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Non-invasive, multimodal analysis of cortical activity, blood volume and neurovascular coupling in infantile spasms using EEG-fNIRS monitoring

Although infantile spasms can be caused by a variety of etiologies, the clinical features are stereotypical. The neuronal and vascular mechanisms that contribute to the emergence of infantile spasms are not well understood. We performed a multimodal study by simultaneously recording electroencephalo...

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Autores principales: Bourel-Ponchel, Emilie, Mahmoudzadeh, Mahdi, Delignières, Aline, Berquin, Patrick, Wallois, Fabrice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5447509/
https://www.ncbi.nlm.nih.gov/pubmed/28580292
http://dx.doi.org/10.1016/j.nicl.2017.05.004
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author Bourel-Ponchel, Emilie
Mahmoudzadeh, Mahdi
Delignières, Aline
Berquin, Patrick
Wallois, Fabrice
author_facet Bourel-Ponchel, Emilie
Mahmoudzadeh, Mahdi
Delignières, Aline
Berquin, Patrick
Wallois, Fabrice
author_sort Bourel-Ponchel, Emilie
collection PubMed
description Although infantile spasms can be caused by a variety of etiologies, the clinical features are stereotypical. The neuronal and vascular mechanisms that contribute to the emergence of infantile spasms are not well understood. We performed a multimodal study by simultaneously recording electroencephalogram and functional Near-infrared spectroscopy in an intentionally heterogeneous population of six children with spasms in clusters. Regardless of the etiology, spasms were accompanied by two phases of hemodynamic changes; an initial change in the cerebral blood volume (simultaneously with each spasm) followed by a neurovascular coupling in all children except for the one with a large porencephalic cyst. Changes in cerebral blood volume, like the neurovascular coupling, occurred over frontal areas in all patients regardless of any brain damage suggesting a diffuse hemodynamic cortical response. The simultaneous motor activation and changes in cerebral blood volume might result from the involvement of the brainstem. The inconstant neurovascular coupling phase suggests a diffuse activation of the brain likely resulting too from the brainstem involvement that might trigger diffuse changes in cortical excitability.
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spelling pubmed-54475092017-06-02 Non-invasive, multimodal analysis of cortical activity, blood volume and neurovascular coupling in infantile spasms using EEG-fNIRS monitoring Bourel-Ponchel, Emilie Mahmoudzadeh, Mahdi Delignières, Aline Berquin, Patrick Wallois, Fabrice Neuroimage Clin Regular Article Although infantile spasms can be caused by a variety of etiologies, the clinical features are stereotypical. The neuronal and vascular mechanisms that contribute to the emergence of infantile spasms are not well understood. We performed a multimodal study by simultaneously recording electroencephalogram and functional Near-infrared spectroscopy in an intentionally heterogeneous population of six children with spasms in clusters. Regardless of the etiology, spasms were accompanied by two phases of hemodynamic changes; an initial change in the cerebral blood volume (simultaneously with each spasm) followed by a neurovascular coupling in all children except for the one with a large porencephalic cyst. Changes in cerebral blood volume, like the neurovascular coupling, occurred over frontal areas in all patients regardless of any brain damage suggesting a diffuse hemodynamic cortical response. The simultaneous motor activation and changes in cerebral blood volume might result from the involvement of the brainstem. The inconstant neurovascular coupling phase suggests a diffuse activation of the brain likely resulting too from the brainstem involvement that might trigger diffuse changes in cortical excitability. Elsevier 2017-05-13 /pmc/articles/PMC5447509/ /pubmed/28580292 http://dx.doi.org/10.1016/j.nicl.2017.05.004 Text en © 2017 The Authors 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 Regular Article
Bourel-Ponchel, Emilie
Mahmoudzadeh, Mahdi
Delignières, Aline
Berquin, Patrick
Wallois, Fabrice
Non-invasive, multimodal analysis of cortical activity, blood volume and neurovascular coupling in infantile spasms using EEG-fNIRS monitoring
title Non-invasive, multimodal analysis of cortical activity, blood volume and neurovascular coupling in infantile spasms using EEG-fNIRS monitoring
title_full Non-invasive, multimodal analysis of cortical activity, blood volume and neurovascular coupling in infantile spasms using EEG-fNIRS monitoring
title_fullStr Non-invasive, multimodal analysis of cortical activity, blood volume and neurovascular coupling in infantile spasms using EEG-fNIRS monitoring
title_full_unstemmed Non-invasive, multimodal analysis of cortical activity, blood volume and neurovascular coupling in infantile spasms using EEG-fNIRS monitoring
title_short Non-invasive, multimodal analysis of cortical activity, blood volume and neurovascular coupling in infantile spasms using EEG-fNIRS monitoring
title_sort non-invasive, multimodal analysis of cortical activity, blood volume and neurovascular coupling in infantile spasms using eeg-fnirs monitoring
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5447509/
https://www.ncbi.nlm.nih.gov/pubmed/28580292
http://dx.doi.org/10.1016/j.nicl.2017.05.004
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