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Intercentre reproducibility of cardiac apparent diffusion coefficient and fractional anisotropy in healthy volunteers

BACKGROUND: Diffusion tensor cardiac magnetic resonance (DT-CMR) enables probing of the microarchitecture of the myocardium, but the apparent diffusion coefficient (ADC) and fractional anisotropy (FA) reported in healthy volunteers have been inconsistent. The aim of this study was to validate a stim...

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Autores principales: Tunnicliffe, Elizabeth M, Scott, Andrew D, Ferreira, Pedro, Ariga, Rina, McGill, Laura-Ann, Nielles-Vallespin, Sonia, Neubauer, Stefan, Pennell, Dudley J, Robson, Matthew D, Firmin, David N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4028111/
https://www.ncbi.nlm.nih.gov/pubmed/24886285
http://dx.doi.org/10.1186/1532-429X-16-31
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author Tunnicliffe, Elizabeth M
Scott, Andrew D
Ferreira, Pedro
Ariga, Rina
McGill, Laura-Ann
Nielles-Vallespin, Sonia
Neubauer, Stefan
Pennell, Dudley J
Robson, Matthew D
Firmin, David N
author_facet Tunnicliffe, Elizabeth M
Scott, Andrew D
Ferreira, Pedro
Ariga, Rina
McGill, Laura-Ann
Nielles-Vallespin, Sonia
Neubauer, Stefan
Pennell, Dudley J
Robson, Matthew D
Firmin, David N
author_sort Tunnicliffe, Elizabeth M
collection PubMed
description BACKGROUND: Diffusion tensor cardiac magnetic resonance (DT-CMR) enables probing of the microarchitecture of the myocardium, but the apparent diffusion coefficient (ADC) and fractional anisotropy (FA) reported in healthy volunteers have been inconsistent. The aim of this study was to validate a stimulated-echo diffusion sequence using phantoms, and to assess the intercentre reproducibility of in-vivo diffusion measures using the sequence. METHODS AND RESULTS: A stimulated-echo, cardiac-gated DT-CMR sequence with a reduced-field-of-view, single-shot EPI readout was used at two centres with 3 T MRI scanners. Four alkane phantoms with known diffusivities were scanned at a single centre using a stimulated echo sequence and a spin-echo Stejskal-Tanner diffusion sequence. The median (maximum, minimum) difference between the DT-CMR sequence and Stejskal-Tanner sequence was 0.01 (0.04, 0.0006) × 10(-3) mm(2)/s (2%), and between the DT-CMR sequence and literature diffusivities was 0.02 (0.05, 0.006) × 10(-3) mm(2)/s (4%). The same ten healthy volunteers were scanned using the DT-CMR sequence at the two centres less than seven days apart. Average ADC and FA were calculated in a single mid-ventricular, short axis slice. Intercentre differences were tested for statistical significance at the p < 0.05 level using paired t-tests. The mean ADC ± standard deviation for all subjects averaged over both centres was 1.10 ± 0.06 × 10(-3) mm(2)/s in systole and 1.20 ± 0.09 × 10(-3) mm(2)/s in diastole; FA was 0.41 ± 0.04 in systole and 0.54 ± 0.03 in diastole. With similarly-drawn regions-of-interest, systolic ADC (difference 0.05 × 10(-3) mm(2)/s), systolic FA (difference 0.003) and diastolic FA (difference 0.01) were not statistically significantly different between centres (p > 0.05), and only the diastolic ADC showed a statistically significant, but numerically small, difference of 0.07 × 10(-3) mm(2)/s (p = 0.047). The intercentre, intrasubject coefficients of variance were: systolic ADC 7%, FA 6%; diastolic ADC 7%, FA 3%. CONCLUSIONS: This is the first study to demonstrate the accuracy of a stimulated-echo DT-CMR sequence in phantoms, and demonstrates the feasibility of obtaining reproducible ADC and FA in healthy volunteers at separate centres with well-matched sequences and processing.
