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Gradient Spin Echo (GraSE) imaging for fast myocardial T2 mapping

BACKGROUND: Quantitative Cardiovascular Magnetic Resonance (CMR) techniques have gained high interest in CMR research. Myocardial T2 mapping is thought to be helpful in diagnosis of acute myocardial conditions associated with myocardial edema. In this study we aimed to establish a technique for myoc...

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Autores principales: Sprinkart, Alois M, Luetkens, Julian A, Träber, Frank, Doerner, Jonas, Gieseke, Jürgen, Schnackenburg, Bernhard, Schmitz, Georg, Thomas, Daniel, Homsi, Rami, Block, Wolfgang, Schild, Hans, Naehle, Claas P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326516/
https://www.ncbi.nlm.nih.gov/pubmed/25885268
http://dx.doi.org/10.1186/s12968-015-0127-z
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author Sprinkart, Alois M
Luetkens, Julian A
Träber, Frank
Doerner, Jonas
Gieseke, Jürgen
Schnackenburg, Bernhard
Schmitz, Georg
Thomas, Daniel
Homsi, Rami
Block, Wolfgang
Schild, Hans
Naehle, Claas P
author_facet Sprinkart, Alois M
Luetkens, Julian A
Träber, Frank
Doerner, Jonas
Gieseke, Jürgen
Schnackenburg, Bernhard
Schmitz, Georg
Thomas, Daniel
Homsi, Rami
Block, Wolfgang
Schild, Hans
Naehle, Claas P
author_sort Sprinkart, Alois M
collection PubMed
description BACKGROUND: Quantitative Cardiovascular Magnetic Resonance (CMR) techniques have gained high interest in CMR research. Myocardial T2 mapping is thought to be helpful in diagnosis of acute myocardial conditions associated with myocardial edema. In this study we aimed to establish a technique for myocardial T2 mapping based on gradient-spin-echo (GraSE) imaging. METHODS: The local ethics committee approved this prospective study. Written informed consent was obtained from all subjects prior to CMR. A modified GraSE sequence allowing for myocardial T2 mapping in a single breath-hold per slice using ECG-triggered acquisition of a black blood multi-echo series was developed at 1.5 Tesla. Myocardial T2 relaxation time (T2-RT) was determined by maximum likelihood estimation from magnitude phased-array multi-echo data. Four GraSE sequence variants with varying number of acquired echoes and resolution were evaluated in-vitro and in 20 healthy volunteers. Inter-study reproducibility was assessed in a subset of five volunteers. The sequence with the best overall performance was further evaluated by assessment of intra- and inter-observer agreement in all volunteers, and then implemented into the clinical CMR protocol of five patients with acute myocardial injury (myocarditis, takotsubo cardiomyopathy and myocardial infarction). RESULTS: In-vitro studies revealed the need for well defined sequence settings to obtain accurate T2-RT measurements with GraSE. An optimized 6-echo GraSE sequence yielded an excellent agreement with the gold standard Carr-Purcell-Meiboom-Gill sequence. Global myocardial T2 relaxation times in healthy volunteers was 52.2 ± 2.0 ms (mean ± standard deviation). Mean difference between repeated examinations (n = 5) was −0.02 ms with 95% limits of agreement (LoA) of [−4.7; 4.7] ms. Intra-reader and inter-reader agreement was excellent with mean differences of −0.1 ms, 95% LoA = [−1.3; 1.2] ms and 0.1 ms, 95% LoA = [−1.5; 1.6] ms, respectively (n = 20). In patients with acute myocardial injury global myocardial T2-RTs were prolonged (mean: 61.3 ± 6.7 ms). CONCLUSION: Using an optimized GraSE sequence CMR allows for robust, reliable, fast myocardial T2 mapping and quantitative tissue characterization. Clinically, the GraSE-based T2-mapping has the potential to complement qualitative CMR in patients with acute myocardial injuries. