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Abnormal eye movements in spinocerebellar ataxia type 3

BACKGROUND: Abnormal eye movements are common in spinocerebellar ataxias Type 3 (SCA3). We conducted the research to explore the frequency of abnormal eye movements in Chinese patients with SCA3, to compare the demographic and clinical characteristics between SCA3 patients with and without each type...

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Autores principales: Lin, Junyu, Zhang, Lingyu, Cao, Bei, Wei, Qianqian, Ou, Ruwei, Hou, Yanbing, Xu, Xinran, Liu, Kuncheng, Gu, Xiaojing, Shang, Huifang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814728/
https://www.ncbi.nlm.nih.gov/pubmed/33468086
http://dx.doi.org/10.1186/s12883-021-02057-3
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author Lin, Junyu
Zhang, Lingyu
Cao, Bei
Wei, Qianqian
Ou, Ruwei
Hou, Yanbing
Xu, Xinran
Liu, Kuncheng
Gu, Xiaojing
Shang, Huifang
author_facet Lin, Junyu
Zhang, Lingyu
Cao, Bei
Wei, Qianqian
Ou, Ruwei
Hou, Yanbing
Xu, Xinran
Liu, Kuncheng
Gu, Xiaojing
Shang, Huifang
author_sort Lin, Junyu
collection PubMed
description BACKGROUND: Abnormal eye movements are common in spinocerebellar ataxias Type 3 (SCA3). We conducted the research to explore the frequency of abnormal eye movements in Chinese patients with SCA3, to compare the demographic and clinical characteristics between SCA3 patients with and without each type of abnormal eye movement, and to explore the correlation between abnormal eye movements and the severity of ataxia. METHODS: Seventy-four patients with SCA3 were enrolled in this cross-sectional study. Six types of abnormal eye movements including impaired smooth pursuit, increased square-wave jerks (SWJ), gaze-evoked nystagmus (GEN), slowing of saccades, saccadic hypo/hypermetria and supranuclear gaze palsy were evaluated by experienced neurologists. The severity of ataxia was evaluated by Scale for the Assessment and Rating of Ataxia (SARA). RESULTS: The prevalence of impaired smooth pursuit, increased SWJ, GEN, slowing of saccades, saccadic hypo/hypermetria and supranuclear gaze palsy in Chinese SCA3 patients was 28.4, 13.5, 78.4, 41.9, 23.0, and 5.4%, respectively. SCA3 patients with GEN had higher scores of International Cooperative Ataxia Rating Scale (ICARS-IV) and total ICARS, and longer length of CAG repeat than patients without GEN. SCA3 patients with slowing of saccades had a longer disease duration, higher scores of ICARS-I, ICARS-II, total ICARS and SARA than patients without slowing of saccades. SCA3 patients with saccadic hypo/hypermetria had higher scores of ICARS-III, ICARS-IV, and SARA than patients without saccadic hypo/hypermetria. The demographic and clinical characteristics did not differ significantly between SCA3 patients with and without impaired smooth pursuit, increased SWJ, or supranuclear gaze palsy. Multivariate linear regression showed that the number of abnormal eye movements (0–6), disease duration, Hamilton Depression Rating Scale-24 (HDRS-24) score, and CAG repeat length were positively correlated with SARA score, whereas Montreal Cognitive Assessment (MoCA) score was negatively correlated with SARA score in SCA3. CONCLUSIONS: An increased number of abnormal eye movement types correlated with the severity of ataxia in SCA3. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12883-021-02057-3.
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spelling pubmed-78147282021-01-21 Abnormal eye movements in spinocerebellar ataxia type 3 Lin, Junyu Zhang, Lingyu Cao, Bei Wei, Qianqian Ou, Ruwei Hou, Yanbing Xu, Xinran Liu, Kuncheng Gu, Xiaojing Shang, Huifang BMC Neurol Research Article BACKGROUND: Abnormal eye movements are common in spinocerebellar ataxias Type 3 (SCA3). We conducted the research to explore the frequency of abnormal eye movements in Chinese patients with SCA3, to compare the demographic and clinical characteristics between SCA3 patients with and without each type of abnormal eye movement, and to explore the correlation between abnormal eye movements and the severity of ataxia. METHODS: Seventy-four patients with SCA3 were enrolled in this cross-sectional study. Six types of abnormal eye movements including impaired smooth pursuit, increased square-wave jerks (SWJ), gaze-evoked nystagmus (GEN), slowing of saccades, saccadic hypo/hypermetria and supranuclear gaze palsy were evaluated by experienced neurologists. The severity of ataxia was evaluated by Scale for the Assessment and Rating of Ataxia (SARA). RESULTS: The prevalence of impaired smooth pursuit, increased SWJ, GEN, slowing of saccades, saccadic hypo/hypermetria and supranuclear gaze palsy in Chinese SCA3 patients was 28.4, 13.5, 78.4, 41.9, 23.0, and 5.4%, respectively. SCA3 patients with GEN had higher scores of International Cooperative Ataxia Rating Scale (ICARS-IV) and total ICARS, and longer length of CAG repeat than patients without GEN. SCA3 patients with slowing of saccades had a longer disease duration, higher scores of ICARS-I, ICARS-II, total ICARS and SARA than patients without slowing of saccades. SCA3 patients with saccadic hypo/hypermetria had higher scores of ICARS-III, ICARS-IV, and SARA than patients without saccadic hypo/hypermetria. The demographic and clinical characteristics did not differ significantly between SCA3 patients with and without impaired smooth pursuit, increased SWJ, or supranuclear gaze palsy. Multivariate linear regression showed that the number of abnormal eye movements (0–6), disease duration, Hamilton Depression Rating Scale-24 (HDRS-24) score, and CAG repeat length were positively correlated with SARA score, whereas Montreal Cognitive Assessment (MoCA) score was negatively correlated with SARA score in SCA3. CONCLUSIONS: An increased number of abnormal eye movement types correlated with the severity of ataxia in SCA3. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12883-021-02057-3. BioMed Central 2021-01-19 /pmc/articles/PMC7814728/ /pubmed/33468086 http://dx.doi.org/10.1186/s12883-021-02057-3 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Lin, Junyu
Zhang, Lingyu
Cao, Bei
Wei, Qianqian
Ou, Ruwei
Hou, Yanbing
Xu, Xinran
Liu, Kuncheng
Gu, Xiaojing
Shang, Huifang
Abnormal eye movements in spinocerebellar ataxia type 3
title Abnormal eye movements in spinocerebellar ataxia type 3
title_full Abnormal eye movements in spinocerebellar ataxia type 3
title_fullStr Abnormal eye movements in spinocerebellar ataxia type 3
title_full_unstemmed Abnormal eye movements in spinocerebellar ataxia type 3
title_short Abnormal eye movements in spinocerebellar ataxia type 3
title_sort abnormal eye movements in spinocerebellar ataxia type 3
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814728/
https://www.ncbi.nlm.nih.gov/pubmed/33468086
http://dx.doi.org/10.1186/s12883-021-02057-3
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