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Published on: May 23, 2025
The association of depression with platelet activation: evidence for a treatment effect
M-C Morel-Kopp1, L McLean, Q Chen
1Northern Blood Research Centre, Department of Haematology and Transfusion Medicine, University of Sydney, Sydney, NSW, Australia. mmorelko@med.usyd.edu.au
Insights
Depression increases platelet activation, a key factor in cardiovascular disease. Treating depression with medication or psychotherapy significantly reduces this platelet activation, offering insights into the depression-cardiovascular link.
Area of Science:
- Cardiovascular Medicine
- Psychiatry
- Hematology
Background:
- Depression is a known risk factor for cardiovascular disease (CVD).
- Prothrombotic and inflammatory mechanisms are suspected links between depression and CVD.
- Platelet activation plays a critical role in the development of CVD.
Purpose of the Study:
- To investigate whether depressed individuals exhibit higher platelet activation compared to non-depressed individuals.
- To determine if treatment for depression leads to a reduction in platelet activation levels.
Main Methods:
- 108 depressed outpatients and 45 control subjects without CVD history were recruited.
- Flow cytometry assessed platelet activation markers (CD62p, CD63) and platelet-leukocyte aggregates.
- Depression severity and platelet activation were measured at baseline, 4 weeks, and 6 months during treatment (medication/psychotherapy).
Main Results:
- Depressed patients showed significantly higher levels of circulating CD62p and CD63 positive platelets compared to controls.
- Increased platelet-leukocyte aggregates were observed in depressed individuals.
- Platelet hyperreactivity to adenosine 5'-diphosphate (ADP) stimulation was noted in depression.
- Treatment for depression led to a significant decrease in circulating CD62p and CD63 positive platelets and reduced ADP-induced platelet activation.
Conclusions:
- Depression is associated with heightened in vivo platelet activation.
- Successful treatment of depression, via medication and/or psychotherapy, effectively reduces platelet activation.
- These findings elucidate a potential mechanism linking depression to increased cardiovascular risk.
Background:
Depression is associated with an increased risk of cardiovascular disease (CVD). Although the mechanism is uncertain, prothrombotic and inflammatory factors may play a role.
Objectives:
As platelets play a key role in CVD, we determined first, whether depressed individuals had more activated platelets than non-depressed individuals and second, whether treatment of depression reduced platelet activation levels.
Patients/Methods:
We recruited 108 depressed outpatients and 45 control subjects all without a history of CVD. After psychological assessment, the depressed patients were offered treatment with medication and/or psychotherapy. Flow cytometric markers of platelet activation and level of depression were assessed at baseline and at 4 weeks and 6 months after treatment.
Results:
Depression was associated with increased platelet activation with a higher number of circulating CD62p (0.76x10(9) L(-1) vs. 0.46, P=0.019) and CD63 (P=0.05) positive platelets compared with controls. Patients with depression also had more circulating platelet-leukocyte aggregates than controls (P<0.001). There was a positive correlation between the severity of depression and the level of platelet activation. Platelets from depressed patients were also hyperreactive to adenosine 5 -diphosphate (ADP) stimulation with increased CD62p and CD63 exposure (P=0.003 and 0.019, respectively). Six months of treatment resulted in a reduced number of circulating CD62p and CD63 positive platelets (29.84% and 53.38% decrease) and a 20.9% reduction in CD63 exposure after ADP activation.
Conclusions:
Depression is associated with increased in vivo platelet activation and resolution of depression using psychotherapy and/or medication reduces platelet activation. These findings provide insights into the link between depression and cardiovascular risk.
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