Antonino Mark J, Mahla Elisabeth, Bliden Kevin P, Tantry Udaya S, Gurbel Paul A
Sinai Center for Thrombosis Research, Baltimore, Maryland, USA.
Am J Cardiol. 2009 Jun 1;103(11):1546-50. doi: 10.1016/j.amjcard.2009.01.367. Epub 2009 Apr 8.
A clopidogrel loading dose administered during stenting attenuates inflammation marker release. However, less is known of the anti-inflammatory effect of clopidogrel maintenance therapy. Platelet reactivity to adenosine diphosphate and inflammation markers were measured in 110 consecutive patients (69 clopidogrel-naive patients and 41 patients receiving long-term clopidogrel therapy for >6 months) before nonemergent stenting by turbidimetric aggregometry and flow cytometry and multianalyte profiling, respectively. All patients were treated with aspirin. Prestenting adenosine diphosphate-induced platelet aggregation, P-selectin, and activated glycoprotein IIb/IIIa expression were lower in patients receiving long-term clopidogrel therapy compared with the clopidogrel-naive group (p <0.001), accompanied by lower levels of selected inflammation markers (p < or = 0.05). Additionally, there were strong correlations between platelet aggregation and flow cytometric measurements (p < or = 0.04) and between specific inflammation markers (p < or = 0.02). In conclusion, in addition to markedly lowering platelet reactivity to adenosine diphosphate, long-term clopidogrel therapy is associated with an anti-inflammatory effect.
在支架置入过程中给予氯吡格雷负荷剂量可减少炎症标志物的释放。然而,关于氯吡格雷维持治疗的抗炎作用,人们了解较少。在110例连续患者(69例未服用过氯吡格雷的患者和41例接受氯吡格雷长期治疗超过6个月的患者)非急诊支架置入术前,分别通过比浊法聚集试验、流式细胞术和多分析物谱分析测量血小板对二磷酸腺苷的反应性和炎症标志物。所有患者均接受阿司匹林治疗。与未服用氯吡格雷的组相比,接受氯吡格雷长期治疗的患者术前二磷酸腺苷诱导的血小板聚集、P-选择素和活化糖蛋白IIb/IIIa表达较低(p<0.001),同时某些炎症标志物水平也较低(p≤0.05)。此外,血小板聚集与流式细胞术测量结果之间(p≤0.04)以及特定炎症标志物之间(p≤0.02)存在强相关性。总之,除了显著降低血小板对二磷酸腺苷的反应性外,氯吡格雷长期治疗还具有抗炎作用。