Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass.
Shaan KhurshidJulieta LazarteJames P PirruccelloLu-Chen WangSeung Hoan ChoiAmelia W HallXin WangSamuel Freesun FriedmanVictor NauffalKiran J BiddingerKrishna G AragamPuneet BatraJennifer E HoAnthony A PhilippakisPatrick T EllinorSteven A LubitzPublished in: Nature communications (2023)
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 th 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.
Keyphrases
- left ventricular
- magnetic resonance
- heart failure
- hypertrophic cardiomyopathy
- cardiac resynchronization therapy
- acute myocardial infarction
- mitral valve
- left atrial
- aortic stenosis
- genome wide
- deep learning
- cardiovascular events
- genome wide association study
- cardiovascular disease
- contrast enhanced
- dna methylation
- machine learning
- coronary artery disease
- gene expression
- magnetic resonance imaging
- percutaneous coronary intervention
- acute coronary syndrome
- transcription factor