Evidence map›Paper›PMID 41191868›Full record

SynthesisInternational clinical psychopharmacology2026

Impact of selected second and third generation antipsychotics on cognitive dysfunction in schizophrenia-spectrum disorders. Systematic review and network meta-analysis.

Paolo Olgiati, Antonino Messina, Vincenzo Oliva, Maria Luca, Antonina Luca, Bernhard T Baune, Raffaele Ferri, Alessandro Serretti

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in International clinical psychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Paolo OlgiatiDepartment of Medicine and Surgery, Kore University of Enna, Enna.
Antonino MessinaDepartment of Medicine and Surgery, Kore University of Enna, Enna.
Vincenzo OlivaDepartment of Psychiatry and Psychology, Institute of Neuroscience, Hospital Clínic de Barcelona.
Maria LucaCentre for Addiction, Adrano-Bronte, Italy.
Antonina LucaDepartment of Medicine and Surgery, Kore University of Enna, Enna.
Bernhard T BauneDepartment of Psychiatry and Psychotherapy, University of Münster, Münster, Germany.
Raffaele FerriOASI Research Institute - IRCCS, Troina.
Alessandro SerrettiDepartment of Medicine and Surgery, Kore University of Enna, Enna.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cognitive dysfunction is a core feature of schizophrenia spectrum disorders and a major determinant of functional outcomes. This study aimed to: (a) systematically review randomized controlled trials (RCTs) evaluating the cognitive effects of third-generation antipsychotics (TGAs: brexpiprazole, cariprazine, lumateperone, and lurasidone) and xanomeline-trospium; and (b) perform a network meta-analysis (NMA) including additional second-generation antipsychotics with potential procognitive effects. A systematic literature search identified eligible RCTs, which were combined with trials on aripiprazole, olanzapine, quetiapine, risperidone, and ziprasidone from a previous meta-analysis. A frequentist NMA (random-effects model) was conducted using standardized mean differences (SMDs) in pre-post cognitive scores. Associations between cognitive outcomes, follow-up duration, and SMDs for psychotic symptoms were examined; metaregression controlled for age and psychosis severity. Fourteen RCTs ( n  = 2464) met the inclusion criteria. Lurasidone (Hedges' g  = 0.46) and xanomeline ( g  = 0.30) outperformed placebo in improving global cognitive performance, whereas quetiapine ( g  = 0.64) and cariprazine ( g  = 0.20) had the most favorable impacts on attention. Cognitive SMDs were unrelated to follow-up duration or improvements in psychotic symptoms. Age and baseline psychosis severity did not influence cognitive response. In conclusion, selected second and TGAs, including M1/M4 receptor agonists such as xanomeline, may offer promising treatment options for cognitive dysfunction. Further research should personalize pharmacological strategies based on cognitive profiles.

Indexed as

Antipsychotic AgentsCognitive DysfunctionSchizophreniaHumansNetwork Meta-Analysis as TopicRandomized Controlled Trials as TopicAntipsychotic Agentsattention deficitcognitive dysfunctionmeta-analysisschizophreniathird-generation antipsychoticsxanomeline

Identifiers

PMID41191868
PMCPMC13015811

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.