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Article: Development and validation of risk prediction model for recurrent cardiovascular events among Chinese: the Personalized CARdiovascular DIsease risk Assessment for Chinese model

TitleDevelopment and validation of risk prediction model for recurrent cardiovascular events among Chinese: the Personalized CARdiovascular DIsease risk Assessment for Chinese model
Authors
KeywordsCardiovascular diseases
Machine learning
Recurrent cardiovascular events
Risk prediction score
Issue Date1-May-2024
PublisherOxford University Press
Citation
European Heart Journal – Digital Health, 2024, v. 5, n. 3, p. 363-370 How to Cite?
Abstract

Aims

Cardiovascular disease (CVD) is a leading cause of mortality, especially in developing countries. This study aimed to develop and validate a CVD risk prediction model, Personalized CARdiovascular DIsease risk Assessment for Chinese (P-CARDIAC), for recurrent cardiovascular events using machine learning technique.

Methods and results

Three cohorts of Chinese patients with established CVD were included if they had used any of the public healthcare services provided by the Hong Kong Hospital Authority (HA) since 2004 and categorized by their geographical locations. The 10-year CVD outcome was a composite of diagnostic or procedure codes with specific International Classification of Diseases, Ninth Revision, Clinical Modification. Multivariate imputation with chained equations and XGBoost were applied for the model development. The comparison with Thrombolysis in Myocardial Infarction Risk Score for Secondary Prevention (TRS-2°P) and Secondary Manifestations of ARTerial disease (SMART2) used the validation cohorts with 1000 bootstrap replicates. A total of 48 799, 119 672 and 140 533 patients were included in the derivation and validation cohorts, respectively. A list of 125 risk variables were used to make predictions on CVD risk, of which 8 classes of CVD-related drugs were considered interactive covariates. Model performance in the derivation cohort showed satisfying discrimination and calibration with a C statistic of 0.69. Internal validation showed good discrimination and calibration performance with C statistic over 0.6. The P-CARDIAC also showed better performance than TRS-2°P and SMART2.

Conclusion

Compared with other risk scores, the P-CARDIAC enables to identify unique patterns of Chinese patients with established CVD. We anticipate that the P-CARDIAC can be applied in various settings to prevent recurrent CVD events, thus reducing the related healthcare burden.


Persistent Identifierhttp://hdl.handle.net/10722/344122

 

DC FieldValueLanguage
dc.contributor.authorZhou, Yekai-
dc.contributor.authorLin, Celia Jiaxi-
dc.contributor.authorYu, Qiuyan-
dc.contributor.authorBlais, Joseph Edgar-
dc.contributor.authorWan, Eric Yuk Fai-
dc.contributor.authorLee, Marco-
dc.contributor.authorWong, Emmanuel-
dc.contributor.authorSiu, David Chung-Wah-
dc.contributor.authorWong, Vincent-
dc.contributor.authorChan, Esther Wai Yin-
dc.contributor.authorLam, Tak-Wah-
dc.contributor.authorChui, William-
dc.contributor.authorWong, Ian Chi Kei-
dc.contributor.authorLuo, Ruibang-
dc.contributor.authorChui, Celine Sze Ling-
dc.date.accessioned2024-07-03T08:40:50Z-
dc.date.available2024-07-03T08:40:50Z-
dc.date.issued2024-05-01-
dc.identifier.citationEuropean Heart Journal – Digital Health, 2024, v. 5, n. 3, p. 363-370-
dc.identifier.urihttp://hdl.handle.net/10722/344122-
dc.description.abstract<p>Aims</p><p>Cardiovascular disease (CVD) is a leading cause of mortality, especially in developing countries. This study aimed to develop and validate a CVD risk prediction model, Personalized CARdiovascular DIsease risk Assessment for Chinese (P-CARDIAC), for recurrent cardiovascular events using machine learning technique.</p><p>Methods and results</p><p>Three cohorts of Chinese patients with established CVD were included if they had used any of the public healthcare services provided by the Hong Kong Hospital Authority (HA) since 2004 and categorized by their geographical locations. The 10-year CVD outcome was a composite of diagnostic or procedure codes with specific International Classification of Diseases, Ninth Revision, Clinical Modification. Multivariate imputation with chained equations and XGBoost were applied for the model development. The comparison with Thrombolysis in Myocardial Infarction Risk Score for Secondary Prevention (TRS-2°P) and Secondary Manifestations of ARTerial disease (SMART2) used the validation cohorts with 1000 bootstrap replicates. A total of 48 799, 119 672 and 140 533 patients were included in the derivation and validation cohorts, respectively. A list of 125 risk variables were used to make predictions on CVD risk, of which 8 classes of CVD-related drugs were considered interactive covariates. Model performance in the derivation cohort showed satisfying discrimination and calibration with a C statistic of 0.69. Internal validation showed good discrimination and calibration performance with C statistic over 0.6. The P-CARDIAC also showed better performance than TRS-2°P and SMART2.</p><p>Conclusion</p><p>Compared with other risk scores, the P-CARDIAC enables to identify unique patterns of Chinese patients with established CVD. We anticipate that the P-CARDIAC can be applied in various settings to prevent recurrent CVD events, thus reducing the related healthcare burden.</p>-
dc.languageeng-
dc.publisherOxford University Press-
dc.relation.ispartofEuropean Heart Journal – Digital Health-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectCardiovascular diseases-
dc.subjectMachine learning-
dc.subjectRecurrent cardiovascular events-
dc.subjectRisk prediction score-
dc.titleDevelopment and validation of risk prediction model for recurrent cardiovascular events among Chinese: the Personalized CARdiovascular DIsease risk Assessment for Chinese model-
dc.typeArticle-
dc.identifier.doi10.1093/ehjdh/ztae018-
dc.identifier.scopuseid_2-s2.0-85194150118-
dc.identifier.volume5-
dc.identifier.issue3-
dc.identifier.spage363-
dc.identifier.epage370-
dc.identifier.eissn2634-3916-
dc.identifier.issnl2634-3916-

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