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Free-breathing T2 mapping at 3T for the monitoring of cardiac allograft rejection: initial results

  • Ruud B van Heeswijk
  • Gabriella Vincenti
  • Pierre Monney
  • Jihen Kourda
  • Samuel Rotman
  • Matthias Stuber
  • Juerg Schwitter
  • Roger Hullin
Open Access
Moderated poster presentation

Keywords

Cardiac Magnetic Resonance Allograft Rejection Acute Cellular Rejection Orthotopic Heart Transplantation Acute Allograft Rejection 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Background

After orthotopic heart transplantation, acute allograft rejection can lead to loss of function. Histological reading of endomyocardial biopsy remains the "gold standard" for guiding immunosuppression, despite its methodological limitations (sampling error and interobserver variability). The measurement of the T2 relaxation time has been suggested for detection of allograft rejection, on the pathophysiological basis that the T2 relaxation time prolongs with local edema resulting from acute allograft rejection. Using breath-held cardiac magnetic resonance T2 mapping at 1.5T, Usman et al. (CircCardiovascImaging2012) detected moderate allograft rejection (grade 2R, ISHLT 2004). With modern immunosuppression grade 2R rejection has become a rare event, but the need remains for a technique that permits the discrimination of absent (grade 0R) and mild rejection (grade 1R). We therefore investigated whether an increase of magnetic field strength to 3T and the use of real-time navigator-gated respiration compensation allow for an increase in the sensitivity of T2 relaxation time detection that is necessary to achieve this discrimination.

Methods

Eighteen patients received EMB (Tan et al., ArchPatholLabMed2007) and cardiac T2 mapping on the same day. Reading of T2 maps was blinded to the histological results. For final analysis, 3 cases with known 2R rejection at the time of T2 mapping were added, yielding 21 T2 mapping sessions. A respiration-navigator-gated radial gradient-recalled-echo pulse sequence (resolution 1.17 mm2, matrix 2562, trigger time 3 heartbeats, T2 preparation duration TET2Prep = 60/30/0 ms) was applied to obtain 3 short-axis T2 maps (van Heeswijk et al., JACCCardiovascImaging2012), which were segmented according to AHA guidelines (Cerqueira et al, Circulation2001). The highest segmental T2 values were grouped according to histological rejection grade and differences were analyzed by Student's t-test, except for the non-blinded cases with 2R rejection. The degree of discrimination was determined using the Spearman's ranked correlation test.

Results

The high-quality T2 maps allowed for visual differentiation of the rejection degrees (Figure 1), and the correlation of T2 mapping with the histological grade of acute cellular rejection was significant (Spearman's ρ = 0.56, p = 0.007). The 0R (n = 15) and 1R (n = 3) degrees demonstrated significantly different T2 values (46.9 ± 5.0 and 54.3 ± 3.0 ms, p = 0.02, Figure 2). Cases with 2R rejection showed clear T2 elevation (T2 = 60.3 ± 16.2 ms).
Figure 1

Mid-ventricular short-axis T 2 maps of varying degrees of rejection. The color bar (right side) indicates the T2 values in ms. a) No rejection (0R) in a 39-year-old female. b) Mild rejection (1R) in a 61-year-old male. c) Moderate rejection in a 66-year-old male.

Figure 2

Bar plot of the average T 2 value per rejection degree and its standard deviation.

Conclusions

This pilot study demonstrates that non-invasive free-breathing cardiac T2 mapping at 3T discriminates between no and mild cardiac allograft rejection. Confirmation of these encouraging results in a larger cohort should consider a study able to show equivalency or superiority of T2 mapping.

Funding

Emma Muschamp Foundation (RBvH), Swiss National Science Foundation (RH, 320030_147121/1).

Copyright information

© van Heeswijk 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.

Authors and Affiliations

  • Ruud B van Heeswijk
    • 1
    • 2
  • Gabriella Vincenti
    • 3
    • 4
  • Pierre Monney
    • 3
    • 4
  • Jihen Kourda
    • 5
  • Samuel Rotman
    • 5
  • Matthias Stuber
    • 1
    • 2
  • Juerg Schwitter
    • 3
    • 4
  • Roger Hullin
    • 3
  1. 1.Department of RadiologyUniversity Hospital (CHUV) and University of Lausanne (UNIL)LausanneSwitzerland
  2. 2.Center for Biomedical Imaging (CIBM)Lausanne and GenevaSwitzerland
  3. 3.Cardiology Service, Department of Internal MedicineUniversity Hospital (CHUV) and University of Lausanne (UNIL)LausanneSwitzerland
  4. 4.Center for Cardiac Magnetic Resonance (CRMC)University Hospital of Lausanne (CHUV)LausanneSwitzerland
  5. 5.Institute of PathologyUniversity Hospital (CHUV) and University of Lausanne (UNIL)LausanneSwitzerland

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