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Olfactory function deteriorates in patients with Parkinson's disease complicated with REM sleep behavior disorder

INTRODUCTION: It is not concluded whether the association between olfactory dysfunction and REM sleep behavior disorder (RBD) were worsen cognitive function in patients with Parkinson's disease (PD). We sought to evaluate the impact of these symptoms in PD. METHODS: We examined 62 patients with...

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Autores principales: Nomura, Takashi, Nomura, Yuki, Oguri, Masayoshi, Hirooka, Yasuaki, Hanajima, Ritsuko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417891/
https://www.ncbi.nlm.nih.gov/pubmed/32802972
http://dx.doi.org/10.1016/j.ensci.2020.100261
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author Nomura, Takashi
Nomura, Yuki
Oguri, Masayoshi
Hirooka, Yasuaki
Hanajima, Ritsuko
author_facet Nomura, Takashi
Nomura, Yuki
Oguri, Masayoshi
Hirooka, Yasuaki
Hanajima, Ritsuko
author_sort Nomura, Takashi
collection PubMed
description INTRODUCTION: It is not concluded whether the association between olfactory dysfunction and REM sleep behavior disorder (RBD) were worsen cognitive function in patients with Parkinson's disease (PD). We sought to evaluate the impact of these symptoms in PD. METHODS: We examined 62 patients with PD using an olfactory test (Odor Stick Identification Test for Japanese: OSIT-J) and polysomnography (PSG). We divided the patients into 3 groups: PD with clinical RBD (n = 32), PD with subclinical RBD (n = 11), and PD with normal REM sleep (n = 19). We compared their clinical backgrounds, results of OSIT-J, autonomic functions, and cognitive functions such as Montreal cognitive assessment Japanese version (MoCA-J). Some factors associated with RBD were analyzed by multiple regression. RESULTS: There were significant differences in the results of OSIT-J, and autonomic and cognitive functions between the 3 groups. There were significant differences in the total OSIT-J score between the 3 groups (PD with clinical RBD: 3.3 ± 2.2, PD with subclinical RBD: 4.0 ± 2.6, PD with normal REM sleep: 6.7 ± 3.0, p < 0.001). Patients in the group with PD with clinical RBD had a significantly lower score than those with normal REM sleep (p < 0.001). Logistic regression analysis showed that OSIT-J score was significantly associated with RBD. The PD group with clinical RBD had more patients with mild cognitive impairment than the group with normal REM sleep. Multiple regression analysis revealed that olfactory dysfunction was correlated with MoCA-J. CONCLUSIONS: Olfactory dysfunction is associated with RBD. Especially, it is important to screen olfactory function in RBD complicated patients with PD in view of cognitive impairment.
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spelling pubmed-74178912020-08-14 Olfactory function deteriorates in patients with Parkinson's disease complicated with REM sleep behavior disorder Nomura, Takashi Nomura, Yuki Oguri, Masayoshi Hirooka, Yasuaki Hanajima, Ritsuko eNeurologicalSci Original Article INTRODUCTION: It is not concluded whether the association between olfactory dysfunction and REM sleep behavior disorder (RBD) were worsen cognitive function in patients with Parkinson's disease (PD). We sought to evaluate the impact of these symptoms in PD. METHODS: We examined 62 patients with PD using an olfactory test (Odor Stick Identification Test for Japanese: OSIT-J) and polysomnography (PSG). We divided the patients into 3 groups: PD with clinical RBD (n = 32), PD with subclinical RBD (n = 11), and PD with normal REM sleep (n = 19). We compared their clinical backgrounds, results of OSIT-J, autonomic functions, and cognitive functions such as Montreal cognitive assessment Japanese version (MoCA-J). Some factors associated with RBD were analyzed by multiple regression. RESULTS: There were significant differences in the results of OSIT-J, and autonomic and cognitive functions between the 3 groups. There were significant differences in the total OSIT-J score between the 3 groups (PD with clinical RBD: 3.3 ± 2.2, PD with subclinical RBD: 4.0 ± 2.6, PD with normal REM sleep: 6.7 ± 3.0, p < 0.001). Patients in the group with PD with clinical RBD had a significantly lower score than those with normal REM sleep (p < 0.001). Logistic regression analysis showed that OSIT-J score was significantly associated with RBD. The PD group with clinical RBD had more patients with mild cognitive impairment than the group with normal REM sleep. Multiple regression analysis revealed that olfactory dysfunction was correlated with MoCA-J. CONCLUSIONS: Olfactory dysfunction is associated with RBD. Especially, it is important to screen olfactory function in RBD complicated patients with PD in view of cognitive impairment. Elsevier 2020-08-03 /pmc/articles/PMC7417891/ /pubmed/32802972 http://dx.doi.org/10.1016/j.ensci.2020.100261 Text en © 2020 Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Nomura, Takashi
Nomura, Yuki
Oguri, Masayoshi
Hirooka, Yasuaki
Hanajima, Ritsuko
Olfactory function deteriorates in patients with Parkinson's disease complicated with REM sleep behavior disorder
title Olfactory function deteriorates in patients with Parkinson's disease complicated with REM sleep behavior disorder
title_full Olfactory function deteriorates in patients with Parkinson's disease complicated with REM sleep behavior disorder
title_fullStr Olfactory function deteriorates in patients with Parkinson's disease complicated with REM sleep behavior disorder
title_full_unstemmed Olfactory function deteriorates in patients with Parkinson's disease complicated with REM sleep behavior disorder
title_short Olfactory function deteriorates in patients with Parkinson's disease complicated with REM sleep behavior disorder
title_sort olfactory function deteriorates in patients with parkinson's disease complicated with rem sleep behavior disorder
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417891/
https://www.ncbi.nlm.nih.gov/pubmed/32802972
http://dx.doi.org/10.1016/j.ensci.2020.100261
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