Genetic architecture of cardiac dynamic flow volumes.
Bruna GomesAditya SinghJack William O'SullivanTheresia M SchnurrPagé C GoddardShaun LoongDavid AmarJ Weston HughesMykhailo KosturFrancois HaddadMichael SalernoRoger Sik Yin FooStephen B MontgomeryVictoria N ParikhBenjamin MederEuan A AshleyPublished in: Nature genetics (2023)
Cardiac blood flow is a critical determinant of human health. However, the definition of its genetic architecture is limited by the technical challenge of capturing dynamic flow volumes from cardiac imaging at scale. We present DeepFlow, a deep-learning system to extract cardiac flow and volumes from phase-contrast cardiac magnetic resonance imaging. A mixed-linear model applied to 37,653 individuals from the UK Biobank reveals genome-wide significant associations across cardiac dynamic flow volumes spanning from aortic forward velocity to aortic regurgitation fraction. Mendelian randomization reveals a causal role for aortic root size in aortic valve regurgitation. Among the most significant contributing variants, localizing genes (near ELN, PRDM6 and ADAMTS7) are implicated in connective tissue and blood pressure pathways. Here we show that DeepFlow cardiac flow phenotyping at scale, combined with genotyping data, reinforces the contribution of connective tissue genes, blood pressure and root size to aortic valve function.
Keyphrases
- aortic valve
- genome wide
- left ventricular
- transcatheter aortic valve replacement
- aortic stenosis
- transcatheter aortic valve implantation
- blood pressure
- aortic valve replacement
- magnetic resonance imaging
- blood flow
- human health
- deep learning
- heart failure
- risk assessment
- dna methylation
- magnetic resonance
- computed tomography
- machine learning
- insulin resistance
- type diabetes
- gene expression
- heart rate
- high throughput
- adipose tissue
- hypertensive patients
- coronary artery disease
- pulmonary arterial hypertension
- skeletal muscle
- mass spectrometry
- big data
- data analysis
- diffusion weighted imaging