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Functional significance of post-myocardial infarction inflammation evaluated by 18 F-fluorodeoxyglucose imaging in swine model.

Authors :
Xi XY
Zhang F
Wang J
Gao W
Tian Y
Xu H
Xu M
Wang Y
Yang MF
Source :
Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology [J Nucl Cardiol] 2020 Apr; Vol. 27 (2), pp. 519-531. Date of Electronic Publication: 2019 Nov 18.
Publication Year :
2020

Abstract

Background: The aim of the study was to investigate the relationship between post-myocardial infarction (MI) inflammation and left ventricular (LV) remodeling in a swine model by <superscript>18</superscript> F-fluorodeoxyglucose (FDG) imaging.<br />Methods: MI was induced in swine by balloon occlusion of the left anterior descending coronary artery. A series of FDG positron emission tomography (PET) images were taken within 2 weeks post-MI, employing a comprehensive strategy to suppress the physiological uptake of cardiomyocytes. Echocardiography was applied to evaluate LV volume, global and regional function. CD68 <superscript>+</superscript> macrophage and glucose transporters (GLUT-1, -3 and -4) were investigated by immunostaining.<br />Results: The physiological uptake of myocardium was adequately suppressed in 92.3% of PET scans verified by visual analysis, which was further confirmed by the minimal expression of myocardial GLUT-4. Higher FDG uptake was observed in the infarct than in the remote area and persisted within the observational period of 2 weeks. The FDG uptake of infarcted myocardium on day 1 post-MI was correlated with LV global remodeling, and the FDG uptake of infarcted myocardium on days 1 and 8 post-MI had a trend of correlating with regional remodeling of the infarct area.<br />Conclusions: We here report a feasible swine model for investigating post-MI inflammation. FDG signal in the infarct area of swine persisted for a longer duration than has been reported in small animals. FDG activity in the infarct area could predict LV remodeling.

Details

Language :
English
ISSN :
1532-6551
Volume :
27
Issue :
2
Database :
MEDLINE
Journal :
Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology
Publication Type :
Academic Journal
Accession number :
31741330
Full Text :
https://doi.org/10.1007/s12350-019-01952-0