Interleukin-1β gene rs1143634 polymorphism and cardiovascular complications in patients with coronary artery atherosclerosis

E. V. Khazova, O. V. Bulashova, E. Valeeva
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Abstract

The course of heart failure, regardless of its etiology, is associated with local and systemic activation of inflammatory signaling cascades. Identification of the association of candidate cytokine genes with the risk of developing coronary heart disease and chronic heart failure remains a subject of interest for many researchers. The review presents an analysis of studies of the rs1143634 polymorphism of the IL-β gene in relation to the risk of atherosclerotic cardiovascular complications. The presence of the minor allele T is associated with an increase in the concentration of IL-1β in the blood serum. Data on the role of the rs1143634 polymorphism of the IL-β gene in atherosclerotic coronary heart disease, including in combination with chronic heart failure syndrome, are presented, taking into account ethnic characteristics and gender of patients. The carriage of the T allele was associated with the risk of developing atherosclerosis and myocardial infarction. At the same time, it is reported that the C allele and the CC genotype of the rs1143634 polymorphism of the IL-1β gene were a genetic risk factor for the development and progression of heart failure. In a number of studies and meta-analyses, the association of this polymorphism with diseases of the cardiovascular system was not confirmed, but certain trajectories of the risk of complications were identified due to differences in the rs1143634 polymorphism of the IL-β gene in heart failure.
白细胞介素-1β基因 rs1143634 多态性与冠状动脉粥样硬化患者的心血管并发症
无论病因如何,心力衰竭的病程都与局部和全身的炎症信号级联激活有关。确定候选细胞因子基因与冠心病和慢性心力衰竭发病风险的关系仍然是许多研究人员感兴趣的课题。本综述分析了有关 IL-β 基因 rs1143634 多态性与动脉粥样硬化性心血管并发症风险的研究。小等位基因 T 的存在与血清中 IL-1β 浓度的增加有关。考虑到患者的种族特征和性别,本文提供了有关 IL-β 基因 rs1143634 多态性在动脉粥样硬化性冠心病(包括合并慢性心力衰竭综合征)中的作用的数据。携带 T 等位基因与动脉粥样硬化和心肌梗死的发病风险有关。同时,据报道,IL-1β 基因 rs1143634 多态性的 C 等位基因和 CC 基因型是心衰发生和发展的遗传风险因素。在一些研究和荟萃分析中,该多态性与心血管系统疾病的关联并未得到证实,但由于心衰患者 IL-β 基因 rs1143634 多态性的差异,确定了某些并发症风险的轨迹。
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