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EEG functional network topology is associated with disability in patients with amyotrophic lateral sclerosis

Amyotrophic Lateral Sclerosis (ALS) is one of the most severe neurodegenerative diseases, which is known to affect upper and lower motor neurons. In contrast to the classical tenet that ALS represents the outcome of extensive and progressive impairment of a fixed set of motor connections, recent neu...

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Autores principales: Fraschini, Matteo, Demuru, Matteo, Hillebrand, Arjan, Cuccu, Lorenza, Porcu, Silvia, Di Stefano, Francesca, Puligheddu, Monica, Floris, Gianluca, Borghero, Giuseppe, Marrosu, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5141491/
https://www.ncbi.nlm.nih.gov/pubmed/27924954
http://dx.doi.org/10.1038/srep38653
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author Fraschini, Matteo
Demuru, Matteo
Hillebrand, Arjan
Cuccu, Lorenza
Porcu, Silvia
Di Stefano, Francesca
Puligheddu, Monica
Floris, Gianluca
Borghero, Giuseppe
Marrosu, Francesco
author_facet Fraschini, Matteo
Demuru, Matteo
Hillebrand, Arjan
Cuccu, Lorenza
Porcu, Silvia
Di Stefano, Francesca
Puligheddu, Monica
Floris, Gianluca
Borghero, Giuseppe
Marrosu, Francesco
author_sort Fraschini, Matteo
collection PubMed
description Amyotrophic Lateral Sclerosis (ALS) is one of the most severe neurodegenerative diseases, which is known to affect upper and lower motor neurons. In contrast to the classical tenet that ALS represents the outcome of extensive and progressive impairment of a fixed set of motor connections, recent neuroimaging findings suggest that the disease spreads along vast non-motor connections. Here, we hypothesised that functional network topology is perturbed in ALS, and that this reorganization is associated with disability. We tested this hypothesis in 21 patients affected by ALS at several stages of impairment using resting-state electroencephalography (EEG) and compared the results to 16 age-matched healthy controls. We estimated functional connectivity using the Phase Lag Index (PLI), and characterized the network topology using the minimum spanning tree (MST). We found a significant difference between groups in terms of MST dissimilarity and MST leaf fraction in the beta band. Moreover, some MST parameters (leaf, hierarchy and kappa) significantly correlated with disability. These findings suggest that the topology of resting-state functional networks in ALS is affected by the disease in relation to disability. EEG network analysis may be of help in monitoring and evaluating the clinical status of ALS patients.
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spelling pubmed-51414912016-12-16 EEG functional network topology is associated with disability in patients with amyotrophic lateral sclerosis Fraschini, Matteo Demuru, Matteo Hillebrand, Arjan Cuccu, Lorenza Porcu, Silvia Di Stefano, Francesca Puligheddu, Monica Floris, Gianluca Borghero, Giuseppe Marrosu, Francesco Sci Rep Article Amyotrophic Lateral Sclerosis (ALS) is one of the most severe neurodegenerative diseases, which is known to affect upper and lower motor neurons. In contrast to the classical tenet that ALS represents the outcome of extensive and progressive impairment of a fixed set of motor connections, recent neuroimaging findings suggest that the disease spreads along vast non-motor connections. Here, we hypothesised that functional network topology is perturbed in ALS, and that this reorganization is associated with disability. We tested this hypothesis in 21 patients affected by ALS at several stages of impairment using resting-state electroencephalography (EEG) and compared the results to 16 age-matched healthy controls. We estimated functional connectivity using the Phase Lag Index (PLI), and characterized the network topology using the minimum spanning tree (MST). We found a significant difference between groups in terms of MST dissimilarity and MST leaf fraction in the beta band. Moreover, some MST parameters (leaf, hierarchy and kappa) significantly correlated with disability. These findings suggest that the topology of resting-state functional networks in ALS is affected by the disease in relation to disability. EEG network analysis may be of help in monitoring and evaluating the clinical status of ALS patients. Nature Publishing Group 2016-12-07 /pmc/articles/PMC5141491/ /pubmed/27924954 http://dx.doi.org/10.1038/srep38653 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Fraschini, Matteo
Demuru, Matteo
Hillebrand, Arjan
Cuccu, Lorenza
Porcu, Silvia
Di Stefano, Francesca
Puligheddu, Monica
Floris, Gianluca
Borghero, Giuseppe
Marrosu, Francesco
EEG functional network topology is associated with disability in patients with amyotrophic lateral sclerosis
title EEG functional network topology is associated with disability in patients with amyotrophic lateral sclerosis
title_full EEG functional network topology is associated with disability in patients with amyotrophic lateral sclerosis
title_fullStr EEG functional network topology is associated with disability in patients with amyotrophic lateral sclerosis
title_full_unstemmed EEG functional network topology is associated with disability in patients with amyotrophic lateral sclerosis
title_short EEG functional network topology is associated with disability in patients with amyotrophic lateral sclerosis
title_sort eeg functional network topology is associated with disability in patients with amyotrophic lateral sclerosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5141491/
https://www.ncbi.nlm.nih.gov/pubmed/27924954
http://dx.doi.org/10.1038/srep38653
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