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Role of C807T polymorphism of ITGA2 gene of collagen receptor and platelet aggregation activity in patients with arterial hypertension

机译:胶原蛋白受体和血小板聚集活性ITGA2基因C807T多态性在动脉高血压患者中的作用

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Aim. To study the prevalence of various C807T polymorphism variants of the ITGA2 gene and to analyze the association of this polymorphism with platelet aggregation activity in hypertensive patients. Methods. 47 patients with arterial hypertension treated at the Clinical Cardiology Dispensary (Perm) were included in the study. Genotyping of C807T polymorphism (rs 1126643) was carried out by the method of polymerase chain reaction with the subsequent identification of the single nucleotide polymorphic variant of ITGA2 gene by the method of allele-specific polymerase chain reaction. Platelet aggregation activity was investigated by the impedance method using TRAP-6 reagent as an inducer of aggregation. Results. The prevalence of C/C, C/T, T/T genotypes of ITGA2 gene among hypertensive patients was 18 (38.3%), 23 (48.9%) and 6 (12.8%), respectively. A comparative analysis of platelet aggregation activity with TRAP-6 reagent revealed statistically significant differences between the groups of patients carrying different genotypes [103.5 (67.0; 121.0) AU in homozygotes –807CC versus 52.5 (48; 83) AU in homozygotes –807TT, p=0.045]. In the group of patients with reduced platelet aggregation activity (TRAP-test less than 94 AU), the carriage of the unfavorable T allele prevailed in comparison with the group of patients with its normal level (OR=3.81, 95% CI 1.38–10.54; p=0.008). In patients of this group, there was a significant increase in the frequency of occurrence of heterozygotes –807CT (OR=4.75, 95% CI 1.24–18.19; p=0.009), as well as an increase in the frequency of occurrence of homozygotes for the variant allele -807TT (OR=2.88, 95% CI 0.31–27.07; p=0.009) compared with the group of patients with a normal level of aggregation. Conclusion. The prevalence of C/C, C/T, T/T genotypes of ITGA2 gene among patients with arterial hypertension is comparable to the data of European researchers: carriers of T allele of ITGA2 gene may have a higher risk of developing cardiovascular events; the molecular mechanism of the relationship of reduced platelet aggregation activity and carriage of the unfavorable T allele of ITGA2 gene requires further studies.
机译:目标。研究ITGA2基因各种C807T多态性变异的患病率,分析这种多态性与高血压患者血小板聚集活性的关联。方法。 47例在临床心脏病病变治疗(烫发)中治疗的动脉高血压患者均包括在该研究中。通过通过等级特异性聚合酶链反应的方法,通过聚合酶链反应的聚合酶链反应方法进行C807T多态性(RS 1126643)的基因分型。通过使用Trap-6试剂作为聚集诱导剂的阻抗法研究了血小板聚集活性。结果。高血压患者ITGA2基因的C / C,C / T,T / T基因型的患病率分别为18(38.3%),23(48.9%)和6(12.8%)。陷阱 - 6试剂的血小板聚集活性的对比分析显示携带不同基因型的患者组之间的统计学上显着差异[103.5(67.0; 121.0)Au在纯合蛋白-807cc与52.5(48; 83)Au在homozygotes -807tt,p = 0.045]。在减少血小板聚集活性的患者(陷阱试验小于94 AU)中,与其正常水平的患者组(或= 3.81,95%CI 1.38-10.54)相比,不利的T等位基因的运输普遍存在; p = 0.008)。在该组的患者中,杂合子的发生频率显着增加-807Ct(或= 4.75,95%CI 1.24-18.19; p = 0.009),以及纯合的发生频率与具有正常聚集水平的患者相比,变体等位基因-807TT(或= 2.88,95%CI 0.31-27.07; p = 0.009)。结论。动脉高血压患者的ITGA2基因的C / C,C / T,T / T基因型的患病率与欧洲研究人员的数据相媲美:ITGA2基因的等位基因的载体可能具有更高的发育心血管事件的风险;降低血小板聚集活性关系的分子机制和ITGA2基因不利等位基因的载体需要进一步研究。

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