Lesion-Level Association Between Artificial Intelligence–Derived Coronary Calcium Volume and Plaque Vulnerability
Abstract
BACKGROUND: Extensively calcified lesions are typically at low risk for lesion-level acute events, which may be related to less vulnerable plaques. OBJECTIVES: This study sought to evaluate the lesion-level association between total calcification volume and plaque vulnerability. METHODS: Data were derived from the prospective, observational PECTUS-obs study, in which patients with myocardial infarction underwent intracoronary optical coherence tomography (OCT) imaging of all fractional flow reserve-negative nonculprit lesions. OCT images were analyzed by a core laboratory for plaque vulnerability features (lipid-rich plaque, thin-cap fibroatheroma, layered plaque, macrophage accumulation, microvessel, and cholesterol crystal) and by a validated artificial intelligence algorithm (OCT-AID) for automated volumetric calcium quantification. Total calcium volume was indexed for lesion length and stratified by quartiles (Q1-Q4), from lowest to highest. RESULTS: /mm (IQR: 0.63-1.18) in Q4. The lower quartiles demonstrated the highest prevalence of lipid-rich plaques, macrophage accumulation, and microvessels. Thin-cap fibroatheroma and layered plaques accumulated predominantly in the middle quartiles (Q2-Q3). Cholesterol crystals showed no significant differences between quartiles. Overall, Q1-Q3 lesions demonstrated a greater mean number of plaque vulnerability features than Q4 lesions (P < 0.001 for all). CONCLUSIONS: Most severely calcified nonculprit lesions demonstrate a significantly lower prevalence of plaque vulnerability features as compared to less calcified, more lipid-rich lesions, which may contribute to the lower lesion-level acute event rate observed in heavily calcified lesions.
Fields of Study & Subjects
Cardiac Imaging and Diagnostics
Coronary Interventions and Diagnostics
Cerebrovascular and Carotid Artery Diseases
Publication details
- Journal / source
- JACC Advances
- Publisher
- Elsevier BV
- Volume
- 5
- Issue
- 8
- Pages
- 103077–103077
- Publication date
- 28 July 2026
- Language
- EN