Evidence map›Paper›PMID 42178548›Full record

ArticleBMC medicine2026

Executive function profiles identify stable schizophrenia subtypes with distinct symptoms, biological markers and treatment responses: a cross-time clustering and validation study.

Tongyi Zhang, Xiaoning Huo, Ji Chen, Xin Zhao

Abstract readValidation Study
In one paragraph

Article in BMC medicine, 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

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Tongyi ZhangSchool of Psychology, Northwest Normal University, Lanzhou, China.
Xiaoning HuoThe Third People's Hospital of Lanzhou, Lanzhou, China.
Ji ChenCenter for Brain Health and Brain Technology, Global Institute of Future Technology, Shanghai Jiao Tong University, Shanghai, China. chen.ji@sjtu.edu.cn.ORCID 0000-0002-9476-1737
Xin ZhaoSchool of Psychology, Northwest Normal University, Lanzhou, China. psyzhaoxin@nwnu.edu.cn.ORCID 0000-0001-9585-8306

Funding

Brain Science and Brain-like Intelligence Technology-National Science and Technology Major Project 2022ZD0214000National Natural Science Foundation of China 32260207National Natural Science Foundation of China 82371506Shanghai Rising-Star Program 24QA2704700
6 · The paper itself

Abstract

backgroundExecutive function (EF) is a heterogeneous neuropsychological construct, and impairments in EF dimensions represent a core aspect of psychopathology in schizophrenia that varies across individual patients. Currently, how this inter-individual variability characterizes schizophrenia subgroups, along with their distinctions in clinical characteristics and prognostic outcomes, remains unclear.

methodsThree EF dimensions (inhibitory control, working memory, cognitive flexibility) were assessed in the main sample (N = 329), its follow-up subset, and an independently "recurring local validation" patient sample (N = 114). Fuzzy clustering was applied to baseline EF assessments to discover and validate the core subtypes after excluding cluster-ambiguous cases in the main and independent samples, respectively. Subtype-based classification trained on the main sample was then tested in the independent sample. Importantly, the stability of these subtypes and their remission statuses, along with associated longitudinal changes in clinical and biological factors, were evaluated, and baseline subtype statuses were also used to predict outcomes.

resultsTwo longitudinally stable, independently validated core EF subtypes were identified, with Subtype I exhibiting selective deficits limited to response inhibition and cognitive flexibility ("EF-Focal") and Subtype II showing broad EF impairments across all dimensions ("EF-Global"). Compared to the "EF-Global" subtype, patients within the "EF-Focal" subtype presented significantly milder positive, affective, and cognitive symptoms, worse working memory updating, lower inflammatory markers, and better metabolic profiles at baseline. Models trained on baseline EF assessments from the main sample accurately classified patient subtypes in the independent sample (area under the curve [AUC] = 0.79); these baseline subtypes moreover classified patients' remission statuses independently of overall severity at intake (AUC = 0.78). Remitted patients were observed to have significantly greater reductions in negative and cognitive symptoms, improved working memory maintenance, lower peripheral inflammatory levels, and superior metabolic functions over time.

conclusionsEF subtyping was associated with symptomatic, biochemical, and prognostic variations in individuals with schizophrenia, which could help to stratify patients within this disorder for targeted treatments.

Indexed as

Executive FunctionSchizophreniaSchizophrenic PsychologyAdultBiomarkersCluster AnalysisClustering AlgorithmsCognitive FlexibilityFemaleHumansMaleMemory, Short-TermPrognosisBiomarkersExecutive dysfunctionMachine learning clusteringPeripheral immune-metabolicPrognostic predictionSchizophreniaSubtyping

Identifiers

PMID42178548
PMCPMC13393924

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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.