Affiliations 

  • 1 UCL Centre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, WC1E 6DD, UK
  • 2 School of Biosciences and Medicine, University of Surrey, Guildford, GU2 7XH, UK
  • 3 School of Biomedical Engineering & Imaging Sciences, King's College London, London, SE1 7EH, UK
  • 4 UCL Elizabeth Garrett Anderson Institute for Women's Health, London, WC1E 6BT, UK
  • 5 Division of Cardiovascular Medicine, Department of Medicine, Stanford University, Stanford, CA, 94305, USA
  • 6 The Hatter Cardiovascular Institute, University College London, 67 Chenies Mews, London, WC1E 6HX, UK
Adv Sci (Weinh), 2021 Jun;8(11):e2003987.
PMID: 34105284 DOI: 10.1002/advs.202003987

Abstract

Early measurements of tissue viability after myocardial infarction (MI) are essential for accurate diagnosis and treatment planning but are challenging to obtain. Here, manganese, a calcium analogue and clinically approved magnetic resonance imaging (MRI) contrast agent, is used as an imaging biomarker of myocardial viability in the first hours after experimental MI. Safe Mn2+ dosing is confirmed by measuring in vitro beating rates, calcium transients, and action potentials in cardiomyocytes, and in vivo heart rates and cardiac contractility in mice. Quantitative T1 mapping-manganese-enhanced MRI (MEMRI) reveals elevated and increasing Mn2+ uptake in viable myocardium remote from the infarct, suggesting MEMRI offers a quantitative biomarker of cardiac inotropy. MEMRI evaluation of infarct size at 1 h, 1 and 14 days after MI quantifies myocardial viability earlier than the current gold-standard technique, late-gadolinium-enhanced MRI. These data, coupled with the re-emergence of clinical Mn2+ -based contrast agents open the possibility of using MEMRI for direct evaluation of myocardial viability early after ischemic onset in patients.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.