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Clinical Course of Optical Coherence Tomography-Detected Lipid-Rich Coronary Plaque After Optimal Medical Therapy.

Authors :
Sugiura J
Soeda T
Kyodo A
Nakamura T
Okamura A
Nogi K
Hashimoto Y
Ueda T
Watanabe M
Saito Y
Source :
Circulation reports [Circ Rep] 2021 Dec 03; Vol. 4 (1), pp. 29-37. Date of Electronic Publication: 2021 Dec 03 (Print Publication: 2022).
Publication Year :
2021

Abstract

Background: The aim of this study was to evaluate optical coherence tomography (OCT)-detected lipid-rich coronary plaques (LRCPs) with coronary computed tomography angiography (CCTA) 10 months after optimal medical therapy (OMT). Methods and Results: Baseline OCT detected 28 LRCPs in non-culprit lesions. High-risk plaque features (HRPFs), such as positive remodeling, very low attenuation plaques, napkin-ring sign, and spotty calcification, were observed in 67.9%, 67.9%, 21.4%, and 64.3% of LRCPs, respectively, at the 10-month follow-up CCTA. Lesions with ≥3 HRPFs were defined as high-risk LRCPs (n=12); the remaining were defined as low-risk LRCPs (n=16). The maximum lipid arc on baseline OCT was larger in high- than low-risk LRCPs (221±62° vs. 179±44°, respectively; P=0.04). Receiver operating characteristic curve analysis indicated that a maximum lipid arc >154° on baseline OCT was the optimal cut-off value to predict high-risk LRCPs 10 months after OMT. Patients with high-risk LRCPs had worse clinical outcomes, defined as a composite of cardiac death, target lesion-related myocardial infarction, and target lesion-related revascularization, during follow-up than those with low-risk LRCPs (33.3% vs. 0%; P=0.01). Conclusions: A high-risk LRCP at follow-up CCTA was correlated with a larger maximum lipid arc on baseline OCT. Further aggressive treatment for patients with large LRCPs may reduce vulnerable plaque features and prevent future cardiac events.<br />Competing Interests: None declared.<br /> (Copyright © 2022, THE JAPANESE CIRCULATION SOCIETY.)

Details

Language :
English
ISSN :
2434-0790
Volume :
4
Issue :
1
Database :
MEDLINE
Journal :
Circulation reports
Publication Type :
Academic Journal
Accession number :
35083386
Full Text :
https://doi.org/10.1253/circrep.CR-21-0147