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基质金属蛋白酶-3 基因启动子多态性与大脑中动脉狭窄的相关性研究。

The association of the metalloproteinase-3 gene promoter polymorphisms and the middle cerebral artery stenosis.

机构信息

Department of Neurology, The First Hospital of Jilin University, 77 Xinmin street, Changchun, 130021, Jilin province, China.

出版信息

Cell Biochem Biophys. 2011 Apr;59(3):185-9. doi: 10.1007/s12013-010-9131-y.

Abstract

To investigate the association of single nucleotide polymorphism in the matrix metalloproteinase-3 (MMP3) gene promoter with the susceptibility to the middle cerebral artery stenosis. A case-control study was performed by determining the genotype of MMP3 gene promoter region using polymerase chain reaction-restriction fragment length polymorphism in 119 patients with middle cerebral artery stenosis documented by transcranial Doppler compared to 92 control patients. The frequencies of 5A and 6A alleles in MMP3 promoter region were 16.0 and 84.0% respectively in case group compared to 15.8 and 84.2% in control group with no significant difference between the two groups (P > 0.05). No significant difference was also observed in the distribution of genotypes 5A/5A,5A/6A, and 6A/6A between middle cerebral artery stenosis and control groups. Compared to 5A/5A + 5A/6A genotypes,the 6A/6A genotype did not significantly modify the risk of developing the middle cerebral artery stenosis. The MMP3-1171 dupA promoter polymorphisms are not valuable markers of susceptibility of the middle cerebral artery stenosis in this sample of population studied.

摘要

为了研究基质金属蛋白酶-3(MMP3)基因启动子中单核苷酸多态性与大脑中动脉狭窄易感性的关系。采用聚合酶链反应-限制性片段长度多态性方法,对 119 例经颅多普勒检查证实的大脑中动脉狭窄患者(病例组)和 92 例对照组 MMP3 基因启动子区基因型进行了测定。病例组 MMP3 启动子区 5A 和 6A 等位基因的频率分别为 16.0%和 84.0%,对照组分别为 15.8%和 84.2%,两组间无显著性差异(P>0.05)。两组间 MMP3 基因型 5A/5A、5A/6A 和 6A/6A 的分布也无显著性差异。与 5A/5A+5A/6A 基因型相比,6A/6A 基因型并未显著改变大脑中动脉狭窄的发病风险。在本研究人群样本中,MMP3-1171dupA 启动子多态性不是大脑中动脉狭窄易感性的有价值标志物。

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