Characterization of dynamic changes in cardiac microstructure after reperfused ST-elevation myocardial infarction by biphasic diffusion tensor cardiovascular magnetic resonance
医学
磁共振成像
磁共振弥散成像
心脏磁共振
心脏病学
心肌梗塞
内科学
核磁共振
放射科
物理
作者
Ramyah Rajakulasingam,Pedro Ferreira,Andrew D. Scott,Zohya Khalique,Alessia Azzu,Maria Molto,Miriam Conway,Emanuela Falaschetti,Kevin Cheng,Daniel Hammersley,Emily-Jane Cantor,Alexander Tindale,Catherine Beattie,Arjun Banerjee,Ricardo Wage,Rajkumar Soundarajan,Miles Dalby,Sònia Nielles‐Vallespin,Dudley J. Pennell,Ranil de Silva
出处
期刊:European Heart Journal [Oxford University Press] 日期:2024-10-15卷期号:46 (5): 454-469被引量:4
Abstract Background and Aims Microstructural disturbances underlie dysfunctional contraction and adverse left ventricular (LV) remodelling after ST-elevation myocardial infarction (STEMI). Biphasic diffusion tensor cardiovascular magnetic resonance (DT-CMR) quantifies dynamic reorientation of sheetlets (E2A) from diastole to systole during myocardial thickening, and markers of tissue integrity [mean diffusivity (MD) and fractional anisotropy (FA)]. This study investigated whether microstructural alterations identified by biphasic DT-CMR: (i) enable contrast-free detection of acute myocardial infarction (MI); (ii) associate with severity of myocardial injury and contractile dysfunction; and (iii) predict adverse LV remodelling. Methods Biphasic DT-CMR was acquired 4 days (n = 70) and 4 months (n = 66) after reperfused STEMI and in healthy volunteers (HVOLs) (n = 22). Adverse LV remodelling was defined as an increase in LV end-diastolic volume ≥ 20% at 4 months. MD and FA maps were compared with late gadolinium enhancement images. Results Widespread microstructural disturbances were detected post-STEMI. In the acute MI zone, diastolic E2A was raised and systolic E2A reduced, resulting in reduced E2A mobility (all P < .001 vs. adjacent and remote zones and HVOLs). Acute global E2A mobility was the only independent predictor of adverse LV remodelling (odds ratio .77; 95% confidence interval .63–.94; P = .010). MD and FA maps had excellent sensitivity and specificity (all > 90%) and interobserver agreement for detecting MI presence and location. Conclusions Biphasic DT-CMR identifies microstructural alterations in both diastole and systole after STEMI, enabling detection of MI presence and location as well as predicting adverse LV remodelling. DT-CMR has potential to provide a single contrast-free modality for MI detection and prognostication of patients after acute STEMI.