Enlargement of cerebral ventricles as an early indicator of encephalomyelitis.

Inflammatory disorders of the central nervous system such as multiple sclerosis and acute disseminated encephalomyelitis involve an invasion of immune cells that ultimately leads to white matter demyelination, neurodegeneration and development of neurological symptoms. A clinical diagnosis is often...

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Main Authors: Stefano Lepore, Helmar Waiczies, Jan Hentschel, Yiyi Ji, Julia Skodowski, Andreas Pohlmann, Jason M Millward, Friedemann Paul, Jens Wuerfel, Thoralf Niendorf, Sonia Waiczies
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23991157/pdf/?tool=EBI
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spelling doaj-620621b02c554a37817544c4df20a70b2021-03-03T22:58:05ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0188e7284110.1371/journal.pone.0072841Enlargement of cerebral ventricles as an early indicator of encephalomyelitis.Stefano LeporeHelmar WaicziesJan HentschelYiyi JiJulia SkodowskiAndreas PohlmannJason M MillwardFriedemann PaulJens WuerfelThoralf NiendorfSonia WaicziesInflammatory disorders of the central nervous system such as multiple sclerosis and acute disseminated encephalomyelitis involve an invasion of immune cells that ultimately leads to white matter demyelination, neurodegeneration and development of neurological symptoms. A clinical diagnosis is often made when neurodegenerative processes are already ongoing. In an attempt to seek early indicators of disease, we studied the temporal and spatial distribution of brain modifications in experimental autoimmune encephalomyelitis (EAE). In a thorough magnetic resonance imaging study performed with EAE mice, we observed significant enlargement of the ventricles prior to disease clinical manifestation and an increase in free water content within the cerebrospinal fluid as demonstrated by changes in T2 relaxation times. The increase in ventricle size was seen in the lateral, third and fourth ventricles. In some EAE mice the ventricle size started returning to normal values during disease remission. In parallel to this macroscopic phenomenon, we studied the temporal evolution of microscopic lesions commonly observed in the cerebellum also starting prior to disease onset. Our data suggest that changes in ventricle size during the early stages of brain inflammation could be an early indicator of the events preceding neurological disease and warrant further exploration in preclinical and clinical studies.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23991157/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Stefano Lepore
Helmar Waiczies
Jan Hentschel
Yiyi Ji
Julia Skodowski
Andreas Pohlmann
Jason M Millward
Friedemann Paul
Jens Wuerfel
Thoralf Niendorf
Sonia Waiczies
spellingShingle Stefano Lepore
Helmar Waiczies
Jan Hentschel
Yiyi Ji
Julia Skodowski
Andreas Pohlmann
Jason M Millward
Friedemann Paul
Jens Wuerfel
Thoralf Niendorf
Sonia Waiczies
Enlargement of cerebral ventricles as an early indicator of encephalomyelitis.
PLoS ONE
author_facet Stefano Lepore
Helmar Waiczies
Jan Hentschel
Yiyi Ji
Julia Skodowski
Andreas Pohlmann
Jason M Millward
Friedemann Paul
Jens Wuerfel
Thoralf Niendorf
Sonia Waiczies
author_sort Stefano Lepore
title Enlargement of cerebral ventricles as an early indicator of encephalomyelitis.
title_short Enlargement of cerebral ventricles as an early indicator of encephalomyelitis.
title_full Enlargement of cerebral ventricles as an early indicator of encephalomyelitis.
title_fullStr Enlargement of cerebral ventricles as an early indicator of encephalomyelitis.
title_full_unstemmed Enlargement of cerebral ventricles as an early indicator of encephalomyelitis.
title_sort enlargement of cerebral ventricles as an early indicator of encephalomyelitis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Inflammatory disorders of the central nervous system such as multiple sclerosis and acute disseminated encephalomyelitis involve an invasion of immune cells that ultimately leads to white matter demyelination, neurodegeneration and development of neurological symptoms. A clinical diagnosis is often made when neurodegenerative processes are already ongoing. In an attempt to seek early indicators of disease, we studied the temporal and spatial distribution of brain modifications in experimental autoimmune encephalomyelitis (EAE). In a thorough magnetic resonance imaging study performed with EAE mice, we observed significant enlargement of the ventricles prior to disease clinical manifestation and an increase in free water content within the cerebrospinal fluid as demonstrated by changes in T2 relaxation times. The increase in ventricle size was seen in the lateral, third and fourth ventricles. In some EAE mice the ventricle size started returning to normal values during disease remission. In parallel to this macroscopic phenomenon, we studied the temporal evolution of microscopic lesions commonly observed in the cerebellum also starting prior to disease onset. Our data suggest that changes in ventricle size during the early stages of brain inflammation could be an early indicator of the events preceding neurological disease and warrant further exploration in preclinical and clinical studies.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23991157/pdf/?tool=EBI
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