冠心病患者血清基质金属蛋白酶9型的研究

P. Pigarevsky, S. Maltseva, D. Tanyansky, E. Firova, A. Tatarinov, Natalja V. Chivikova
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引用次数: 0

摘要

背景:该研究旨在量化冠心病患者血清中的9型基质金属蛋白酶,因为这种酶能够引发免疫炎症过程,导致动脉粥样硬化斑块的不稳定,不稳定型心绞痛和急性冠状动脉综合征的发展。目的:比较分析不同病程心绞痛和动脉粥样硬化的冠心病患者与相对健康人群血清中MMR-9的定量含量。材料与方法:对66例冠心病患者进行血清检测。根据临床检查将所有患者根据病情严重程度分为3组。采用Thermo Fisher ELISA试剂盒(BMS2016-2)进行定量MMR-9分析。elx800酶联免疫吸附试验板记录血清中MMR-9的含量。数据处理采用Statistica 6.0统计分析软件(statsoft, USA)。结果以均数和均数误差表示。结果:获得的结果表明,与对照组(相对健康的人)相比,病程不稳定的患者血清中MMR-9的浓度显著降低。这可能是由于其对MMR-9抑制剂TIMP-1的含量和活性的影响。进一步的研究将探讨MMR-9是否可以作为动脉粥样硬化斑块不稳定的标志,并作为心血管病理患者急性临床并发症的独立预测因子。结论:与对照组(相对健康的人群)相比,该研究可以确定动脉粥样硬化不稳定病程患者血清中MMR-9的浓度显著降低。此外,在动脉粥样硬化过程不稳定的患者中,与动脉粥样硬化稳定的患者相比,这种酶的浓度有降低的趋势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum matrix metalloproteinase type 9 in patients with coronary heart disease
BACKGROUND: The study sends to quantify type 9 matrix metalloproteinase in serum in patients with coronary heart disease, since this enzyme is able to provoke an immunoinflammatory process leading to destabilization of atherosclerotic plaque, the development of unstable angina and acute coronary syndrome. AIM: Is to conduct a comparative analysis of the quantitative content of MMR-9 in serum in patients with coronary heart disease (CHD) with a different course of angina and atherosclerosis and in relatively healthy individuals. MATERIALS AND METHODS: Blood serum samples of 66 CHD patients were examined. All patients based on clinical examination were divided into 3 groups, depending on the severity of the disease. Quantitative MMR-9 analysis was performed using the Thermo Fisher ELISA kits (BMS2016-2). Determination of the amount of MMR-9 in serum was recorded in the ELX 800 ELISA reader plate. Data processing was carried out using Statistica 6.0 statistical analysis (StatSof, USA). The results were presented as means and mean errors. RESULTS: The obtained results indicate a significant decrease in the concentration of MMR-9 in the serum of patients with an unstable course of the disease compared to the control group (relatively healthy people). This is probably due to the effect on the content and activity of its MMR-9 inhibitor TIMP-1. Further studies will investigate whether MMR-9 can be considered as a marker of destabilization of atherosclerotic plaque and act as an independent predictor of acute clinical complications in patients with cardiovascular pathology. CONCLUSIONS: The study made it possible to establish a significant decrease in the concentration of MMR-9 in the serum of patients with an unstable course of atherosclerosis compared to the control group (relatively healthy people). In addition, in patients with an unstable course of atherosclerosis, a tendency to reduce the concentration of this enzyme compared to persons with stable atherosclerosis was revealed.
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