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作 者:高秋琦[1] 徐力辛[2] 陶志华[3] 张怀勤[2] 陈达开[2] 林锡芳[1]
机构地区:[1]温州医学院第一附属医院ICU,浙江温州325000 [2]温州医学院第一附属医院心内科 [3]温州医学院第一附属医院检验科
出 处:《温州医学院学报》2008年第4期321-324,共4页Journal of Wenzhou Medical College
摘 要:目的:研究中国南方人群基质溶解素-1基因启动子16125A/6A多态性与急性心肌梗死的相关性。方法:采用DNA测序法检测116例急性心肌梗死患者和105例对照的基质溶解素-1基因启动子序列。结果:①基质溶解素-1基因启动子16125A/6A多态性的三种基因型(5A/5A、5A/6A、6A/6A)符合Hardy-Weinberg分布。②与对照组相比,心梗组的基质溶解素-1基因5A/5A和5A/6A基因型较多见,差异有显著性,P<0.01。③基因型的相对风险分析发现,5A/5A或5A/6A基因型携带者患急性心肌梗死风险是6A/6A基因型的3.050倍(95%可信区间:1.653-5.627)。结论:基质溶解素-1基因启动子16125A/6A多态性可能与中国南方急性心肌梗死的遗传易感性相关联,5A等位基因是急性心肌梗死发病的一个独立危险因素。Objective: To investigate the relationship between the polymorphism of 1 612 5A/6A in the promoter of the stromelysin-1 gene and the acute myocardial infarction (AMI) in population of southern Chinese. Methods: Using DNA sequencing, the polymorphism of the stromelysin-1 gene was detected in both 116 AMI patients and 105 control subjects. Results: (1) The allelic distribution of the stromelysin-1 gene in both groups matched the Hardy-Weinberg equilibrium (P〉0.05).(2) The number of 5A allele of the promoter of the stromelysin-1 gene in patients with AMI was higher than that of the control group (P〈0.01).(3) The odds ratio of the 5A/6A+SA/SA was 3.050(95% CI, 1.653 to 5.627). Conclusion: The 1612 5A/6A polymorphism in the promoter of the stromelysin-1 gene is associated with AMI in southern Chinese. The 1612 5A allele in the promoter of the stromelysin-1 gene may play an important role in the pathogenesis of AMI.
关 键 词:基质金属蛋白酶基因 基因多态性 急性心肌梗死 危险因素
分 类 号:R541[医药卫生—心血管疾病]
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