Automated Extracellular Volume Fraction Mapping Provides Insights Into the Pathophysiology of Left Ventricular Remodeling Post–Reperfused ST‐Elevation Myocardial Infarction

Author:

Bulluck Heerajnarain123,Rosmini Stefania3,Abdel‐Gadir Amna3,White Steven K.123,Bhuva Anish N.3,Treibel Thomas A.3,Fontana Marianna3,Gonzalez‐Lopez Esther4,Reant Patricia5,Ramlall Manish123,Hamarneh Ashraf123,Sirker Alex23,Herrey Anna S.3,Manisty Charlotte3,Yellon Derek M.12,Kellman Peter6,Moon James C.23,Hausenloy Derek J.12378

Affiliation:

1. The Hatter Cardiovascular Institute, Institute of Cardiovascular Science, University College London, London, United Kingdom

2. The National Institute of Health Research University College London Hospitals Biomedical Research Center, London, United Kingdom

3. Barts Heart Center, St Bartholomew's Hospital, London, United Kingdom

4. Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain

5. CHU de Bordeaux, University of Bordeaux, France

6. National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD

7. Cardiovascular and Metabolic Disorders Program, Duke–National University of Singapore, Singapore

8. National Heart Research Institute Singapore, National Heart Center Singapore, Singapore

Abstract

Background Whether the remote myocardium of reperfused ST ‐segment elevation myocardial infarction ( STEMI ) patients plays a part in adverse left ventricular ( LV ) remodeling remains unclear. We aimed to use automated extracellular volume fraction ( ECV ) mapping to investigate whether changes in the ECV of the remote ( ECV R emote ) and infarcted myocardium ( ECV I nfarct ) impacted LV remodeling. Methods and Results Forty‐eight of 50 prospectively recruited reperfused STEMI patients completed a cardiovascular magnetic resonance at 4±2 days and 40 had a follow‐up scan at 5±2 months. Twenty healthy volunteers served as controls. Mean segmental values for native T1, T2, and ECV were obtained. Adverse LV remodeling was defined as ≥20% increase in LV end‐diastolic volume. ECV R emote was higher on the acute scan when compared to control (27.9±2.1% vs 26.4±2.1%; P =0.01). Eight patients developed adverse LV remodeling and had higher ECV R emote acutely (29.5±1.4% vs 27.4±2.0%; P =0.01) and remained higher at follow‐up (28.6±1.5% vs 26.6±2.1%; P =0.02) compared to those without. Patients with a higher ECV R emote and a lower myocardial salvage index ( MSI ) acutely were significantly associated with adverse LV remodeling, independent of T1 Remote , T1 Core and microvascular obstruction, whereas a higher ECV I nfarct was significantly associated with worse wall motion recovery. Conclusions ECV R emote was increased acutely in reperfused STEMI patients. Those with adverse LV remodeling had higher ECV R emote acutely, and this remained higher at follow‐up than those without adverse LV remodeling. A higher ECV R emote and a lower MSI acutely were significantly associated with adverse LV remodeling whereas segments with higher ECV I nfarct were less likely to recover wall motion.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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