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Development and external validation of machine learning approaches for risk prediction of cardiovascular disease in individuals with schizophrenia: a nationwide Swedish and Danish study
Department of Applied Mathematics and Computer Science, Technical University of Denmark, Lyngby, Denmark; Copenhagen Research Center for Biological and Precision Psychiatry, Mental Health Centre Copenhagen, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Örebro University, School of Medical Sciences.ORCID iD: 0000-0002-3887-9669
Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden; ME Cardiology, Heart and Vascular Theme, Karolinska University Hospital, Stockholm, Sweden.
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
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2026 (English)In: BMJ Mental Health, E-ISSN 2755-9734, Vol. 29, no 1, article id e301964Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: Currently available cardiovascular disease (CVD) risk prediction tools may underestimate the risk in individuals with schizophrenia.

OBJECTIVE: To develop and externally validate 5-year CVD risk prediction models for people with schizophrenia using large-scale register data in Sweden and Denmark with a machine learning (ML) approach.

METHODS: Individuals with a diagnosis of schizophrenia, aged 30 and older and without prior CVD, were followed for up to 5 years. We investigated whether adding additional health-related and socio-demographic predictors to the established CVD risk factors improved predictions and compared ML models with logistic regression. External validation was performed across countries. FINDINGS: A lasso penalised logistic regression including additional predictors achieved the highest predictive performance, both on Swedish and Danish data, while complex ML models with interaction terms did not provide additional improvements. The area under the receiver operating characteristic curve (AUC) on the internal validation data was 0.745 (95% CI (0.742 to 0.749)) in the Swedish model, and 0.722, 95% CI (0.719 to 0.726) in the Danish model. External validation showed similar performance, yielding an AUC of 0.746, 95% CI (0.741 to 0.751) using the Danish model on the Swedish data, and an AUC of 0.720, 95% CI (0.712 to 0.726) using the Swedish model on the Danish validation data.

CONCLUSIONS: Incorporating additional health-related information, such as psychiatric comorbidities and medication use, improved 5-year CVD risk prediction for people with schizophrenia in both countries. CLINICAL IMPLICATIONS: The models can be deployed between Denmark and Sweden without loss of performance compared with training a model on each country.

Place, publisher, year, edition, pages
BMJ Publishing Group Ltd, 2026. Vol. 29, no 1, article id e301964
Keywords [en]
Psychiatry, Schizophrenia, Schizophrenia Spectrum and Other Psychotic Disorders
National Category
Psychiatry
Identifiers
URN: urn:nbn:se:oru:diva-126405DOI: 10.1136/bmjment-2025-301964ISI: 001664095700001PubMedID: 41545227OAI: oai:DiVA.org:oru-126405DiVA, id: diva2:2029656
Funder
Swedish Research Council, 2025-03176Vinnova, 2022-00541
Note

This work was supported by unrestricted grants from the Lundbeck Foundation (Grant Number: R278-2018-1411). The project has also received funding from the Swedish Research Council (2025-03176). MD acknowledges funding from VINNOVA (Sweden's Innovation Agency; grant number: 2022-00541) under the framework of ERA PerMed, ERAP-ERMED2022-087-BIPCOM.

Available from: 2026-01-19 Created: 2026-01-19 Last updated: 2026-01-29Bibliographically approved

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Dobrosavljevic, MajaLarsson, Henrik

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