Division of Cardiology, University of Texas Medical School at Houston, Memorial Hermann Hospital Heart & Vascular Institute at the Texas Medical Center, USA.
Biomark Med. 2011 Feb;5(1):43-51. doi: 10.2217/bmm.11.1.
Dual antiplatelet therapy with aspirin and a P2Y(12) receptor antagonist is the cornerstone of management in patients with acute coronary syndrome and those with coronary artery disease who have undergone coronary stent implantation. Clopidogrel is the most commonly used P2Y(12) antagonist. Despite clopidogrel's clinical effectiveness in reducing recurrent cardiovascular events in patients with coronary artery disease, the pharmacodynamic effect of clopidogrel is heterogeneous. Various platelet function tests that provide a quantitative measure of the downstream effects of clopidogrel on the P2Y(12) receptor are available. The consistent observation that a lack of clopidogrel effect based on these tests is associated with poor clinical outcome has led to the promise of an individualized, patient-centered approach to antiplatelet therapy. Over the past few years, a wealth of data have helped bring this promise closer to reality, and upcoming clinical trials of platelet function testing could at last bring personalized medicine into routine clinical practice.
双重抗血小板治疗,即阿司匹林联合 P2Y(12)受体拮抗剂,是急性冠脉综合征和经冠状动脉支架植入术治疗的冠状动脉疾病患者的治疗基石。氯吡格雷是最常用的 P2Y(12)拮抗剂。尽管氯吡格雷在减少冠状动脉疾病患者复发性心血管事件方面具有临床疗效,但氯吡格雷的药效学作用存在异质性。目前已有多种血小板功能检测方法可定量评估氯吡格雷对 P2Y(12)受体的下游作用。一致观察到,这些检测方法显示氯吡格雷缺乏作用与临床预后不良相关,这为个体化、以患者为中心的抗血小板治疗方法带来了希望。在过去几年中,大量数据使这一希望更接近现实,即将进行的血小板功能检测临床试验最终可能将个体化医疗纳入常规临床实践。