A deep learning algorithm to translate and classify cardiac electrophysiology
Year: 2021
Type: article
Abstract: The development of induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) has been a critical in vitro advance in the study of patient-specific physiology, pathophysiology, and pharmacology. We designed a new deep learning multitask network approach intended to address the low throughput, high variability, and immature phenotype of the iPSC-CM platform. The rationale for combining translation and classification tasks is because the most likely application of the deep learning technology we describe here is to translate iPSC-CMs following application of a perturbation. The deep learning network was trained using simulated action potential (AP) data and applied to classify cells into the drug-free and drugged categories and to predict the impact of electrophysiological perturbation across the continuum of aging from the immature iPSC-CMs to the adult ventricular myocytes. The phase of the AP extremely sensitive to perturbation due to a steep rise of the membrane resistance was found to contain the key information required for successful network multitasking. We also demonstrated successful translation of both experimental and simulated iPSC-CM AP data validating our network by prediction of experimental drug-induced effects on adult cardiomyocyte APs by the latter.
Source: eLife
DOI: 10.7554/elife.68335
Language: English
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,500
Funders: National Science Foundation, American Heart Association, Oracle, National Centre for Supercomputing Applications, Scheme for Promotion of Academic and Research Collaboration, National Institutes of Health, Japan Society for the Promotion of Science, National Heart, Lung, and Blood Institute, Common Fund
Awards: G1351713346, G2288730888, G3554245083, A multidisciplinary approaches for drug-induced arrhythmia using human iPS cells, G4085294414, G5514250563, Cellular and molecular analysis of skeletal muscle protection by female sex hormones, Elucidation of molecular mechanisms of sex-based arrhythmias, G725283979, G7421814563, G7855795961, G9000019190, G9000039216, G9000047255, G9000055623, G9000098431, G9000216659
OpenAlex ID: W3176661463
