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AI-Enabled Echocardiography Identifies Prominent Epicardial Adipose Tissue Associated With an Adverse Cardiometabolic
Background:
Excess epicardial adipose tissue (EAT) is associated with cardiovascular-kidney-metabolic (CKM) dysfunction, but its assessment has traditionally required advanced imaging.
Objectives:
We investigated whether AI-enabled echocardiography could characterize epicardial adiposity and identify residual cardiometabolic risk beyond body mass index (BMI).
Methods:
We developed PanAdipo, a video-based deep learning model in 1,114,441 videos from 28,797 studies across the Yale-New Haven Health System (YNHHS; 2016-2022), using report-derived expert reader labels of prominent EAT (2.3% of studies). PanAdipo was evaluated in five cohorts: a temporally distinct YNHHS transthoracic echocardiography (TTE) set (n=4,588 patients contributing 5,130 studies), an emergency department point-of-care ultrasound (POCUS) cohort (n=10,957), the geographically distinct MIMIC-IV dataset (n=4,549), the community-based Multi-Ethnic Study of Atherosclerosis (MESA Exam 6, n=2,740), and in held-out YNHHS patients with paired coronary CT angiography within 12 months (n=5,167). Analyses examined discrimination of the report label and of CT-defined high indexed EAT volume, correlation with paired cardiac CT phenotypes, and BMI-adjusted associations with cardiometabolic biomarkers and newly documented metabolic disease.
Results:
In the held-out health system test set, PanAdipo identified prominent EAT documented in clinical reports with an area under the receiver operating characteristic curve (AUROC) of 0.86 (95% CI, 0.82-0.91) across all views and of up to 0.93 when combining apical 4-chamber and parasternal views. Against paired CT-derived measurements, PanAdipo discriminated age- and sex-specific high EAT (EAT/heart volume ≥95th percentile) with AUROCs of 0.91 to 0.95 across age-sex groups and correlated more strongly with indexed EAT volume (ρ=0.76) than with BMI (ρ=0.41, all P<0.001); PanAdipo alone explained 53% of indexed EAT volume variance, versus 23% for age, sex, and BMI combined. In MESA, higher scores were associated with an adverse metabolic profile (higher HOMA-IR [β=0.17 per SD; 95% CI, 0.11-0.22]) after adjustment for age, sex, and BMI. In health system TTE and POCUS cohorts, higher scores were associated with newly documented MASLD/MASH (BMI-adjusted pooled HR 1.31 [1.03-1.67] per SD of log[PanAdipo]) and hyperlipidemia (1.11 [1.04-1.18]).
Conclusions:
AI-enabled echocardiography provides a scalable digital biomarker that characterizes prominent epicardial adiposity and is associated with an adverse cardiometabolic profile, highlighting a role for echocardiography in metabolic risk stratification.
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