Association of ITGA2 C807T and ITGB3 T1565C polymorphisms with platelet characteristics in hypertensive Azerbaijani patients.

Vafa Nazirova, Zumrud Ismibayli, Ismayil Gafarov, Faig Guliyev
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Abstract

Objective: Cardiovascular diseases (CVDs) are a leading cause of mortality worldwide, including in Azerbaijan. This study investigates the association of ITGA2 (C807T) and ITGB3 (T1565C) gene polymorphisms with platelet characteristics in Azerbaijani patients with arterial hypertension (AH), focusing on potential thrombotic risk. Methods: A total of 100 participants were examined, including 76 hypertensive patients and 24 controls. The hypertensive group was further subdivided based on comorbidities: ischemic heart disease (IHD) and type 2 diabetes mellitus (T2DM). Genotyping was performed using the massARRAY method. Platelet indices, including mean platelet volume (MPV), plateletcrit (PCT), and platelet large cell ratio (P-LCR), platelet distribution width (PDWsd) were evaluated. Statistical analysis was conducted using IBM SPSS Statistics 26, with correlation tests, ANOVA, and Chi-square tests to examine genotype distribution and platelet characteristics. Results: Carriers of the homozygous C/C genotype of the ITGA2 gene and T/T genotype of the ITGB3 gene exhibited the highest platelet counts and elevated MPV, suggesting a tendency toward increased platelet aggregation. Although all platelet parameters remained within the normal range, significant correlations were found between the ITGA2 T allele and MPV, PDWsd, and LPCR in hypertensive patients (p < 0.05). The study indicates that patients with the T/T genotype of ITGA2 and ITGB3 may have an elevated risk of thromboembolism. Conclusion: Integrin gene polymorphisms, particularly in ITGA2 and ITGB3, are associated with altered platelet characteristics in Azerbaijani patients with arterial hypertension. These genetic markers could serve as predictors for thrombotic complications, providing insights into targeted prevention strategies in CVD management.

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ITGA2 C807T和ITGB3 T1565C多态性与阿塞拜疆高血压患者血小板特征的关系
目的:心血管疾病(cvd)是全世界(包括阿塞拜疆)死亡的主要原因。本研究探讨了ITGA2 (C807T)和ITGB3 (T1565C)基因多态性与阿塞拜疆动脉高血压(AH)患者血小板特征的关系,重点关注潜在的血栓形成风险。方法:对100名参与者进行调查,其中高血压患者76人,对照组24人。高血压组根据合并症进一步细分:缺血性心脏病(IHD)和2型糖尿病(T2DM)。采用massARRAY方法进行基因分型。评估血小板指标,包括平均血小板体积(MPV)、血小板电积(PCT)、血小板大细胞比(P-LCR)、血小板分布宽度(PDWsd)。采用IBM SPSS Statistics 26进行统计学分析,采用相关检验、方差分析和卡方检验检验基因型分布和血小板特征。结果:ITGA2基因纯合子C/C基因型和ITGB3基因纯合子T/T基因型携带者血小板计数最高,MPV升高,提示血小板聚集增加的趋势。虽然所有血小板参数保持在正常范围内,但发现ITGA2 T等位基因与高血压患者MPV、PDWsd和LPCR之间存在显著相关性(p ITGA2和ITGB3可能增加血栓栓塞的风险。结论:整合素基因多态性,特别是在ITGA2和ITGB3中,与阿塞拜疆动脉高血压患者血小板特征的改变有关。这些遗传标记可以作为血栓性并发症的预测因子,为心血管疾病管理的针对性预防策略提供见解。
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来源期刊
Global Cardiology Science & Practice
Global Cardiology Science & Practice Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.60
自引率
0.00%
发文量
20
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