Cuisset Thomas, Frere Corinne, Quilici Jacques, Gaborit Bénédicte, Castelli Christel, Poyet Raphael, Bali Laurent, Morange Pierre-Emmanuel, Alessi Marie-Christine, Bonnet Jean-Louis
Department of Cardiology, CHU Timone, Marseille, France.
Am J Cardiol. 2009 Oct 15;104(8):1078-82. doi: 10.1016/j.amjcard.2009.06.007.
A low response to clopidogrel has been associated with an increased risk of stent thrombosis. However, the definition of a nonresponse to clopidogrel remains controversial, and different tests have been used to assess the clopidogrel response. The present study was designed to assess the predictive value of adenosine diphosphate (ADP)-induced platelet aggregation (ADP-Ag) and the Platelet Reactivity Index of vasodilator-stimulated phosphoprotein for the occurrence of stent thrombosis in patients admitted for non-ST-elevation acute coronary syndrome undergoing percutaneous coronary intervention. A total of 598 consecutive patients with non-ST-elevation acute coronary syndrome undergoing coronary stenting were prospectively included. They received 600 mg of clopidogrel >or=12 hours before percutaneous coronary intervention. Acute or subacute definite or probable stent thrombosis occurred in 11 patients (1.8%). These patients had significantly greater ADP-Ag compared to patients free of stent thrombosis (68 +/- 14% vs 56 +/- 19%, p = 0.002) but only a trend toward a greater Platelet Reactivity Index of vasodilator-stimulated phosphoprotein (62 +/- 14% vs 53 +/- 23%, p = 0.19). The construction of receiver operating characteristic curves to examine the most predictive value of ADP-Ag for stent thrombosis gave a threshold of ADP-Ag of >67% to identify low responders. These patients were at a greater risk of stent thrombosis than the clopidogrel responders (4.3% vs 0.8%, odds ratio 5.8, 95% confidence interval 1.9 to 24.6, p = 0.003). In conclusion, in patients with non-ST-elevation acute coronary syndrome undergoing percutaneous coronary intervention, ADP-Ag is a good parameter to identify clopidogrel nonresponders who are at increased risk of stent thrombosis, with a cutoff value of ADP-Ag of >67%.
对氯吡格雷反应低下与支架内血栓形成风险增加相关。然而,氯吡格雷无反应的定义仍存在争议,并且已使用不同的检测方法来评估氯吡格雷反应。本研究旨在评估二磷酸腺苷(ADP)诱导的血小板聚集(ADP-Ag)和血管扩张剂刺激磷蛋白的血小板反应指数对因非ST段抬高急性冠状动脉综合征入院并接受经皮冠状动脉介入治疗患者发生支架内血栓形成的预测价值。前瞻性纳入了总共598例连续接受冠状动脉支架置入术的非ST段抬高急性冠状动脉综合征患者。他们在经皮冠状动脉介入治疗前≥12小时接受了600mg氯吡格雷。11例患者(1.8%)发生了急性或亚急性明确或可能的支架内血栓形成。与无支架内血栓形成的患者相比,这些患者的ADP-Ag显著更高(68±14%对56±19%,p = 0.002),但血管扩张剂刺激磷蛋白的血小板反应指数仅呈升高趋势(62±14%对53±23%,p = 0.19)。构建受试者工作特征曲线以检验ADP-Ag对支架内血栓形成的最大预测价值,得出ADP-Ag>67%的阈值来识别低反应者。这些患者发生支架内血栓形成的风险高于氯吡格雷反应者(4.3%对0.8%,比值比5.8,95%置信区间1.9至24.6,p = 0.003)。总之,在接受经皮冠状动脉介入治疗的非ST段抬高急性冠状动脉综合征患者中,ADP-Ag是识别支架内血栓形成风险增加的氯吡格雷无反应者的良好参数,ADP-Ag的截断值>67%。