Evidence map›Paper›PMID 41698795›Full record

ArticleOpen heart2026

External validation of the SMART2 model for recurrent cardiovascular risk: performance in socioeconomic, ethnic and psychiatric subgroups.

Jasper Wilhelmus Adrianus van Egeraat, Nan van Geloven, Steven H J Hageman, Tobias N Bonten, Wiepke Cahn, Rimke C Vos, Janet Kist, Albert Mairuhu, Hendrikus van Os

Abstract readValidation Study
In one paragraph

Article in Open heart, 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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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Jasper Wilhelmus Adrianus van EgeraatPublic Health and Primary Care, Leiden University Medical Center, Leiden, Zuid Holland, The Netherlands j.w.a.van_egeraat@lumc.nl.ORCID 0000-0002-0540-4237
Nan van GelovenDepartment of Biomedical Data Sciences, Section Medical Statistics, Leiden University Medical Center, Leiden, The Netherlands.
Steven H J HagemanDepartment of Vascular Medicine, University Medical Centre Utrecht, Utrecht, The Netherlands.ORCID 0000-0003-2299-6745
Tobias N BontenPublic Health and Primary Care, Leiden University Medical Center, Leiden, Zuid Holland, The Netherlands.
Wiepke CahnDepartment of Psychiatry, University Medical Centre Utrecht, Utrecht, The Netherlands.
Rimke C VosPublic Health and Primary Care, Leiden University Medical Center, Leiden, Zuid Holland, The Netherlands.
Janet KistPublic Health and Primary Care, Leiden University Medical Center, Leiden, Zuid Holland, The Netherlands.
Albert MairuhuHagaZiekenhuis, The Hague, Zuid Holland, The Netherlands.
Hendrikus van OsPublic Health and Primary Care, Leiden University Medical Center, Leiden, Zuid Holland, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSecondary prevention is critical for patients with established atherosclerotic cardiovascular diseases (ASCVD). The SMART2 model predicts recurrent ASCVD risk but does not account for psychiatric disorders, socioeconomic deprivation or ethnicity. We aimed to evaluate SMART2 model performance overall and in subgroups defined by these factors.

methodsSMART2 was externally validated using electronic health records of patients aged 40-80 in the Leiden-The Hague region. Patients hospitalised for cardiovascular disease or coronary interventions between 1 January 2010 and 31 December 2021 were included. Model performance was assessed using discrimination (10-year area under ROC curve (AUC)) and calibration (observed/expected (OE) ratios and plots, adjusted for competing risks), both overall and in subgroups defined by three factors: psychiatric history, socioeconomic status (SES) and ethnicity.

resultsAmong 15 528 patients (66% male, mean age 65) with established ASCVD, median follow-up was 6.0 years. Recurrent cardiovascular events occurred in 2220 patients, and 1820 had competing events. Overall AUC was 0.63 (95% CI 0.61 to 0.65). OE ratio was 0.96 (95% CI 0.92 to 1.00). The model underestimated risk in patients with low SES (OE 1.09, 95% CI 1.02 to 1.17) and in non-Western patients (OE 1.16, 95% CI 1.02 to 1.31). Calibration was adequate in patients with psychiatric history, but the model was substantially underestimating for patients with multiple vulnerabilities-combinations of low SES, non-Western ethnicity and psychiatric history-with OE ranging from 1.19 to 1.29, depending on the combination.

conclusionThe SMART2 model is well-calibrated in the general population but underestimates risk, especially in subgroups with multiple vulnerabilities. Patients in these vulnerable subgroups may require intensified monitoring. Clinicians should consider social, ethnic and psychiatric factors when interpreting risk estimates.

Indexed as

Cardiovascular DiseasesEthnicityMental DisordersSecondary PreventionAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedNetherlandsRecurrenceReproducibility of ResultsRetrospective StudiesRisk AssessmentElectronic Health RecordsMyocardial InfarctionSTROKE

Identifiers

PMID41698795
PMCPMC12911681

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