4.5 Article

Impact of clopidogrel and aspirin treatment on the expression of proteins in platelets from type-2 diabetic patients with stable coronary ischemia

Journal

JOURNAL OF PHARMACEUTICAL SCIENCES
Volume 101, Issue 8, Pages 2821-2832

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1002/jps.23201

Keywords

mass spectrometry; drug interaction; metabolism; drug effects; proteomics

Funding

  1. Brystol-Myers Squibb
  2. Fondo de Investigacion de la Seguridad Social (Redes Tematicas de Investigacion Cooperativa, Red Heracles) [RD06/0009/0010, FIS EC07/90573, FIS PI08/0942]

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The purpose of this study was to compare the effect of dual antiplatelet therapy [clopidogrel + aspirin (ASA)] with respect to ASA on the protein expression of platelets from controlled type-2 diabetic patients with stable coronary ischemia. Patients had been taking ASA (100 mg day) and they were randomized to receive (n = 29) or not (n = 28) 75 mg day clopidogrel for 12 +/- 2 weeks in a blind form. Protein expression was analyzed by two-dimensional electrophoresis and mass spectrometry. The protein expression of a limited number of proteins such as actin-binding protein isotypes 2 and 5, lactate dehydrogenase, serotransferrin isotype 4, protein disulfide isomerase-A3 isotype 1, fibrinogen beta chain isotype 5, Ras-related protein Rab-7b isotypes 1 and 6, and immunoglobulin heavy chain was changed after dual antiplatelet therapy. Plasma level of platelet factor 4 (PF4), an in vivo marker of platelet activity, was not different between both groups. These changes suggest lower platelet reactivity after dual antiplatelet therapy in the studied patients. However, the variation in platelet proteome was lower than it would be initially expected, taking into account the apparent clinical beneficial effects of dual antiplatelet therapy. PF4 plasma level was not further decreased in the platelets treated for a longer time than 912 months with ASA + clopidogrel, as compared with ASA alone. (C) 2012 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 101:28212832, 2012

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