Variability in platelet responsiveness to clopidogrel among 544 individuals

被引:633
作者
Serebruany, VL
Steinhubl, SR
Berger, PB
Malinin, AI
Bhatt, DL
Topol, EJ
机构
[1] HeartDrug Res Labs, Towson, MD 21204 USA
[2] Univ Kentucky, Lexington, KY USA
[3] Duke Clin Res Inst, Durham, NC USA
[4] Cleveland Clin, Cleveland, OH 44106 USA
关键词
D O I
10.1016/j.jacc.2004.09.067
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES We sought to describe the responses of patients to clopidogrel using ex vivo measures of platelet aggregation and activation in a large, heterogeneous population. BACKGROUND Recently, a number of reports, using various definitions, have dichotomized patients who are treated with clopidogrel into a minority of "non-responders" and a majority of "responders." Such classifications imply that treatment leads to an all-or-none response, with potentially important clinical implications. METHODS We conducted secondary post-hoc analyses of a dataset consisting of volunteers (n = 94) and patients after coronary stenting (n = 405), with heart failure (n = 25), and after stroke (n 20). RESULTS The response of subjects to clopidogrel followed a normal, bell-shaped distribution, with a mean and standard deviation of 41.9 +/- 20.8% when aggregation was induced by 5 mumol/l of adenosine diphosphate. When hyporesponsiveness and hyper-responsiveness to clopidogrel were considered to be two standard deviations less than and greater than the mean, respectively, the prevalence of hyporesponsiveness and hyper-responsiveness in these patients was 4.2% and 4.8%, respectively. Pretreatment platelet activity and clinical characteristics were not associated with responsiveness to clopidogrel. CONCLUSIONS Individuals receiving clopidogrel exhibit a wide variability in response that follows a normal distribution. The clinical implications of this variability are unknown but potentially are important. Clinical trials are needed to define whether hyporesponders to clopidogrel are at increased risk for thrombotic events and whether hyper-responders are at increased risk for bleeding. If so, the individualization of antiplatelet therapy, including clopidogrel dosing, may be possible in the future but will require the ability to easily and reproducibly measure responsiveness by a method that has been proven to be predictive of clinical events. (C) 2005 by the American College of Cardiology Foundation.
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收藏
页码:246 / 251
页数:6
相关论文
共 13 条
[1]   Adenosine diphosphate-induced platelet aggregation is associated with P2Y12 gene sequence variations in healthy subjects [J].
Fontana, P ;
Dupont, A ;
Gandrille, S ;
Bachelot-Loza, C ;
Reny, JL ;
Aiach, M ;
Gaussem, P .
CIRCULATION, 2003, 108 (08) :989-995
[2]   A randomised, blinded, trial of clopidogrel versus aspirin in patients at risk of ischaemic events (CAPRIE) [J].
Gent, M ;
Beaumont, D ;
Blanchard, J ;
Bousser, MG ;
Coffman, J ;
Easton, JD ;
Hampton, JR ;
Harker, LA ;
Janzon, L ;
Kusmierek, JJE ;
Panak, E ;
Roberts, RS ;
Shannon, JS ;
Sicurella, J ;
Tognoni, G ;
Topol, EJ ;
Verstraete, M ;
Warlow, C .
LANCET, 1996, 348 (9038) :1329-1339
[3]   2-YEAR FOLLOW-UP OF ASPIRIN RESPONDER AND ASPIRIN NONRESPONDER - A PILOT-STUDY INCLUDING 180 POSTSTROKE PATIENTS [J].
GROTEMEYER, KH ;
SCHARAFINSKI, HW ;
HUSSTEDT, IW .
THROMBOSIS RESEARCH, 1993, 71 (05) :397-403
[4]   A prospective, blinded determination of the natural history of aspirin resistance among stable patients with cardiovascular disease [J].
Gum, PA ;
Kottke-Marchant, K ;
Welsh, PA ;
White, J ;
Topol, EJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2003, 41 (06) :961-965
[5]   Clopidogrel for coronary stenting - Response variability, drug resistance, and the effect of pretreatment platelet reactivity [J].
Gurbel, PA ;
Bliden, KP ;
Hiatt, BL ;
O'Connor, CM .
CIRCULATION, 2003, 107 (23) :2908-2913
[6]   Individual variations of platelet inhibition after loading doses of clopidogrel [J].
Järemo, P ;
Lindahl, TL ;
Fransson, SG ;
Richter, A .
JOURNAL OF INTERNAL MEDICINE, 2002, 252 (03) :233-238
[7]   Platelet GP IIIa PlA polymorphisms display different sensitivities to agonists [J].
Michelson, AD ;
Furman, MI ;
Goldschmidt-Clermont, P ;
Mascelli, MA ;
Hendrix, C ;
Coleman, L ;
Hamlington, J ;
Barnard, MR ;
Kickler, T ;
Christie, DJ ;
Kundu, S ;
Bray, PF .
CIRCULATION, 2000, 101 (09) :1013-1018
[8]   Prevalence of clopidogrel non-responders among patients with stable angina pectoris scheduled for elective coronary stent placement [J].
Müller, I ;
Besta, F ;
Schulz, C ;
Massberg, S ;
Schönig, A ;
Gawaz, M .
THROMBOSIS AND HAEMOSTASIS, 2003, 89 (05) :783-787
[9]   Genetic and environmental contributions to platelet aggregation - The Framingham Heart Study [J].
O'Donnell, CJ ;
Larson, MG ;
Feng, DL ;
Sutherland, PA ;
Lindpaintner, K ;
Myers, RH ;
D'Agostino, RA ;
Levy, D ;
Tofler, GH .
CIRCULATION, 2001, 103 (25) :3051-3056
[10]   SALICYLATES AND BLEEDING - ASPIRIN TOLERANCE TEST [J].
QUICK, AJ .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1966, 252 (03) :265-&