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Topography-specific spindle frequency changes in Obstructive Sleep Apnea
BACKGROUND: Sleep spindles, as detected on scalp electroencephalography (EEG), are considered to be markers of thalamo-cortical network integrity. Since obstructive sleep apnea (OSA) is a known cause of brain dysfunction, the aim of this study was to investigate sleep spindle frequency distribution...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496607/ https://www.ncbi.nlm.nih.gov/pubmed/22985414 http://dx.doi.org/10.1186/1471-2202-13-89 |
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author | V, Suzana Carvalho, Diego Z de Santa-Helena, Emerson L Lemke, Ney L Gerhardt, Günther J |
author_facet | V, Suzana Carvalho, Diego Z de Santa-Helena, Emerson L Lemke, Ney L Gerhardt, Günther J |
author_sort | V, Suzana |
collection | PubMed |
description | BACKGROUND: Sleep spindles, as detected on scalp electroencephalography (EEG), are considered to be markers of thalamo-cortical network integrity. Since obstructive sleep apnea (OSA) is a known cause of brain dysfunction, the aim of this study was to investigate sleep spindle frequency distribution in OSA. Seven non-OSA subjects and 21 patients with OSA (11 mild and 10 moderate) were studied. A matching pursuit procedure was used for automatic detection of fast (≥13Hz) and slow (<13Hz) spindles obtained from 30min samples of NREM sleep stage 2 taken from initial, middle and final night thirds (sections I, II and III) of frontal, central and parietal scalp regions. RESULTS: Compared to non-OSA subjects, Moderate OSA patients had higher central and parietal slow spindle percentage (SSP) in all night sections studied, and higher frontal SSP in sections II and III. As the night progressed, there was a reduction in central and parietal SSP, while frontal SSP remained high. Frontal slow spindle percentage in night section III predicted OSA with good accuracy, with OSA likelihood increased by 12.1%for every SSP unit increase (OR 1.121, 95% CI 1.013 - 1.239, p=0.027). CONCLUSIONS: These results are consistent with diffuse, predominantly frontal thalamo-cortical dysfunction during sleep in OSA, as more posterior brain regions appear to maintain some physiological spindle frequency modulation across the night. Displaying changes in an opposite direction to what is expected from the aging process itself, spindle frequency appears to be informative in OSA even with small sample sizes, and to represent a sensitive electrophysiological marker of brain dysfunction in OSA. |
format | Online Article Text |
id | pubmed-3496607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34966072012-11-19 Topography-specific spindle frequency changes in Obstructive Sleep Apnea V, Suzana Carvalho, Diego Z de Santa-Helena, Emerson L Lemke, Ney L Gerhardt, Günther J BMC Neurosci Research Article BACKGROUND: Sleep spindles, as detected on scalp electroencephalography (EEG), are considered to be markers of thalamo-cortical network integrity. Since obstructive sleep apnea (OSA) is a known cause of brain dysfunction, the aim of this study was to investigate sleep spindle frequency distribution in OSA. Seven non-OSA subjects and 21 patients with OSA (11 mild and 10 moderate) were studied. A matching pursuit procedure was used for automatic detection of fast (≥13Hz) and slow (<13Hz) spindles obtained from 30min samples of NREM sleep stage 2 taken from initial, middle and final night thirds (sections I, II and III) of frontal, central and parietal scalp regions. RESULTS: Compared to non-OSA subjects, Moderate OSA patients had higher central and parietal slow spindle percentage (SSP) in all night sections studied, and higher frontal SSP in sections II and III. As the night progressed, there was a reduction in central and parietal SSP, while frontal SSP remained high. Frontal slow spindle percentage in night section III predicted OSA with good accuracy, with OSA likelihood increased by 12.1%for every SSP unit increase (OR 1.121, 95% CI 1.013 - 1.239, p=0.027). CONCLUSIONS: These results are consistent with diffuse, predominantly frontal thalamo-cortical dysfunction during sleep in OSA, as more posterior brain regions appear to maintain some physiological spindle frequency modulation across the night. Displaying changes in an opposite direction to what is expected from the aging process itself, spindle frequency appears to be informative in OSA even with small sample sizes, and to represent a sensitive electrophysiological marker of brain dysfunction in OSA. BioMed Central 2012-07-31 /pmc/articles/PMC3496607/ /pubmed/22985414 http://dx.doi.org/10.1186/1471-2202-13-89 Text en Copyright ©2012 Schönwald et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article V, Suzana Carvalho, Diego Z de Santa-Helena, Emerson L Lemke, Ney L Gerhardt, Günther J Topography-specific spindle frequency changes in Obstructive Sleep Apnea |
title | Topography-specific spindle frequency changes in Obstructive Sleep Apnea |
title_full | Topography-specific spindle frequency changes in Obstructive Sleep Apnea |
title_fullStr | Topography-specific spindle frequency changes in Obstructive Sleep Apnea |
title_full_unstemmed | Topography-specific spindle frequency changes in Obstructive Sleep Apnea |
title_short | Topography-specific spindle frequency changes in Obstructive Sleep Apnea |
title_sort | topography-specific spindle frequency changes in obstructive sleep apnea |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496607/ https://www.ncbi.nlm.nih.gov/pubmed/22985414 http://dx.doi.org/10.1186/1471-2202-13-89 |
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