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Changes in Interictal Pretreatment and Posttreatment EEG in Childhood Absence Epilepsy
Spike and wave discharges (SWDs) are a characteristic manifestation of childhood absence epilepsy (CAE). It has long been believed that they unpredictably emerge from otherwise almost normal interictal EEG. Herein, we demonstrate that pretreatment closed-eyes theta and beta EEG wavelet powers of CAE...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082231/ https://www.ncbi.nlm.nih.gov/pubmed/32231515 http://dx.doi.org/10.3389/fnins.2020.00196 |
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author | Glaba, Pawel Latka, Miroslaw Krause, Małgorzata J. Kuryło, Marta Jernajczyk, Wojciech Walas, Wojciech West, Bruce J. |
author_facet | Glaba, Pawel Latka, Miroslaw Krause, Małgorzata J. Kuryło, Marta Jernajczyk, Wojciech Walas, Wojciech West, Bruce J. |
author_sort | Glaba, Pawel |
collection | PubMed |
description | Spike and wave discharges (SWDs) are a characteristic manifestation of childhood absence epilepsy (CAE). It has long been believed that they unpredictably emerge from otherwise almost normal interictal EEG. Herein, we demonstrate that pretreatment closed-eyes theta and beta EEG wavelet powers of CAE patients (20 girls and 10 boys, mean age 7.4 ± 1.9 years) are much higher than those of age-matched healthy controls at multiple sites of the 10–20 system. For example, at the C4 site, we observed a 100 and 63% increase in power of theta and beta rhythms, respectively. We were able to compare the baseline and posttreatment wavelet power in 16 patients. Pharmacotherapy brought about a statistically significant decrease in delta and theta wavelet power in all the channels, e.g., for C4 the reduction was equal to 45% (delta) and 63% (theta). The less pronounced attenuation of posttreatment beta waves was observed in 13 channels (36% at C4 site). The beta and theta wavelet power were positively correlated with the percentage of time in seizure (defined as the ratio of the duration of all absences which patients experienced to the duration of recording) for majority of channels. We hypothesize that the increased theta and beta powers result from cortical hyperexcitability and propensity for epileptic spike generation, respectively. We argue that the distinct features of CAE wavelet power spectrum may be used to define an EEG biomarker which could be used for diagnosis and monitoring of patients. |
format | Online Article Text |
id | pubmed-7082231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70822312020-03-30 Changes in Interictal Pretreatment and Posttreatment EEG in Childhood Absence Epilepsy Glaba, Pawel Latka, Miroslaw Krause, Małgorzata J. Kuryło, Marta Jernajczyk, Wojciech Walas, Wojciech West, Bruce J. Front Neurosci Neuroscience Spike and wave discharges (SWDs) are a characteristic manifestation of childhood absence epilepsy (CAE). It has long been believed that they unpredictably emerge from otherwise almost normal interictal EEG. Herein, we demonstrate that pretreatment closed-eyes theta and beta EEG wavelet powers of CAE patients (20 girls and 10 boys, mean age 7.4 ± 1.9 years) are much higher than those of age-matched healthy controls at multiple sites of the 10–20 system. For example, at the C4 site, we observed a 100 and 63% increase in power of theta and beta rhythms, respectively. We were able to compare the baseline and posttreatment wavelet power in 16 patients. Pharmacotherapy brought about a statistically significant decrease in delta and theta wavelet power in all the channels, e.g., for C4 the reduction was equal to 45% (delta) and 63% (theta). The less pronounced attenuation of posttreatment beta waves was observed in 13 channels (36% at C4 site). The beta and theta wavelet power were positively correlated with the percentage of time in seizure (defined as the ratio of the duration of all absences which patients experienced to the duration of recording) for majority of channels. We hypothesize that the increased theta and beta powers result from cortical hyperexcitability and propensity for epileptic spike generation, respectively. We argue that the distinct features of CAE wavelet power spectrum may be used to define an EEG biomarker which could be used for diagnosis and monitoring of patients. Frontiers Media S.A. 2020-03-13 /pmc/articles/PMC7082231/ /pubmed/32231515 http://dx.doi.org/10.3389/fnins.2020.00196 Text en Copyright © 2020 Glaba, Latka, Krause, Kuryło, Jernajczyk, Walas and West. 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) and the copyright owner(s) 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 Glaba, Pawel Latka, Miroslaw Krause, Małgorzata J. Kuryło, Marta Jernajczyk, Wojciech Walas, Wojciech West, Bruce J. Changes in Interictal Pretreatment and Posttreatment EEG in Childhood Absence Epilepsy |
title | Changes in Interictal Pretreatment and Posttreatment EEG in Childhood Absence Epilepsy |
title_full | Changes in Interictal Pretreatment and Posttreatment EEG in Childhood Absence Epilepsy |
title_fullStr | Changes in Interictal Pretreatment and Posttreatment EEG in Childhood Absence Epilepsy |
title_full_unstemmed | Changes in Interictal Pretreatment and Posttreatment EEG in Childhood Absence Epilepsy |
title_short | Changes in Interictal Pretreatment and Posttreatment EEG in Childhood Absence Epilepsy |
title_sort | changes in interictal pretreatment and posttreatment eeg in childhood absence epilepsy |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082231/ https://www.ncbi.nlm.nih.gov/pubmed/32231515 http://dx.doi.org/10.3389/fnins.2020.00196 |
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