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Mesial temporal sclerosis is linked with more widespread white matter changes in temporal lobe epilepsy()

Temporal lobe epilepsy patients with unilateral mesial temporal sclerosis (TLE + uMTS) have been demonstrated to have extensive white matter abnormalities both ipsilateral and contralateral to the seizure onset zone. However, comparatively less is known about the white matter integrity of TLE patien...

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Autores principales: Liu, Min, Concha, Luis, Lebel, Catherine, Beaulieu, Christian, Gross, Donald W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757721/
https://www.ncbi.nlm.nih.gov/pubmed/24179742
http://dx.doi.org/10.1016/j.nicl.2012.09.010
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author Liu, Min
Concha, Luis
Lebel, Catherine
Beaulieu, Christian
Gross, Donald W.
author_facet Liu, Min
Concha, Luis
Lebel, Catherine
Beaulieu, Christian
Gross, Donald W.
author_sort Liu, Min
collection PubMed
description Temporal lobe epilepsy patients with unilateral mesial temporal sclerosis (TLE + uMTS) have been demonstrated to have extensive white matter abnormalities both ipsilateral and contralateral to the seizure onset zone. However, comparatively less is known about the white matter integrity of TLE patients without MTS (non-lesional TLE, nl-TLE). The purpose of the study was to investigate the diffusion properties of thirteen major white matter tracts in patients with TLE + uMTS and nl-TLE. Diffusion tensor imaging (DTI) was performed on 23 TLE + uMTS (15 left MTS and 8 right MTS), 15 nl-TLE and 21 controls. Thirteen tracts were delineated by tractography and their diffusion parameters compared for the two TLE groups relative to controls, with left and right hemispheres combined per tract. A subgroup analysis investigated left and right MTS separately. Compared to controls, reduced anisotropy was detected in ten tracts for TLE + uMTS, but only the parahippocampal cingulum and tapetum for nl-TLE. Right MTS subgroup showed reduced anisotropy in 7 tracts bilaterally (3 limbic, 3 association, 1 projection) and 2 tracts ipsilaterally (1 association, 1 projection) and the body of the corpus callosum whereas the left MTS subgroup showed reduced anisotropy in 4 tracts bilaterally (2 limbic, 1 association, 1 projection) and 2 tracts ipsilaterally (1 limbic, 1 association). Diffusion abnormalities in tracts were observed within and beyond the temporal lobe in TLE + uMTS and were more widespread than in nl-TLE. Patients with right MTS had more extensive, bilateral abnormalities in comparison to left MTS. These findings suggest different dysfunctional networks in TLE patients with and without MTS.
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spelling pubmed-37577212013-10-31 Mesial temporal sclerosis is linked with more widespread white matter changes in temporal lobe epilepsy() Liu, Min Concha, Luis Lebel, Catherine Beaulieu, Christian Gross, Donald W. Neuroimage Clin Article Temporal lobe epilepsy patients with unilateral mesial temporal sclerosis (TLE + uMTS) have been demonstrated to have extensive white matter abnormalities both ipsilateral and contralateral to the seizure onset zone. However, comparatively less is known about the white matter integrity of TLE patients without MTS (non-lesional TLE, nl-TLE). The purpose of the study was to investigate the diffusion properties of thirteen major white matter tracts in patients with TLE + uMTS and nl-TLE. Diffusion tensor imaging (DTI) was performed on 23 TLE + uMTS (15 left MTS and 8 right MTS), 15 nl-TLE and 21 controls. Thirteen tracts were delineated by tractography and their diffusion parameters compared for the two TLE groups relative to controls, with left and right hemispheres combined per tract. A subgroup analysis investigated left and right MTS separately. Compared to controls, reduced anisotropy was detected in ten tracts for TLE + uMTS, but only the parahippocampal cingulum and tapetum for nl-TLE. Right MTS subgroup showed reduced anisotropy in 7 tracts bilaterally (3 limbic, 3 association, 1 projection) and 2 tracts ipsilaterally (1 association, 1 projection) and the body of the corpus callosum whereas the left MTS subgroup showed reduced anisotropy in 4 tracts bilaterally (2 limbic, 1 association, 1 projection) and 2 tracts ipsilaterally (1 limbic, 1 association). Diffusion abnormalities in tracts were observed within and beyond the temporal lobe in TLE + uMTS and were more widespread than in nl-TLE. Patients with right MTS had more extensive, bilateral abnormalities in comparison to left MTS. These findings suggest different dysfunctional networks in TLE patients with and without MTS. Elsevier 2012-10-01 /pmc/articles/PMC3757721/ /pubmed/24179742 http://dx.doi.org/10.1016/j.nicl.2012.09.010 Text en © 2012 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Liu, Min
Concha, Luis
Lebel, Catherine
Beaulieu, Christian
Gross, Donald W.
Mesial temporal sclerosis is linked with more widespread white matter changes in temporal lobe epilepsy()
title Mesial temporal sclerosis is linked with more widespread white matter changes in temporal lobe epilepsy()
title_full Mesial temporal sclerosis is linked with more widespread white matter changes in temporal lobe epilepsy()
title_fullStr Mesial temporal sclerosis is linked with more widespread white matter changes in temporal lobe epilepsy()
title_full_unstemmed Mesial temporal sclerosis is linked with more widespread white matter changes in temporal lobe epilepsy()
title_short Mesial temporal sclerosis is linked with more widespread white matter changes in temporal lobe epilepsy()
title_sort mesial temporal sclerosis is linked with more widespread white matter changes in temporal lobe epilepsy()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757721/
https://www.ncbi.nlm.nih.gov/pubmed/24179742
http://dx.doi.org/10.1016/j.nicl.2012.09.010
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