[趋化因子基因多态性标记物及其受体和CD14基因与冠状动脉粥样硬化的关系]。

Genetika Pub Date : 2016-08-01
T R Nasibullin, L F Yagafarova, I R Yagafarov, Ya R Timasheva, V V Erdman, I A Tuktarova, O E Mustafina
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引用次数: 0

摘要

动脉粥样硬化是动脉血流中内皮层紊乱引起的炎症反应。在本研究中,我们对冠状动脉粥样硬化(CA)患者(217名受试者)和对照组(250名受试者)中控制动脉粥样硬化发病过程中蛋白质合成的基因多态性标记进行了关联分析。检测以下基因:rs991804 (CCL2基因)、rs1126579 (CXCR2基因)、rs4074 (CXCL1基因)、rs4073 (CXCL8基因)、rs333 (CCR5基因)、rs2471859 (CXCR4基因)、rs1801157 (CXCL12基因)、rs2569190 (CD14基因)。采用蒙特卡洛和马尔科夫链(APSampler)方法,揭示了与低、高CA风险相关的等位基因/基因型组合。最重要的结果包括:CXCR4*T/T + CCL2*C + CCR5*I/I (P perm = 1 × 10-6, OR = 0.44, 95% CI 0.3 ~ 0.63)、CXCR2*C + CD14*C + CXCL12*G + CCL2*C + CCR5*D (P perm = 4 × 10-6, OR = 5.78, 95% CI 2.34 ~ 14.28)、CD14*C + CCL2*C/C + CCR5*D (P perm = 6.3 × 10-6, OR = 5.81, 95% CI 2.17 ~ 15.56)、CXCL8*A + CXCR2*C + CD14*T + CXCR4*C (P perm = 0.01, OR = 3.21, 95% CI 1.63 ~ 6.31)。
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[Association of polymorphic markers of chemokine genes, their receptors, and CD14 gene with coronary atherosclerosis].

Atherosclerosis represents an inflammatory response to the disturbance of the endothelial layer in the arterial bloodstream. In the present study, an analysis of associations of polymorphic markers for the genes controlling synthesis of proteins involved in atherosclerosis pathogenesis in coronary atherosclerosis (CA) patients (217 subjects) and in a control group (250 subjects) was conducted. The following genes were examined: rs991804 (CCL2 gene), rs1126579 (CXCR2 gene), rs4074 (CXCL1 gene), rs4073 (CXCL8 gene), rs333 (CCR5 gene), rs2471859 (CXCR4 gene), rs1801157 (CXCL12 gene), and rs2569190 (CD14 gene). Using the Monte Carlo and Markov chain (APSampler) method, allele/genotype combinations associated with both low and high CA risk were revealed. The most important findings included the following: CXCR4*T/T + CCL2*C + CCR5*I/I (P perm = 1 × 10–6, OR = 0.44, 95% CI 0.3–0.63), CXCR2*C + CD14*C + CXCL12*G + CCL2*C + CCR5*D (P perm = 4 × 10–6, OR = 5.78, 95% CI 2.34–14.28), CD14*C + CCL2*C/C + CCR5*D (P perm = 6.3 × 10–6, OR = 5.81, 95% CI 2.17–15.56), CXCL8*A + CXCR2*C + CD14*T + CXCR4*C (P perm = 0.01, OR = 3.21, 95% CI 1.63–6.31).

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