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Antithrombotic agents may reduce symptoms in severe mental illness, but evidence is very low certainty

Antithrombotic agents may reduce symptoms in severe mental illness, but evidence is very low certain…
Photo by Pawel Czerwinski / Unsplash
Key Takeaway
Interpret very low-certainty evidence on antithrombotics for SMI with extreme caution.

A systematic review and meta-analysis examined the effects of antithrombotic agents (aspirin, cilostazol, dipyridamole) versus placebo in 742 patients with severe mental illness, including schizophrenia, major depression, and bipolar disorder. The primary outcomes were symptom severity, risk of recurrence, and tolerability.

For depressive symptoms, treatment with antithrombotic agents was associated with a reduction, with a standardized mean difference (SMD) of -0.62 (95% CI -1.11 to -0.13). For the PANSS total score, a reduction was also observed, with an SMD of -0.57 (95% CI -0.86 to -0.28). Absolute numbers for these outcomes were not reported. Tolerability, based on very low-certainty evidence from 9 studies, may not differ from placebo (risk ratio 0.89; 95% CI 0.57-1.40). Data on specific adverse events, serious adverse events, and discontinuations were not reported.

Key limitations include the very low-certainty of the evidence (per GRADE framework), meaning effect estimates should be interpreted with caution and the therapeutic potential of these agents in severe mental illness remains uncertain. The study setting and follow-up duration were not reported. In practice, these findings are hypothesis-generating. Well-powered randomized controlled trials investigating clinically relevant outcomes in clearly defined populations are needed before any clinical application can be considered.

Study Details

Study typeMeta analysis
Sample sizen = 742
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
Evidence suggests shared pathophysiologic mechanisms between severe mental illness (SMI) and cardiovascular disease (CVD). Drugs used for CVD, such as antithrombotic agents (ATAs), may therefore be repurposed for the treatment of SMI. We conducted the first systematic review and meta-analysis (PROSPERO registration CRD42024524420) of ATAs for SMI and reported results according to PRISMA guidelines. We searched MEDLINE, Embase, and PsycINFO (October 10, 2024) and performed random-effects meta-analysis. Risk of bias was assessed using the Cochrane Risk of Bias 2 tool, and the certainty of evidence was evaluated using the Grading of Recommendations, Assessment, Development, and Evaluations (GRADE) framework. Primary outcomes were symptom severity, risk of recurrence, and tolerability. We included 12 randomized trials investigating aspirin, cilostazol, and dipyridamole in a total of 742 patients with schizophrenia, major depression, and bipolar disorder. Results showed that ATA treatment may reduce depressive symptoms in patients with SMI (SMD -0.62; 95 % CI -1.11 to -0.13; 8 studies; very low-certainty evidence). Based on studies with low risk of bias, ATA treatment may reduce PANSS total score compared with placebo (SMD -0.57; 95 % CI -0.86 to -0.28; 3 studies; very low-certainty evidence). Tolerability of ATAs may not differ from placebo (RR 0.89; 95 % CI 0.57-1.40; 9 studies; very low-certainty evidence). Given the low certainty of the evidence, effect estimates should be interpreted with caution. The therapeutic potential of ATAs in SMI remains uncertain. Well-powered RCTs investigating clinically relevant outcomes in clearly defined populations are needed.
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