Angiolillo Dominick J, Costa Marco A, Shoemaker Steven B, Desai Bhaloo, Bernardo Esther, Suzuki Yoshie, Charlton Ronald K, Zenni Martin M, Guzman Luis A, Bass Theodore A
Division of Cardiology, University of Florida College of Medicine at Shands Jacksonville, Jacksonville, Florida, USA.
Am J Cardiol. 2008 Feb 15;101(4):440-5. doi: 10.1016/j.amjcard.2007.09.087. Epub 2007 Dec 20.
Updated guidelines on percutaneous coronary intervention recommend increasing the dose of clopidogrel to 150 mg in high-risk patients if <50% platelet inhibition is demonstrated. However, to date, the functional impact of this recommendation has been poorly explored. The aim of this study was to assess the functional implications associated with the use of clopidogrel 150 mg/day in patients with inadequate platelet inhibition while receiving standard 75 mg/day maintenance treatment. Patients with diabetes mellitus have a higher prevalence of inadequate clopidogrel-induced antiplatelet effects and stent thrombosis compared with those without diabetes and were selected for this analysis. Platelet inhibition was assessed using the VerifyNow P2Y12 assay in patients with type 2 diabetes receiving dual-antiplatelet therapy. Patients (n = 17) with <50% platelet inhibition were treated with clopidogrel 150 mg/day for 1 month. Adenosine diphosphate-induced aggregation and the P2Y12 reactivity ratio were also assessed. Platelet function profiles were compared with that of a control group (n = 17) with >or=50% inhibition. Platelet inhibition increased from 27.1 +/- 12% to 40.6 +/- 18% in patients treated with clopidogrel 150 mg/day (p = 0.009; primary end point). All other functional measures also showed enhanced clopidogrel-induced antiplatelet effects. The degree of platelet inhibition achieved after treatment with clopidogrel 150 mg/day varied broadly, and only 35% of patients yielded a degree of platelet inhibition >or=50%. Increasing the dose in patients with inadequate response to clopidogrel did not reach the same degree of antiplatelet effects as those achieved in patients with adequate response while receiving 75 mg/day. In conclusion, the use of a 150 mg maintenance dose of clopidogrel in patients with type 2 diabetes with <50% platelet inhibition is associated with enhanced antiplatelet effects. However, the antiplatelet effects achieved are nonuniform, and a considerable number of patients persist with inadequate platelet inhibition.
经皮冠状动脉介入治疗的更新指南建议,如果血小板抑制率<50%,高危患者应将氯吡格雷剂量增加至150mg。然而,迄今为止,这一建议的功能影响尚未得到充分研究。本研究的目的是评估在接受标准75mg/天维持治疗但血小板抑制不足的患者中使用150mg/天氯吡格雷的功能影响。与非糖尿病患者相比,糖尿病患者氯吡格雷诱导的抗血小板作用不足和支架血栓形成的发生率更高,因此选择糖尿病患者进行本分析。在接受双联抗血小板治疗的2型糖尿病患者中,使用VerifyNow P2Y12检测法评估血小板抑制情况。血小板抑制率<50%的患者(n = 17)接受150mg/天氯吡格雷治疗1个月。同时评估二磷酸腺苷诱导的聚集和P2Y12反应性比值。将血小板功能谱与血小板抑制率≥50%的对照组(n = 17)进行比较。接受150mg/天氯吡格雷治疗的患者血小板抑制率从27.1±12%增至40.6±18%(p = 0.009;主要终点)。所有其他功能指标也显示氯吡格雷诱导的抗血小板作用增强。接受150mg/天氯吡格雷治疗后达到的血小板抑制程度差异很大,只有35%的患者血小板抑制率≥50%。氯吡格雷反应不足的患者增加剂量后,抗血小板作用程度不及接受75mg/天治疗且反应充分的患者。总之,血小板抑制率<50%的2型糖尿病患者使用150mg维持剂量氯吡格雷与抗血小板作用增强相关。然而,所达到的抗血小板作用并不一致,相当一部分患者血小板抑制仍不足。