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  • Workshop presentation
  • Open Access

Myocardial iron quantification using modified Look-Locker inversion recovery (MOLLI) T1 mapping at 3 Tesla

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Journal of Cardiovascular Magnetic Resonance201315 (Suppl 1) :W8

https://doi.org/10.1186/1532-429X-15-S1-W8

  • Published:

Keywords

  • Iron Overload
  • Hemochromatosis
  • Susceptibility Artifact
  • Iron Chelate Therapy
  • Myocardial Iron

Background

Quantification of myocardial iron overload is critical for the management of patients with hemochromatosis. The effects of excess iron on T1 and T2* relaxation times correlate directly with tissue iron concentration. T2* became the clinical standard at 1.5T as it can be easily obtained in a fast one breath-hold ECG gated multi-echo GRE sequence. At 3T, however, T2* quantification can be limited by pronounced susceptibility artifacts and signal sampling restraints due to shorter T2* times at higher iron concentrations . Since myocardial T1 time is up to thirty times longer than T2*, it can be quantified with short echo-time inversion-recovery sequences even at high iron concentrations, and is less sensitive to susceptibility artifacts. We aimed to validate a recently developed modified Look-Locker inversion recovery (MOLLI) sequence to quantify myocardial T1 in healthy controls and patients with iron overload at 3T, comparing to standard GRE based multi-echo T2* times at 1.5T.

Methods

A total of 15 normal volunteers and 7 chronic anemia patients (with a myocardial T2* measure <20 ms at 1.5T in the last 2 years, five of these on iron chelating therapy) were prospectively enrolled. Myocardial T2* and T1 times were quantified in the same day, the former using a breath-hold multi-echo GRE sequence at 1.5T (Symphony, Siemens, Erlangen, Germany) and the latter using the T1 mapping -MOLLI sequence at 3T (Verio, Siemens, Erlangen, Germany). All ROIs were placed at mid-interventricular septum, carefully avoiding the blood pool (Fig 1). All analyses were blinded.
Figure 1
Figure 1

T1 map at 3T of a patient with iron overload showing reduced T1 time within the interventricular septum (781.6 ms), in agreement with a significantly reduced T2* time at 1.5T (8.5 ms - not shown).

Results

All patients had regular heart rhythm and all MRI exams showed diagnostic image quality. Volunteers and patients had significantly different mean myocardial T2* (27.2 ms +/- 3.9 vs. 15.4 ms +/- 6.3 p<0.05 respectively) and T1 times 1175.7 ms +/- 22.8 vs. 952.1 ms +/- 173.2 p<0.05 respectively). 3T T1 times strongly correlated with 1.5T T2* times (r=0.95 and Fig 2). Using the 3T T1 cut-off of 1130 ms, sensitivity and specificity for 3T T1 to predict a T2*<20 ms at 1.5T (standard reference) were both 100%.
Figure 2
Figure 2

Correlation curve between T1 at 3T and T2* at 1.5T. The whole data were best fitted by a quadratic curve with r=0.95. Red lines delimitate true positives (TP), true negatives (TN), false positives (FP) and false negatives (FN) based on a T1 cutpoint of 1130 ms for the prediction of a T2* < 20 ms.

Conclusions

Myocardial T1 value obtained with a MOLLI sequence has excellent iron quantification capability at 3T.

Funding

Internal.

Authors’ Affiliations

(1)
CDPI - Clínica de Diagnóstico por Imagem, Rio de Janeiro, Brazil
(2)
Medicine/Cardiology, Johns Hopkins University, Baltimore, MD, USA
(3)
Cardiology, Hospital Universitário Clementino Fraga Filho - UFRJ, Rio de Janeiro, RJ, Brazil
(4)
Siemens Healthcare, Erlangen, Germany
(5)
Siemens LTDA, Sao Paulo, SP, Brazil

Copyright

© Camargo et al; licensee BioMed Central Ltd. 2013

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.

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