| Literature DB >> 32916098 |
Niek Verweij1, Jan-Walter Benjamins2, Michael P Morley3, Yordi J van de Vegte2, Alexander Teumer4, Teresa Trenkwalder5, Wibke Reinhard6, Thomas P Cappola7, Pim van der Harst8.
Abstract
The electrocardiogram (ECG) is one of the most useful non-invasive diagnostic tests for a wide array of cardiac disorders. Traditional approaches to analyzing ECGs focus on individual segments. Here, we performed comprehensive deep phenotyping of 77,190 ECGs in the UK Biobank across the complete cycle of cardiac conduction, resulting in 500 spatial-temporal datapoints, across 10 million genetic variants. In addition to characterizing polygenic risk scores for the traditional ECG segments, we identified over 300 genetic loci that are statistically associated with the high-dimensional representation of the ECG. We established the genetic ECG signature for dilated cardiomyopathy, associated the BAG3, HSPB7/CLCNKA, PRKCA, TMEM43, and OBSCN loci with disease risk and confirmed this association in an independent cohort. In total, our work demonstrates that a high-dimensional analysis of the entire ECG provides unique opportunities for studying cardiac biology and disease and furthering drug development. A record of this paper's transparent peer review process is included in the Supplemental Information.Entities:
Keywords: cardiac conduction; cardiovascular risk; complex disease; dilated cardiomyopathy; electrocardiogram; electrophysiology; genetics; genome wide association
Mesh:
Year: 2020 PMID: 32916098 PMCID: PMC7530085 DOI: 10.1016/j.cels.2020.08.005
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 11.091