Cardiovascular Magnetic Resonance Relaxometry Predicts Regional Functional Outcome After Experimental Myocardial Infarction

Author:

Haberkorn Sebastian M.1,Jacoby Christoph1,Ding Zhaoping1,Keul Petra1,Bönner Florian1,Polzin Amin1,Levkau Bodo1,Schrader Jürgen1,Kelm Malte1,Flögel Ulrich1

Affiliation:

1. From the Department of Molecular Cardiology (S.M.H., Z.D., J.S., U.F.) and Cardiovascular Research Institute Düsseldorf, Germany (J.S., M.K., U.F.), Heinrich Heine University Düsseldorf, Germany; Department of Cardiology, Pneumology and Angiology, University Hospital Düsseldorf, Germany (S.M.H., C.J., F.B., A.P., M.K., U.F.); and Department of Pathophysiology, University Hospital Essen, Germany (P.K., B.L.).

Abstract

Background— Cardiovascular magnetic resonance with gadolinium-based contrast agents has established as gold standard for tissue characterization after myocardial infarction (MI). Beyond accurate diagnosis, the value of cardiovascular magnetic resonance to predict the outcome after MI has yet to be substantiated. Methods and Results— Recent cardiovascular magnetic resonance approaches were systematically compared for quantification of tissue injury and functional impairment after MI using murine models with permanent left anterior descending coronary artery ligation (n=14) or 50 minutes ischemia/reperfusion (n=13). Cardiovascular magnetic resonance included native/postcontrast T1 maps, T2 maps, and late gadolinium enhancement at days 1 and 21 post-MI. For regional correlation of parametric and functional measures, the left ventricle was analyzed over 200 sectors. For T1 mapping, we used retrospective triggering with variable flip angle analysis. Sectoral analysis of native T1 maps already revealed in the acute phase after MI substantial discrepancies in myocardial tissue texture between the 2 MI models (native T1 day 1: permanent ligation, 1280.0±162.6 ms; ischemia/reperfusion, 1115.0±140.5 ms; P <0.001; n=14/13), which were later associated with differential functional outcome (left ventricular ejection fraction day 21: permanent ligation, 24.5±7.0%; ischemia/reperfusion, 33.7±11.6%; P <0.05; n=14/13). At this early time, any other parameter was indicative for the subsequent worsening of left ventricular ejection fraction in permanent ligation mice. Linear regression of acute individual measures with contractile function in corresponding areas at day 21 demonstrated for early native T1 values the best correlation with the later functional impairment ( R 2 =0.94). Conclusions— The present T1 mapping approach permits accurate characterization of local tissue injury and holds the potential for sensitive and graduated prognosis of the functional outcome after MI without gadolinium-based contrast agents.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging

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