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A computational biomarker of juvenile myoclonic epilepsy from resting-state MEG
OBJECTIVE: For people with idiopathic generalized epilepsy, functional networks derived from their resting-state scalp electrophysiological recordings have shown an inherent higher propensity to generate seizures than those from healthy controls when assessed using the concept of brain network ictog...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992031/ https://www.ncbi.nlm.nih.gov/pubmed/33636607 http://dx.doi.org/10.1016/j.clinph.2020.12.021 |
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author | Lopes, Marinho A. Krzemiński, Dominik Hamandi, Khalid Singh, Krish D. Masuda, Naoki Terry, John R. Zhang, Jiaxiang |
author_facet | Lopes, Marinho A. Krzemiński, Dominik Hamandi, Khalid Singh, Krish D. Masuda, Naoki Terry, John R. Zhang, Jiaxiang |
author_sort | Lopes, Marinho A. |
collection | PubMed |
description | OBJECTIVE: For people with idiopathic generalized epilepsy, functional networks derived from their resting-state scalp electrophysiological recordings have shown an inherent higher propensity to generate seizures than those from healthy controls when assessed using the concept of brain network ictogenicity (BNI). Herein we tested whether the BNI framework is applicable to resting-state magnetoencephalography (MEG) from people with juvenile myoclonic epilepsy (JME). METHODS: The BNI framework consists in deriving a functional network from apparently normal brain activity, placing a mathematical model of ictogenicity into the network and then computing how often such network generates seizures in silico. We considered data from 26 people with JME and 26 healthy controls. RESULTS: We found that resting-state MEG functional networks from people with JME are characterized by a higher propensity to generate seizures (i.e., higher BNI) than those from healthy controls. We found a classification accuracy of 73%. CONCLUSIONS: The BNI framework is applicable to MEG and was capable of differentiating people with epilepsy from healthy controls. SIGNIFICANCE: The BNI framework may be applied to resting-state MEG to aid in epilepsy diagnosis. |
format | Online Article Text |
id | pubmed-7992031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-79920312021-04-01 A computational biomarker of juvenile myoclonic epilepsy from resting-state MEG Lopes, Marinho A. Krzemiński, Dominik Hamandi, Khalid Singh, Krish D. Masuda, Naoki Terry, John R. Zhang, Jiaxiang Clin Neurophysiol Article OBJECTIVE: For people with idiopathic generalized epilepsy, functional networks derived from their resting-state scalp electrophysiological recordings have shown an inherent higher propensity to generate seizures than those from healthy controls when assessed using the concept of brain network ictogenicity (BNI). Herein we tested whether the BNI framework is applicable to resting-state magnetoencephalography (MEG) from people with juvenile myoclonic epilepsy (JME). METHODS: The BNI framework consists in deriving a functional network from apparently normal brain activity, placing a mathematical model of ictogenicity into the network and then computing how often such network generates seizures in silico. We considered data from 26 people with JME and 26 healthy controls. RESULTS: We found that resting-state MEG functional networks from people with JME are characterized by a higher propensity to generate seizures (i.e., higher BNI) than those from healthy controls. We found a classification accuracy of 73%. CONCLUSIONS: The BNI framework is applicable to MEG and was capable of differentiating people with epilepsy from healthy controls. SIGNIFICANCE: The BNI framework may be applied to resting-state MEG to aid in epilepsy diagnosis. Elsevier 2021-04 /pmc/articles/PMC7992031/ /pubmed/33636607 http://dx.doi.org/10.1016/j.clinph.2020.12.021 Text en © 2021 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lopes, Marinho A. Krzemiński, Dominik Hamandi, Khalid Singh, Krish D. Masuda, Naoki Terry, John R. Zhang, Jiaxiang A computational biomarker of juvenile myoclonic epilepsy from resting-state MEG |
title | A computational biomarker of juvenile myoclonic epilepsy from resting-state MEG |
title_full | A computational biomarker of juvenile myoclonic epilepsy from resting-state MEG |
title_fullStr | A computational biomarker of juvenile myoclonic epilepsy from resting-state MEG |
title_full_unstemmed | A computational biomarker of juvenile myoclonic epilepsy from resting-state MEG |
title_short | A computational biomarker of juvenile myoclonic epilepsy from resting-state MEG |
title_sort | computational biomarker of juvenile myoclonic epilepsy from resting-state meg |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992031/ https://www.ncbi.nlm.nih.gov/pubmed/33636607 http://dx.doi.org/10.1016/j.clinph.2020.12.021 |
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