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抗血小板治疗的药物遗传学。

Pharmacogenetics of Antiplatelet Therapy.

机构信息

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA; email:

Department of Clinical Pharmacy, University of Michigan College of Pharmacy, Ann Arbor, Michigan, USA.

出版信息

Annu Rev Pharmacol Toxicol. 2023 Jan 20;63:211-229. doi: 10.1146/annurev-pharmtox-051921-092701. Epub 2022 Jan 8.

Abstract

Antiplatelet therapy is used in the treatment of patients with acute coronary syndromes, stroke, and those undergoing percutaneous coronary intervention. Clopidogrel is the most widely used antiplatelet P2Y12 inhibitor in clinical practice. Genetic variation in may influence its enzymatic activity, resulting in individuals who are carriers of loss-of-function alleles and thus have reduced active clopidogrel metabolites, high on-treatment platelet reactivity, and increased ischemic risk. Prospective studies have examined the utility of genetic testing to guide antiplatelet therapy, and more recently published meta-analyses suggest that pharmacogenetics represents a key treatment strategy to individualize antiplatelet therapy. Rapid genetic tests, including bedside genotyping platforms that are validated and have high reproducibility, are available to guide selection of P2Y12 inhibitors in clinical practice. The aim of this review is to provide an overview of the background and rationale for the role of a guided antiplatelet approach to enhance patient care.

摘要

抗血小板治疗用于治疗急性冠脉综合征、中风和接受经皮冠状动脉介入治疗的患者。氯吡格雷是临床实践中最广泛使用的抗血小板 P2Y12 抑制剂。可能影响其酶活性的遗传变异导致携带功能丧失等位基因的个体,从而使氯吡格雷活性代谢物减少、治疗中血小板反应性高和缺血风险增加。前瞻性研究已经检查了基因检测在指导抗血小板治疗中的效用,最近发表的荟萃分析表明,药物遗传学是个体化抗血小板治疗的关键治疗策略。快速基因检测,包括经过验证且具有高重现性的床边基因分型平台,可用于指导临床实践中 P2Y12 抑制剂的选择。本综述的目的是提供对抗血小板治疗方法的背景和原理的概述,以增强患者护理。

相似文献

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Pharmacogenetics of Antiplatelet Therapy.抗血小板治疗的药物遗传学。
Annu Rev Pharmacol Toxicol. 2023 Jan 20;63:211-229. doi: 10.1146/annurev-pharmtox-051921-092701. Epub 2022 Jan 8.

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From genes to drugs: and pharmacogenetics in clinical practice.从基因到药物:以及临床实践中的药物遗传学。
Front Pharmacol. 2024 Feb 14;15:1326776. doi: 10.3389/fphar.2024.1326776. eCollection 2024.

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