Cargando…

Extra-Cerebellar Signs and Non-motor Features in Chinese Patients With Spinocerebellar Ataxia Type 3

Objectives: Our study attempted to systematically explore the prevalence of extra-cerebellar signs and non-motor symptoms, such as anxiety, depression, fatigue, excessive daytime sleepiness (EDS) and sleep disturbances in a cohort of Chinese patients with spinocerebellar ataxia type 3 (SCA3), and fu...

Descripción completa

Detalles Bibliográficos
Autores principales: Yuan, Xiaoqin, Ou, Ruwei, Hou, Yanbing, Chen, Xueping, Cao, Bei, Hu, Xun, Shang, Huifang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388540/
https://www.ncbi.nlm.nih.gov/pubmed/30833927
http://dx.doi.org/10.3389/fneur.2019.00110
_version_ 1783397785030098944
author Yuan, Xiaoqin
Ou, Ruwei
Hou, Yanbing
Chen, Xueping
Cao, Bei
Hu, Xun
Shang, Huifang
author_facet Yuan, Xiaoqin
Ou, Ruwei
Hou, Yanbing
Chen, Xueping
Cao, Bei
Hu, Xun
Shang, Huifang
author_sort Yuan, Xiaoqin
collection PubMed
description Objectives: Our study attempted to systematically explore the prevalence of extra-cerebellar signs and non-motor symptoms, such as anxiety, depression, fatigue, excessive daytime sleepiness (EDS) and sleep disturbances in a cohort of Chinese patients with spinocerebellar ataxia type 3 (SCA3), and further investigated the correlations between non-motor symptoms and clinical characteristics in SCA3 patients. Methods: This study included 68 molecular-proven SCA3 patients. Extra-cerebellar signs were evaluated with the Inventory of Non-Ataxia Symptoms (INAS). The INAS count indicated the number of non-ataxia signs in each patient. The severity of ataxia, fatigue, EDS, sleep quality, anxiety, and depression were assessed using the Scale for the assessment and rating of ataxia (SARA), Fatigue Severity Scale (FSS), Epworth Sleepiness Scale (ESS), Pittsburgh Sleep Quality Index (PSQI), Hamilton Anxiety Rating Scale (HAMA), and the Hamilton Depression Rating Scale (HAMD) (24 items), respectively. Results: Extra-cerebellar signs were detected in 91.2% of all SCA3 patients and the mean total INAS count was 2.72 ± 1.88. Rigidity was the most frequent extra-cerebellar sign (47.1%, N = 32). Sensory symptoms (2.9%, N = 2) and chorea (5.9%, N = 4) were rare, and myoclonus (0%) was not found in this cohort. High frequencies of sleep disturbances (64.7%), fatigue (52.9%), depression (48.5%), and anxiety (42.6%) were detected in SCA3 patients. The Spearman correlation indicated that the HAMD score was associated with the CAG repeat length and HAMA score, while the PSQI score was correlated with the SARA and FSS score. In addition, multivariate linear regression analysis showed that the CAG repeat length, age of onset, sleep disturbances and depression were significant predictors of fatigue in SCA3 patients. Conclusions: Our study indicates that the vast majority of SCA3 patients display extra-cerebellar signs. Except for EDS, anxiety, depression, fatigue and impaired sleep quality are present in SCA3 patients. The CAG repeat length, age of onset, sleep disturbances and depression are predictors of fatigue in SCA3 patients.
format Online
Article
Text
id pubmed-6388540
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-63885402019-03-04 Extra-Cerebellar Signs and Non-motor Features in Chinese Patients With Spinocerebellar Ataxia Type 3 Yuan, Xiaoqin Ou, Ruwei Hou, Yanbing Chen, Xueping Cao, Bei Hu, Xun Shang, Huifang Front Neurol Neurology Objectives: Our study attempted to systematically explore the prevalence of extra-cerebellar signs and non-motor symptoms, such as anxiety, depression, fatigue, excessive daytime sleepiness (EDS) and sleep disturbances in a cohort of Chinese patients with spinocerebellar ataxia type 3 (SCA3), and further investigated the