中国人复发性心血管事件风险预测模型的开发与验证:中国人个性化心血管疾病风险评估模型。

IF 3.9 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
European heart journal. Digital health Pub Date : 2024-04-08 eCollection Date: 2024-05-01 DOI:10.1093/ehjdh/ztae018
Yekai Zhou, Celia Jiaxi Lin, Qiuyan Yu, Joseph Edgar Blais, Eric Yuk Fai Wan, Marco Lee, Emmanuel Wong, David Chung-Wah Siu, Vincent Wong, Esther Wai Yin Chan, Tak-Wah Lam, William Chui, Ian Chi Kei Wong, Ruibang Luo, Celine Sze Ling Chui
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引用次数: 0

摘要

目的:心血管疾病(CVD)是导致死亡的主要原因,尤其是在发展中国家。本研究旨在利用机器学习技术开发并验证心血管疾病风险预测模型--中国人个性化心血管疾病风险评估(P-CARDIAC),以预测复发性心血管事件:自2004年以来,三组已确诊心血管疾病的华人患者均使用过香港医院管理局(医管局)提供的任何公营医疗服务,并按地理位置进行了分类。10年心血管疾病结果是诊断或手术代码的综合结果,并附有特定的《国际疾病分类,第九版,临床修正》。在建立模型时,使用了链式方程和 XGBoost 进行多变量归因。与用于二级预防的心肌梗死溶栓风险评分(TRS-2°P)和动脉疾病继发表现(SMART2)进行比较时,使用了 1000 次引导复制的验证队列。推导队列和验证队列中分别纳入了 48 799、119 672 和 140 533 名患者。预测心血管疾病风险时使用了 125 个风险变量,其中 8 类心血管疾病相关药物被视为交互协变量。推导队列中的模型表现出了令人满意的区分度和校准性,C统计量为0.69。内部验证显示出良好的区分度和校准性能,C 统计量超过 0.6。P-CARDIAC 的性能也优于 TRS-2°P 和 SMART2:结论:与其他风险评分相比,P-CARDIAC 能够识别中国已确诊心血管疾病患者的独特模式。我们预计,P-CARDIAC 可应用于各种场合,以预防心血管疾病的复发,从而减轻相关的医疗负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and validation of risk prediction model for recurrent cardiovascular events among Chinese: the Personalized CARdiovascular DIsease risk Assessment for Chinese model.

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.

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