Pharmacological interventions for social cognitive impairments in schizophrenia: A systematic review and network meta-analysis of randomized controlled trials

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Authors: Yuji Yamada, Norio Watanabe, Yui Tomo, Hisateru Tachimori, Toru Horinouchi, Takashi Uchino, Ryotaro Kubota, Hiroki Okano, Shuhei Ishikawa, Ryo Sawagashira, Keisuke Takanobu, Yumi Hasegawa
+7 more Yohei Sasaki, Motohiro Nishiuchi, Tomiki Sumiyoshi, Naoki Hashimoto, Satoru Ikezawa, Takahiro Nemoto, Ryo Okubo
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Abstract

BACKGROUND: Social cognitive impairments are a fundamental aspect of schizophrenia, exerting a substantial influence on patients' functional outcomes. However, to date, there have been no meta-analyses of comprehensive pharmacological interventions covering all domains of social cognition. The aim of the present study was to address this knowledge gap by conducting a network meta-analysis, a comprehensive approach that systematically compares the efficacy of pharmacological interventions across all domains of social cognition. METHODS: A literature search for randomized controlled trials (RCTs) was conducted using PubMed, Embase, the Cochrane Central Register of Controlled Trials, PsycINFO, ClinicalTrials.gov, and the International Clinical Trials Registry Platform. The Preferred Reporting Items for Systematic Reviews and Meta-Analysis guidelines were followed. RESULTS: A total of 8,752 records were screened, and 60 RCTs involving 4,270 subjects were included in the systematic review. Thirty-six pharmacological interventions were extracted, but no compounds had a significant ameliorative effect on social cognition in comparison with placebo. In each domain of social cognition, the following compounds were identified as the most probable candidates for treatment selection: selective glycine uptake inhibitor (standardized mean difference [SMD], 0.46; 95% credible interval [CI], -0.52 to 1.44) and stimulant (SMD, 0.44; 95% CI, -0.57 to 1.45) for emotion perception in comparison with placebo. In the context of emotion processing, γ-aminobutyric acid (A) α2/α3 partial agonist (SMD, 0.33; 95% CI, -0.53 to 1.19) emerged as the top compound. CONCLUSIONS: To date, no pharmacological interventions have demonstrated efficacy for social cognitive impairments in schizophrenia.

Fields of Study & Subjects

Schizophrenia research and treatment Mental Health and Psychiatry Neurotransmitter Receptor Influence on Behavior

Publication details

Journal / source
European Psychiatry
Volume
69
Issue
1
Pages
e43–e43
Publication date
1 January 2026
Language
EN