Clopidogrel resistance in Japanese patients scheduled for percutaneous coronary intervention

Circ J. 2009 Feb;73(2):336-42. doi: 10.1253/circj.cj-08-0559. Epub 2008 Dec 24.

Abstract

Background: Dual antiplatelet therapy with acetylsalicylic acid (ASA) and a P2Y(12) ADP-receptor blocker is standard for prevention of coronary stent thrombosis. Clopidogrel, a 2(nd)-generation P2Y(12) blocker, has recently become available in Japan and this study aimed to evaluate its antiplatelet effects in Japanese patients.

Methods and results: Thirty Japanese patients scheduled for elective coronary stent implantation were enrolled. Under low-dose ASA therapy, 300 mg clopidogrel was loaded on the 1(st) day and a daily 75-mg dose was administered on the following days. Assessed by optical aggregometer, rapid inhibition occurred at 4 h, when the inhibition of platelet aggregation rate (IPA) was 16.4+/-12.8% using 5 mumol/L ADP as the stimulus. The antiplatelet efficacy of clopidogrel was reasonably constant in each patient throughout the study period, although there was a broad inter-individual variation. At 48 h after clopidogrel loading, the ratios of responders (IPA > or =30%), hypo-responders (10%< or =IPA<30%), and non-responders (IPA <10%) were 36%, 50%, and 14%, respectively.

Conclusions: The antiplatelet effectiveness of clopidogrel appeared individual-specific with wide inter-individual variation. The rate of clopidogrel non-responders was 14% among the examined Japanese patients.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Angioplasty, Balloon, Coronary*
  • Cell Adhesion Molecules / metabolism
  • Clopidogrel
  • Coronary Stenosis / ethnology*
  • Coronary Stenosis / prevention & control*
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Male
  • Microfilament Proteins / metabolism
  • Middle Aged
  • Myocardial Ischemia / therapy*
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Platelet Aggregation / drug effects
  • Platelet Aggregation Inhibitors / pharmacology
  • Platelet Aggregation Inhibitors / therapeutic use*
  • Stents*
  • Ticlopidine / analogs & derivatives*
  • Ticlopidine / pharmacology
  • Ticlopidine / therapeutic use
  • Treatment Outcome

Substances

  • Cell Adhesion Molecules
  • Microfilament Proteins
  • Phosphoproteins
  • Platelet Aggregation Inhibitors
  • vasodilator-stimulated phosphoprotein
  • Clopidogrel
  • Ticlopidine