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Overnight Distribution of REM Sleep Features in People with Parkinson’s Disease (PD) and Non-PD Controls

BACKGROUND: Rapid eye movement (REM) sleep behavior disorder (RBD) is a leading predictor of Parkinson’s disease (PD). Diagnosis is performed in the sleep laboratory by detecting pathological REM sleep without atonia (RSWA). The evidence on the overnight distribution of RSWA% is conflicting. OBJECTI...

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Autores principales: Dagay, Andrew, Oz, Shani, Katzav, Shlomit, Wasserman, Danielle, Tauman, Riva, Thaler, Avner, Giladi, Nir, Mirelman, Anat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657693/
https://www.ncbi.nlm.nih.gov/pubmed/37807787
http://dx.doi.org/10.3233/JPD-230116
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author Dagay, Andrew
Oz, Shani
Katzav, Shlomit
Wasserman, Danielle
Tauman, Riva
Thaler, Avner
Giladi, Nir
Mirelman, Anat
author_facet Dagay, Andrew
Oz, Shani
Katzav, Shlomit
Wasserman, Danielle
Tauman, Riva
Thaler, Avner
Giladi, Nir
Mirelman, Anat
author_sort Dagay, Andrew
collection PubMed
description BACKGROUND: Rapid eye movement (REM) sleep behavior disorder (RBD) is a leading predictor of Parkinson’s disease (PD). Diagnosis is performed in the sleep laboratory by detecting pathological REM sleep without atonia (RSWA). The evidence on the overnight distribution of RSWA% is conflicting. OBJECTIVE: To investigate the temporal distribution of the number of ocular movements per REM sleep minute (REM density), and RSWA% in people with PD and non-PD controls. METHODS: All participants underwent a single overnight evaluation in a sleep laboratory. Clinical evaluation was performed on a separate day. REM density and RSWA% were compared between PD and controls both across four sleep periods and individual REM cycles. RESULTS: A total of 51 participants with recorded RSWA in polysomnography laboratory were included, 28 with PD aged 64±9 years with a disease duration of 3.3±2.9 years, and 23 controls aged 55±8 years. People with PD had lower REM density and higher RSWA% compared to controls. As expected, REM density was higher towards the morning. In contrast, RSWA% was equally distributed across the night, for both PD and controls. CONCLUSIONS: PD pathology affects REM sleep features, but not the overnight distribution of those features. While REM density increased towards the end of the night, RSWA% was equally distributed across the night for both PD and controls. Our findings have clinical implications for diagnosing RBD, as quantification of RSWA% in any sleep cycle is sufficient for reliably evaluating total RSWA% and reduced REM density may be a marker of PD.
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spelling pubmed-106576932023-11-19 Overnight Distribution of REM Sleep Features in People with Parkinson’s Disease (PD) and Non-PD Controls Dagay, Andrew Oz, Shani Katzav, Shlomit Wasserman, Danielle Tauman, Riva Thaler, Avner Giladi, Nir Mirelman, Anat J Parkinsons Dis Research Report BACKGROUND: Rapid eye movement (REM) sleep behavior disorder (RBD) is a leading predictor of Parkinson’s disease (PD). Diagnosis is performed in the sleep laboratory by detecting pathological REM sleep without atonia (RSWA). The evidence on the overnight distribution of RSWA% is conflicting. OBJECTIVE: To investigate the temporal distribution of the number of ocular movements per REM sleep minute (REM density), and RSWA% in people with PD and non-PD controls. METHODS: All participants underwent a single overnight evaluation in a sleep laboratory. Clinical evaluation was performed on a separate day. REM density and RSWA% were compared between PD and controls both across four sleep periods and individual REM cycles. RESULTS: A total of 51 participants with recorded RSWA in polysomnography laboratory were included, 28 with PD aged 64±9 years with a disease duration of 3.3±2.9 years, and 23 controls aged 55±8 years. People with PD had lower REM density and higher RSWA% compared to controls. As expected, REM density was higher towards the morning. In contrast, RSWA% was equally distributed across the night, for both PD and controls. CONCLUSIONS: PD pathology affects REM sleep features, but not the overnight distribution of those features. While REM density increased towards the end of the night, RSWA% was equally distributed across the night for both PD and controls. Our findings have clinical implications for diagnosing RBD, as quantification of RSWA% in any sleep cycle is sufficient for reliably evaluating total RSWA% and reduced REM density may be a marker of PD. IOS Press 2023-11-03 /pmc/articles/PMC10657693/ /pubmed/37807787 http://dx.doi.org/10.3233/JPD-230116 Text en © 2023 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Report
Dagay, Andrew
Oz, Shani
Katzav, Shlomit
Wasserman, Danielle
Tauman, Riva
Thaler, Avner
Giladi, Nir
Mirelman, Anat
Overnight Distribution of REM Sleep Features in People with Parkinson’s Disease (PD) and Non-PD Controls
title Overnight Distribution of REM Sleep Features in People with Parkinson’s Disease (PD) and Non-PD Controls
title_full Overnight Distribution of REM Sleep Features in People with Parkinson’s Disease (PD) and Non-PD Controls
title_fullStr Overnight Distribution of REM Sleep Features in People with Parkinson’s Disease (PD) and Non-PD Controls
title_full_unstemmed Overnight Distribution of REM Sleep Features in People with Parkinson’s Disease (PD) and Non-PD Controls
title_short Overnight Distribution of REM Sleep Features in People with Parkinson’s Disease (PD) and Non-PD Controls
title_sort overnight distribution of rem sleep features in people with parkinson’s disease (pd) and non-pd controls
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657693/
https://www.ncbi.nlm.nih.gov/pubmed/37807787
http://dx.doi.org/10.3233/JPD-230116
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