1型和2型基质金属蛋白酶编码基因多态性变异与缺血性卒中风险的关联研究分析:俄罗斯中部人群的试点研究

L. Rymarova, E. Klyosova, A. Volkova, O. Bushueva, I. Azarova, V. Laskov, A. Polonikov
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引用次数: 0

摘要

基质金属蛋白酶基因的多态性变异是一个有吸引力的对象,用于检测与缺血性卒中风险的关联。迄今为止,还没有研究评估基质金属蛋白酶基因多态性在俄罗斯人缺血性中风发展中的作用。本研究的目的是分析编码基质金属蛋白酶1型(MMP1 rs1799750)和2型(MMP2 rs243865)基因多态性变异与俄罗斯中部俄罗斯人缺血性卒中(IS)风险之间的关系。本研究的结果以及在其他人群中进行的研究清楚地表明,协同作用在基质金属蛋白酶基因多态性变异之间的相互作用中在缺血性卒中易感性中起着至关重要的作用,因此需要在这一方向上进行进一步的研究。
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Analysis of association study between polymorphic variants of genes encoding matrix metalloproteinases types 1 and 2 and the risk of ischemic stroke: pilot study in the central Russia population
Polymorphic variants of matrix metalloproteinase genes are an attractive object for testing associations with the risk of ischemic stroke. To date, no studies have been done to assess the contribution of polymorphisms of matrix metalloproteinase genes in the development of ischemic stroke in Russians. The purpose of this study was to analyze the association between polymorphic variants of the genes encoding matrix metalloproteinases type 1 (MMP1 rs1799750) and 2 (MMP2 rs243865) and the risk of ischemic stroke (IS) in Russians from Central Russia. The results of this study, as well as studies performed in oth-er populations clearly demonstrate the crucial role of synergy in the interaction between polymorphic variants of matrix metalloproteinase genes in the predisposition to ischemic stroke, thereby dictating the need for further research in this direction.
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