片段长度多态性分析方法,检测 MMP-2、MMP-3、MMP-9 和 MMP-13 基因的 5 个功能启动子多态性和 TIMP-2 基因的一个潜在功能启动子多态性。采用多变量 logistic 回归分析其与 MMD 的关系。

结果

共纳入 208 例确诊的 MMD 患者(包括 31 例家族性 MMD,FMMD)和 224 例健康对照者。与健康对照组相比,MMD 患者 MMP-3 5A/6A 和 5A/5A 基因型的频率在显性遗传模型中显著降低(OR=0.57,95%CI 0.38-0.86,p(corr)=0.042)。在显性遗传模型中,FMMD 患者 MMP-3 5A/6A 多态性与对照组之间也存在显著差异(OR=0.23,95%CI 0.08-0.68,p(corr)=0.048)和加性遗传模型(OR=0.24,95%CI 0.08-0.69,p(corr)=0.048)。

结论

MMP-3 启动子的功能多态性可能与汉族人群 MMD 和 FMMD 的易感性有关。这些发现需要在包括来自不同人群的更多受试者的进一步研究中得到验证。

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