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The structural plasticity of white matter networks following anterior temporal lobe resection

Anterior temporal lobe resection is an effective treatment for refractory temporal lobe epilepsy. The structural consequences of such surgery in the white matter, and how these relate to language function after surgery remain unknown. We carried out a longitudinal study with diffusion tensor imaging...

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Autores principales: Yogarajah, Mahinda, Focke, Niels K., Bonelli, Silvia B., Thompson, Pamela, Vollmar, Christian, McEvoy, Andrew W., Alexander, Daniel C., Symms, Mark R., Koepp, Matthias J., Duncan, John S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198261/
https://www.ncbi.nlm.nih.gov/pubmed/20826432
http://dx.doi.org/10.1093/brain/awq175
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author Yogarajah, Mahinda
Focke, Niels K.
Bonelli, Silvia B.
Thompson, Pamela
Vollmar, Christian
McEvoy, Andrew W.
Alexander, Daniel C.
Symms, Mark R.
Koepp, Matthias J.
Duncan, John S.
author_facet Yogarajah, Mahinda
Focke, Niels K.
Bonelli, Silvia B.
Thompson, Pamela
Vollmar, Christian
McEvoy, Andrew W.
Alexander, Daniel C.
Symms, Mark R.
Koepp, Matthias J.
Duncan, John S.
author_sort Yogarajah, Mahinda
collection PubMed
description Anterior temporal lobe resection is an effective treatment for refractory temporal lobe epilepsy. The structural consequences of such surgery in the white matter, and how these relate to language function after surgery remain unknown. We carried out a longitudinal study with diffusion tensor imaging in 26 left and 20 right temporal lobe epilepsy patients before and a mean of 4.5 months after anterior temporal lobe resection. The whole-brain analysis technique tract-based spatial statistics was used to compare pre- and postoperative data in the left and right temporal lobe epilepsy groups separately. We observed widespread, significant, mean 7%, decreases in fractional anisotropy in white matter networks connected to the area of resection, following both left and right temporal lobe resections. However, we also observed a widespread, mean 8%, increase in fractional anisotropy after left anterior temporal lobe resection in the ipsilateral external capsule and posterior limb of the internal capsule, and corona radiata. These findings were confirmed on analysis of the native clusters and hand drawn regions of interest. Postoperative tractography seeded from this area suggests that this cluster is part of the ventro-medial language network. The mean pre- and postoperative fractional anisotropy and parallel diffusivity in this cluster were significantly correlated with postoperative verbal fluency and naming test scores. In addition, the percentage change in parallel diffusivity in this cluster was correlated with the percentage change in verbal fluency after anterior temporal lobe resection, such that the bigger the increase in parallel diffusivity, the smaller the fall in language proficiency after surgery. We suggest that the findings of increased fractional anisotropy in this ventro-medial language network represent structural reorganization in response to the anterior temporal lobe resection, which may damage the more susceptible dorso-lateral language pathway. These findings have important implications for our understanding of brain injury and rehabilitation, and may also prove useful in the prediction and minimization of postoperative language deficits.
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spelling pubmed-31982612011-10-23 The structural plasticity of white matter networks following anterior temporal lobe resection Yogarajah, Mahinda Focke, Niels K. Bonelli, Silvia B. Thompson, Pamela Vollmar, Christian McEvoy, Andrew W. Alexander, Daniel C. Symms, Mark R. Koepp, Matthias J. Duncan, John S. Brain Original Articles Anterior temporal lobe resection is an effective treatment for refractory temporal lobe epilepsy. The structural consequences of such surgery in the white matter, and how these relate to language function after surgery remain unknown. We carried out a longitudinal study with diffusion tensor imaging in 26 left and 20 right temporal lobe epilepsy patients before and a mean of 4.5 months after anterior temporal lobe resection. The whole-brain analysis technique tract-based spatial statistics was used to compare pre- and postoperative data in the left and right temporal lobe epilepsy groups separately. We observed widespread, significant, mean 7%, decreases in fractional anisotropy in white matter networks connected to the area of resection, following both left and right temporal lobe resections. However, we also observed a widespread, mean 8%, increase in fractional anisotropy after left anterior temporal lobe resection in the ipsilateral external capsule and posterior limb of the internal capsule, and corona radiata. These findings were confirmed on analysis of the native clusters and hand drawn regions of interest. Postoperative tractography seeded from this area suggests that this cluster is part of the ventro-medial language network. The mean pre- and postoperative fractional anisotropy and parallel diffusivity in this cluster were significantly correlated with postoperative verbal fluency and naming test scores. In addition, the percentage change in parallel diffusivity in this cluster was correlated with the percentage change in verbal fluency after anterior temporal lobe resection, such that the bigger the increase in parallel diffusivity, the smaller the fall in language proficiency after surgery. We suggest that the findings of increased fractional anisotropy in this ventro-medial language network represent structural reorganization in response to the anterior temporal lobe resection, which may damage the more susceptible dorso-lateral language pathway. These findings have important implications for our understanding of brain injury and rehabilitation, and may also prove useful in the prediction and minimization of postoperative language deficits. Oxford University Press 2010-08 2010-07-24 /pmc/articles/PMC3198261/ /pubmed/20826432 http://dx.doi.org/10.1093/brain/awq175 Text en © The Author(s) 2010. Published by Oxford University Press on behalf of Brain. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Yogarajah, Mahinda
Focke, Niels K.
Bonelli, Silvia B.
Thompson, Pamela
Vollmar, Christian
McEvoy, Andrew W.
Alexander, Daniel C.
Symms, Mark R.
Koepp, Matthias J.
Duncan, John S.
The structural plasticity of white matter networks following anterior temporal lobe resection
title The structural plasticity of white matter networks following anterior temporal lobe resection
title_full The structural plasticity of white matter networks following anterior temporal lobe resection
title_fullStr The structural plasticity of white matter networks following anterior temporal lobe resection
title_full_unstemmed The structural plasticity of white matter networks following anterior temporal lobe resection
title_short The structural plasticity of white matter networks following anterior temporal lobe resection
title_sort structural plasticity of white matter networks following anterior temporal lobe resection
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198261/
https://www.ncbi.nlm.nih.gov/pubmed/20826432
http://dx.doi.org/10.1093/brain/awq175
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