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基质金属蛋白酶 12 基因多态性与汉族人群颈动脉斑块易感性之间无独立关系。

Lack of independent relationship between the MMP-12 gene polymorphism and carotid plaque susceptibility in the Chinese Han population.

机构信息

Department of Neurology, Taizhou Hospital, Affiliated Hospital of Wenzhou Medical College, Taizhou, Zhejiang, PR China.

出版信息

Vasc Med. 2012 Oct;17(5):310-6. doi: 10.1177/1358863X12451513. Epub 2012 Aug 3.

DOI:10.1177/1358863X12451513
PMID:22863605
Abstract

The purpose of this study was to investigate whether a polymorphism in the matrix metalloproteinase-12 gene (MMP-12 -82A/G) is correlated with serum protein levels or with the susceptibility for carotid plaques in the Chinese Han population. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was performed on the -82A/G polymorphism in the MMP-12 gene for 1314 patients with acute cerebral infarctions; 710 of these cases were diagnosed with stable plaques, 340 cases were diagnosed with vulnerable plaques and 264 cases had no plaques. At the same time, serum MMP-12 levels were measured using the enzyme-linked immunosorbent assay (ELISA). Compared to the AA genotype, the frequency of the AG+GG genotypes was not significantly different between the three groups (χ(2) = 1.242, p = 0.537), and the frequency of the G allele of the MMP-12 gene was not different within the three subgroups (χ(2) = 1.218, p = 0.544). There were no significant differences in MMP-12 protein levels among the three groups (F = 0.675, p = 0.510); similarly, there was no difference in MMP-12 protein levels between the stable plaque group and the vulnerable plaque group (p = 0.755). There was also no difference between the vulnerable plaque group and the no plaque group (p = 0.420). The current data suggest that the inter-individual variability in the MMP-12 gene variation may not be a risk factor for vulnerable plaques in the Chinese Han population.

摘要

本研究旨在探讨基质金属蛋白酶-12 基因(MMP-12-82A/G)多态性是否与血清蛋白水平或中国汉族人群颈动脉斑块易感性相关。对 1314 例急性脑梗死患者的 MMP-12 基因-82A/G 多态性进行聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析;其中 710 例诊断为稳定斑块,340 例诊断为易损斑块,264 例无斑块。同时,采用酶联免疫吸附试验(ELISA)检测血清 MMP-12 水平。与 AA 基因型相比,三组间 AG+GG 基因型的频率无显著差异(χ(2) = 1.242,p = 0.537),三组内 MMP-12 基因 G 等位基因的频率也无差异(χ(2) = 1.218,p = 0.544)。三组间 MMP-12 蛋白水平无显著差异(F = 0.675,p = 0.510);同样,稳定斑块组与易损斑块组 MMP-12 蛋白水平也无差异(p = 0.755)。易损斑块组与无斑块组之间也无差异(p = 0.420)。目前的数据表明,MMP-12 基因变异的个体间变异性可能不是中国汉族人群易损斑块的危险因素。

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