Thin-cap fibroatheroma predicts clinical events in diabetic patients with normal fractional flow reserve: the COMBINE OCT–FFR trial

医学 部分流量储备 内科学 心脏病学 心肌梗塞 冠状动脉造影
作者
Elvin Kedhi,Balázs Berta,Tomasz Roleder,Renicus S. Hermanides,Enrico Fabris,Alexander Ijsselmuiden,Floris Kauer,Fernándo Alfonso,Clemens von Birgelen,Javier Escaned,Cyril Camaro,Mark Kennedy,Bruno Pereira,Michael Magro,Holger Nef,Sebastian Reith,Arif Al Nooryani,Fernando Rivero,Krzysztof Piotr Malinowski,Giuseppe De Luca
出处
期刊:European Heart Journal [Oxford University Press]
卷期号:42 (45): 4671-4679 被引量:185
标识
DOI:10.1093/eurheartj/ehab433
摘要

Abstract Aims The aim of this study was to understand the impact of optical coherence tomography (OCT)-detected thin-cap fibroatheroma (TCFA) on clinical outcomes of diabetes mellitus (DM) patients with fractional flow reserve (FFR)-negative lesions. Methods and results COMBINE OCT-FFR study was a prospective, double-blind, international, natural history study. After FFR assessment, and revascularization of FFR-positive lesions, patients with ≥1 FFR-negative lesions (target lesions) were classified in two groups based on the presence or absence of ≥1 TCFA lesion. The primary endpoint compared FFR-negative TCFA-positive patients with FFR-negative TCFA-negative patients for a composite of cardiac mortality, target vessel myocardial infarction, clinically driven target lesion revascularization or unstable angina requiring hospitalization at 18 months. Among 550 patients enrolled, 390 (81%) patients had ≥1 FFR-negative lesions. Among FFR-negative patients, 98 (25%) were TCFA positive and 292 (75%) were TCFA negative. The incidence of the primary endpoint was 13.3% and 3.1% in TCFA-positive vs. TCFA-negative groups, respectively (hazard ratio 4.65; 95% confidence interval, 1.99–10.89; P < 0.001). The Cox regression multivariable analysis identified TCFA as the strongest predictor of major adverse clinical events (MACE) (hazard ratio 5.12; 95% confidence interval 2.12–12.34; P < 0.001). Conclusions Among DM patients with ≥1 FFR-negative lesions, TCFA-positive patients represented 25% of this population and were associated with a five-fold higher rate of MACE despite the absence of ischaemia. This discrepancy between the impact of vulnerable plaque and ischaemia on future adverse events may represent a paradigm shift for coronary artery disease risk stratification in DM patients.
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