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Network of ictal head version in mesial temporal lobe epilepsy
OBJECTIVE: Ictal head version is a common clinical manifestation of mesial temporal lobe epilepsy (MTLE). Nevertheless, the location of the symptomatogenic zone and the network involved in head version remains unclear. We attempt to explain these problems by analyzing interictal (18)FDG‐PET imaging...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667364/ https://www.ncbi.nlm.nih.gov/pubmed/32857475 http://dx.doi.org/10.1002/brb3.1820 |
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author | Wang, Yao Wang, Xiu Sang, Lin Zhang, Chao Zhao, Bao‐tian Mo, Jia‐jie Hu, Wen‐han Shao, Xiao‐qiu Wang, Feng Ai, Lin Zhang, Jian‐guo Zhang, Kai |
author_facet | Wang, Yao Wang, Xiu Sang, Lin Zhang, Chao Zhao, Bao‐tian Mo, Jia‐jie Hu, Wen‐han Shao, Xiao‐qiu Wang, Feng Ai, Lin Zhang, Jian‐guo Zhang, Kai |
author_sort | Wang, Yao |
collection | PubMed |
description | OBJECTIVE: Ictal head version is a common clinical manifestation of mesial temporal lobe epilepsy (MTLE). Nevertheless, the location of the symptomatogenic zone and the network involved in head version remains unclear. We attempt to explain these problems by analyzing interictal (18)FDG‐PET imaging and ictal stereo‐electroencephalography (SEEG) recordings in MTLE patients. METHODS: Fifty‐eight patients with MTLE were retrospectively analyzed. The patients were divided into version (+) and (−) groups according to the occurrence of versive head movements. The interictal PET data were compared among 18 healthy controls and the (+) and (−) groups. Furthermore, epileptogenicity index (EI) values and correlations with the onset time of head version were analyzed with SEEG. RESULTS: Intergroup comparisons showed that PET differences were observed in the middle temporal neocortex (MTN), posterior temporal neocortex (PTN), supramarginal gyrus (SMG), and inferior parietal lobe (IPL). The EI values in the SMG, MTN, and PTN were significantly higher in the version (+) group than in the version (−) group. A linear relationship was observed between head version onset and ipsilateral onset time in the SMG, orbitofrontal cortex (OFC), MTN, and PTN. A linear relationship was observed between EI, the difference between version onset and temporal neocortex onset, and the y‐axis of the MNI coordinate. CONCLUSION: The generation of ictal head version contributes to the propagation of ictal discharges to the intraparietal sulcus (IPS) area. The network of version originates from a mesial temporal lobe structure, passes through the MTN, PTN, and SMG, and likely ends at the IPS. |
format | Online Article Text |
id | pubmed-7667364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76673642020-11-20 Network of ictal head version in mesial temporal lobe epilepsy Wang, Yao Wang, Xiu Sang, Lin Zhang, Chao Zhao, Bao‐tian Mo, Jia‐jie Hu, Wen‐han Shao, Xiao‐qiu Wang, Feng Ai, Lin Zhang, Jian‐guo Zhang, Kai Brain Behav Original Research OBJECTIVE: Ictal head version is a common clinical manifestation of mesial temporal lobe epilepsy (MTLE). Nevertheless, the location of the symptomatogenic zone and the network involved in head version remains unclear. We attempt to explain these problems by analyzing interictal (18)FDG‐PET imaging and ictal stereo‐electroencephalography (SEEG) recordings in MTLE patients. METHODS: Fifty‐eight patients with MTLE were retrospectively analyzed. The patients were divided into version (+) and (−) groups according to the occurrence of versive head movements. The interictal PET data were compared among 18 healthy controls and the (+) and (−) groups. Furthermore, epileptogenicity index (EI) values and correlations with the onset time of head version were analyzed with SEEG. RESULTS: Intergroup comparisons showed that PET differences were observed in the middle temporal neocortex (MTN), posterior temporal neocortex (PTN), supramarginal gyrus (SMG), and inferior parietal lobe (IPL). The EI values in the SMG, MTN, and PTN were significantly higher in the version (+) group than in the version (−) group. A linear relationship was observed between head version onset and ipsilateral onset time in the SMG, orbitofrontal cortex (OFC), MTN, and PTN. A linear relationship was observed between EI, the difference between version onset and temporal neocortex onset, and the y‐axis of the MNI coordinate. CONCLUSION: The generation of ictal head version contributes to the propagation of ictal discharges to the intraparietal sulcus (IPS) area. The network of version originates from a mesial temporal lobe structure, passes through the MTN, PTN, and SMG, and likely ends at the IPS. John Wiley and Sons Inc. 2020-08-28 /pmc/articles/PMC7667364/ /pubmed/32857475 http://dx.doi.org/10.1002/brb3.1820 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Wang, Yao Wang, Xiu Sang, Lin Zhang, Chao Zhao, Bao‐tian Mo, Jia‐jie Hu, Wen‐han Shao, Xiao‐qiu Wang, Feng Ai, Lin Zhang, Jian‐guo Zhang, Kai Network of ictal head version in mesial temporal lobe epilepsy |
title | Network of ictal head version in mesial temporal lobe epilepsy |
title_full | Network of ictal head version in mesial temporal lobe epilepsy |
title_fullStr | Network of ictal head version in mesial temporal lobe epilepsy |
title_full_unstemmed | Network of ictal head version in mesial temporal lobe epilepsy |
title_short | Network of ictal head version in mesial temporal lobe epilepsy |
title_sort | network of ictal head version in mesial temporal lobe epilepsy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667364/ https://www.ncbi.nlm.nih.gov/pubmed/32857475 http://dx.doi.org/10.1002/brb3.1820 |
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