Abstract
Objective: This work investigates the possibility of disentangled representation learning of inter-subject anatomical variations within electrocardiographic (ECG) data. Methods: Since ground truth anatomical factors are generally not known in clinical ECG for assessing the disentangling ability of the models, the presented work first proposes the SimECG data set, a 12-lead ECG data set procedurally generated with a controlled set of anatomical generative factors. Second, to perform such disentanglement, the presented method evaluates and compares deep generative models with latent density modeled by nonparametric Indian Buffet Process to account for the complex generative process of ECG data. Results: In the simulated data, the experiments demonstrate, for the first time, concrete evidence of the possibility to disentangle key generative anatomical factors within ECG data in separation from task-relevant generative factors. We achieve a disentanglement score of 92.1% while disentangling five anatomical generative factors and the task-relevant generative factor. In both simulated and real-data experiments, this work further provides quantitative evidence for the benefit of disentanglement learning on the downstream clinical task of localizing the origin of ventricular activation. Overall, the presented method achieves an improvement of around 18.5%, and 11.3% for the simulated dataset, and around 7.2%, and 3.6% for the real dataset, over baseline CNN, and standard generative model, respectively. Conclusion: These results demonstrate the importance as well as the feasibility of the disentangled representation learning of inter-subject anatomical variations within ECG data. Significance: This work suggests the important research direction to deal with the well-known challenge posed by the presence of significant inter-subject variations during an automated analysis of ECG data.
Original language | English |
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Pages (from-to) | 860-870 |
Number of pages | 11 |
Journal | IEEE Transactions on Biomedical Engineering |
Volume | 69 |
Issue number | 2 |
DOIs | |
Publication status | Published - Feb 1 2022 |
Bibliographical note
Funding Information:Manuscript received June 23, 2021; revised August 18, 2021; accepted August 22, 2021. Date of publication August 30, 2021; date of current version January 20, 2022. This work was supported by the National Institute of Health (National Heart, Lung, and Blood Institute) under Award R15HL140500 and R01HL145590. (Corresponding author: Prashnna K. Gyawali.) Prashnna K. Gyawali was with the Rochester Institute of Technology, Stanford, CA 94305 USA. He is now with Stanford University, Stanford, CA 94305 USA (e-mail: pkg2182@rit.edu).
Publisher Copyright:
© 1964-2012 IEEE.
ASJC Scopus Subject Areas
- Biomedical Engineering
PubMed: MeSH publication types
- Journal Article
- Research Support, N.I.H., Extramural