Evidence map›Paper›PMID 41923472›Full record

ArticleNeuropsychopharmacology reports2026

Beyond Diagnosis: Transdiagnostic Cognitive Subgroups in Mood Disorders Linked to Work-Related Disability.

Ryo Sawagashira, Takuro Tsutsumi, Hayato Watanabe, Atsuhito Toyomaki, Ryo Okubo, Naoki Hashimoto, Takahiro A Kato

Abstract read
In one paragraph

Article in Neuropsychopharmacology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Ryo SawagashiraDepartment of Psychiatry, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.ORCID https://orcid.org/0000-0003-2930-1192
Takuro TsutsumiDepartment of Chemistry, Faculty of Science, Hokkaido University, Sapporo, Japan.
Hayato WatanabeDepartment of Psychiatry, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Atsuhito ToyomakiDepartment of Psychiatry, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.ORCID https://orcid.org/0000-0001-9333-8833
Ryo OkuboDepartment of Psychiatry, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Naoki HashimotoDepartment of Psychiatry, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Takahiro A KatoDepartment of Psychiatry, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.ORCID https://orcid.org/0000-0001-5169-2930

Funding

Japan Society for the Promotion of Science 24K10699
6 · The paper itself

Abstract

aimCognitive dysfunction is a transdiagnostic feature of mood disorders and a key determinant of functional outcomes. This study aimed to identify transdiagnostic cognitive heterogeneity among patients with mood disorders using a data-driven approach and to examine its association with social functioning. Characterizing cognitive subtypes and their association with subjective functional disability is an essential first step toward stratified interventions and personalized care.

methodsWe analyzed data from 264 age- and sex-matched patients (132 each with major depressive disorder [MDD] or bipolar disorder [BD]). Participants completed six neurocognitive tests to assess executive function, memory, attention, and processing speed. Cognitive variables were adjusted for age and sex, and unsupervised K-means clustering was used to identify transdiagnostic subgroups. Functional impairment was evaluated using the Sheehan Disability Scale.

resultsAfter matching participants based on age and sex, we compared the cognitive performance between the diagnostic groups. Significant differences were observed in only two cognitive variables with a small effect size (mean |Cohen's d| = 0.14). No differences were found in the social functioning measures. Cluster analysis identified two cognitive subtypes: higher-performance group (n = 200) and lower-performance group (n = 64) with a large effect size (mean |Cohen's d| = 0.99). Both clusters included patients with MDD and BD in similar proportions (p = 0.11), indicating a diagnostic overlap. The lower-performance group also showed significantly greater work-related and total functional impairments.

conclusionUnsupervised clustering revealed transdiagnostic cognitive subgroups in mood disorders independent of diagnostic labels. Cognitive phenotyping may inform personalized treatment strategies and improve functional outcomes by identifying high-risk patients for cognitive remediation or neuromodulation therapies.

Indexed as

Bipolar DisorderCognitive DysfunctionMajor Depressive DisorderMood DisordersAdultCluster AnalysisClustering AlgorithmsExecutive FunctionFemaleHumansMaleMiddle AgedNeuropsychological TestsProcessing Speedcluster analysiscognitive heterogeneitymood disordersneurocognition

Identifiers

PMID41923472
PMCPMC13045375

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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.