Gao Bo, Li Zhong-cheng
Tianjin Tianhe Hospital, Tianjin 300050, China.
Zhongguo Wei Zhong Bing Ji Jiu Yi Xue. 2004 Sep;16(9):536-9.
To investigate the association between serum matrix metalloproteinase-3(MMP-3) concentrations and the promoter 5A/6A polymorphism in patients with coronary heart disease (CHD).
The study enrolled 137 CHD patients and 106 control subjects without CHD. The diagnosis of both groups were confirmed by coronary artery angiography. One hundred and thirty-seven CHD patients were divided into acute myocardial infarction (AMI)group, unstable angina pectoris (UAP) group and stable angina (SA) group according to World Health Organization criteria. Serum concentration of MMP-3 was measured by enzyme linked immunoadsorbent assay (ELISA). MMP-3 promoter gene containing the 5A/6A polymorphism was amplified by polymerase chain reaction (PCR). PCR products were digested by Tth111 I and then were separated by electrophoresis on agarose gel.
The distribution of MMP-3 genotype was not significantly different between CHD patients and controls, so was it between AMI patients and controls. Serum MMP-3 level was significantly higher in AMI group than controls, UAP group and SA group (56.815+/-38.932)microg/L, (39.149+/-24.155)microg/L, (41.640+/-29.180)microg/L, (33.336+/-20.755)microg/L; P<0.01, P<0.05, P<0.01). Serum MMP-3 levels were not significantly different among genotypes and among controls, UAP and SA groups. No significantly differences in serum MMP-3 levels were found among patients with different numbers of coronary arteries that were involved in CHD.
No marked association could be found between 5A/6A polymorphism in MMP-3 gene and risk of CHD and AMI. Higher serum level of MMP-3 is strong associated with AMI, while not with number of coronary arteries that are involved in CHD. These data suggest that MMP-3 is a useful marker for AMI, and it might play an important role in the induction of disruption of atherosclerosis plaque.
探讨冠心病(CHD)患者血清基质金属蛋白酶-3(MMP-3)浓度与启动子5A/6A多态性之间的关联。
本研究纳入137例CHD患者和106例无CHD的对照者。两组的诊断均经冠状动脉造影证实。137例CHD患者根据世界卫生组织标准分为急性心肌梗死(AMI)组、不稳定型心绞痛(UAP)组和稳定型心绞痛(SA)组。采用酶联免疫吸附测定(ELISA)法检测血清MMP-3浓度。通过聚合酶链反应(PCR)扩增包含5A/6A多态性的MMP-3启动子基因。PCR产物用Tth111 I酶切,然后在琼脂糖凝胶上进行电泳分离。
CHD患者与对照者之间MMP-3基因型分布无显著差异,AMI患者与对照者之间也无显著差异。AMI组血清MMP-3水平显著高于对照组、UAP组和SA组(分别为56.815±38.932)μg/L、(39.149±24.155)μg/L、(41.640±29.180)μg/L、(33.336±20.755)μg/L;P<0.01,P<0.05,P<0.01)。基因型之间以及对照组、UAP组和SA组之间血清MMP-3水平无显著差异。CHD患者中不同冠状动脉受累数目患者的血清MMP-3水平无显著差异。
MMP-3基因的5A/6A多态性与CHD和AMI风险之间未发现明显关联。血清MMP-3水平升高与AMI密切相关,而与CHD患者冠状动脉受累数目无关。这些数据表明,MMP-3是AMI的一个有用标志物,它可能在动脉粥样硬化斑块破裂的诱导中起重要作用。