Malinin A, Pokov A, Swaim L, Kotob M, Serebruany V
Heart Drug Research Laboratories, Baltimore, Maryland, USA.
Methods Find Exp Clin Pharmacol. 2006 Jun;28(5):315-22. doi: 10.1358/mf.2006.28.5.990205.
Despite common use of clopidogrel in patients with vascular disease, monitoring of platelet inhibition is still not conventional in clinical practice. Considering substantial response variability, when some patients may experience inadequate protection, and/or increased risk of bleeding, simple and reliable methods to control adequate antiplatelet regimen is mandatory. We validated a new VerifyNow-P2Y12 assay to measure inhibition of the P2Y12 platelet receptors by clopidogrel by evaluating its receptor specificity, precision, and potential interference with platelet count, hematocrit, age, cholesterol, triglycerides, and other antiplatelet agents. Platelet aggregation induced by ADP or ADP + prostaglandin E1 (ADP + PGE1) in the presence of specific P2Y12 inhibitor 2-methylthio-AMP (2MeSAMP) for the assessment of assay specificity was performed in 10 volunteers. Seventeen medications were used for the VerifyNow-P2Y12 interference testing, and assay interplay with blood constituents was evaluated in a clinical setting in 131 patients with coronary artery disease. In the presence of 2MeSAMP, the average residual aggregation level across the 10 donors was 27% for ADP and 5% for ADP + PGE1. There also was a strong agreement between ADP + PGE1 aggregometry and VerifyNow-P2Y12 assay (93% vs. 95% average inhibition across all donors). The coefficient of variation for the test precision was less than 8%. The VerifyNow-P2Y12 readings were not influenced by age, platelet count, hematocrit, fibrinogen, cholesterol, or triglycerides level. There was an interference with abciximab before P2Y12 inhibition; however, after platelet suppression with cilostazol, the interference with all tested substances was minimal. VerifyNow-P2Y12 is a reliable, simple, and sensitive device suitable for monitoring of P2Y12 platelet receptor inhibitors in the clinical arena.
尽管氯吡格雷在血管疾病患者中被广泛使用,但在临床实践中,血小板抑制监测仍未成为常规操作。考虑到个体反应差异较大,部分患者可能得不到充分的保护,和/或出血风险增加,因此必须采用简单可靠的方法来控制适当的抗血小板治疗方案。我们通过评估一种新的VerifyNow-P2Y12检测法的受体特异性、精密度以及与血小板计数、血细胞比容、年龄、胆固醇、甘油三酯和其他抗血小板药物之间的潜在干扰,验证了该检测法用于测量氯吡格雷对P2Y12血小板受体的抑制作用。在10名志愿者中,使用特异性P2Y12抑制剂2-甲硫基-AMP(2MeSAMP)评估检测特异性,检测由ADP或ADP + 前列腺素E1(ADP + PGE1)诱导的血小板聚集。使用17种药物进行VerifyNow-P2Y12干扰测试,并在131例冠心病患者的临床环境中评估该检测法与血液成分之间的相互作用。在2MeSAMP存在的情况下,10名供体的ADP平均残余聚集水平为27%,ADP + PGE1为5%。ADP + PGE1血小板聚集测定法与VerifyNow-P2Y12检测法之间也具有高度一致性(所有供体的平均抑制率分别为93%和95%)。检测精密度的变异系数小于8%。VerifyNow-P2Y12读数不受年龄、血小板计数、血细胞比容、纤维蛋白原、胆固醇或甘油三酯水平的影响。在P2Y12抑制之前,阿昔单抗存在干扰;然而,在用西洛他唑抑制血小板后,对所有测试物质的干扰最小。VerifyNow-P2Y12是一种可靠、简单且灵敏的设备,适用于临床领域中P2Y12血小板受体抑制剂的监测。