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The Genetic Makeup of the Electrocardiogram.
Verweij, Niek; Benjamins, Jan-Walter; Morley, Michael P; van de Vegte, Yordi J; Teumer, Alexander; Trenkwalder, Teresa; Reinhard, Wibke; Cappola, Thomas P; van der Harst, Pim.
Affiliation
  • Verweij N; University of Groningen, University Medical Center Groningen, Department of Cardiology, Groningen, the Netherlands; Genomics plc, Oxford, UK. Electronic address: mail@niekverweij.com.
  • Benjamins JW; University of Groningen, University Medical Center Groningen, Department of Cardiology, Groningen, the Netherlands.
  • Morley MP; Cardiovascular Institute, Perelman School of Medicine , University of Pennsylvania, Philadelphia, USA.
  • van de Vegte YJ; University of Groningen, University Medical Center Groningen, Department of Cardiology, Groningen, the Netherlands.
  • Teumer A; Institute for Community Medicine, University Medicine Greifswald, Greifswald, Germany; DZHK (German Center for Cardiovascular Research), partner site Greifswald, Greifswald, Germany.
  • Trenkwalder T; Klinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technical University Munich, Munich, Germany; DZHK (German Center for Cardiovascular Research), partner site Munich Heart Alliance, Munich, Germany.
  • Reinhard W; Klinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technical University Munich, Munich, Germany.
  • Cappola TP; Division of Cardiovascular Medicine at the Perelman School of Medicine at the University of Pennsylvania, Philadelphia, USA.
  • van der Harst P; University of Groningen, University Medical Center Groningen, Department of Cardiology, Groningen, the Netherlands; Department of Cardiology, Heart and Lung Division, University Medical Center Utrecht, Utrecht, the Netherlands.
Cell Syst ; 11(3): 229-238.e5, 2020 09 23.
Article in En | MEDLINE | ID: mdl-32916098
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Electrocardiography Type of study: Prognostic_studies Limits: Humans Language: En Journal: Cell Syst Year: 2020 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Electrocardiography Type of study: Prognostic_studies Limits: Humans Language: En Journal: Cell Syst Year: 2020 Document type: Article Country of publication: United States