Biological effect of increased maintenance dose of clopidogrel in cardiovascular outpatients and influence of the cytochrome P450 2C19*2 allele on clopidogrel responsiveness

被引:71
作者
Fontana, Pierre [1 ,2 ]
Senouf, David [2 ,3 ]
Mach, Francois [2 ,3 ]
机构
[1] Ctr Med Univ Geneva, Div Angiol & Haemostasis, Dept Internal Med, Fac Med, CH-1211 Geneva 14, Switzerland
[2] Univ Hosp Geneva, Geneva, Switzerland
[3] Fac Med, Dept Internal Med, Div Cardiol, Geneva, Switzerland
关键词
clopidogrel; dose; platelets; resistance;
D O I
10.1016/j.thromres.2007.06.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The first aim of this study is to evaluate the biological effect of doubling the maintenance dose of clopidogrel in pre-defined clopidogrel "low responders", compared to the biological effect of the standard dose in "responders". The second aim is to test the influence of the CYP 2C19*2 allele on clopiclogrel responsiveness. Materials and methods: The platelet reactivity index (PRI), based on the phosphorylation status of the vasodilatator phosphoprotein, was determined in 81 consecutive cardiovascular outpatients who had been taking clopidogrel 75 mg/day for at least 15 days (visit 1). Patients with PRI >= 50% ("low responders") were then given clopidogret 150 mg/day. All the patients were again evaluated 15 days later (visit 2) and were genotyped for the CYP 2C19*2 allele. Results: At visit 1, PRI values ranged from 12.6% to 80.4%. In "low responders" (n=45), the mean PRI fell from 62.0 +/- 6.7% to 49.4 +/- 11.3% (P < 0.001) after 15 days of clopidogrel 150 mg/day, while no significant change was observed in the other patients ("responders"), who remained on the standard dose (mean PRI: 37.7 +/- 10.4% and 39.9 +/- 10.8%, P=0.22, in visit 1 and 2, respectively). The CYP 2C19*2 allele was not associated with clopiclogrel responsiveness. Conclusions: Increasing the maintenance dose of clopidogrel from 75 to 150 mg/day for 15 days in "low responders" is associated with a relative 20%-increase in its biological effect, independently of the CYP2C19 genotype, but without reaching the levels observed in "responders". The CYP 2C19*2 allele is not associated with clopidogrel responsiveness in our population of cardiovascular outpatients. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:463 / 468
页数:6
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