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The topograpy of demyelination and neurodegeneration in the multiple sclerosis brain

Multiple sclerosis is a chronic inflammatory disease with primary demyelination and neurodegeneration in the central nervous system. In our study we analysed demyelination and neurodegeneration in a large series of multiple sclerosis brains and provide a map that displays the frequency of different...

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Autores principales: Haider, Lukas, Zrzavy, Tobias, Hametner, Simon, Höftberger, Romana, Bagnato, Francesca, Grabner, Günther, Trattnig, Siegfried, Pfeifenbring, Sabine, Brück, Wolfgang, Lassmann, Hans
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766379/
https://www.ncbi.nlm.nih.gov/pubmed/26912645
http://dx.doi.org/10.1093/brain/awv398
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author Haider, Lukas
Zrzavy, Tobias
Hametner, Simon
Höftberger, Romana
Bagnato, Francesca
Grabner, Günther
Trattnig, Siegfried
Pfeifenbring, Sabine
Brück, Wolfgang
Lassmann, Hans
author_facet Haider, Lukas
Zrzavy, Tobias
Hametner, Simon
Höftberger, Romana
Bagnato, Francesca
Grabner, Günther
Trattnig, Siegfried
Pfeifenbring, Sabine
Brück, Wolfgang
Lassmann, Hans
author_sort Haider, Lukas
collection PubMed
description Multiple sclerosis is a chronic inflammatory disease with primary demyelination and neurodegeneration in the central nervous system. In our study we analysed demyelination and neurodegeneration in a large series of multiple sclerosis brains and provide a map that displays the frequency of different brain areas to be affected by these processes. Demyelination in the cerebral cortex was related to inflammatory infiltrates in the meninges, which was pronounced in invaginations of the brain surface (sulci) and possibly promoted by low flow of the cerebrospinal fluid in these areas. Focal demyelinated lesions in the white matter occurred at sites with high venous density and additionally accumulated in watershed areas of low arterial blood supply. Two different patterns of neurodegeneration in the cortex were identified: oxidative injury of cortical neurons and retrograde neurodegeneration due to axonal injury in the white matter. While oxidative injury was related to the inflammatory process in the meninges and pronounced in actively demyelinating cortical lesions, retrograde degeneration was mainly related to demyelinated lesions and axonal loss in the white matter. Our data show that accumulation of lesions and neurodegeneration in the multiple sclerosis brain does not affect all brain regions equally and provides the pathological basis for the selection of brain areas for monitoring regional injury and atrophy development in future magnetic resonance imaging studies.
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spelling pubmed-47663792016-02-26 The topograpy of demyelination and neurodegeneration in the multiple sclerosis brain Haider, Lukas Zrzavy, Tobias Hametner, Simon Höftberger, Romana Bagnato, Francesca Grabner, Günther Trattnig, Siegfried Pfeifenbring, Sabine Brück, Wolfgang Lassmann, Hans Brain Original Articles Multiple sclerosis is a chronic inflammatory disease with primary demyelination and neurodegeneration in the central nervous system. In our study we analysed demyelination and neurodegeneration in a large series of multiple sclerosis brains and provide a map that displays the frequency of different brain areas to be affected by these processes. Demyelination in the cerebral cortex was related to inflammatory infiltrates in the meninges, which was pronounced in invaginations of the brain surface (sulci) and possibly promoted by low flow of the cerebrospinal fluid in these areas. Focal demyelinated lesions in the white matter occurred at sites with high venous density and additionally accumulated in watershed areas of low arterial blood supply. Two different patterns of neurodegeneration in the cortex were identified: oxidative injury of cortical neurons and retrograde neurodegeneration due to axonal injury in the white matter. While oxidative injury was related to the inflammatory process in the meninges and pronounced in actively demyelinating cortical lesions, retrograde degeneration was mainly related to demyelinated lesions and axonal loss in the white matter. Our data show that accumulation of lesions and neurodegeneration in the multiple sclerosis brain does not affect all brain regions equally and provides the pathological basis for the selection of brain areas for monitoring regional injury and atrophy development in future magnetic resonance imaging studies. Oxford University Press 2016-03 2016-02-08 /pmc/articles/PMC4766379/ /pubmed/26912645 http://dx.doi.org/10.1093/brain/awv398 Text en © The Author (2016). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/ ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
Haider, Lukas
Zrzavy, Tobias
Hametner, Simon
Höftberger, Romana
Bagnato, Francesca
Grabner, Günther
Trattnig, Siegfried
Pfeifenbring, Sabine
Brück, Wolfgang
Lassmann, Hans
The topograpy of demyelination and neurodegeneration in the multiple sclerosis brain
title The topograpy of demyelination and neurodegeneration in the multiple sclerosis brain
title_full The topograpy of demyelination and neurodegeneration in the multiple sclerosis brain
title_fullStr The topograpy of demyelination and neurodegeneration in the multiple sclerosis brain
title_full_unstemmed The topograpy of demyelination and neurodegeneration in the multiple sclerosis brain
title_short The topograpy of demyelination and neurodegeneration in the multiple sclerosis brain
title_sort topograpy of demyelination and neurodegeneration in the multiple sclerosis brain
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766379/
https://www.ncbi.nlm.nih.gov/pubmed/26912645
http://dx.doi.org/10.1093/brain/awv398
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