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spelling pubmed-40281112014-05-30 Intercentre reproducibility of cardiac apparent diffusion coefficient and fractional anisotropy in healthy volunteers Tunnicliffe, Elizabeth M Scott, Andrew D Ferreira, Pedro Ariga, Rina McGill, Laura-Ann Nielles-Vallespin, Sonia Neubauer, Stefan Pennell, Dudley J Robson, Matthew D Firmin, David N J Cardiovasc Magn Reson Research BACKGROUND: Diffusion tensor cardiac magnetic resonance (DT-CMR) enables probing of the microarchitecture of the myocardium, but the apparent diffusion coefficient (ADC) and fractional anisotropy (FA) reported in healthy volunteers have been inconsistent. The aim of this study was to validate a stimulated-echo diffusion sequence using phantoms, and to assess the intercentre reproducibility of in-vivo diffusion measures using the sequence. METHODS AND RESULTS: A stimulated-echo, cardiac-gated DT-CMR sequence with a reduced-field-of-view, single-shot EPI readout was used at two centres with 3 T MRI scanners. Four alkane phantoms with known diffusivities were scanned at a single centre using a stimulated echo sequence and a spin-echo Stejskal-Tanner diffusion sequence. The median (maximum, minimum) difference between the DT-CMR sequence and Stejskal-Tanner sequence was 0.01 (0.04, 0.0006) × 10(-3) mm(2)/s (2%), and between the DT-CMR sequence and literature diffusivities was 0.02 (0.05, 0.006) × 10(-3) mm(2)/s (4%). The same ten healthy volunteers were scanned using the DT-CMR sequence at the two centres less than seven days apart. Average ADC and FA were calculated in a single mid-ventricular, short axis slice. Intercentre differences were tested for statistical significance at the p < 0.05 level using paired t-tests. The mean ADC ± standard deviation for all subjects averaged over both centres was 1.10 ± 0.06 × 10(-3) mm(2)/s in systole and 1.20 ± 0.09 × 10(-3) mm(2)/s in diastole; FA was 0.41 ± 0.04 in systole and 0.54 ± 0.03 in diastole. With similarly-drawn regions-of-interest, systolic ADC (difference 0.05 × 10(-3) mm(2)/s), systolic FA (difference 0.003) and diastolic FA (difference 0.01) were not statistically significantly different between centres (p > 0.05), and only the diastolic ADC showed a statistically significant, but numerically small, difference of 0.07 × 10(-3) mm(2)/s (p = 0.047). The intercentre, intrasubject coefficients of variance were: systolic ADC 7%, FA 6%; diastolic ADC 7%, FA 3%. CONCLUSIONS: This is the first study to demonstrate the accuracy of a stimulated-echo DT-CMR sequence in phantoms, and demonstrates the feasibility of obtaining reproducible ADC and FA in healthy volunteers at separate centres with well-matched sequences and processing. BioMed Central 2014-05-06 /pmc/articles/PMC4028111/ /pubmed/24886285 http://dx.doi.org/10.1186/1532-429X-16-31 Text en Copyright © 2014 Tunnicliffe et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 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 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
Tunnicliffe, Elizabeth M
Scott, Andrew D
Ferreira, Pedro
Ariga, Rina
McGill, Laura-Ann
Nielles-Vallespin, Sonia
Neubauer, Stefan
Pennell, Dudley J
Robson, Matthew D
Firmin, David N
Intercentre reproducibility of cardiac apparent diffusion coefficient and fractional anisotropy in healthy volunteers
title Intercentre reproducibility of cardiac apparent diffusion coefficient and fractional anisotropy in healthy volunteers
title_full Intercentre reproducibility of cardiac apparent diffusion coefficient and fractional anisotropy in healthy volunteers
title_fullStr Intercentre reproducibility of cardiac apparent diffusion coefficient and fractional anisotropy in healthy volunteers
title_full_unstemmed Intercentre reproducibility of cardiac apparent diffusion coefficient and fractional anisotropy in healthy volunteers
title_short Intercentre reproducibility of cardiac apparent diffusion coefficient and fractional anisotropy in healthy volunteers
title_sort intercentre reproducibility of cardiac apparent diffusion coefficient and fractional anisotropy in healthy volunteers
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4028111/
https://www.ncbi.nlm.nih.gov/pubmed/24886285
http://dx.doi.org/10.1186/1532-429X-16-31
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