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Brain Viscoelasticity Alteration in Chronic-Progressive Multiple Sclerosis

INTRODUCTION: Viscoelastic properties indicate structural alterations in biological tissues at multiple scales with high sensitivity. Magnetic Resonance Elastography (MRE) is a novel technique that directly visualizes and quantitatively measures biomechanical tissue properties in vivo. MRE recently...

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Autores principales: Streitberger, Kaspar-Josche, Sack, Ingolf, Krefting, Dagmar, Pfüller, Caspar, Braun, Jürgen, Paul, Friedemann, Wuerfel, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262797/
https://www.ncbi.nlm.nih.gov/pubmed/22276134
http://dx.doi.org/10.1371/journal.pone.0029888
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author Streitberger, Kaspar-Josche
Sack, Ingolf
Krefting, Dagmar
Pfüller, Caspar
Braun, Jürgen
Paul, Friedemann
Wuerfel, Jens
author_facet Streitberger, Kaspar-Josche
Sack, Ingolf
Krefting, Dagmar
Pfüller, Caspar
Braun, Jürgen
Paul, Friedemann
Wuerfel, Jens
author_sort Streitberger, Kaspar-Josche
collection PubMed
description INTRODUCTION: Viscoelastic properties indicate structural alterations in biological tissues at multiple scales with high sensitivity. Magnetic Resonance Elastography (MRE) is a novel technique that directly visualizes and quantitatively measures biomechanical tissue properties in vivo. MRE recently revealed that early relapsing-remitting multiple sclerosis (MS) is associated with a global decrease of the cerebral mechanical integrity. This study addresses MRE and MR volumetry in chronic-progressive disease courses of MS. METHODS: We determined viscoelastic parameters of the brain parenchyma in 23 MS patients with primary or secondary chronic progressive disease course in comparison to 38 age- and gender-matched healthy individuals by multifrequency MRE, and correlated the results with clinical data, T2 lesion load and brain volume. Two viscoelastic parameters, the shear elasticity μ and the powerlaw exponent α, were deduced according to the springpot model and compared to literature values of relapsing-remitting MS. RESULTS: In chronic-progressive MS patients, μ and α were reduced by 20.5% and 6.1%, respectively, compared to healthy controls. MR volumetry yielded a weaker correlation: Total brain volume loss in MS patients was in the range of 7.5% and 1.7% considering the brain parenchymal fraction. All findings were significant (P<0.001). CONCLUSIONS: Chronic-progressive MS disease courses show a pronounced reduction of the cerebral shear elasticity compared to early relapsing-remitting disease. The powerlaw exponent α decreased only in the chronic-progressive stage of MS, suggesting an alteration in the geometry of the cerebral mechanical network due to chronic neuroinflammation.
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spelling pubmed-32627972012-01-24 Brain Viscoelasticity Alteration in Chronic-Progressive Multiple Sclerosis Streitberger, Kaspar-Josche Sack, Ingolf Krefting, Dagmar Pfüller, Caspar Braun, Jürgen Paul, Friedemann Wuerfel, Jens PLoS One Research Article INTRODUCTION: Viscoelastic properties indicate structural alterations in biological tissues at multiple scales with high sensitivity. Magnetic Resonance Elastography (MRE) is a novel technique that directly visualizes and quantitatively measures biomechanical tissue properties in vivo. MRE recently revealed that early relapsing-remitting multiple sclerosis (MS) is associated with a global decrease of the cerebral mechanical integrity. This study addresses MRE and MR volumetry in chronic-progressive disease courses of MS. METHODS: We determined viscoelastic parameters of the brain parenchyma in 23 MS patients with primary or secondary chronic progressive disease course in comparison to 38 age- and gender-matched healthy individuals by multifrequency MRE, and correlated the results with clinical data, T2 lesion load and brain volume. Two viscoelastic parameters, the shear elasticity μ and the powerlaw exponent α, were deduced according to the springpot model and compared to literature values of relapsing-remitting MS. RESULTS: In chronic-progressive MS patients, μ and α were reduced by 20.5% and 6.1%, respectively, compared to healthy controls. MR volumetry yielded a weaker correlation: Total brain volume loss in MS patients was in the range of 7.5% and 1.7% considering the brain parenchymal fraction. All findings were significant (P<0.001). CONCLUSIONS: Chronic-progressive MS disease courses show a pronounced reduction of the cerebral shear elasticity compared to early relapsing-remitting disease. The powerlaw exponent α decreased only in the chronic-progressive stage of MS, suggesting an alteration in the geometry of the cerebral mechanical network due to chronic neuroinflammation. Public Library of Science 2012-01-20 /pmc/articles/PMC3262797/ /pubmed/22276134 http://dx.doi.org/10.1371/journal.pone.0029888 Text en Streitberger 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Streitberger, Kaspar-Josche
Sack, Ingolf
Krefting, Dagmar
Pfüller, Caspar
Braun, Jürgen
Paul, Friedemann
Wuerfel, Jens
Brain Viscoelasticity Alteration in Chronic-Progressive Multiple Sclerosis
title Brain Viscoelasticity Alteration in Chronic-Progressive Multiple Sclerosis
title_full Brain Viscoelasticity Alteration in Chronic-Progressive Multiple Sclerosis
title_fullStr Brain Viscoelasticity Alteration in Chronic-Progressive Multiple Sclerosis
title_full_unstemmed Brain Viscoelasticity Alteration in Chronic-Progressive Multiple Sclerosis
title_short Brain Viscoelasticity Alteration in Chronic-Progressive Multiple Sclerosis
title_sort brain viscoelasticity alteration in chronic-progressive multiple sclerosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262797/
https://www.ncbi.nlm.nih.gov/pubmed/22276134
http://dx.doi.org/10.1371/journal.pone.0029888
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