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Updated: Jul 2, 2026

Optical Coherence Tomography Based Biomechanical Fluid-Structure Interaction Analysis of Coronary Atherosclerosis Progression
Published on: January 15, 2022
Serial OCT-based coronary physiology and plaque composition in vessels with nonobstructive coronary lesions following
Pruthvi C Revaiah1, Yuliya Vengrenyuk1, Vemuri Krishna Santosh1
1Icahn School of Medicine at Mount Sinai and Fuster Heart Hospital at Mount Sinai, New York, NY, USA.
Background And Aims:
Non-obstructive coronary plaques are a major source of future coronary events, particularly when characterized by high lipid burden and adverse plaque morphology. While intensive lipid-lowering therapy promotes plaque regression, serial data linking quantitative plaque compositional changes to coronary physiology are limited. We aimed to evaluate the impact of maximal lipid-lowering therapy on coronary plaque composition and coronary physiology, using artificial intelligence (AI) based tissue characterization derived from OCT and optical flow ratio (OFR).
Methods:
This was a serial intravascular imaging sub-study of YELLOW III. Stable coronary artery disease patients with lipid-rich, non-obstructive plaques (diameter stenosis of 30-50% on angiography) received Evolocumab in addition to high-intensity statin therapy. Paired baseline and 26-week follow-up OCT and NIRS-IVUS imaging were available for 105 coronary segments. AI-based OCT was used for quantitative plaque characterization, and OFR was computed as a surrogate of invasive fractional flow reserve. Changes in plaque composition and coronary physiology were assessed, and correlations between compositional changes and OFR improvement were evaluated.
Results:
Amongst 105 paired coronary segments, total plaque volume decreased significantly over follow-up (201.2 ± 81.8 vs 191.3 ± 72.4 mm3; p < 0.001), driven primarily by reductions in lipid volume (p < 0.001) and macrophage volume (p = 0.006). Fibrous tissue volume showed a modest reduction, while its relative proportion increased, consistent with preferential lipid regression. Calcified plaque volume remained unchanged. Coronary physiology improved modestly, with an improvement in OFR (0.924 ± 0.062 to 0.932 ± 0.060; p < 0.001) and a reduction in lesion-level ΔOFR (p < 0.001). Improvement in OFR correlated inversely with reductions in total plaque volume (ρ = -0.286; p = 0.003), lipid volume (ρ = -0.257; p = 0.008), and lesion-level lipid burden assessed by LCBI (r = -0.23; p = 0.021).
Conclusions:
Maximal lipid-lowering therapy induces favorable quantitative changes in plaque composition and modest but significant improvements in coronary physiology in non-obstructive coronary lesions. AI-based OCT with OFR provides an integrated approach to link plaque biology with functional remodeling.
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