Case control polysomnographic studies of sleep disorders in Parkinson's disease.

BACKGROUND: The relationship between a number of primary sleep disorders and Parkinson's disease (PD) is still debated. There are limited case control polysomnographic studies in PD and most of these study sample sizes are small. METHODOLOGY/FINDINGS: We conducted one of the largest case-contro...

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Main Authors: Ming-Hui Yong, Stephanie Fook-Chong, Ratnagopal Pavanni, Li-Ling Lim, Eng-King Tan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3142152?pdf=render
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author Ming-Hui Yong
Stephanie Fook-Chong
Ratnagopal Pavanni
Li-Ling Lim
Eng-King Tan
author_facet Ming-Hui Yong
Stephanie Fook-Chong
Ratnagopal Pavanni
Li-Ling Lim
Eng-King Tan
author_sort Ming-Hui Yong
collection DOAJ
description BACKGROUND: The relationship between a number of primary sleep disorders and Parkinson's disease (PD) is still debated. There are limited case control polysomnographic studies in PD and most of these study sample sizes are small. METHODOLOGY/FINDINGS: We conducted one of the largest case-control studies involving overnight polysomnographic evaluation, with prospective recruitment of unselected Parkinson's disease patients and healthy controls from an Asian population. The cases were recruited from the specialized movement disorder outpatient clinics in a tertiary referral center, and controls from the same geographical locations. All subjects underwent an overnight polysomnographic study and a multiple sleep latency test. A total of 124 subjects including 56 patients and 68 controls frequency-matched for age and sex were included. Multivariate analysis revealed that patients had significantly shorter total sleep time than controls (p = 0.01), lower sleep efficiency (p = 0.001) and increased REM latency (p = 0.007). In patients, multivariate analysis showed that reduced total sleep time was significantly associated with increased age (p = 0.001) and increased levodopa dose (p = 0.032). The mean Insomnia Severity Index was higher in PD patients (9.0±7.1) compared to controls (3.3±3.9, p<0.001). The mean Epworth Sleepiness Scale score was higher in PD patients (9.3±5.9 vs. 5.7±4.8, p<0.001). Nocturnal arousals, obstructive sleep apnea, periodic leg movements and objective abnormal sleepiness were not increased in our patients. CONCLUSIONS/SIGNIFICANCE: Our case-control polysomnographic study, the first-ever performed in an Asian population, revealed altered sleep architecture and reduced sleep in PD patients compared to controls. Reduced total sleep time was associated with increased age and levodopa dose. However, nocturnal arousals, primary sleep disorders and abnormal sleepiness were not increased in our PD patients suggesting that ethnic/genetic differences may be a factor in the pathophysiology of these conditions.
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spelling doaj.art-8dfaa52a6a424551a19e71d1a95930bf2022-12-21T23:16:03ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0167e2251110.1371/journal.pone.0022511Case control polysomnographic studies of sleep disorders in Parkinson's disease.Ming-Hui YongStephanie Fook-ChongRatnagopal PavanniLi-Ling LimEng-King TanBACKGROUND: The relationship between a number of primary sleep disorders and Parkinson's disease (PD) is still debated. There are limited case control polysomnographic studies in PD and most of these study sample sizes are small. METHODOLOGY/FINDINGS: We conducted one of the largest case-control studies involving overnight polysomnographic evaluation, with prospective recruitment of unselected Parkinson's disease patients and healthy controls from an Asian population. The cases were recruited from the specialized movement disorder outpatient clinics in a tertiary referral center, and controls from the same geographical locations. All subjects underwent an overnight polysomnographic study and a multiple sleep latency test. A total of 124 subjects including 56 patients and 68 controls frequency-matched for age and sex were included. Multivariate analysis revealed that patients had significantly shorter total sleep time than controls (p = 0.01), lower sleep efficiency (p = 0.001) and increased REM latency (p = 0.007). In patients, multivariate analysis showed that reduced total sleep time was significantly associated with increased age (p = 0.001) and increased levodopa dose (p = 0.032). The mean Insomnia Severity Index was higher in PD patients (9.0±7.1) compared to controls (3.3±3.9, p<0.001). The mean Epworth Sleepiness Scale score was higher in PD patients (9.3±5.9 vs. 5.7±4.8, p<0.001). Nocturnal arousals, obstructive sleep apnea, periodic leg movements and objective abnormal sleepiness were not increased in our patients. CONCLUSIONS/SIGNIFICANCE: Our case-control polysomnographic study, the first-ever performed in an Asian population, revealed altered sleep architecture and reduced sleep in PD patients compared to controls. Reduced total sleep time was associated with increased age and levodopa dose. However, nocturnal arousals, primary sleep disorders and abnormal sleepiness were not increased in our PD patients suggesting that ethnic/genetic differences may be a factor in the pathophysiology of these conditions.http://europepmc.org/articles/PMC3142152?pdf=render
spellingShingle Ming-Hui Yong
Stephanie Fook-Chong
Ratnagopal Pavanni
Li-Ling Lim
Eng-King Tan
Case control polysomnographic studies of sleep disorders in Parkinson's disease.
PLoS ONE
title Case control polysomnographic studies of sleep disorders in Parkinson's disease.
title_full Case control polysomnographic studies of sleep disorders in Parkinson's disease.
title_fullStr Case control polysomnographic studies of sleep disorders in Parkinson's disease.
title_full_unstemmed Case control polysomnographic studies of sleep disorders in Parkinson's disease.
title_short Case control polysomnographic studies of sleep disorders in Parkinson's disease.
title_sort case control polysomnographic studies of sleep disorders in parkinson s disease
url http://europepmc.org/articles/PMC3142152?pdf=render
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