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Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
Antiplatelet Effects of Clopidogrel Vs Aspirin in Virologically Controlled HIV: A Randomized Controlled Trial
Emanuela Marcantoni1, Michael S Garshick1,2, Tamar Schwartz1
1Leon H. Charney Division of Cardiology, Department of Medicine, New York University School of Medicine, New York, New York, USA.
Insights
Clopidogrel significantly reduced platelet activation and inflammation in HIV patients, unlike aspirin. Further clinical trials are recommended to explore clopidogrel for preventing cardiovascular disease in this population.
Area of Science:
- Cardiovascular Medicine
- Hematology
- Infectious Diseases
Background:
- Patients with Human Immunodeficiency Virus (HIV) show increased platelet activation.
- This platelet activation is linked to a higher risk of cardiovascular disease (CVD).
- Effective prevention strategies for CVD in HIV patients remain largely unknown.
Purpose of the Study:
- To investigate the effects of antiplatelet agents on platelet activation and endothelial inflammation in HIV patients.
- To compare the efficacy of clopidogrel and aspirin in modulating platelet phenotype and inflammatory responses.
Main Methods:
- A randomized trial involving 55 HIV-positive patients.
- Participants were assigned to receive clopidogrel, aspirin, or no treatment for 14 days.
- Platelet activation markers (P-selectin, PAC-1) and platelet-induced endothelial inflammation were assessed.
Main Results:
- Clopidogrel significantly reduced platelet activation compared to aspirin and no treatment.
- Platelet-induced proinflammatory gene expression in endothelial cells decreased with clopidogrel.
- No significant changes in these markers were observed in the aspirin or no-treatment groups.
Conclusions:
- Clopidogrel demonstrates potent antiplatelet and anti-inflammatory effects in HIV patients.
- These findings suggest a potential role for clopidogrel in managing cardiovascular risk in HIV.
- Clinical trials evaluating clopidogrel for CVD prevention in HIV are warranted.
Abstract:
Patients with HIV exhibit platelet activation and increased risk of cardiovascular disease, the prevention of which is not fully known. Fifty-five HIV-positive patients were randomized to clopidogrel, aspirin, or no-treatment for 14 days, and the platelet phenotype and ability to induce endothelial inflammation assessed. Clopidogrel as opposed to aspirin and no-treatment reduced platelet activation (P-selectin and PAC-1 expression). Compared with baseline, platelet-induced proinflammatory transcript expression of cultured endothelial cells were reduced in those assigned to clopidogrel, with no change in the aspirin and no-treatment arms. In HIV, clinical trials of clopidogrel to prevent cardiovascular disease are warranted. (Antiplatelet Therapy in HIV; NCT02559414).
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