Early molecular imaging of interstitial changes in patients after myocardial infarction: Comparison with delayed contrast-enhanced magnetic resonance imaging

Johan Verjans, Sander Wolters, Ward Laufer, Mark Schellings, Michelle Lax, Dagfinn Lovhaug, Hendrikus Boersma, Gerrit J. Kemerink, Simon Schalla, Paul Gordon, Jaap Teule, Jagat Narula*, Leonard Hofstra

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review


The clinical feasibility of noninvasive imaging of interstitial alterations after myocardial infarction (MI) was assessed using a technetium-99m-labeled RGD imaging peptide (RIP). In experimental studies, RIP has been shown to target integrins associated with collagen-producing myofibroblasts (MFB). Ten patients underwent myocardial perfusion imaging (MPI) within the first week after MI. At 3 and 8 weeks after MI, RIP was administered intravenously and SPECT images acquired for interstitial imaging. RIP imaging was compared to initial MPI and to the extent of scar formation defined by late gadolinium-enhanced (LGE) cardiac magnetic resonance (CMR) imaging 1 year after MI. RIP uptake was observed in 7 of the 10 patients at both 3 and 8 weeks. Although, RIP uptake corresponded to areas of perfusion defects, it usually extended beyond the infarct zone to a variable extent; 2 of 7 patients showed tracer uptake throughout myocardium. In all positive cases, RIP uptake was similar to the extent of scar observed at 1 year by LGE-CMR imaging. This study demonstrates that RGD-based imaging early after MI may predict the eventual extent of scar formation, which often exceeds initial MPI deficit but colocalizes with LGE in CMR imaging performed subsequently.
Original languageEnglish
Pages (from-to)1065-1072
JournalJournal of Nuclear Cardiology
Issue number6
Publication statusPublished - Dec 2010


  • Molecular imaging
  • infarction
  • myocardial
  • heart failure

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