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Updated: Jun 17, 2026

Optical Coherence Tomography Based Biomechanical Fluid-Structure Interaction Analysis of Coronary Atherosclerosis Progression
Published on: January 15, 2022
Long-term prognostic impact of optical coherence tomography detected plaque rupture in nonculprit coronary segments
Flavio Giuseppe Biccirè1, Eloisa Arbustini2, Yukio Ozaki3
1Cardiovascular Sciences Department, San Giovanni Addolorata Hospital, Rome, Italy; Centro per la Lotta Contro L'Infarto, CLI Foundation, Rome, Italy.
Insights
Nonculprit plaque rupture, identified by optical coherence tomography, was not an independent predictor of cardiac events. Its presence did not improve risk prediction beyond established features like thin-cap fibroatheroma.
Area of Science:
- Cardiology
- Vascular Biology
- Medical Imaging
Background:
- Atherosclerotic plaque rupture is a primary cause of acute coronary syndrome.
- The prognostic impact of plaque rupture in nonculprit coronary arteries is not well understood.
Purpose of the Study:
- To investigate the long-term clinical outcomes associated with nonculprit plaque rupture detected by optical coherence tomography (OCT).
- To determine if nonculprit plaque rupture independently predicts cardiac events.
Main Methods:
- Prospective investigation within the CLIMA study.
- Optical coherence tomography (OCT) used to detect nonculprit plaque rupture.
- 5-year follow-up for major adverse cardiac events (MACE), including cardiac death and target-segment myocardial infarction (TS-MI).
Main Results:
- Nonculprit plaque rupture was identified in 7.3% of patients.
- Associated factors included three-vessel disease, total plaque length, thin-cap fibroatheroma (TCFA), and large lipid arc.
- While associated with MACE in univariable analysis, it was not an independent predictor in multivariable models.
- Nonculprit plaque rupture did not improve the predictive accuracy of TCFA for cardiac events.
Conclusions:
- Nonculprit plaque rupture is not an independent predictor of cardiac events at 5-year follow-up.
- Its identification does not enhance the predictive value of existing high-risk morphological features like TCFA.
- Further research is warranted to fully elucidate the clinical relevance of nonculprit plaque rupture.
Background And Aims:
Atherosclerotic plaque rupture is largely acknowledged as the main mechanism of acute coronary syndrome. However, the prognostic significance of plaque rupture detected in nonculprit coronary sites remains largely unknown.
Methods:
We investigated the long-term clinical outcomes of nonculprit plaque rupture detected by optical coherence tomography in the prospective CLIMA study. The primary composite endpoint was cardiac death or target-segment myocardial infarction (TS-MI) through 5-year follow-up.
Results:
Among 1003 patients (age 64.8y; 24.6% women), nonculprit plaque rupture was observed in 7.3% of patients. Three-vessel disease, total plaque length, thin-cap fibroatheroma and large lipid arc were independently associated with nonculprit plaque rupture. The presence of nonculprit plaque rupture was associated with the primary endpoint at univariable (HR 2.09, 95%CI 1.07-4.08, p = 0.030) but not clinical (adjusted HR 1.70, 95%CI 0.83-3.48, p = 0.145) and morphological (adjusted HR 1.63, 95%CI 0.83-3.21, p = 0.156) multivariable analysis. The individual rates of cardiac death (HR 1.64, 95%CI 0.70-3.85, p = 0.252) and TS-MI (HR 2.87, 95%CI 0.97-8.47, p = 0.057) did not significantly differ between patients with vs without nonculprit plaque rupture. At the Kaplan-meier analysis, the presence of nonculprit plaque rupture was significantly associated with the primary endpoint only in presence of a thin-cap fibroatheroma (TCFA). The presence of nonculprit plaque rupture did not improve the predictive accuracy of any TCFA in multiple prediction models.
Conclusions:
Nonculprit plaque rupture was associated with cardiac events at univariable but not multivariable analysis. Identification of nonculprit PR did not improve the predictive value of established high-risk morphological features such as TCFA; however, future ad hoc studies are needed to further clarify its potential independent clinical relevance.
Clinical Trial Registration:
URL: https://www.
Clinicaltrials:
gov; Unique identifier: NCT02883088.
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