Cargando…

Physiological and pathological high-frequency oscillations have distinct sleep-homeostatic properties

OBJECTIVE: The stage of sleep is a known modulator of high-frequency oscillations (HFOs). For instance, high amplitude slow waves during NREM sleep and the subtypes of REM sleep were shown to contribute to a better separation between physiological and pathological HFOs. This study investigated rates...

Descripción completa

Detalles Bibliográficos
Autores principales: von Ellenrieder, Nicolás, Dubeau, François, Gotman, Jean, Frauscher, Birgit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349616/
https://www.ncbi.nlm.nih.gov/pubmed/28337411
http://dx.doi.org/10.1016/j.nicl.2017.02.018
_version_ 1782514509187907584
author von Ellenrieder, Nicolás
Dubeau, François
Gotman, Jean
Frauscher, Birgit
author_facet von Ellenrieder, Nicolás
Dubeau, François
Gotman, Jean
Frauscher, Birgit
author_sort von Ellenrieder, Nicolás
collection PubMed
description OBJECTIVE: The stage of sleep is a known modulator of high-frequency oscillations (HFOs). For instance, high amplitude slow waves during NREM sleep and the subtypes of REM sleep were shown to contribute to a better separation between physiological and pathological HFOs. This study investigated rates and spatial spread of the different HFO types (physiological and pathological ripples in the 80–250 Hz frequency band, and fast ripples above 250 Hz) depending on time spent in sleep across the different sleep cycles. METHODS: Fifteen patients with focal pharmaco-resistant epilepsy underwent one night of video-polysomnography during chronic intracranial EEG recording for presurgical epilepsy evaluation. The HFO rate and spread across the different sleep cycles were determined with an automatic HFO detector. We built models to explain the observed rate and spread based on time in sleep and other variables i.e. sleep stage, delta band and sigma band activity, and slow wave amplitude. Statistical significance of the different variables was determined by a model comparison using the Akaike information criterion. RESULTS: The rate of HFOs depends significantly on the accumulated time of sleep. As the night advanced, the rate of pathological ripples and fast ripples decreased during NREM sleep (up to 15% per hour spent in the respective sleep stages), while the rate of physiological ripples increased during REM sleep (8% per hour spent in REM sleep). Interestingly, the stage of sleep but not the sleep cycle determined the extent of spread of HFOs, showing a larger field during NREM sleep and a more restricted field during REM sleep. CONCLUSION: The different dependence with sleep time for physiological and pathological ripples is in keeping with their distinct underlying generating mechanisms. From a practical point of view, the first sleep cycle seems to be best suitable for studying HFOs in epilepsy, given that the contrast between physiological and pathological ripple rates is largest during this time.
format Online
Article
Text
id pubmed-5349616
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-53496162017-03-23 Physiological and pathological high-frequency oscillations have distinct sleep-homeostatic properties von Ellenrieder, Nicolás Dubeau, François Gotman, Jean Frauscher, Birgit Neuroimage Clin Regular Article OBJECTIVE: The stage of sleep is a known modulator of high-frequency oscillations (HFOs). For instance, high amplitude slow waves during NREM sleep and the subtypes of REM sleep were shown to contribute to a better separation between physiological and pathological HFOs. This study investigated rates and spatial spread of the different HFO types (physiological and pathological ripples in the 80–250 Hz frequency band, and fast ripples above 250 Hz) depending on time spent in sleep across the different sleep cycles. METHODS: Fifteen patients with focal pharmaco-resistant epilepsy underwent one night of video-polysomnography during chronic intracranial EEG recording for presurgical epilepsy evaluation. The HFO rate and spread across the different sleep cycles were determined with an automatic HFO detector. We built models to explain the observed rate and spread based on time in sleep and other variables i.e. sleep stage, delta band and sigma band activity, and slow wave amplitude. Statistical significance of the different variables was determined by a model comparison using the Akaike information criterion. RESULTS: The rate of HFOs depends significantly on the accumulated time of sleep. As the night advanced, the rate of pathological ripples and fast ripples decreased during NREM sleep (up to 15% per hour spent in the respective sleep stages), while the rate of physiological ripples increased during REM sleep (8% per hour spent in REM sleep). Interestingly, the stage of sleep but not the sleep cycle determined the extent of spread of HFOs, showing a larger field during NREM sleep and a more restricted field during REM sleep. CONCLUSION: The different dependence with sleep time for physiological and pathological ripples is in keeping with their distinct underlying generating mechanisms. From a practical point of view, the first sleep cycle seems to be best suitable for studying HFOs in epilepsy, given that the contrast between physiological and pathological ripple rates is largest during this time. Elsevier 2017-02-24 /pmc/articles/PMC5349616/ /pubmed/28337411 http://dx.doi.org/10.1016/j.nicl.2017.02.018 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
von Ellenrieder, Nicolás
Dubeau, François
Gotman, Jean
Frauscher, Birgit
Physiological and pathological high-frequency oscillations have distinct sleep-homeostatic properties
title Physiological and pathological high-frequency oscillations have distinct sleep-homeostatic properties
title_full Physiological and pathological high-frequency oscillations have distinct sleep-homeostatic properties
title_fullStr Physiological and pathological high-frequency oscillations have distinct sleep-homeostatic properties
title_full_unstemmed Physiological and pathological high-frequency oscillations have distinct sleep-homeostatic properties
title_short Physiological and pathological high-frequency oscillations have distinct sleep-homeostatic properties
title_sort physiological and pathological high-frequency oscillations have distinct sleep-homeostatic properties
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349616/
https://www.ncbi.nlm.nih.gov/pubmed/28337411
http://dx.doi.org/10.1016/j.nicl.2017.02.018
work_keys_str_mv AT vonellenriedernicolas physiologicalandpathologicalhighfrequencyoscillationshavedistinctsleephomeostaticproperties
AT dubeaufrancois physiologicalandpathologicalhighfrequencyoscillationshavedistinctsleephomeostaticproperties
AT gotmanjean physiologicalandpathologicalhighfrequencyoscillationshavedistinctsleephomeostaticproperties
AT frauscherbirgit physiologicalandpathologicalhighfrequencyoscillationshavedistinctsleephomeostaticproperties