IMPACT OF THE SINGLE-NUCLEOTIDE POLYMORPHISM OF GENES IL1β, EDN1, AND NOS3 GENES ON THE INDIVIDUAL GENETIC PROFILE OF PATIENTS WITH CORONARY HEART DISEASE IN THE REPUBLIC OF CRIMEA

E. A. Zakharyan, O. Y. Gritskevich
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Abstract

Abstracts. Introduction. Coronary heart disease prevalence rate grows, which determines the importance of researchers’ inquiries aiming to improve the prevention, diagnosis, and treatment of this pathology. Aim. This study was aimed at identifying the associations of polymorphisms of genes interleukin 1-beta, endothelin-1, and endothelial nitric oxide synthase in patients with coronary heart disease. Materials and Methods. We studied polymorphic markers of endothelin-1 (rs5370), endothelial nitric oxide synthase (rs2070244), and interleukin 1-beta genes (rs1143634 and rs16944) in patients with ischemic heart disease (n=229) and in controls (n=56) by multiplex allele-specific polymerase chain reaction with electrophoretic detection. Odds ratio (OR) was used to state the association of genotypes with the disease; 95% confidence interval limits were calculated to assess the significance of OR. Results and Discussion. Analysis of the T-511C polymorphism in the interleukin 1-beta gene demonstrated a trend towards an increased risk of coronary heart disease associated with the TT genotype in the study group (Odds ratio=2.2, 95%. Confidence interval: 1.3-3.6). At the same time, the CC genotype can be associated with a protective effect (Odds Ratio=0.3, 95%. Confidence Interval: 0.2-0.6). When analyzing the C3953T polymorphism in the interleukin 1-beta gene, the TT genotype showed a significantly increased disease development risk within the pathology under study (Odds Ratio=6.4, 95%. Confidence Interval: 1.7-23.4). Analysis of the polymorphic marker C786T in the NOS3 gene showed a correlation between the TT genotype and susceptibility to coronary heart disease (Odds ratio=2.07, 95%. Confidence interval: 1.3-3.2), while the CC genotype showed a protective effect (Odds ratio=0.3, 95%. Confidence interval: 0.2-0.5). A similar result was obtained in an experiment with the Lys198Asn polymorphism in the endothelin-1 gene. TT genotype showed an association with the increased risk of coronary heart disease (Odds ratio=6.5, 95%. Confidence Interval: 3.4-12.4). Odds ratio analysis of the effect of heterozygotes showed no risk of coronary heart disease (Odds ratio=0.3, 95%. Confidence Interval: 0.1-0.5). Conclusions. This study allowed us to find an association between the polymorphic markers of genes endothelin-1 (rs5370), eNOS (rs2070244), and interleukin-1β (rs114634 and rs16944) and the coronary heart disease risk in the population, which may be useful for both stratification and selection of further therapeutic strategies.
IL1β、EDN1 和 NOS3 基因的单核苷酸多聚酶对克里米亚共和国冠心病患者个体遗传特征的影响
摘要。简介冠心病的发病率在不断上升,这就决定了研究人员为改善这一病症的预防、诊断和治疗而进行调查的重要性。研究目的本研究旨在确定冠心病患者体内白细胞介素 1-beta、内皮素-1 和内皮一氧化氮合酶基因多态性的相关性。材料与方法我们通过多重等位基因特异性聚合酶链反应和电泳检测,研究了缺血性心脏病患者(229 人)和对照组(56 人)中内皮素-1(rs5370)、内皮一氧化氮合酶(rs2070244)和白细胞介素 1-beta 基因(rs1143634 和 rs16944)的多态性标记。用比值比(OR)来说明基因型与疾病的相关性;计算95%置信区间限来评估OR的显著性。结果与讨论对白细胞介素 1-beta 基因 T-511C 多态性的分析表明,研究组中 TT 基因型的人患冠心病的风险有增加的趋势(Odds ratio=2.2,95% 置信区间:1.3-3.6)。与此同时,CC 基因型可起到保护作用(Odds Ratio=0.3,95%. 置信区间:0.2-0.6)。在分析白细胞介素 1-beta 基因中的 C3953T 多态性时,TT 基因型显示在所研究的病理范围内,疾病发展风险显著增加(Odds Ratio=6.4,95%。置信区间:1.7-23.4)。对 NOS3 基因多态性标记 C786T 的分析表明,TT 基因型与冠心病易感性之间存在相关性(Odds ratio=2.07,95% 置信区间:1.3-3.2),而 CC 基因型则显示出保护作用(Odds ratio=0.3,95% 置信区间:0.2-0.5)。内皮素-1 基因中 Lys198Asn 多态性的实验也得出了类似的结果。TT 基因型显示与冠心病风险增加有关(Odds ratio=6.5,95%。置信区间:3.4-12.4)。对杂合子影响的比值分析表明,没有患冠心病的风险(比值比=0.3,95%。 置信区间:0.1-0.5)。结论。这项研究让我们发现了内皮素-1(rs5370)、eNOS(rs2070244)和白细胞介素-1β(rs114634 和 rs16944)基因的多态性标记与人群冠心病风险之间的关联,这可能有助于分层和选择进一步的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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