Shevchenko A V, Golovanova O V, Konenkov V I, Tolkacheva O M, Maksimov V N, Voevoda M I, Romashchenko A G
Ter Arkh. 2010;82(1):31-4.
To analyze the gene polymorphisms of matrix metalloproteinase-2 and -9 in patients with coronary heart disease (CHD).
The influence of single nucleotide polymorphism in the promoter region of the gene of matrix metalloproteinase (MMP)-2 at position -1306 and that of MMP-9 at position -1562 on the development of complications was studied in 181patients with atherosclerosis by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis of amplification products.
A significant genotype increase with enhanced MMP-9 gene transcriptional activity was found in the patients aged 55 years inclusively who had been diagnosed as having myocardial infarction as compared with an older age group and, on the contrary, a rise in the MMP-2 genotype with a high promoter activity in the older age group.
The findings suggest that the functional polymorphism in the promoter region of the MMP-2 and MMP-9 genes plays a certain role in the development of acute coronary events.
分析冠心病(CHD)患者基质金属蛋白酶-2和-9的基因多态性。
采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析扩增产物,研究181例动脉粥样硬化患者基质金属蛋白酶(MMP)-2基因启动子区域-1306位点及MMP-9基因启动子区域-1562位点的单核苷酸多态性对并发症发生的影响。
与年龄较大组相比,年龄在55岁及以上且被诊断为心肌梗死的患者中,MMP-9基因转录活性增强的基因型显著增加;相反,年龄较大组中启动子活性高的MMP-2基因型增加。
研究结果表明,MMP-2和MMP-9基因启动子区域的功能多态性在急性冠状动脉事件的发生中起一定作用。