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Daytime sleepiness in Japanese patients with multiple system atrophy: prevalence and determinants

BACKGROUND: The recent SLEEMSA study that evaluated excessive daytime sleepiness (EDS) in Caucasian patients with multiple system atrophy (MSA) demonstrated that EDS was more frequent in patients (28%) than in healthy subjects (2%). However, the prevalence and determinants of EDS in other ethnic pop...

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Autores principales: Shimohata, Takayoshi, Nakayama, Hideaki, Tomita, Masahiko, Ozawa, Tetsutaro, Nishizawa, Masatoyo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3517378/
https://www.ncbi.nlm.nih.gov/pubmed/23116490
http://dx.doi.org/10.1186/1471-2377-12-130
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author Shimohata, Takayoshi
Nakayama, Hideaki
Tomita, Masahiko
Ozawa, Tetsutaro
Nishizawa, Masatoyo
author_facet Shimohata, Takayoshi
Nakayama, Hideaki
Tomita, Masahiko
Ozawa, Tetsutaro
Nishizawa, Masatoyo
author_sort Shimohata, Takayoshi
collection PubMed
description BACKGROUND: The recent SLEEMSA study that evaluated excessive daytime sleepiness (EDS) in Caucasian patients with multiple system atrophy (MSA) demonstrated that EDS was more frequent in patients (28%) than in healthy subjects (2%). However, the prevalence and determinants of EDS in other ethnic populations have not been reported to date. METHODS: We performed a single-hospital prospective study on patients with probable MSA. To ascertain the prevalence and determinants of EDS in Japanese MSA patients, we assessed the patients’ degree of daytime sleepiness by using the Japanese version of the Epworth Sleepiness Scale (ESS). In addition, we investigated the effects of sleep-disordered breathing (SDB) and abnormal periodic leg movements in sleep (PLMS), which were measured by polysomnography, on the patients’ ESS scores. RESULTS: A total of 25 patients with probable MSA (21 patients with cerebellar MSA and 4 patients with parkinsonian MSA) were included in this study. All patients underwent standard polysomnography. The mean ESS score was 6.2 ± 0.9, and EDS was identified in 24% of the patients. SDB and abnormal PLMS were identified in 24 (96%) and 11 (44%) patients, respectively. The prevalences of EDS in patients with SDB and abnormal PLMS were 25% and 18%, respectively. No correlations were observed between ESS scores and the parameters of SDB or abnormal PLMS. CONCLUSIONS: The frequency of EDS in Japanese patients with MSA was similar to that in Caucasian MSA patients. SDB and abnormal PLMS were frequently observed in MSA patients, although the severities of these factors were not correlated with EDS. Further investigations using objective sleep tests need to be performed.
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spelling pubmed-35173782012-12-08 Daytime sleepiness in Japanese patients with multiple system atrophy: prevalence and determinants Shimohata, Takayoshi Nakayama, Hideaki Tomita, Masahiko Ozawa, Tetsutaro Nishizawa, Masatoyo BMC Neurol Research Article BACKGROUND: The recent SLEEMSA study that evaluated excessive daytime sleepiness (EDS) in Caucasian patients with multiple system atrophy (MSA) demonstrated that EDS was more frequent in patients (28%) than in healthy subjects (2%). However, the prevalence and determinants of EDS in other ethnic populations have not been reported to date. METHODS: We performed a single-hospital prospective study on patients with probable MSA. To ascertain the prevalence and determinants of EDS in Japanese MSA patients, we assessed the patients’ degree of daytime sleepiness by using the Japanese version of the Epworth Sleepiness Scale (ESS). In addition, we investigated the effects of sleep-disordered breathing (SDB) and abnormal periodic leg movements in sleep (PLMS), which were measured by polysomnography, on the patients’ ESS scores. RESULTS: A total of 25 patients with probable MSA (21 patients with cerebellar MSA and 4 patients with parkinsonian MSA) were included in this study. All patients underwent standard polysomnography. The mean ESS score was 6.2 ± 0.9, and EDS was identified in 24% of the patients. SDB and abnormal PLMS were identified in 24 (96%) and 11 (44%) patients, respectively. The prevalences of EDS in patients with SDB and abnormal PLMS were 25% and 18%, respectively. No correlations were observed between ESS scores and the parameters of SDB or abnormal PLMS. CONCLUSIONS: The frequency of EDS in Japanese patients with MSA was similar to that in Caucasian MSA patients. SDB and abnormal PLMS were frequently observed in MSA patients, although the severities of these factors were not correlated with EDS. Further investigations using objective sleep tests need to be performed. BioMed Central 2012-11-01 /pmc/articles/PMC3517378/ /pubmed/23116490 http://dx.doi.org/10.1186/1471-2377-12-130 Text en Copyright ©2012 Shimohata 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
Shimohata, Takayoshi
Nakayama, Hideaki
Tomita, Masahiko
Ozawa, Tetsutaro
Nishizawa, Masatoyo
Daytime sleepiness in Japanese patients with multiple system atrophy: prevalence and determinants
title Daytime sleepiness in Japanese patients with multiple system atrophy: prevalence and determinants
title_full Daytime sleepiness in Japanese patients with multiple system atrophy: prevalence and determinants
title_fullStr Daytime sleepiness in Japanese patients with multiple system atrophy: prevalence and determinants
title_full_unstemmed Daytime sleepiness in Japanese patients with multiple system atrophy: prevalence and determinants
title_short Daytime sleepiness in Japanese patients with multiple system atrophy: prevalence and determinants
title_sort daytime sleepiness in japanese patients with multiple system atrophy: prevalence and determinants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3517378/
https://www.ncbi.nlm.nih.gov/pubmed/23116490
http://dx.doi.org/10.1186/1471-2377-12-130
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