Effects of Clopidogrel and Aspirin in Combination Versus Aspirin Alone on Platelet Activation and Major Receptor Expression in Patients After Recent Ischemic Stroke: for the Plavix Use for Treatment of Stroke (PLUTO-Stroke) Trial
Overview
Neurology
Authors
Affiliations
Background And Purpose: Clopidogrel is widely used in patients after recent ischemic stroke; however, its ability to yield additional antiplatelet protection on top of aspirin has never been explored in a controlled study. To determine whether clopidogrel with aspirin (C+ASA) will produce more potent platelet inhibition than aspirin alone (ASA) in patients after ischemic stroke, we conducted the Plavix Use for Treatment of Stroke trial.
Methods: Seventy patients after ischemic stroke were randomly assigned to C+ASA or ASA groups. Platelet studies included aggregometry; cartridge-based analyzers; expression of PECAM-1, P-selectin, GP IIb/IIIa (antigen and activity), vitronectin receptor, and formation of platelet-leukocyte microparticles by flow cytometry. Platelet tests were performed at baseline and after 30 days after randomization.
Results: There were no deaths, hospitalizations, or serious adverse events. There were no differences in the baseline platelet characteristics between C+ASA and ASA groups, or significant changes in platelet parameters in the ASA group, except diminished collagen-induced aggregation (P=0.001). In contrast, therapy with C+ASA resulted in a significant inhibition of platelet activity assessed by ADP- (P=0.00001) and collagen-induced (P=0.02) aggregation; closure time prolongation (P=0.03), and reduction of platelet activation units with Ultegra (P=0.00001); expression of PECAM-1 (P=0.01), and GP IIb/IIIa activity with PAC-1 (P=0.02) when compared with ASA group. Therapy with C+ASA also resulted in the reduced formation of platelet-leukocyte microparticles (P=0.02).
Conclusions: Treatment with C+ASA for 1 month provides significantly greater inhibition of platelet activity than ASA alone in patients after recent ischemic stroke in the frame of the small randomized trial.
Andersson A, Hossain I, Marklund N Acta Neurochir (Wien). 2024; 166(1):377.
PMID: 39316131 PMC: 11422287. DOI: 10.1007/s00701-024-06269-7.
Different Contribution of Monocyte- and Platelet-Derived Microvesicles to Endothelial Behavior.
Brambilla M, Talmon M, Canzano P, Fresu L, Brunelleschi S, Tremoli E Int J Mol Sci. 2022; 23(9).
PMID: 35563201 PMC: 9105732. DOI: 10.3390/ijms23094811.
Jung S, Kim B, Kim C, Shim S, Jung J Ann Transl Med. 2022; 10(5):245.
PMID: 35402589 PMC: 8987873. DOI: 10.21037/atm-21-3748.
Marcinczyk N, Misztal T, Gromotowicz-Poplawska A, Zebrowska A, Rusak T, Radziwon P Int J Mol Sci. 2021; 22(17).
PMID: 34502520 PMC: 8431756. DOI: 10.3390/ijms22179611.
Antiplatelet Drugs for Neurointerventions: Part 2 Clinical Applications.
Pearce S, Maingard J, Kok H, Barras C, Russell J, Hirsch J Clin Neuroradiol. 2021; 31(3):545-558.
PMID: 33646319 DOI: 10.1007/s00062-021-00997-4.