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Parkinson's Disease with Fatigue: Clinical Characteristics and Potential Mechanisms Relevant to α-Synuclein Oligomer

BACKGROUND AND PURPOSE: The aim of this study was to identify the clinical characteristics and potential mechanisms relevant to pathological proteins in Parkinson's disease (PD) patients who experience fatigue. METHODS: PD patients (n=102) were evaluated using a fatigue severity scale and scale...

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Autores principales: Zuo, Li-Jun, Yu, Shu-Yang, Wang, Fang, Hu, Yang, Piao, Ying-Shan, Du, Yang, Lian, Teng-Hong, Wang, Rui-Dan, Yu, Qiu-Jin, Wang, Ya-Jie, Wang, Xiao-Min, Chan, Piu, Chen, Sheng-Di, Wang, Yongjun, Zhang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828563/
https://www.ncbi.nlm.nih.gov/pubmed/26869370
http://dx.doi.org/10.3988/jcn.2016.12.2.172
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author Zuo, Li-Jun
Yu, Shu-Yang
Wang, Fang
Hu, Yang
Piao, Ying-Shan
Du, Yang
Lian, Teng-Hong
Wang, Rui-Dan
Yu, Qiu-Jin
Wang, Ya-Jie
Wang, Xiao-Min
Chan, Piu
Chen, Sheng-Di
Wang, Yongjun
Zhang, Wei
author_facet Zuo, Li-Jun
Yu, Shu-Yang
Wang, Fang
Hu, Yang
Piao, Ying-Shan
Du, Yang
Lian, Teng-Hong
Wang, Rui-Dan
Yu, Qiu-Jin
Wang, Ya-Jie
Wang, Xiao-Min
Chan, Piu
Chen, Sheng-Di
Wang, Yongjun
Zhang, Wei
author_sort Zuo, Li-Jun
collection PubMed
description BACKGROUND AND PURPOSE: The aim of this study was to identify the clinical characteristics and potential mechanisms relevant to pathological proteins in Parkinson's disease (PD) patients who experience fatigue. METHODS: PD patients (n=102) were evaluated using a fatigue severity scale and scales for motor and nonmotor symptoms. The levels of three pathological proteins—α-synuclein oligomer, β-amyloid (Aβ)(1-42), and tau—were measured in 102 cerebrospinal fluid (CSF) samples from these PD patients. Linear regression analyses were performed between fatigue score and the CSF levels of the above-listed pathological proteins in PD patients. RESULTS: The frequency of fatigue in the PD patients was 62.75%. The fatigue group had worse motor symptoms and anxiety, depression, and autonomic dysfunction. The CSF level of α-synuclein oligomer was higher and that of Aβ(1-42) was lower in the fatigue group than in the non-fatigue group. In multiple linear regression analyses, fatigue severity was significantly and positively correlated with the α-synuclein oligomer level in the CSF of PD patients, after adjusting for confounders. CONCLUSIONS: PD patients experience a high frequency of fatigue. PD patients with fatigue have worse motor and part nonmotor symptoms. Fatigue in PD patients is associated with an increased α-synuclein oligomer level in the CSF.
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spelling pubmed-48285632016-04-21 Parkinson's Disease with Fatigue: Clinical Characteristics and Potential Mechanisms Relevant to α-Synuclein Oligomer Zuo, Li-Jun Yu, Shu-Yang Wang, Fang Hu, Yang Piao, Ying-Shan Du, Yang Lian, Teng-Hong Wang, Rui-Dan Yu, Qiu-Jin Wang, Ya-Jie Wang, Xiao-Min Chan, Piu Chen, Sheng-Di Wang, Yongjun Zhang, Wei J Clin Neurol Original Article BACKGROUND AND PURPOSE: The aim of this study was to identify the clinical characteristics and potential mechanisms relevant to pathological proteins in Parkinson's disease (PD) patients who experience fatigue. METHODS: PD patients (n=102) were evaluated using a fatigue severity scale and scales for motor and nonmotor symptoms. The levels of three pathological proteins—α-synuclein oligomer, β-amyloid (Aβ)(1-42), and tau—were measured in 102 cerebrospinal fluid (CSF) samples from these PD patients. Linear regression analyses were performed between fatigue score and the CSF levels of the above-listed pathological proteins in PD patients. RESULTS: The frequency of fatigue in the PD patients was 62.75%. The fatigue group had worse motor symptoms and anxiety, depression, and autonomic dysfunction. The CSF level of α-synuclein oligomer was higher and that of Aβ(1-42) was lower in the fatigue group than in the non-fatigue group. In multiple linear regression analyses, fatigue severity was significantly and positively correlated with the α-synuclein oligomer level in the CSF of PD patients, after adjusting for confounders. CONCLUSIONS: PD patients experience a high frequency of fatigue. PD patients with fatigue have worse motor and part nonmotor symptoms. Fatigue in PD patients is associated with an increased α-synuclein oligomer level in the CSF. Korean Neurological Association 2016-04 2016-02-04 /pmc/articles/PMC4828563/ /pubmed/26869370 http://dx.doi.org/10.3988/jcn.2016.12.2.172 Text en Copyright © 2016 Korean Neurological Association http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Zuo, Li-Jun
Yu, Shu-Yang
Wang, Fang
Hu, Yang
Piao, Ying-Shan
Du, Yang
Lian, Teng-Hong
Wang, Rui-Dan
Yu, Qiu-Jin
Wang, Ya-Jie
Wang, Xiao-Min
Chan, Piu
Chen, Sheng-Di
Wang, Yongjun
Zhang, Wei
Parkinson's Disease with Fatigue: Clinical Characteristics and Potential Mechanisms Relevant to α-Synuclein Oligomer
title Parkinson's Disease with Fatigue: Clinical Characteristics and Potential Mechanisms Relevant to α-Synuclein Oligomer
title_full Parkinson's Disease with Fatigue: Clinical Characteristics and Potential Mechanisms Relevant to α-Synuclein Oligomer
title_fullStr Parkinson's Disease with Fatigue: Clinical Characteristics and Potential Mechanisms Relevant to α-Synuclein Oligomer
title_full_unstemmed Parkinson's Disease with Fatigue: Clinical Characteristics and Potential Mechanisms Relevant to α-Synuclein Oligomer
title_short Parkinson's Disease with Fatigue: Clinical Characteristics and Potential Mechanisms Relevant to α-Synuclein Oligomer
title_sort parkinson's disease with fatigue: clinical characteristics and potential mechanisms relevant to α-synuclein oligomer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828563/
https://www.ncbi.nlm.nih.gov/pubmed/26869370
http://dx.doi.org/10.3988/jcn.2016.12.2.172
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