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

J Nucl Cardiol. 2020 Apr;27(2):519-531. doi: 10.1007/s12350-019-01952-0. Epub 2019 Nov 18.

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 18F-fluorodeoxyglucose (FDG) imaging.

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+ macrophage and glucose transporters (GLUT-1, -3 and -4) were investigated by immunostaining.

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.

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.

Keywords: FDG; Inflammation; Myocardial infarction; PET.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / biosynthesis
  • Antigens, Differentiation, Myelomonocytic / biosynthesis
  • Coronary Vessels / pathology
  • Echocardiography
  • Fluorodeoxyglucose F18*
  • Glucose Transporter Type 1 / biosynthesis
  • Glucose Transporter Type 3 / biosynthesis
  • Glucose Transporter Type 4 / biosynthesis
  • Heart / diagnostic imaging
  • Heart Ventricles / diagnostic imaging*
  • Image Processing, Computer-Assisted
  • Inflammation / diagnostic imaging*
  • Muscle Cells / pathology
  • Myocardial Infarction / diagnostic imaging*
  • Myocardial Perfusion Imaging / methods*
  • Myocytes, Cardiac / metabolism
  • Necrosis
  • Positron-Emission Tomography
  • Radiopharmaceuticals
  • Swine

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD68 antigen, human
  • Glucose Transporter Type 1
  • Glucose Transporter Type 3
  • Glucose Transporter Type 4
  • Radiopharmaceuticals
  • Fluorodeoxyglucose F18