PMID- 26512599 OWN - NLM STAT- MEDLINE DCOM- 20160208 LR - 20221005 IS - 1536-5964 (Electronic) IS - 0025-7974 (Print) IS - 0025-7974 (Linking) VI - 94 IP - 43 DP - 2015 Oct TI - Characterization of Benign Myocarditis Using Quantitative Delayed-Enhancement Imaging Based on Molli T1 Mapping. PG - e1868 LID - 10.1097/MD.0000000000001868 [doi] LID - e1868 AB - Delayed contrast enhancement after injection of a gadolinium-chelate (Gd-chelate) is a reference imaging method to detect myocardial tissue changes. Its localization within the thickness of the myocardial wall allows differentiating various pathological processes such as myocardial infarction (MI), inflammatory myocarditis, and cardiomyopathies. The aim of the study was first to characterize benign myocarditis using quantitative delayed-enhancement imaging and then to investigate whether the measure of the extracellular volume fraction (ECV) can be used to discriminate between MI and myocarditis.In 6 patients with acute benign myocarditis (32.2 +/- 13.8 year-old, subepicardial late gadolinium enhancement [LGE]) and 18 patients with MI (52.3 +/- 10.9 year-old, subendocardial/transmural LGE), myocardial T1 was determined using the Modified Look-Locker Imaging (MOLLI) sequence at 3 Tesla before and after Gd-chelate injection. T1 values were compared in LGE and normal regions of the myocardium. The myocardial T1 values were normalized to the T1 of blood, and the ECV was calculated from T1 values of myocardium and blood pre- and post-Gd injection.In both myocarditis and MI, the T1 was lower in LGE regions than in normal regions of the left ventricle. T1 of LGE areas was significantly higher in myocarditis than in MI (446.8 +/- 45.8 vs 360.5 +/- 66.9 ms, P = 0.003) and ECV was lower in myocarditis than in MI (34.5 +/- 3.3 vs 53.8 +/- 13.0 %, P = 0.004).Both inflammatory process and chronic fibrosis induce LGE (subepicardial in myocarditis and subendocardial in MI). The present study demonstrates that the determination of T1 and ECV is able to differentiate the 2 histological patterns.Further investigation will indicate whether the severity of ECV changes might help refine the predictive risk of LGE in myocarditis. FAU - Toussaint, Marcel AU - Toussaint M AD - From the Hopital Pitie-Salpetriere, Institut de Myologie and CEA, NMR Laboratory, Paris (MT, RJG, NA, BM, PGC); Hopital Sud-Francilien, Corbeil-Essonnes (MT); MIRCen, I2BM, CEA, Paris, France (NA, BM, PGC); CHWAPI, Tournai, Belgium (RJG); Siemens Healthcare, Saint-Denis, France (AV); and Siemens AG Healthcare Sector, Erlangen, Germany (AG). FAU - Gilles, Raymond J AU - Gilles RJ FAU - Azzabou, Noura AU - Azzabou N FAU - Marty, Benjamin AU - Marty B FAU - Vignaud, Alexandre AU - Vignaud A FAU - Greiser, Andreas AU - Greiser A FAU - Carlier, Pierre G AU - Carlier PG LA - eng PT - Clinical Trial PT - Journal Article PT - Observational Study PL - United States TA - Medicine (Baltimore) JT - Medicine JID - 2985248R RN - AU0V1LM3JT (Gadolinium) SB - IM MH - Adolescent MH - Adult MH - *Cardiac Imaging Techniques MH - Extracellular Fluid MH - Female MH - Gadolinium MH - Humans MH - Magnetic Resonance Imaging/*methods MH - Male MH - Middle Aged MH - Myocardial Infarction/*diagnosis MH - Myocarditis/*pathology MH - Myocardium/*pathology MH - Young Adult PMC - PMC4985413 COIS- The authors have no conflicts of interest to declare. EDAT- 2015/10/30 06:00 MHDA- 2016/02/09 06:00 PMCR- 2015/10/30 CRDT- 2015/10/30 06:00 PHST- 2015/10/30 06:00 [entrez] PHST- 2015/10/30 06:00 [pubmed] PHST- 2016/02/09 06:00 [medline] PHST- 2015/10/30 00:00 [pmc-release] AID - 00005792-201510270-00054 [pii] AID - 10.1097/MD.0000000000001868 [doi] PST - ppublish SO - Medicine (Baltimore). 2015 Oct;94(43):e1868. doi: 10.1097/MD.0000000000001868.