Resistance to antiplatelet drugs. Can it be assessed?

Rossella Marcucci
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引用次数: 3

Abstract

High platelet reactivity (HPR) during dual antiplatelet therapy is a marker of vascular risk, in particular stent thrombosis in patients with acute coronary syndromes. Genetic determinants (CYP2C19*2 polymorphism), advanced age, female gender, diabetes and reduced ventricular function are related to a higher risk to develop HPR. In addition, inflammation and increased platelet turnover, as revealed by the elevated percentage of reticulate platelets in patients' blood that characterize the acute phase of ACS, are associated with HPR. To overcome the limitation of Clopidogrel, new antiplatelet agents (Prasugrel and Ticagrelor) were synthesized and the demonstration of their superiority over Clopidogrel was obtained in two randomized trials TRITON TIMI 38 and PLATO. Due to the current possibility of choosing between multiple antiplatelet strategies, the future prospect is to include the definition of platelet function during treatment in order to set a tailored therapy, in addition to clinical data and classical risk factors.

抗血小板药物耐药性。它可以被评估吗?
双重抗血小板治疗期间的高血小板反应性(HPR)是血管危险的标志,特别是急性冠状动脉综合征患者的支架血栓形成。遗传决定因素(CYP2C19*2多态性)、高龄、女性、糖尿病和心室功能降低与HPR发生的高风险相关。此外,炎症和血小板周转增加,如ACS急性期患者血液中网状血小板百分比升高所显示的,与HPR相关。为了克服氯吡格雷的局限性,我们合成了新的抗血小板药物(Prasugrel和Ticagrelor),并在TRITON TIMI 38和PLATO两项随机试验中证明了它们优于氯吡格雷。由于目前可以在多种抗血小板策略之间进行选择,未来的前景是在治疗过程中除了临床数据和经典危险因素外,还包括血小板功能的定义,以便制定量身定制的治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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