Effect of dopamine partial agonist antipsychotics on suicide risk in persons with schizophrenia and schizoaffective disorders: A systematic review and meta-analysis.

Schizophr ResSep 8, 2026 (epub)
Clinical ResearchPsychiatryOpen access

Jeff W Jin, Charlotte J Winkler, Heather B Blunt et al.

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In 30 seconds

This systematic review and meta-analysis examined whether dopamine partial agonist antipsychotics (DPAs) affect suicide outcomes in people with schizophrenia or schizoaffective disorders. Twenty articles were included; 13 excluded participants at higher suicide risk. In randomized controlled trials, DPAs did not significantly alter primary outcomes (suicide deaths and attempts) versus placebo (RR = 0.65, p = 0.38), or secondary outcomes (suicidal ideation; RR = 0.63, p = 0.15). Open-label extension studies showed increased incidence of both outcome groups, but substantial heterogeneity limits interpretation. The authors conclude that current trial evidence does not show a significant effect.

Key findings

  • In randomized trials, primary suicide outcomes did not differ significantly from placebo (RR = 0.65, p = 0.38).
  • Secondary outcomes, including suicidal ideation, were not significantly changed in randomized trials (RR = 0.63, p = 0.15).
  • Open-label extensions showed increased incidence of primary (Ip = 0.004, p = 0.048) and secondary outcomes (Ip = 0.024, p = 0.0013), with marked heterogeneity.

Why it matters

Suicide prevention remains an important treatment challenge in schizophrenia. This synthesis finds no significant randomized-trial evidence that dopamine partial agonists reduce or increase suicide outcomes, so their potential role in suicide prevention remains uncertain. The open-label signal warrants cautious interpretation rather than being treated as evidence of a causal effect.

What to keep in mind

Thirteen included articles excluded participants at higher suicide risk, limiting applicability to that group. Open-label extension findings had marked study heterogeneity.

Source

Published in Schizophr Res. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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