医学
生命银行
心脏磁共振
磁共振成像
心脏病学
内科学
放射科
生物信息学
生物
作者
Alan Le Goallec,Jean-Baptiste Prost,Sasha Collin,Samuel Diai,Théo Vincent,Chirag B. Patel
出处
期刊:Circulation
[Lippincott Williams & Wilkins]
日期:2021-11-16
卷期号:144 (Suppl_1)
被引量:3
标识
DOI:10.1161/circ.144.suppl_1.12758
摘要
Introduction: Heart disease is the first cause of death after age 65 and, with the world population aging, its prevalence is expected to starkly increase. Methods: We used deep learning to build a heart age predictor on 45,000 heart magnetic resonance videos [MRI] and electrocardiograms [ECG] from the UK Biobank cohort (age range 45-81 years). (Figure 1) Results: We predicted age with a root mean squared error [RMSE] of 2.81±0.02 years (R-Squared=85.6±0.2%) and found that accelerated heart aging is heritable at more than 35%. MRI-based anatomical features predicted age better than ECG-based electro-physiological features (RMSE=2.89±0.02 years vs. 6.09±.0.02 years), and heart anatomical and electrical aging are weakly correlated (Pearson correlation=.249±.002). Our attention maps highlighted the aorta, the mitral valve, and the interventricular septum as key anatomical features driving heart age prediction (Figure 2). We identified genetic (e.g titin gene) and non-genetic correlates (e.g smoking) of accelerated heart aging. Conclusions: We built the first accurate heart age predictor, and showed that different dimensions of the heart can age at different rates. We identified genetic and non-genetic factors associated with accelerated heart aging. Our predictor can be used the assess the effect of rejuvenating therapies on cardiovascular health.
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