TY - JOUR
T1 - Coronary artery disease severity and location detection using deep-mining-based magnetocardiography pattern features
AU - Han, Xiaole
AU - Pang, Jiaojiao
AU - Xu, Dong
AU - Xie, Fei
AU - Li, Yu
AU - Xiang, Min
AU - Sun, Jinji
AU - Chen, Yuguo
AU - Ning, Xiaolin
N1 - Publisher Copyright:
© 2025
PY - 2025/6
Y1 - 2025/6
N2 - Background and Objective: The objective of this study was to develop an automated, accurate method of assessing coronary artery disease (CAD), including its severity and location, using deep-mining-based magnetocardiography (MCG) pattern features. Methods: The pattern information of MCG was mined deeply, and features were extracted from multiple perspectives. The curl, gradient, and divergence fields were extended based on the current field to visualize hidden pattern information before the singular value decomposition, main field, and image class features were proposed. Finally, the statistical parameters of fine granularity and compound features were introduced. To estimate the CAD severity, stenosis was classified as none, mild, moderate, or severe, and a suitable subset of features for machine learning (ML) modeling was presented. To localize CAD, it was categorized according to the stenosis location, including the left anterior descending (LAD), left circumflex artery (LCX), and right coronary artery (RCA), and the selected subsets of features appropriate for each localization ML model. Results: The test set exhibited an accuracy, precision, sensitivity, specificity, F1 score, and area under the receiver operating characteristic curve of 85.1 %, 77.8 %, 75.9 %, 95.6 %, 75.9 %, and 0.853, respectively, for CAD severity. The model test sets to detect the LAD, LCX, and RCA locations exhibited accuracies of 97.6 %, 81.2 %, and 85.9 %, respectively. Conclusions: Deep-mining-based MCG features can effectively reflect the severity and location of CAD. The proposed ML method can serve as an automated, accurate diagnostic tool for clinicians to improve the interpretation and application of MCG technology in clinical settings.
AB - Background and Objective: The objective of this study was to develop an automated, accurate method of assessing coronary artery disease (CAD), including its severity and location, using deep-mining-based magnetocardiography (MCG) pattern features. Methods: The pattern information of MCG was mined deeply, and features were extracted from multiple perspectives. The curl, gradient, and divergence fields were extended based on the current field to visualize hidden pattern information before the singular value decomposition, main field, and image class features were proposed. Finally, the statistical parameters of fine granularity and compound features were introduced. To estimate the CAD severity, stenosis was classified as none, mild, moderate, or severe, and a suitable subset of features for machine learning (ML) modeling was presented. To localize CAD, it was categorized according to the stenosis location, including the left anterior descending (LAD), left circumflex artery (LCX), and right coronary artery (RCA), and the selected subsets of features appropriate for each localization ML model. Results: The test set exhibited an accuracy, precision, sensitivity, specificity, F1 score, and area under the receiver operating characteristic curve of 85.1 %, 77.8 %, 75.9 %, 95.6 %, 75.9 %, and 0.853, respectively, for CAD severity. The model test sets to detect the LAD, LCX, and RCA locations exhibited accuracies of 97.6 %, 81.2 %, and 85.9 %, respectively. Conclusions: Deep-mining-based MCG features can effectively reflect the severity and location of CAD. The proposed ML method can serve as an automated, accurate diagnostic tool for clinicians to improve the interpretation and application of MCG technology in clinical settings.
KW - Coronary artery disease
KW - Machine learning
KW - Magnetocardiography
KW - Pattern features
KW - Severity and location
UR - https://www.scopus.com/pages/publications/105002735799
U2 - 10.1016/j.cmpb.2025.108764
DO - 10.1016/j.cmpb.2025.108764
M3 - 文章
C2 - 40253808
AN - SCOPUS:105002735799
SN - 0169-2607
VL - 266
JO - Computer Methods and Programs in Biomedicine
JF - Computer Methods and Programs in Biomedicine
M1 - 108764
ER -