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Functional Connectivity of the Corpus Callosum in Epilepsy Patients with Secondarily Generalized Seizures
The corpus callosum (CC) plays an important role in generalization of seizure activity. We used resting-state function magnetic resonance imaging (rs-fMRI) to investigate the regional and interregional functional connectivity of CC in patients with magnetic resonance imaging (MRI)-negative and secon...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582206/ https://www.ncbi.nlm.nih.gov/pubmed/28912749 http://dx.doi.org/10.3389/fneur.2017.00446 |
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author | Peng, Syu-Jyun Hsin, Yue-Loong |
author_facet | Peng, Syu-Jyun Hsin, Yue-Loong |
author_sort | Peng, Syu-Jyun |
collection | PubMed |
description | The corpus callosum (CC) plays an important role in generalization of seizure activity. We used resting-state function magnetic resonance imaging (rs-fMRI) to investigate the regional and interregional functional connectivity of CC in patients with magnetic resonance imaging (MRI)-negative and secondarily generalized seizures. We measured the multi-regional coherences of blood oxygen level-dependent (BOLD) signals via rs-fMRI, cortical thickness via high-resolution T1-weighted MRI, and white matter (WM) integrity via diffusion-tensor imaging in 16 epilepsy patients as well as in 16 age- and gender-matched healthy subjects. All patients had non-lesional MRI, medically well-controlled focal epilepsy and history of secondarily generalized convulsions. Individuals with epilepsy had significant differences in regional and interregional hypersynchronization of BOLD signals intrahemispherically and interhemispherically, but no difference in cortical thickness and WM integrity. The only area with increased regional hypersynchrony in WM was over the anterior CC, which also exhibited lower activation of neighboring resting-state networks. The present study revealed abnormal local and distant synchronization of spontaneous neural activities in epileptic patients with secondarily generalized seizures. |
format | Online Article Text |
id | pubmed-5582206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55822062017-09-14 Functional Connectivity of the Corpus Callosum in Epilepsy Patients with Secondarily Generalized Seizures Peng, Syu-Jyun Hsin, Yue-Loong Front Neurol Neuroscience The corpus callosum (CC) plays an important role in generalization of seizure activity. We used resting-state function magnetic resonance imaging (rs-fMRI) to investigate the regional and interregional functional connectivity of CC in patients with magnetic resonance imaging (MRI)-negative and secondarily generalized seizures. We measured the multi-regional coherences of blood oxygen level-dependent (BOLD) signals via rs-fMRI, cortical thickness via high-resolution T1-weighted MRI, and white matter (WM) integrity via diffusion-tensor imaging in 16 epilepsy patients as well as in 16 age- and gender-matched healthy subjects. All patients had non-lesional MRI, medically well-controlled focal epilepsy and history of secondarily generalized convulsions. Individuals with epilepsy had significant differences in regional and interregional hypersynchronization of BOLD signals intrahemispherically and interhemispherically, but no difference in cortical thickness and WM integrity. The only area with increased regional hypersynchrony in WM was over the anterior CC, which also exhibited lower activation of neighboring resting-state networks. The present study revealed abnormal local and distant synchronization of spontaneous neural activities in epileptic patients with secondarily generalized seizures. Frontiers Media S.A. 2017-08-30 /pmc/articles/PMC5582206/ /pubmed/28912749 http://dx.doi.org/10.3389/fneur.2017.00446 Text en Copyright © 2017 Peng and Hsin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Peng, Syu-Jyun Hsin, Yue-Loong Functional Connectivity of the Corpus Callosum in Epilepsy Patients with Secondarily Generalized Seizures |
title | Functional Connectivity of the Corpus Callosum in Epilepsy Patients with Secondarily Generalized Seizures |
title_full | Functional Connectivity of the Corpus Callosum in Epilepsy Patients with Secondarily Generalized Seizures |
title_fullStr | Functional Connectivity of the Corpus Callosum in Epilepsy Patients with Secondarily Generalized Seizures |
title_full_unstemmed | Functional Connectivity of the Corpus Callosum in Epilepsy Patients with Secondarily Generalized Seizures |
title_short | Functional Connectivity of the Corpus Callosum in Epilepsy Patients with Secondarily Generalized Seizures |
title_sort | functional connectivity of the corpus callosum in epilepsy patients with secondarily generalized seizures |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582206/ https://www.ncbi.nlm.nih.gov/pubmed/28912749 http://dx.doi.org/10.3389/fneur.2017.00446 |
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