comparison of myocardial t1 mapping techniques at 1.5t to detect interstitial fibrosis in patients...

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POSTER PRESENTATION Open Access Comparison of myocardial T1 mapping techniques at 1.5T to detect interstitial fibrosis in patients with orthotopic cardiac transplant Patrizia Pedrotti 2 , Gabriella Masciocco 2 , Giuseppina Quattrocchi 2 , Angela Milazzo 2 , Maria Frigerio 2 , Paola Campadello 2 , Alberto Roghi 2 , Ornella Rimoldi 1,3* From 17th Annual SCMR Scientific Sessions New Orleans, LA, USA. 16-19 January 2014 Background Apoptotic death of interstitial cells and myocytes is a detrimental effect of the interstitial inflammatory infiltrate accompanying heart transplant rejection. This inflamma- tory 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. Methods 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 cover- age. 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, para- meters 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 Results 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 hypertro- phy P = 0.02. ECV, but not T1 pre or post, was inversely correlated to IVRT (msec) at echo p < 0.003. Conclusions 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 pre- sence 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 Funding CNR. 1 IBFM, CNR, Segrate, Italy Full list of author information is available at the end of the article Pedrotti et al. Journal of Cardiovascular Magnetic Resonance 2014, 16(Suppl 1):P391 http://www.jcmr-online.com/content/16/S1/P391 © 2014 Pedrotti et al.; licensee 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.

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POSTER PRESENTATION Open Access

Comparison of myocardial T1 mappingtechniques at 1.5T to detect interstitial fibrosis inpatients with orthotopic cardiac transplantPatrizia Pedrotti2, Gabriella Masciocco2, Giuseppina Quattrocchi2, Angela Milazzo2, Maria Frigerio2,Paola Campadello2, Alberto Roghi2, Ornella Rimoldi1,3*

From 17th Annual SCMR Scientific SessionsNew Orleans, LA, USA. 16-19 January 2014

BackgroundApoptotic death of interstitial cells and myocytes is adetrimental effect of the interstitial inflammatory infiltrateaccompanying heart transplant rejection. This inflamma-tory reaction is followed by both replacement fibrosis andinterstitial fibrosis which in the long term can impairdiastolic and systolic ventricular (LV) function. Cardiacmagnetic resonance (CMR) with gadolinium quantifiesreplacement fibrosis and new sequences with T1 mappingare proposed for the quantification of more elusiveinterstitial fibrosis. We aimed at determining the optimalT1 mapping approach to assess characteristic tissuecomposition in these patients.

MethodsWe studied 60 patients who underwent orthotopic hearttransplant (HTx) and were free of active rejection, meantime from Tx 79 ± 79 mo (range 6 ÷307) age 47 ± 13and 10 Normals (N) 39 ± 11 p = ns. Standard volumesand LGE-CMR scans were carried out on a 1.5-T scanner(Siemens, Erlangen, Germany), with full myocardial cover-age. The IR LGE images were acquired after intravenousGadobutrol (0.15 mmol/kg) in identical short-axis planesto cine. MOLLI T1 maps (Messroghli, 2007) weregenerated from 3 short axis slices at Base, Mid and Apexand acquired pre and 15 minutes post contrast, para-meters were TR = 2.5 msec, TE = 1.1 msec, Flip Angle35°, Voxel size 2.2×1.4×6 mm, GRAPPA = 2. Regions ofinterest (ROIs) were defined defined according to AHAavoiding areas with coarse LGE or artifacts. Extracellularvolume (ECV) was derived from T1-maps acquired

pre- and post-contrast calibrated by blood hematocrit.Data are mean ± SD

ResultsSystolic function was similar in both groups HTx 64 ±11 vs N 68 ± 5 p = 0.32, LV Mass Index was slightlyhigher in HTx 75 ± 14 vs 69 ± 16 N p = 0.2. In HTxnative pre -contrast T1 was 1007 ± 75 vs (N) 957 ± 44msec 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). Whereaswithin Htx population T1 precontrast was more accurateto identify previous systemic CMV infection Se 77% andSp 75% (cut-off 993 msec) (Figure 1B). T1 Pre wassignificantly higher in HTx with left ventricular hypertro-phy P = 0.02. ECV, but not T1 pre or post, was inverselycorrelated to IVRT (msec) at echo p < 0.003.

ConclusionsHTx patients with no active rejection show a significantincrease of ECV and T1 relaxation time, an indicationof increased interstitial fibrosis. In this population ECVseems to better identify deposition of collagen, whereasnon contrast T1 mapping is also influenced by the pre-sence of tissue inflammation. These preliminary findingsneed further confirmation in large scale studies that willassess both the diagnostic and prognostic values of T1mapping derived parameters

FundingCNR.

1IBFM, CNR, Segrate, ItalyFull list of author information is available at the end of the article

Pedrotti et al. Journal of Cardiovascular MagneticResonance 2014, 16(Suppl 1):P391http://www.jcmr-online.com/content/16/S1/P391

© 2014 Pedrotti et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the CreativeCommons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, andreproduction 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.

Authors’ details1IBFM, CNR, Segrate, Italy. 2Dipartimento Cardiologico A. De Gasperis,Ospedale Niguarda Cà Granda, Milan, Italy. 3Universita Vita Salute, SanRaffaele, Milan, Italy.

Published: 16 January 2014

doi:10.1186/1532-429X-16-S1-P391Cite this article as: Pedrotti et al.: Comparison of myocardial T1mapping techniques at 1.5T to detect interstitial fibrosis in patientswith orthotopic cardiac transplant. Journal of Cardiovascular MagneticResonance 2014 16(Suppl 1):P391.

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Pedrotti et al. Journal of Cardiovascular MagneticResonance 2014, 16(Suppl 1):P391http://www.jcmr-online.com/content/16/S1/P391

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