correlations between non-motor symptoms and clinical characteristics in SCA3 patients. Methods: This study included 68 molecular-proven SCA3 patients. Extra-cerebellar signs were evaluated with the Inventory of Non-Ataxia Symptoms (INAS). The INAS count indicated the number of non-ataxia signs in each patient. The severity of ataxia, fatigue, EDS, sleep quality, anxiety, and depression were assessed using the Scale for the assessment and rating of ataxia (SARA), Fatigue Severity Scale (FSS), Epworth Sleepiness Scale (ESS), Pittsburgh Sleep Quality Index (PSQI), Hamilton Anxiety Rating Scale (HAMA), and the Hamilton Depression Rating Scale (HAMD) (24 items), respectively. Results: Extra-cerebellar signs were detected in 91.2% of all SCA3 patients and the mean total INAS count was 2.72 ± 1.88. Rigidity was the most frequent extra-cerebellar sign (47.1%, N = 32). Sensory symptoms (2.9%, N = 2) and chorea (5.9%, N = 4) were rare, and myoclonus (0%) was not found in this cohort. High frequencies of sleep disturbances (64.7%), fatigue (52.9%), depression (48.5%), and anxiety (42.6%) were detected in SCA3 patients. The Spearman correlation indicated that the HAMD score was associated with the CAG repeat length and HAMA score, while the PSQI score was correlated with the SARA and FSS score. In addition, multivariate linear regression analysis showed that the CAG repeat length, age of onset, sleep disturbances and depression were significant predictors of fatigue in SCA3 patients. Conclusions: Our study indicates that the vast majority of SCA3 patients display extra-cerebellar signs. Except for EDS, anxiety, depression, fatigue and impaired sleep quality are present in SCA3 patients. The CAG repeat length, age of onset, sleep disturbances and depression are predictors of fatigue in SCA3 patients. Frontiers Media S.A. 2019-02-18 /pmc/articles/PMC6388540/ /pubmed/30833927 http://dx.doi.org/10.3389/fneur.2019.00110 Text en Copyright © 2019 Yuan, Ou, Hou, Chen, Cao, Hu and Shang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Yuan, Xiaoqin
Ou, Ruwei
Hou, Yanbing
Chen, Xueping
Cao, Bei
Hu, Xun
Shang, Huifang
Extra-Cerebellar Signs and Non-motor Features in Chinese Patients With Spinocerebellar Ataxia Type 3
title Extra-Cerebellar Signs and Non-motor Features in Chinese Patients With Spinocerebellar Ataxia Type 3
title_full Extra-Cerebellar Signs and Non-motor Features in Chinese Patients With Spinocerebellar Ataxia Type 3
title_fullStr Extra-Cerebellar Signs and Non-motor Features in Chinese Patients With Spinocerebellar Ataxia Type 3
title_full_unstemmed Extra-Cerebellar Signs and Non-motor Features in Chinese Patients With Spinocerebellar Ataxia Type 3
title_short Extra-Cerebellar Signs and Non-motor Features in Chinese Patients With Spinocerebellar Ataxia Type 3
title_sort extra-cerebellar signs and non-motor features in chinese patients with spinocerebellar ataxia type 3
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388540/
https://www.ncbi.nlm.nih.gov/pubmed/30833927
http://dx.doi.org/10.3389/fneur.2019.00110
work_keys_str_mv AT yuanxiaoqin extracerebellarsignsandnonmotorfeaturesinchinesepatientswithspinocerebellarataxiatype3
AT ouruwei extracerebellarsignsandnonmotorfeaturesinchinesepatientswithspinocerebellarataxiatype3
AT houyanbing extracerebellarsignsandnonmotorfeaturesinchinesepatientswithspinocerebellarataxiatype3
AT chenxueping extracerebellarsignsandnonmotorfeaturesinchinesepatientswithspinocerebellarataxiatype3
AT caobei extracerebellarsignsandnonmotorfeaturesinchinesepatientswithspinocerebellarataxiatype3
AT huxun extracerebellarsignsandnonmotorfeaturesinchinesepatientswithspinocerebellarataxiatype3
AT shanghuifang extracerebellarsignsandnonmotorfeaturesinchinesepatientswithspinocerebellarataxiatype3