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Lateralizing Cortical Excitability in Drug Naïve Patients with Generalized or Focal Epilepsy

BACKGROUND AND PURPOSE: Numerous transcranial magnetic stimulation (TMS) studies have defined the characteristic features of TMS in epilepsy. TME parameters were expected to classify the epilepsy syndrome or drug responses. However, the results such as cortical silent periods (CSP) are variable acco...

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Autores principales: Lee, Jung Hwa, Joo, Eun Yeon, Seo, Dae Won, Hong, Seung Bong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Epilepsy Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724855/
https://www.ncbi.nlm.nih.gov/pubmed/26819939
http://dx.doi.org/10.14581/jer.15013
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author Lee, Jung Hwa
Joo, Eun Yeon
Seo, Dae Won
Hong, Seung Bong
author_facet Lee, Jung Hwa
Joo, Eun Yeon
Seo, Dae Won
Hong, Seung Bong
author_sort Lee, Jung Hwa
collection PubMed
description BACKGROUND AND PURPOSE: Numerous transcranial magnetic stimulation (TMS) studies have defined the characteristic features of TMS in epilepsy. TME parameters were expected to classify the epilepsy syndrome or drug responses. However, the results such as cortical silent periods (CSP) are variable according to conditions of patients. Here, we investigate whether specific TMS parameters have localizing or lateralizing values in drug-naïve epilepsy patients. METHODS: We recruited 148 consecutive untreated patients with epilepsy (idiopathic generalized epilepsy (IGE) 38, focal epilepsy (FE) 110, mean age 31.4 years) and 38 age- and gender-matched normal subjects. We obtained resting motor threshold (RMT), motor-evoked potential (MEP), CSP, short interval intracortical inhibition (SICI, inter-stimuli interval 2–5 ms), and intracortical facilitation (ICF, inter-stimuli interval 10–20 ms). TMS were performed during a seizure-free state of more than 48 h. RESULTS: In IGE, no interhemispheric difference in CSP was found (p > 0.05). However, the mean CSP was longer in IGE patients than in normal controls at all stimulus intensities (p < 0.05). The mean CSP in ipsilateral hemisphere (IH) of FE was significantly longer at all stimulus intensities than that in normal controls (p < 0.001). The CSP in IH was longer than that in the contralateral hemisphere of FE. There was no significant difference in CSP between FE and IGE. SICI was significantly reduced only in the IH of FE versus normal subjects. RMT, MEP amplitudes, and ICF did not differ among IGE, FE, and normal controls. CONCLUSIONS: We found that prolonged CSP and reduced SICI in FE indicate asymmetrically increased cortical inhibition and excitation in the epileptic hemispheres. It suggests that CSP among TMS parameters has a crucial role to lateralize the epileptic hemisphere in FE.
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spelling pubmed-47248552016-01-27 Lateralizing Cortical Excitability in Drug Naïve Patients with Generalized or Focal Epilepsy Lee, Jung Hwa Joo, Eun Yeon Seo, Dae Won Hong, Seung Bong J Epilepsy Res Original Article BACKGROUND AND PURPOSE: Numerous transcranial magnetic stimulation (TMS) studies have defined the characteristic features of TMS in epilepsy. TME parameters were expected to classify the epilepsy syndrome or drug responses. However, the results such as cortical silent periods (CSP) are variable according to conditions of patients. Here, we investigate whether specific TMS parameters have localizing or lateralizing values in drug-naïve epilepsy patients. METHODS: We recruited 148 consecutive untreated patients with epilepsy (idiopathic generalized epilepsy (IGE) 38, focal epilepsy (FE) 110, mean age 31.4 years) and 38 age- and gender-matched normal subjects. We obtained resting motor threshold (RMT), motor-evoked potential (MEP), CSP, short interval intracortical inhibition (SICI, inter-stimuli interval 2–5 ms), and intracortical facilitation (ICF, inter-stimuli interval 10–20 ms). TMS were performed during a seizure-free state of more than 48 h. RESULTS: In IGE, no interhemispheric difference in CSP was found (p > 0.05). However, the mean CSP was longer in IGE patients than in normal controls at all stimulus intensities (p < 0.05). The mean CSP in ipsilateral hemisphere (IH) of FE was significantly longer at all stimulus intensities than that in normal controls (p < 0.001). The CSP in IH was longer than that in the contralateral hemisphere of FE. There was no significant difference in CSP between FE and IGE. SICI was significantly reduced only in the IH of FE versus normal subjects. RMT, MEP amplitudes, and ICF did not differ among IGE, FE, and normal controls. CONCLUSIONS: We found that prolonged CSP and reduced SICI in FE indicate asymmetrically increased cortical inhibition and excitation in the epileptic hemispheres. It suggests that CSP among TMS parameters has a crucial role to lateralize the epileptic hemisphere in FE. Korean Epilepsy Society 2015-12-31 /pmc/articles/PMC4724855/ /pubmed/26819939 http://dx.doi.org/10.14581/jer.15013 Text en Copyright © 2015 Korean Epilepsy Society This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Jung Hwa
Joo, Eun Yeon
Seo, Dae Won
Hong, Seung Bong
Lateralizing Cortical Excitability in Drug Naïve Patients with Generalized or Focal Epilepsy
title Lateralizing Cortical Excitability in Drug Naïve Patients with Generalized or Focal Epilepsy
title_full Lateralizing Cortical Excitability in Drug Naïve Patients with Generalized or Focal Epilepsy
title_fullStr Lateralizing Cortical Excitability in Drug Naïve Patients with Generalized or Focal Epilepsy
title_full_unstemmed Lateralizing Cortical Excitability in Drug Naïve Patients with Generalized or Focal Epilepsy
title_short Lateralizing Cortical Excitability in Drug Naïve Patients with Generalized or Focal Epilepsy
title_sort lateralizing cortical excitability in drug naïve patients with generalized or focal epilepsy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724855/
https://www.ncbi.nlm.nih.gov/pubmed/26819939
http://dx.doi.org/10.14581/jer.15013
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