Volume 16 Supplement 1

Abstracts of the 17th Annual SCMR Scientific Sessions

Open Access

Comparison of myocardial T1 mapping techniques at 1.5T to detect interstitial fibrosis in patients with orthotopic cardiac transplant

  • Patrizia Pedrotti2,
  • Gabriella Masciocco2,
  • Giuseppina Quattrocchi2,
  • Angela Milazzo2,
  • Maria Frigerio2,
  • Paola Campadello2,
  • Alberto Roghi2 and
  • Ornella Rimoldi1, 3
Journal of Cardiovascular Magnetic Resonance201416(Suppl 1):P391


Published: 16 January 2014


Apoptotic death of interstitial cells and myocytes is a detrimental effect of the interstitial inflammatory infiltrate accompanying heart transplant rejection. This inflammatory reaction is followed by both replacement fibrosis and interstitial fibrosis which in the long term can impair diastolic and systolic ventricular (LV) function. Cardiac magnetic resonance (CMR) with gadolinium quantifies replacement fibrosis and new sequences with T1 mapping are proposed for the quantification of more elusive interstitial fibrosis. We aimed at determining the optimal T1 mapping approach to assess characteristic tissue composition in these patients.


We studied 60 patients who underwent orthotopic heart transplant (HTx) and were free of active rejection, mean time from Tx 79 ± 79 mo (range 6 ÷307) age 47 ± 13 and 10 Normals (N) 39 ± 11 p = ns. Standard volumes and LGE-CMR scans were carried out on a 1.5-T scanner (Siemens, Erlangen, Germany), with full myocardial coverage. The IR LGE images were acquired after intravenous Gadobutrol (0.15 mmol/kg) in identical short-axis planes to cine. MOLLI T1 maps (Messroghli, 2007) were generated from 3 short axis slices at Base, Mid and Apex and acquired pre and 15 minutes post contrast, parameters were TR = 2.5 msec, TE = 1.1 msec, Flip Angle 35°, Voxel size 2.2×1.4×6 mm, GRAPPA = 2. Regions of interest (ROIs) were defined defined according to AHA avoiding areas with coarse LGE or artifacts. Extracellular volume (ECV) was derived from T1-maps acquired pre- and post-contrast calibrated by blood hematocrit. Data are mean ± SD


Systolic function was similar in both groups HTx 64 ± 11 vs N 68 ± 5 p = 0.32, LV Mass Index was slightly higher in HTx 75 ± 14 vs 69 ± 16 N p = 0.2. In HTx native pre -contrast T1 was 1007 ± 75 vs (N) 957 ± 44 msec p < 0.001, T1 post-contrast was 400 ± 47 msec vs (N) 455 ± 35 msec p < 0.001, ECV was 39.4 ± 4% vs 33.3 ± 3%(N) p < 0.001. ECV had the best Sensitivity(Se) 84% and Specificity(Sp) 78% at ROC analysis (cut-off 35.4%), for identifying HTx patients from N (Figure 1A). Whereas within Htx population T1 precontrast was more accurate to identify previous systemic CMV infection Se 77% and Sp 75% (cut-off 993 msec) (Figure 1B). T1 Pre was significantly higher in HTx with left ventricular hypertrophy P = 0.02. ECV, but not T1 pre or post, was inversely correlated to IVRT (msec) at echo p < 0.003.

Figure 1


HTx patients with no active rejection show a significant increase of ECV and T1 relaxation time, an indication of increased interstitial fibrosis. In this population ECV seems to better identify deposition of collagen, whereas non contrast T1 mapping is also influenced by the presence of tissue inflammation. These preliminary findings need further confirmation in large scale studies that will assess both the diagnostic and prognostic values of T1 mapping derived parameters



Authors’ Affiliations

Dipartimento Cardiologico A. De Gasperis, Ospedale Niguarda Cà Granda
Universita Vita Salute, San Raffaele


© Pedrotti et al.; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.