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The association between cognition and gait disturbance in central nervous system demyelinating disorder with mild disability

INTRODUCTION: Gait disturbance in central nervous system (CNS) demyelinating disorders, including multiple sclerosis (MS) and neuromyelitis optica (NMO) is one of the most troublesome problems that has a direct impact on the quality of life. However, the associations between gait disturbance and oth...

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Autores principales: Chang, Min Cheol, Lee, Byung Joo, Yang, Dongseok, Kim, Chung Reen, Park, Donghwi, Kim, Sunyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148385/
https://www.ncbi.nlm.nih.gov/pubmed/37120584
http://dx.doi.org/10.1186/s12883-023-03210-w
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author Chang, Min Cheol
Lee, Byung Joo
Yang, Dongseok
Kim, Chung Reen
Park, Donghwi
Kim, Sunyoung
author_facet Chang, Min Cheol
Lee, Byung Joo
Yang, Dongseok
Kim, Chung Reen
Park, Donghwi
Kim, Sunyoung
author_sort Chang, Min Cheol
collection PubMed
description INTRODUCTION: Gait disturbance in central nervous system (CNS) demyelinating disorders, including multiple sclerosis (MS) and neuromyelitis optica (NMO) is one of the most troublesome problems that has a direct impact on the quality of life. However, the associations between gait disturbance and other clinical variables of these two diseases have not been fully elucidated. OBJECTIVE: This study aimed to evaluate gait disturbance using a computerized gait analysis system and its association with various clinical variables in patients with MS and NMO. METHODS: A total of 33 patients (14 with MS and 19 with NMO) with minor disabilities, who were able to walk independently and had passed their acute phase, were enrolled in the study. Gait analysis were performed using a computer-based instrumented walkway system. (Walk-way MG-1000, Anima, Japan) Clinical variables, such as disease duration, medication, body mass index (BMI), hand grip power, and muscle mass were recorded. The Montreal Cognitive Assessment (MOCA), Beck Depression Inventory score-II (BDI), and fatigue scale were measured using the Functional Assessment of Chronic Illness Therapy-fatigue scale (FACIT-fatigue) scale. A trained neurologist scored the Expanded Disability Status Scale (EDSS). RESULTS: Gait speed was the single parameter that showed a significant positive correlation with MOCA (p < 0.001). The stance phase time was the single parameter that showed a significant negative correlation with EDSS (p < 0.001). Hand grip strength showed a significant positive correlation with skeletal muscle mass as assessed by bioimpedance analysis (p < 0.05). The FACIT-fatigue scale score showed a significant negative correlation with the BDI (p < 0.001). CONCLUSION: In our patients with MS/NMO with mild disability, cognitive impairment was significantly correlated with gait speed, and the degree of disability was significantly correlated with stance phase time. Our findings may imply that early detection of a decrease in gait speed and an increase in stance phase time can predict the progression of cognitive impairment in patients with MS/NMO with mild disability.
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spelling pubmed-101483852023-04-30 The association between cognition and gait disturbance in central nervous system demyelinating disorder with mild disability Chang, Min Cheol Lee, Byung Joo Yang, Dongseok Kim, Chung Reen Park, Donghwi Kim, Sunyoung BMC Neurol Research INTRODUCTION: Gait disturbance in central nervous system (CNS) demyelinating disorders, including multiple sclerosis (MS) and neuromyelitis optica (NMO) is one of the most troublesome problems that has a direct impact on the quality of life. However, the associations between gait disturbance and other clinical variables of these two diseases have not been fully elucidated. OBJECTIVE: This study aimed to evaluate gait disturbance using a computerized gait analysis system and its association with various clinical variables in patients with MS and NMO. METHODS: A total of 33 patients (14 with MS and 19 with NMO) with minor disabilities, who were able to walk independently and had passed their acute phase, were enrolled in the study. Gait analysis were performed using a computer-based instrumented walkway system. (Walk-way MG-1000, Anima, Japan) Clinical variables, such as disease duration, medication, body mass index (BMI), hand grip power, and muscle mass were recorded. The Montreal Cognitive Assessment (MOCA), Beck Depression Inventory score-II (BDI), and fatigue scale were measured using the Functional Assessment of Chronic Illness Therapy-fatigue scale (FACIT-fatigue) scale. A trained neurologist scored the Expanded Disability Status Scale (EDSS). RESULTS: Gait speed was the single parameter that showed a significant positive correlation with MOCA (p < 0.001). The stance phase time was the single parameter that showed a significant negative correlation with EDSS (p < 0.001). Hand grip strength showed a significant positive correlation with skeletal muscle mass as assessed by bioimpedance analysis (p < 0.05). The FACIT-fatigue scale score showed a significant negative correlation with the BDI (p < 0.001). CONCLUSION: In our patients with MS/NMO with mild disability, cognitive impairment was significantly correlated with gait speed, and the degree of disability was significantly correlated with stance phase time. Our findings may imply that early detection of a decrease in gait speed and an increase in stance phase time can predict the progression of cognitive impairment in patients with MS/NMO with mild disability. BioMed Central 2023-04-29 /pmc/articles/PMC10148385/ /pubmed/37120584 http://dx.doi.org/10.1186/s12883-023-03210-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Chang, Min Cheol
Lee, Byung Joo
Yang, Dongseok
Kim, Chung Reen
Park, Donghwi
Kim, Sunyoung
The association between cognition and gait disturbance in central nervous system demyelinating disorder with mild disability
title The association between cognition and gait disturbance in central nervous system demyelinating disorder with mild disability
title_full The association between cognition and gait disturbance in central nervous system demyelinating disorder with mild disability
title_fullStr The association between cognition and gait disturbance in central nervous system demyelinating disorder with mild disability
title_full_unstemmed The association between cognition and gait disturbance in central nervous system demyelinating disorder with mild disability
title_short The association between cognition and gait disturbance in central nervous system demyelinating disorder with mild disability
title_sort association between cognition and gait disturbance in central nervous system demyelinating disorder with mild disability
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148385/
https://www.ncbi.nlm.nih.gov/pubmed/37120584
http://dx.doi.org/10.1186/s12883-023-03210-w
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