Shevchenko A V, Konenkov V I, Prokof'ev V F, Pokushalov E A
Ter Arkh. 2014;86(4):19-24.
To analyze the association of the promoter polymorphism of the genes of the matrix metalloproteinases (MMP) MMP2 (-1306), MMP3 (-1171), and MMP9 (-1562) and two vascular endothelial growth factor (VEGF) gene regulatory regions (-2578, +936) with the development of myocardial infarction (MI).
DNA was analyzed in 251 patients with a history of MI. Five polymorphic positions were genotyped by restrictase analysis of amplification products, by using specific primers.
In addition to the MMP3 5A5A monogenotype, there were 4 complex genotypes that were significantly different between two analyzed groups and positively associated with acute coronary syndrome. Among them, each of two genotypes included 2 polymorphic positions; two genotypes did 3 analyzed polymorphic positions. Four complex (two-locus (n = 1), three-locus (n = 2), four-locus (n = 1) genotypes that were negatively associated with MI were also identified.
These findings are evidence in favor of our assumption that the increasing number of genotypes as part of the analyzed combined genetic complexes detectable in one patient considerably enhances the clinical significance of the results of immunogenetic analysis.
分析基质金属蛋白酶(MMP)MMP2(-1306)、MMP3(-1171)和MMP9(-1562)基因启动子多态性以及两个血管内皮生长因子(VEGF)基因调控区(-2578,+936)与心肌梗死(MI)发生的相关性。
对251例有MI病史的患者进行DNA分析。通过使用特异性引物对扩增产物进行限制性酶切分析,对5个多态性位点进行基因分型。
除MMP3 5A5A单基因型外,还有4种复合基因型在两个分析组之间存在显著差异,并与急性冠状动脉综合征呈正相关。其中,两种基因型各包含2个多态性位点;两种基因型包含3个分析的多态性位点。还鉴定出4种与MI呈负相关的复合(两位点(n = 1)、三位点(n = 2)、四位点(n = 1))基因型。
这些发现支持了我们的假设,即作为在一名患者中可检测到的分析性复合遗传复合物一部分的基因型数量增加,大大提高了免疫遗传学分析结果的临床意义。