Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass.

Journal: Nature communications
Published Date:

Abstract

Left ventricular mass is a risk marker for cardiovascular events, and may indicate an underlying cardiomyopathy. Cardiac magnetic resonance is the gold-standard for left ventricular mass estimation, but is challenging to obtain at scale. Here, we use deep learning to enable genome-wide association study of cardiac magnetic resonance-derived left ventricular mass indexed to body surface area within 43,230 UK Biobank participants. We identify 12 genome-wide associations (1 known at TTN and 11 novel for left ventricular mass), implicating genes previously associated with cardiac contractility and cardiomyopathy. Cardiac magnetic resonance-derived indexed left ventricular mass is associated with incident dilated and hypertrophic cardiomyopathies, and implantable cardioverter-defibrillator implant. An indexed left ventricular mass polygenic risk score ≥90 percentile is also associated with incident implantable cardioverter-defibrillator implant in separate UK Biobank (hazard ratio 1.22, 95% CI 1.05-1.44) and Mass General Brigham (hazard ratio 1.75, 95% CI 1.12-2.74) samples. Here, we perform a genome-wide association study of cardiac magnetic resonance-derived indexed left ventricular mass to identify 11 novel variants and demonstrate that cardiac magnetic resonance-derived and genetically predicted indexed left ventricular mass are associated with incident cardiomyopathy.

Authors

  • Shaan Khurshid
    Division of Cardiology, Massachusetts General Hospital, Boston, Massachusetts.
  • Julieta Lazarte
    Cardiovascular Research Center, Massachusetts General Hospital, Boston, MA, USA.
  • James P Pirruccello
    Division of Cardiology, Massachusetts General Hospital, Boston, Massachusetts.
  • Lu-Chen Weng
    Cardiovascular Research Center, Massachusetts General Hospital, Boston, MA, USA.
  • Seung Hoan Choi
    Cardiovascular Disease Initiative, Broad Institute, Cambridge, MA, USA.
  • Amelia W Hall
    Cardiovascular Disease Initiative, Broad Institute, Cambridge, MA, USA.
  • Xin Wang
    Key Laboratory of Bio-based Material Science & Technology (Northeast Forestry University), Ministry of Education, Harbin 150040, China.
  • Samuel F Friedman
    Data Sciences Platform, Broad Institute, Cambridge, MA, USA.
  • Victor Nauffal
    Division of Cardiology, Brigham and Women's Hospital, Boston, MA, USA.
  • Kiran J Biddinger
    Cardiovascular Research Center, Massachusetts General Hospital, Boston, MA, USA.
  • Krishna G Aragam
    Cardiovascular Research Center, Massachusetts General Hospital, Boston, MA, USA.
  • Puneet Batra
    Data Sciences Platform, Broad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, Massachusetts.
  • Jennifer E Ho
    Division of Cardiology, Massachusetts General Hospital, Boston, Massachusetts.
  • Anthony A Philippakis
    Data Sciences Platform, Broad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, Massachusetts.
  • Patrick T Ellinor
    Cardiovascular Disease Initiative, Broad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, Massachusetts.
  • Steven A Lubitz
    Cardiovascular Disease Initiative, Broad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, Massachusetts.