评估接受替卡格雷和阿司匹林治疗的急性冠状动脉综合征患者的 ADRB1 多态性。

Personalized medicine Pub Date : 2024-01-01 Epub Date: 2024-04-29 DOI:10.2217/pme-2024-0004
Xiang Zhang, Qi Yuan, Dawei Zhang
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引用次数: 0

摘要

研究背景本研究探讨了 ADRB1 基因 rs1801253 多态性对急性冠状动脉综合征(ACS)患者服用替卡格雷和阿司匹林治疗反应的影响。研究方法通过桑格测序检测基因分型。使用血栓弹力图评估血小板抑制作用。采用 Kaplan-Meier 和 Cox 回归进行预后分析。结果在 200 名参与者中,发现 94 例 rs1801253-CC 基因型和 106 例 CG+GG 基因型。rs1801253-CC组和CG+GG组在ST段抬高型心肌梗死、非ST段抬高型心肌梗死和不稳定型心绞痛患者人数上无明显差异。在显性模型中,两组患者在年龄、性别、病史和用药方面的基本数据无统计学差异。根据 Cox 回归分析结果,rs1801253-CC 基因型是 ACS 患者的风险预后因素。结论检测 ADRB1 多态性对接受替卡格雷和阿司匹林治疗的 ACS 患者至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of ADRB1 polymorphism in patients with acute coronary syndrome treated with ticagrelor and aspirin.

Background: This study investigated the influence of ADRB1 gene rs1801253 polymorphism on the treatment response of ticagrelor and aspirin in patients with acute coronary syndrome (ACS). Methods: Genetic typing was detected by Sanger sequencing. Platelet inhibition was assessed using thromboelastography. Kaplan-Meier and Cox regression were applied for prognosis analysis. Results: Out of 200 participants, 94 cases with rs1801253-CC genotype and 106 cases with CG+GG genotype were found. There was no significant difference between the rs1801253-CC and CG+GG groups in the number of ST-segment elevation myocardial infarction, non-ST-segment elevation myocardial infarction and unstable angina patients. There was no statistical difference in the basic data of patients in the two groups in terms of age, sex, medical history and medicine use in the dominant model. The rs1801253-CC genotype was a risk prognostic factor for ACS patients based on the Cox regression analysis results. Conclusion: Detecting ADRB1 polymorphism is crucial for ACS patients undergoing treatment with ticagrelor and aspirin.

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