Related Experiment Video
Updated: May 17, 2026

Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
Postmenopausal women have an increased maximal platelet reactivity compared to men despite dual antiplatelet therapy
Peter Bobbert1, Caroline Stellbaum, Daniel Steffens
1Department of Cardiology and Pneumology, Diabetes and Nutrition, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin, Hindenburgdamm, Berlin, Germany.
Insights
Women exhibit higher platelet reactivity than men despite dual antiplatelet therapy with acetylsalicylic acid (ASA) and clopidogrel. This sex difference in platelet response, particularly to thrombin receptor-activating peptide (TRAP), persists independently of standard antiplatelet medication.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Hematology
Background:
- Dual antiplatelet therapy (DAPT) with aspirin (ASA) and clopidogrel is standard for stable coronary vessel disease (CVD) post-percutaneous coronary intervention (PCI).
- Subgroups of patients on DAPT show increased risk for adverse cardiovascular events, suggesting variability in treatment response.
- The influence of sex on platelet reactivity and DAPT effectiveness requires further investigation.
Purpose of the Study:
- To investigate the impact of sex on platelet reactivity in patients with CVD undergoing combined ASA and clopidogrel therapy.
- To determine if sex influences the efficacy of ASA and clopidogrel in inhibiting platelet function.
- To identify sex as a potential prognostic marker for cardiovascular events in patients on DAPT.
Main Methods:
- A cohort of 230 patients with CVD on DAPT (ASA 100 mg/day, clopidogrel 75 mg/day) was divided into male (n=128) and female (n=102) groups.
- Platelet reactivity was assessed using impedance aggregometry.
- Multivariate linear regression analysis was employed to identify independent predictors of platelet reactivity.
Main Results:
- Women showed significantly higher thrombin receptor-activating peptide (TRAP)-induced platelet reactivity compared to men (89.3 ± 30.69 U vs. 79.43 ± 28.55 U; P < 0.05).
- No significant differences in adenosine diphosphate (ADP)- or arachidonic acid-induced platelet aggregation were observed between sexes.
- Female sex was identified as a significant independent predictor of increased TRAP-induced platelet reactivity.
Conclusions:
- Women exhibit higher maximal platelet reactivity than men, even when treated with ASA and clopidogrel.
- Sex differences do not appear to affect the inhibitory efficacy of ASA or clopidogrel on platelet function.
- Increased TRAP-induced platelet reactivity in women warrants further research regarding its clinical implications for cardiovascular event risk.
Abstract:
Dual antiplatelet medication with acetylsalicylic acid (ASA) and clopidogrel is the main therapy for patients with stable coronary vessel disease (CVD) after percutaneous coronary intervention (PCI). Despite platelet inhibition subgroups of patients have been shown to exhibit an increase of risk for adverse cardiovascular events. The aim of our study was to elucidate the influence of sex on platelet reactivity in patients with CVD under medication with ASA and clopidogrel. Two hundred and thirty patients with CVD on combined therapy with ASA (100 mg/day) and clopidogrel (75 mg/day) were included into our study. These patients were divided into a male (n = 128) and female (n = 102) group. Platelet reactivity was assessed by impedance aggregometry. Women demonstrated a significantly higher thrombin receptor-activating peptide (TRAP)-induced platelet reactivity than men (male 79.43 ± 28.55 U vs. female 89.3 ± 30.69 U; P < 0.05). The ADP-induced (male 19.81 ± 15.51 U vs. female 23.73 ± 17.68 U; P > 0.05) or arachidonic acid-induced (male 10.3 ± 12.87 U vs. female 12.76 ± 14.44 U; P > 0.05) platelet aggregation did not differ significantly between women and men. A multivariate linear regression model revealed female sex to be a significant prognostic marker for an increased TRAP-induced platelet reactivity, independent of the ASA and clopidogrel-associated platelet function inhibition. Sex differences did not influence the effectiveness of ASA or clopidogrel-mediated platelet function inhibition. Nevertheless, women had a significantly increased maximal platelet reactivity compared to men despite antiplatelet therapy.
Related Concept Videos
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Menopause
Formation of the Platelet Plug
As the injured blood vessel contracts, endothelial cells undergo contraction, revealing collagen fibers in the basement membrane and underlying connective tissue. Furthermore, the plasma membrane of endothelial cells becomes adhesive, preparing the site for platelet adhesion. Platelets...
Coronary Artery Disease V: Interprofessional Care
Pharmacodynamics in Geriatric Patients: Effects of Age
Peripheral Artery Disease III: Interprofessional Care

