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Longitudinal study of multiple sclerosis lesions using ultra-high field (7T) multiparametric MR imaging

Pathophysiology of multiple sclerosis (MS) lesions is dynamic and changes over time. The purpose of this exploratory study was to determine the longitudinal changes in MS lesions over time on ultra-high field MR imaging. Nine patients with MS underwent high-resolution 3D-susceptibility weighted imag...

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Autores principales: Chawla, Sanjeev, Kister, Ilya, Sinnecker, Tim, Wuerfel, Jens, Brisset, Jean-Christophe, Paul, Friedemann, Ge, Yulin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136714/
https://www.ncbi.nlm.nih.gov/pubmed/30212476
http://dx.doi.org/10.1371/journal.pone.0202918
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author Chawla, Sanjeev
Kister, Ilya
Sinnecker, Tim
Wuerfel, Jens
Brisset, Jean-Christophe
Paul, Friedemann
Ge, Yulin
author_facet Chawla, Sanjeev
Kister, Ilya
Sinnecker, Tim
Wuerfel, Jens
Brisset, Jean-Christophe
Paul, Friedemann
Ge, Yulin
author_sort Chawla, Sanjeev
collection PubMed
description Pathophysiology of multiple sclerosis (MS) lesions is dynamic and changes over time. The purpose of this exploratory study was to determine the longitudinal changes in MS lesions over time on ultra-high field MR imaging. Nine patients with MS underwent high-resolution 3D-susceptibility weighted imaging (SWI) and 2D-gradient-echo-T2*-weighted imaging on 7T MRI at baseline and after ~2.4 years of follow-up. Morphologic imaging characteristics, signal intensity patterns and quantitative susceptibility mapping (QSM) values of lesions were recorded at both time points. Lesions were classified as "iron-laden" if they demonstrated hypointense signal on T2*-weighted images and/or SWI as well as hyperintense signal on QSM. Lesions were considered "non-iron-laden" if they were hyperintense on T2*/SWI and isointense or hyperintense on QSM. Total of 162 non-iron-laden and 29 iron-laden lesions were observed at baseline. No change in baseline lesion size during follow up was recorded in 92.7%; no change in lesion-vessel relationship in 86.5%; and no change in signal intensity pattern in 96.9% of lesions. Three lesions which were non-iron-laden at baseline, exhibited iron at follow-up. In two iron-laden lesions, redistribution of iron content was observed at follow-up. Two-thirds of these iron-laden lesions showed an increase in QSM at follow-up relative to baseline, and the remaining one-third exhibited decrease in QSM. Most of the newly formed lesions (11/13, 84.6%) at follow-up were iron-laden. 7T multiparametric MRI is a useful tool for tracking the evolution of MS lesions, especially with regard to changes in iron content.
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spelling pubmed-61367142018-09-27 Longitudinal study of multiple sclerosis lesions using ultra-high field (7T) multiparametric MR imaging Chawla, Sanjeev Kister, Ilya Sinnecker, Tim Wuerfel, Jens Brisset, Jean-Christophe Paul, Friedemann Ge, Yulin PLoS One Research Article Pathophysiology of multiple sclerosis (MS) lesions is dynamic and changes over time. The purpose of this exploratory study was to determine the longitudinal changes in MS lesions over time on ultra-high field MR imaging. Nine patients with MS underwent high-resolution 3D-susceptibility weighted imaging (SWI) and 2D-gradient-echo-T2*-weighted imaging on 7T MRI at baseline and after ~2.4 years of follow-up. Morphologic imaging characteristics, signal intensity patterns and quantitative susceptibility mapping (QSM) values of lesions were recorded at both time points. Lesions were classified as "iron-laden" if they demonstrated hypointense signal on T2*-weighted images and/or SWI as well as hyperintense signal on QSM. Lesions were considered "non-iron-laden" if they were hyperintense on T2*/SWI and isointense or hyperintense on QSM. Total of 162 non-iron-laden and 29 iron-laden lesions were observed at baseline. No change in baseline lesion size during follow up was recorded in 92.7%; no change in lesion-vessel relationship in 86.5%; and no change in signal intensity pattern in 96.9% of lesions. Three lesions which were non-iron-laden at baseline, exhibited iron at follow-up. In two iron-laden lesions, redistribution of iron content was observed at follow-up. Two-thirds of these iron-laden lesions showed an increase in QSM at follow-up relative to baseline, and the remaining one-third exhibited decrease in QSM. Most of the newly formed lesions (11/13, 84.6%) at follow-up were iron-laden. 7T multiparametric MRI is a useful tool for tracking the evolution of MS lesions, especially with regard to changes in iron content. Public Library of Science 2018-09-13 /pmc/articles/PMC6136714/ /pubmed/30212476 http://dx.doi.org/10.1371/journal.pone.0202918 Text en © 2018 Chawla et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are credited.
spellingShingle Research Article
Chawla, Sanjeev
Kister, Ilya
Sinnecker, Tim
Wuerfel, Jens
Brisset, Jean-Christophe
Paul, Friedemann
Ge, Yulin
Longitudinal study of multiple sclerosis lesions using ultra-high field (7T) multiparametric MR imaging
title Longitudinal study of multiple sclerosis lesions using ultra-high field (7T) multiparametric MR imaging
title_full Longitudinal study of multiple sclerosis lesions using ultra-high field (7T) multiparametric MR imaging
title_fullStr Longitudinal study of multiple sclerosis lesions using ultra-high field (7T) multiparametric MR imaging
title_full_unstemmed Longitudinal study of multiple sclerosis lesions using ultra-high field (7T) multiparametric MR imaging
title_short Longitudinal study of multiple sclerosis lesions using ultra-high field (7T) multiparametric MR imaging
title_sort longitudinal study of multiple sclerosis lesions using ultra-high field (7t) multiparametric mr imaging
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136714/
https://www.ncbi.nlm.nih.gov/pubmed/30212476
http://dx.doi.org/10.1371/journal.pone.0202918
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