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Greatest rapid eye movement sleep atonia loss in men and older age

To determine quantitative REM sleep muscle tone in men and women without REM sleep behavior disorder, we quantitatively analyzed REM sleep phasic and tonic muscle activity, phasic muscle burst duration, and automated REM atonia index in submentalis and anterior tibialis muscles in 25 men and 25 wome...

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Autores principales: McCarter, Stuart J, St Louis, Erik K, Boeve, Bradley F, Sandness, David J, Silber, Michael H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241799/
https://www.ncbi.nlm.nih.gov/pubmed/25493286
http://dx.doi.org/10.1002/acn3.93
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author McCarter, Stuart J
St Louis, Erik K
Boeve, Bradley F
Sandness, David J
Silber, Michael H
author_facet McCarter, Stuart J
St Louis, Erik K
Boeve, Bradley F
Sandness, David J
Silber, Michael H
author_sort McCarter, Stuart J
collection PubMed
description To determine quantitative REM sleep muscle tone in men and women without REM sleep behavior disorder, we quantitatively analyzed REM sleep phasic and tonic muscle activity, phasic muscle burst duration, and automated REM atonia index in submentalis and anterior tibialis muscles in 25 men and 25 women without REM sleep behavior disorder. Men showed significantly higher anterior tibialis phasic muscle activity. Higher phasic muscle activity was independently associated with male sex and older age in multivariate analysis. Men and the elderly may be biologically predisposed to altered REM sleep muscle atonia control, and/or some may have occult neurodegenerative disease, possibly underlying the predominance of older men with REM sleep behavior disorder.
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spelling pubmed-42417992014-12-09 Greatest rapid eye movement sleep atonia loss in men and older age McCarter, Stuart J St Louis, Erik K Boeve, Bradley F Sandness, David J Silber, Michael H Ann Clin Transl Neurol Brief Communication To determine quantitative REM sleep muscle tone in men and women without REM sleep behavior disorder, we quantitatively analyzed REM sleep phasic and tonic muscle activity, phasic muscle burst duration, and automated REM atonia index in submentalis and anterior tibialis muscles in 25 men and 25 women without REM sleep behavior disorder. Men showed significantly higher anterior tibialis phasic muscle activity. Higher phasic muscle activity was independently associated with male sex and older age in multivariate analysis. Men and the elderly may be biologically predisposed to altered REM sleep muscle atonia control, and/or some may have occult neurodegenerative disease, possibly underlying the predominance of older men with REM sleep behavior disorder. BlackWell Publishing Ltd 2014-09 2014-09-02 /pmc/articles/PMC4241799/ /pubmed/25493286 http://dx.doi.org/10.1002/acn3.93 Text en © 2014 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Brief Communication
McCarter, Stuart J
St Louis, Erik K
Boeve, Bradley F
Sandness, David J
Silber, Michael H
Greatest rapid eye movement sleep atonia loss in men and older age
title Greatest rapid eye movement sleep atonia loss in men and older age
title_full Greatest rapid eye movement sleep atonia loss in men and older age
title_fullStr Greatest rapid eye movement sleep atonia loss in men and older age
title_full_unstemmed Greatest rapid eye movement sleep atonia loss in men and older age
title_short Greatest rapid eye movement sleep atonia loss in men and older age
title_sort greatest rapid eye movement sleep atonia loss in men and older age
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241799/
https://www.ncbi.nlm.nih.gov/pubmed/25493286
http://dx.doi.org/10.1002/acn3.93
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