Authors
Jorge Dahdal, Teemu Maaniitty, Ruurt A Jukema, Nick S Nurmohamed, Pieter G Raijmakers, Roel S Driessen, Matias Mäenpää, Sarah Bär, R Nils Planken, Niels van Royen, Jeroen J Bax, Antti Saraste, Saloua El Messaoudi, Juhani Knuuti, Paul Knaapen, Ibrahim Danad
Published in
European journal of nuclear medicine and molecular imaging. Aug 30, 2026. Epub Aug 30, 2026.
Abstract
The time-dependent contributions of coronary atherosclerotic plaque burden and myocardial ischemia to clinical outcomes in suspected coronary artery disease (CAD) remain uncertain. This study aimed to evaluate the temporal associations of quantitatively assessed plaque burden and ischemia with cardiovascular events.
We studied 1,385 patients with suspected CAD who underwent coronary computed tomography angiography (CCTA) and [15O]H₂O positron emission tomography (PET) perfusion imaging. Plaque burden was measured as percent atheroma volume (PAV) using AI-based CCTA analysis. Myocardial perfusion was evaluated by regional hyperemic myocardial blood flow (hMBF) using PET. Adjusted Cox regression models, including both PAV and hMBF, were used to assess associations with a composite outcome (death, non-fatal myocardial infarction, unstable angina) at 3, 6, and 9 years.
The median follow-up time was 7.1 years, during which 185 patients (13.4%) experienced the outcome. Higher per-patient PAV (per 1%) was consistently and independently associated with increased event rate across all three timepoints (aHR 1.035-1.047, all p < 0.001). Lower regional hMBF (per 0.1 mL/min/g) was independently associated with events at 3 years (aHR 1.050, p = 0.004) and 6 years (aHR 1.028, p = 0.024), but not at 9 years (aHR 1.020, p = 0.063). After excluding early revascularization patients, regional hMBF remained associated with outcomes at all timepoints.
Plaque burden and regional hMBF are independent markers of cardiovascular risk. Plaque burden remained consistently associated with adverse clinical outcomes throughout follow-up, whereas regional hMBF was primarily related to short- and intermediate-term events, likely influenced by the effects of myocardial revascularization.
PMID:
42669101
Bibliographic data and abstract were imported from PubMed on 31 Aug 2026.
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