AI-derived left atrial volumetric and ratio-based metrics from coronary artery calcium scans provide incremental predictive value for long-term atrial fibrillation and stroke.
Do AI-derived left atrial volume index and chamber ratios from routine CAC scans predict incident atrial fibrillation and stroke beyond established risk scores?
6,812 participants pooled from 2 prospective cohorts (MESA, n=5670; FHS, n=1142)
AI-enabled volumetry (AutoChamber) quantifying left atrial volume index and chamber ratios (LA/RA, LA/LV) from noncontrast coronary artery calcium (CAC) scans
Established risk scores (CHARGE-AF risk score and Framingham Stroke Risk Profile)
Incident atrial fibrillation and incident strokehard clinical
AI-derived left atrial volume and chamber ratios from routine noncontrast CAC scans provide incremental predictive value for long-term atrial fibrillation and stroke beyond established clinical risk scores.
Absolute Event Rate: 0% vs 0%
Background: The AI-CVD initiative aims to extract actionable insights from coronary artery calcium (CAC) scans beyond the traditional CAC score. Although AI-derived cardiac chamber volumes predict atrial fibrillation (AF) and stroke, the long-term prognostic value of chamber ratios is less established. We evaluated the predictive value of AI-derived left atrial volume index and related chamber ratios (left atrial LA/right atrial RA, LA/left ventricular) from routine CAC scans for incident AF and stroke, and their incremental value beyond established risk scores. Methods: Pooled participant-level data from 2 prospective cohorts, the MESA (Multi-Ethnic Study of Atherosclerosis, 2000–2002, n=5670) and the FHS (Framingham Heart Study Offspring cohort, 1998–2001, n=1142), were analyzed. Primary outcomes were incident AF and incident stroke. AI-enabled volumetry (AutoChamber, AI-CVD platform) quantified cardiac chamber metrics from noncontrast CAC scans. Cox proportional hazards models, net reclassification improvement, time-dependent area under the curve, calibration metrics, and least absolute shrinkage and selection operator regression were applied to evaluate predictive performance. Results: Over a median 17-year follow-up, 1302 participants developed AF, and 365 experienced stroke events. Individuals in the ≥95th percentile of chamber metrics had a significantly increased risk. Adjusted hazard ratios for AF were 2.66 (95% CI, 2.23–3.17) for left atrial volume index, 2.04 (95% CI, 1.71–2.45) for LA/left ventricular (LV) ratio, and 1.87 (95% CI, 1.55–2.26) for LA/RA ratio. For stroke, corresponding hazard ratios were 1.96 (95% CI, 1.38–2.77), 1.64 (95% CI, 1.15–2.33), and 1.83 (95% CI, 1.29–2.59), respectively. AI-derived metrics improved reclassification beyond Cohorts for Heart and Aging Research in Genomic Epidemiology Atrial Fibrillation risk score and Framingham Stroke Risk Profile, with greatest improvements for AF from left atrial volume index (net reclassification improvement, 0.48) and stroke from LA/RA ratio (net reclassification improvement, 0.39), driven mainly by nonevent classification. Although discrimination improvements (area under the curve ) were modest, chamber measurements substantially improved Framingham Stroke Risk Profile calibration (slope, 0.448 to 0.834–0.902). Among all chamber metrics (including volumes and ratios), the least absolute shrinkage and selection operator identified left atrial volume index as the strongest predictor for AF, and LA/RA ratio as the strongest for stroke. Conclusions: AI-enabled left atrial volumetric and ratio-based metrics derived opportunistically from CAC scans provide incremental predictive value for AF and stroke prediction.
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Amir Azimi
Kyle Atlas
MACOM (United States)
Anthony P. Reeves
Cornell University
Stroke
Stanford University
Cornell University
University of Southern California
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Azimi et al. (Wed,) reported a other. AI-derived left atrial volumetric and ratio-based metrics from coronary artery calcium scans provide incremental predictive value for long-term atrial fibrillation and stroke.
synapsesocial.com/papers/69d895796c1944d70ce066fd — DOI: https://doi.org/10.1161/strokeaha.125.053401