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12968-015-0127-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-43265162015-02-14 Gradient Spin Echo (GraSE) imaging for fast myocardial T2 mapping Sprinkart, Alois M Luetkens, Julian A Träber, Frank Doerner, Jonas Gieseke, Jürgen Schnackenburg, Bernhard Schmitz, Georg Thomas, Daniel Homsi, Rami Block, Wolfgang Schild, Hans Naehle, Claas P J Cardiovasc Magn Reson Research BACKGROUND: Quantitative Cardiovascular Magnetic Resonance (CMR) techniques have gained high interest in CMR research. Myocardial T2 mapping is thought to be helpful in diagnosis of acute myocardial conditions associated with myocardial edema. In this study we aimed to establish a technique for myocardial T2 mapping based on gradient-spin-echo (GraSE) imaging. METHODS: The local ethics committee approved this prospective study. Written informed consent was obtained from all subjects prior to CMR. A modified GraSE sequence allowing for myocardial T2 mapping in a single breath-hold per slice using ECG-triggered acquisition of a black blood multi-echo series was developed at 1.5 Tesla. Myocardial T2 relaxation time (T2-RT) was determined by maximum likelihood estimation from magnitude phased-array multi-echo data. Four GraSE sequence variants with varying number of acquired echoes and resolution were evaluated in-vitro and in 20 healthy volunteers. Inter-study reproducibility was assessed in a subset of five volunteers. The sequence with the best overall performance was further evaluated by assessment of intra- and inter-observer agreement in all volunteers, and then implemented into the clinical CMR protocol of five patients with acute myocardial injury (myocarditis, takotsubo cardiomyopathy and myocardial infarction). RESULTS: In-vitro studies revealed the need for well defined sequence settings to obtain accurate T2-RT measurements with GraSE. An optimized 6-echo GraSE sequence yielded an excellent agreement with the gold standard Carr-Purcell-Meiboom-Gill sequence. Global myocardial T2 relaxation times in healthy volunteers was 52.2 ± 2.0 ms (mean ± standard deviation). Mean difference between repeated examinations (n = 5) was −0.02 ms with 95% limits of agreement (LoA) of [−4.7; 4.7] ms. Intra-reader and inter-reader agreement was excellent with mean differences of −0.1 ms, 95% LoA = [−1.3; 1.2] ms and 0.1 ms, 95% LoA = [−1.5; 1.6] ms, respectively (n = 20). In patients with acute myocardial injury global myocardial T2-RTs were prolonged (mean: 61.3 ± 6.7 ms). CONCLUSION: Using an optimized GraSE sequence CMR allows for robust, reliable, fast myocardial T2 mapping and quantitative tissue characterization. Clinically, the GraSE-based T2-mapping has the potential to complement qualitative CMR in patients with acute myocardial injuries. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12968-015-0127-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-02-12 /pmc/articles/PMC4326516/ /pubmed/25885268 http://dx.doi.org/10.1186/s12968-015-0127-z Text en © Sprinkart et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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.
spellingShingle Research
Sprinkart, Alois M
Luetkens, Julian A
Träber, Frank
Doerner, Jonas
Gieseke, Jürgen
Schnackenburg, Bernhard
Schmitz, Georg
Thomas, Daniel
Homsi, Rami
Block, Wolfgang
Schild, Hans
Naehle, Claas P
Gradient Spin Echo (GraSE) imaging for fast myocardial T2 mapping
title Gradient Spin Echo (GraSE) imaging for fast myocardial T2 mapping
title_full Gradient Spin Echo (GraSE) imaging for fast myocardial T2 mapping
title_fullStr Gradient Spin Echo (GraSE) imaging for fast myocardial T2 mapping
title_full_unstemmed Gradient Spin Echo (GraSE) imaging for fast myocardial T2 mapping
title_short Gradient Spin Echo (GraSE) imaging for fast myocardial T2 mapping
title_sort gradient spin echo (grase) imaging for fast myocardial t2 mapping
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326516/
https://www.ncbi.nlm.nih.gov/pubmed/25885268
http://dx.doi.org/10.1186/s12968-015-0127-z
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