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Artificial Intelligence-Enabled ECG Algorithm for the Prediction of Coronary Artery Calcification

Authors
 Changho Han  ;  Ki-Woon Kang  ;  Tae Young Kim  ;  Jae-Sun Uhm  ;  Je-Wook Park  ;  In Hyun Jung  ;  Minkwan Kim  ;  SungA Bae  ;  Hong-Seok Lim  ;  Dukyong Yoon 
Citation
 FRONTIERS IN CARDIOVASCULAR MEDICINE, Vol.9 : 849223, 2022-04 
Journal Title
FRONTIERS IN CARDIOVASCULAR MEDICINE
Issue Date
2022-04
Keywords
artificial intelligence ; atherosclerosis ; coronary artery calcium ; coronary artery disease ; deep neural network ; electrocardiogram
Abstract
Coronary artery calcium (CAC), which can be measured in various types of computed tomography (CT) examinations, is a hallmark of coronary artery atherosclerosis. However, despite the clinical value of CAC scores in predicting cardiovascular events, routine measurement of CAC scores is limited due to high cost, radiation exposure, and lack of widespread availability. It would be of great clinical significance if CAC could be predicted by electrocardiograms (ECGs), which are cost-effective and routinely performed during various medical checkups. We aimed to develop binary classification artificial intelligence (AI) models that predict CAC using only ECGs as input. Moreover, we aimed to address the generalizability of our model in different environments by externally validating our model on a dataset from a different institution. Among adult patients, standard 12-lead ECGs were extracted if measured within 60 days before or after the CAC scores, and labeled with the corresponding CAC scores. We constructed deep convolutional neural network models based on residual networks using only the raw waveforms of the ECGs as input, predicting CAC at different levels, namely CAC score ≥100, ≥400 and ≥1,000. Our AI models performed well in predicting CAC in the training and internal validation dataset [area under the receiver operating characteristics curve (AUROC) 0.753 ± 0.009, 0.802 ± 0.027, and 0.835 ± 0.024 for the CAC score ≥100, ≥400, and ≥1,000 model, respectively]. Our models also performed well in the external validation dataset (AUROC 0.718, 0.777 and 0.803 for the CAC score ≥100, ≥400, and ≥1,000 model, respectively), indicating that our model can generalize well to different but plausibly related populations. Model performance in terms of AUROC increased in the order of CAC score ≥100, ≥400, and ≥1,000 model, indicating that higher CAC scores might be associated with more prominent structural changes of the heart detected by the model. With our AI models, a substantial proportion of previously unrecognized CAC can be afforded with a risk stratification of CAC, enabling initiation of prophylactic therapy, and reducing the adverse consequences related to ischemic heart disease.
Files in This Item:
T202201249.pdf Download
DOI
10.3389/fcvm.2022.849223
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Biomedical Systems Informatics (의생명시스템정보학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Minkwan(김민관) ORCID logo https://orcid.org/0000-0002-4079-8219
Park, Je Wook(박제욱)
Bae, SungA(배성아) ORCID logo https://orcid.org/0000-0003-1484-4645
Uhm, Jae Sun(엄재선) ORCID logo https://orcid.org/0000-0002-1611-8172
Yoon, Dukyong(윤덕용)
Jung, In Hyun(정인현) ORCID logo https://orcid.org/0000-0002-1793-215X
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/188466
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