Effects of combined therapy with clopidogrel and acetylsalicylic acid on platelet glycoprotein expression and aggregation

被引:19
作者
Dörr, G
Schmidt, G
Gräfe, M
Regitz-Zagrosek, V
Fleck, E
机构
[1] Humboldt Univ, Charite, Dept Med Cardiol, D-13353 Berlin, Germany
[2] Deutsch Herzzentrum Berlin, Dept Med Cardiol, D-13353 Berlin, Germany
关键词
antibodies; aspirin; clopidogrel; combination; coronary disease; drug therapy; flow cytometry; human; monoclonal; platelet aggregation inhibitors; platelet glycoprotein GPIIb/IIIa complex; P-selectin;
D O I
10.1097/00005344-200204000-00008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study aimed to compare the effects of clopidogrel, acetylsalicylic acid (ASA), and the combination of both substances on platelet aggregation and expression of platelet membrane glycoproteins in patients with chronic coronary artery disease. We investigated platelet activation by flow cytometry and by platelet aggregation and disaggregation in 60 patients randomly assigned to 3 treatment groups: ASA, clopidogrel, combination of clopidogrel and ASA, treated for 14 days. Adenosine diphosphate (ADP)induced expression of P-selectin and of PAC- I was significantly reduced after 2 wk of clopidogrel but not of ASA treatment. Treatment with clopidogrel reduced the ADP-induced platelet aggregation. The combination of clopidogrel and ASA did not increase the inhibition of platelet activation compared with clopidogrel alone. A significant increase in platelet disaggregation was observed with clopidogrel alone and was more pronounced with the combination of clopidogrel and ASA. ADP-induced platelet degranulation, activation of GPIIb/IIIa receptor, and aggregation in vivo are effectively inhibited by clopidogrel. The significantly increased disaggregation under clopidogrel and ASA suggests that the combined therapy may be superior to the monotherapy in patients with coronary artery disease and a high risk for vascular events.
引用
收藏
页码:523 / 532
页数:10
相关论文
共 48 条
  • [1] ABRAMS C, 1991, THROMB HAEMOSTASIS, V65, P467
  • [2] Randomized multicenter comparison of conventional anticoagulation versus antiplatelet therapy in unplanned and elective coronary stenting - The full anticoagulation versus aspirin and ticlopidine (FANTASTIC) study
    Bertrand, ME
    Legrand, V
    Boland, J
    Fleck, E
    Bonnier, J
    Emmanuelson, H
    Vrolix, M
    Missault, L
    Chierchia, S
    Casaccia, M
    Niccoli, L
    Oto, A
    White, C
    Webb-Peploe, M
    Van Belle, E
    McFadden, EP
    [J]. CIRCULATION, 1998, 98 (16) : 1597 - 1603
  • [3] AGGREGATION OF BLOOD PLATELETS BY ADENOSINE DIPHOSPHATE AND ITS REVERSAL
    BORN, GVR
    [J]. NATURE, 1962, 194 (4832) : 927 - &
  • [4] Brass LF, 1997, THROMB HAEMOSTASIS, V78, P581
  • [5] Brass LF, 1991, HEMATOLOGY BASIC PRI, P1176
  • [6] CHARO IF, 1994, HEMOSTASIS THROMBOSI
  • [7] PATHOGENESIS OF THROMBOSIS IN UNSTABLE ANGINA
    CHESEBRO, JH
    ZOLDHELYI, P
    FUSTER, V
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 1991, 68 (07) : B2 - B10
  • [8] Molecular basis for ADP-induced platelet activation I. Evidence for three distinct ADP receptors on human platelets
    Daniel, JL
    Dangelmaier, C
    Jin, JG
    Ashby, B
    Smith, JB
    Kunapuli, SP
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (04) : 2024 - 2029
  • [9] DAVIES M, 1994, HEMOSTASIS THROMBOSI
  • [10] Increased platelet reactivity and circulating monocyte-platelet aggregates in patients with stable coronary artery disease
    Furman, MI
    Benoit, SE
    Barnard, MR
    Valeri, CR
    Borbone, ML
    Becker, RC
    Hechtman, HB
    Michelson, AD
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1998, 31 (02) : 352 - 358