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High-density electroencephalographic recordings during sleep in children with disorders of consciousness

INTRODUCTION: A large number of studies have investigated neural correlates of consciousness in adults. However, knowledge about brain function in children with disorders of consciousness (DOC) is very limited. We suggest that EEG recordings during sleep are a promising approach. In healthy adults a...

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Autores principales: Mouthon, Anne-Laure, van Hedel, Hubertus J.A., Meyer-Heim, Andreas, Kurth, Salome, Ringli, Maya, Pugin, Fiona, Huber, Reto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827803/
https://www.ncbi.nlm.nih.gov/pubmed/27104141
http://dx.doi.org/10.1016/j.nicl.2016.03.012
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author Mouthon, Anne-Laure
van Hedel, Hubertus J.A.
Meyer-Heim, Andreas
Kurth, Salome
Ringli, Maya
Pugin, Fiona
Huber, Reto
author_facet Mouthon, Anne-Laure
van Hedel, Hubertus J.A.
Meyer-Heim, Andreas
Kurth, Salome
Ringli, Maya
Pugin, Fiona
Huber, Reto
author_sort Mouthon, Anne-Laure
collection PubMed
description INTRODUCTION: A large number of studies have investigated neural correlates of consciousness in adults. However, knowledge about brain function in children with disorders of consciousness (DOC) is very limited. We suggest that EEG recordings during sleep are a promising approach. In healthy adults as well as in children, it has been shown that the activity of sleep slow waves (EEG spectral power 1–4.5 Hz), the primary characteristic of deep sleep, is dependent on use during previous wakefulness. Thus the regulation of slow wave activity (SWA) provides indirect insights into brain function during wakefulness. METHODS: In the present study, we investigated high-density EEG recordings during sleep in ten healthy children and in ten children with acquired brain injury, including five children with DOC and five children with acquired brain injury without DOC. We used the build-up of SWA to quantify SWA regulation. RESULTS: Children with DOC showed a global reduction in the SWA build-up when compared to both, healthy children and children with acquired brain injury without DOC. This reduction was most pronounced over parietal brain areas. Comparisons within the group of children with DOC revealed that the parietal SWA build-up was the lowest in patients showing poor outcome. Longitudinal measurements during the recovery period showed an increase in parietal SWA build-up from the first to the second sleep recording. CONCLUSIONS: Our results suggest that the reduced parietal SWA regulation may represent a characteristic topographical marker for brain network dysfunction in children with DOC. In the future, the regulation of SWA might be used as a complementary assessment in adult and paediatric patients with DOC.
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spelling pubmed-48278032016-04-21 High-density electroencephalographic recordings during sleep in children with disorders of consciousness Mouthon, Anne-Laure van Hedel, Hubertus J.A. Meyer-Heim, Andreas Kurth, Salome Ringli, Maya Pugin, Fiona Huber, Reto Neuroimage Clin Regular Article INTRODUCTION: A large number of studies have investigated neural correlates of consciousness in adults. However, knowledge about brain function in children with disorders of consciousness (DOC) is very limited. We suggest that EEG recordings during sleep are a promising approach. In healthy adults as well as in children, it has been shown that the activity of sleep slow waves (EEG spectral power 1–4.5 Hz), the primary characteristic of deep sleep, is dependent on use during previous wakefulness. Thus the regulation of slow wave activity (SWA) provides indirect insights into brain function during wakefulness. METHODS: In the present study, we investigated high-density EEG recordings during sleep in ten healthy children and in ten children with acquired brain injury, including five children with DOC and five children with acquired brain injury without DOC. We used the build-up of SWA to quantify SWA regulation. RESULTS: Children with DOC showed a global reduction in the SWA build-up when compared to both, healthy children and children with acquired brain injury without DOC. This reduction was most pronounced over parietal brain areas. Comparisons within the group of children with DOC revealed that the parietal SWA build-up was the lowest in patients showing poor outcome. Longitudinal measurements during the recovery period showed an increase in parietal SWA build-up from the first to the second sleep recording. CONCLUSIONS: Our results suggest that the reduced parietal SWA regulation may represent a characteristic topographical marker for brain network dysfunction in children with DOC. In the future, the regulation of SWA might be used as a complementary assessment in adult and paediatric patients with DOC. Elsevier 2016-03-19 /pmc/articles/PMC4827803/ /pubmed/27104141 http://dx.doi.org/10.1016/j.nicl.2016.03.012 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Mouthon, Anne-Laure
van Hedel, Hubertus J.A.
Meyer-Heim, Andreas
Kurth, Salome
Ringli, Maya
Pugin, Fiona
Huber, Reto
High-density electroencephalographic recordings during sleep in children with disorders of consciousness
title High-density electroencephalographic recordings during sleep in children with disorders of consciousness
title_full High-density electroencephalographic recordings during sleep in children with disorders of consciousness
title_fullStr High-density electroencephalographic recordings during sleep in children with disorders of consciousness
title_full_unstemmed High-density electroencephalographic recordings during sleep in children with disorders of consciousness
title_short High-density electroencephalographic recordings during sleep in children with disorders of consciousness
title_sort high-density electroencephalographic recordings during sleep in children with disorders of consciousness
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827803/
https://www.ncbi.nlm.nih.gov/pubmed/27104141
http://dx.doi.org/10.1016/j.nicl.2016.03.012
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