Evaluation of Atherosclerotic Cardiovascular Risk Prediction Models in China: Results From the CHERRY Study
- PMID: 36340248
- PMCID: PMC9627894
- DOI: 10.1016/j.jacasi.2021.10.007
Evaluation of Atherosclerotic Cardiovascular Risk Prediction Models in China: Results From the CHERRY Study
Abstract
Background: Updated American or Chinese guidelines recommended calculating atherosclerotic cardiovascular disease (ASCVD) risk using the Pooled Cohort Equations (PCE) or Prediction for Atherosclerotic Cardiovascular Disease Risk in China (China-PAR) models; however, evidence on performance of both models in Asian populations is limited.
Objectives: The authors aimed to evaluate the accuracy of the PCE or China-PAR models in a Chinese contemporary cohort.
Methods: Data were extracted from the CHERRY (CHinese Electronic health Records Research in Yinzhou) study. Participants aged 40 to 79 years without prior ASCVD at baseline from 2010 to 2016 were included. ASCVD was defined as nonfatal or fatal stroke, nonfatal myocardial infarction, and cardiovascular death. Models were assessed for discrimination and calibration.
Results: Among 226,406 participants, 5362 (2.37%) adults developed a first ASCVD event during a median of 4.60 years of follow-up. Both models had good discrimination: C-statistics in men were 0.763 (95% confidence interval [CI]: 0.754-0.773) for PCE and 0.758 (95% CI: 0.749-0.767) for China-PAR; C-statistics in women were 0.820 (95% CI: 0.812-0.829) for PCE and 0.811 (95% CI: 0.802-0.819) for China-PAR. The China-PAR model underpredicted risk by 20% in men and by 40% in women, especially in the highest-risk groups. However, PCE overestimated by 63% in men and inversely underestimated the risk by 34% in women with poor calibration (both P < 0.001). After recalibration, observed and predicted risks by recalibrated PCE were better aligned.
Conclusions: In this large-scale population-based study, both PCE and China-PAR had good discrimination in 5-year ASCVD risk prediction. China-PAR outperformed PCE in calibration, whereas recalibration equalized the performance of PCE and China-PAR. Further specific models are needed to improve accuracy in the highest-risk groups.
Keywords: ACC/AHA, American College of Cardiology/American Heart Association; ASCVD, atherosclerotic cardiovascular disease; Chinese; EHR, electronic health record; EMR, electronic medical record; PCE, pooled cohort equations; atherosclerotic cardiovascular disease; electronic health records; primary prevention; risk assessment.
© 2022 The Authors.
Conflict of interest statement
This study was supported by the Chinese Ministry of Science and Technology (grant number 2020YFC2003503), the National Natural Science Foundation of China (grant numbers 81973132, 81961128006, 91846112), and the Beijing Natural Science Foundation (grant number 7182084). All authors have followed the Recommendations for the Conduct, Reporting, Editing, and Publication of Scholarly Work in Medical Journals formulated by the International Committee of Medical Journal Editors (ICMJE). Dr Tang has served as a consultant for Medtronic. Dr Gao has served as a consultant for Medtronic. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
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References
-
- Lloyd-Jones D.M., Braun L.T., Ndumele C.E., et al. Use of risk assessment tools to guide decision-making in the primary prevention of atherosclerotic cardiovascular disease: a special report from the American Heart Association and American College of Cardiology. J Am Coll Cardiol. 2019;73:3153–3167. - PubMed
-
- Task Force on Chinese Guidelines for the Prevention of Cardiovascular Disease, Editorial Board of Chinese Journal of Cardiology. Chinese guidelines for the prevention of cardiovascular diseases (2017). Article in Chinese. Chin J Cardiol. 2018;46(1):10–25. - PubMed
-
- Yang X., Li J., Hu D., et al. Predicting the 10-year risks of atherosclerotic cardiovascular disease in Chinese population: The China-PAR Project (Prediction for ASCVD Risk in China) Circulation. 2016;134:1430–1440. - PubMed
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