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Real-world risk stratification for coronary heart disease

A one-year prediction model using health information exchange data

Datos Bibliográficos

ID15359662
AutoresYaqi Zhang (0000-0002-7103-9864, Guangdong Polytechnic Normal University, autor de correspondencia), Yifu Mo (0000-0002-2337-4668, China Southern Power Grid (China)), Noriaki Ozawa (Stanford University), Naoto Ozawa, Takumi Ichikawa (Stanford University), Chao-Jung Huang (0000-0002-4293-9492, National Taiwan University), Zhi Han (0000-0002-5340-0070, Stanford University), Lü Tian (0000-0002-5893-0169, Stanford University), Shaun T Alfreds (0000-0003-1752-4823, Gulf of Maine Research Institute), Karl G Sylvester (0000-0002-8559-0155, Stanford University), Doff B McElhinney (0000-0001-7242-0934, Stanford University), Xuefeng B Ling (0000-0002-5386-3884, Stanford Medicine)
Año2025
Volumen25
Número1
Páginas3218-3218
Fecha de publicación2025-09-30
Peer ReviewedSí
Open AccessSí
TipoARTICLE
RevistaBMC Public Health (JOURNAL)
Identificadores de la revistaISSN: 1471-2458 • E-ISSN: 1471-2458
EditorialBioMed Central (PUBLISHER • GB)
DOI10.1186/s12889-025-24266-y
PMID41029641
OpenAlexW4414663968
IdiomaEN
Referencias citadas37

Coronary heart disease (CHD), the most common form of heart disease, progresses over years before culminating in serious cardiac events. Early prediction and intervention are critical to reducing CHD-related morbidity, mortality, and healthcare burden. To develop and validate a machine learning model using statewide electronic health records (EHRs) to predict 1-year risk of CHD in the general population of Maine, enabling targeted preventive strategies. Two population-based cohorts were constructed from the Maine Health Information Exchange (HIE): a retrospective cohort for model training and calibration (2015–2017, N = 1,042,124), and a prospective cohort for external validation (2016–2018, N = 1,040,158). EHR features included demographics, diagnoses, procedures, medications, labs, and utilization metrics. A multistage modeling pipeline—comprising statistical filtering, XGBoost-based feature selection, risk prediction, and isotonic regression calibration—was used to construct the final model. Validation included discrimination, calibration, and survival analysis. The final XGBoost model achieved strong discrimination: AUC = 0.952 (95% CI: 0.950–0.954) in the retrospective cohort and 0.888 (95% CI: 0.885–0.890) in the prospective cohort. Based on calibrated risk probabilities, the population was stratified into five risk categories: very low (92.30%, N = 960,021), low (6.79%, N = 70,676), medium (0.85%, N = 8,888), high (0.05%, N = 554), and very high (0.002%, N = 19). Among the very high-risk group, 11 individuals (57.89%) developed CHD within one year. This statewide, HIE-based CHD risk prediction model demonstrates robust performance and real-world applicability. It enables early identification of high-risk individuals and supports population-scale precision prevention through evidence-informed, proactive care

Biostatistics · Cohort · Cohort study · Framingham Risk Score · Health information exchange · Population · Prospective cohort study · Retrospective cohort study · Risk assessment · Artificial Intelligence in Healthcare · Cardiovascular Health and Risk Factors · Machine Learning in Healthcare

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