Manganese dipyridoxyl-diphosphate (MnDPDP) as a viability marker in patients with myocardial infarction

Arne Skjold1, Brage H Amundsen, Rune Wiseth

  • 1Department of Circulation and Medical Imaging (ISB), Faculty of Medicine, Norwegian University of Science and Technology (NTNU), Trondheim, Norway. Arne.Skjold@stolav.no

Abstract

Insights

Manganese dipyridoxyl-diphosphate (MnDPDP) showed differential contrast accumulation in the heart after myocardial infarction. Viable heart muscle (remote regions) accumulated more contrast than infarcted areas, indicating selective manganese uptake.

Area of Science:

  • Cardiovascular Imaging
  • Medical Diagnostics
  • Biomedical Engineering

Background:

  • Myocardial infarction (MI) can lead to significant changes in left ventricular (LV) myocardium.
  • Assessing myocardial viability and function post-MI is crucial for patient management.
  • Novel contrast agents are being investigated for cardiovascular magnetic resonance imaging (CMR).

Purpose of the Study:

  • To evaluate contrast accumulation in the left ventricular (LV) myocardium.
  • To assess the behavior of manganese dipyridoxyl-diphosphate (MnDPDP) after myocardial infarction.
  • To correlate contrast enhancement patterns with myocardial function.

Main Methods:

  • MnDPDP was administered to 10 patients with recent myocardial infarction.
  • Longitudinal relaxivity rates (R(1)) and signal changes were measured using fast gradient echo sequences.
  • LV volume and wall thickening were assessed, and infarct localization was compared using vector analyses.

Main Results:

  • Reduced myocardial wall thickening correlated with reduced precontrast R(1) and contrast enhancement.
  • Both infarcted and remote regions showed rapid initial MnDPDP accumulation.
  • Remote regions exhibited a slower, sustained increase in R(1) compared to infarcted regions.

Conclusions:

  • Remote myocardial regions demonstrated greater increases in R(1) than infarcted regions.
  • This suggests selective and slow manganese accumulation in viable myocytes.
  • MnDPDP shows potential for differentiating viable from infarcted myocardium post-MI.

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