Year: 2022
Type: preprint
Study design: Observational Study
Abstract: ABSTRACT The electrocardiogram (ECG) is an inexpensive and widely available diagnostic tool, and therefore has great potential to facilitate disease detection in large-scale populations. Both cardiac and noncardiac diseases may alter the appearance of the ECG, though the extent to which diseases across the human phenotypic landscape can be detected on the ECG remains unclear. We developed a deep learning variational autoencoder model that encodes and reconstructs ECG waveform data within a multidimensional latent space. We then systematically evaluated whether associations between ECG encodings and a broad range of disease phenotypes could be detected using the latent space model by deriving disease vectors and projecting individual ECG encodings onto the vectors. We developed models for both 12- and single-lead ECGs, akin to those used in wearable ECG technology. We leveraged phecodes to generate disease labels using International Classification of Disease (ICD) codes for about 1,600 phenotypes in three different datasets linked to electronic health record data. We tested associations between ECG encodings and disease phenotypes using a phenome-wide association study approach in each dataset, and meta-analyzed the results. We observed that the latent space ECG model identified associations for 645 (40%) diseases tested in the 12-lead model. Associations were enriched for diseases of the circulatory (n=140, 82% of category-specific diseases), respiratory (n=53, 62%), and endocrine/metabolic (n=73, 45%) systems, with additional associations evident across the human phenome; results were similar for the single-lead models. The top ECG latent space association was with hypertension in the 12-lead ECG model, and cardiomyopathy in the single-lead ECG model (p<2.2×10 -308 for each). The ECG latent space model demonstrated a greater number of associations than ECG models using standard ECG intervals alone, and generally resulted in improvements in discrimination of diseases compared to models comprising only age, sex, and race. We further demonstrate how a latent space model can be used to generate disease-specific ECG waveforms and facilitate disease profiling for individual patients.
Source: medRxiv
Authors: Rachael A. Venn, Xin Wang, Sam Freesun Friedman, Nate Diamant, Shaan Khurshid, Paolo Di Achille, Lu-Chen Weng, Seung Hoan Choi, Christopher Reeder, James P. Pirruccello, Pulkit Singh, Emily S. Lau, Anthony Philippakis, Christopher D. Anderson, Patrick T. Ellinor, Jennifer E. Ho, Puneet Batra, Steven A. Lubitz
Language: English
Topic: ECG Monitoring and Analysis
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: green
Awards: Precision Medicine in Ischemic Stroke and Atrial Fibrillation (PreMISe-AF), ERICH-GENE, Sequencing Annotation and Functional Analysis in Risk of Intracerebral Hemorrhage, G3897532131, G4077987447, G5961991630, Advancing Atrial Fibrillation Precision Medicine, G6486946130, Mentoring in Arrhythmia Research, G8630864450, HFpEF Susceptibility in Women: The Role of Inflammation, IDENTIFICATION OF COMMON GENETIC VARIANTS FOR ATRIAL FIBRILLATION AND PR INTERVAL, Using Electrocardiogram Genetics to Inform Arrhythmia Risk, Genomics of Cardiac Arrhythmias
OpenAlex ID: W4312198228
