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Weaker Braking Force, A New Marker of Worse Gait Stability in Alzheimer Disease

Background: Braking force is a gait marker associated with gait stability. This study aimed to determine the alteration of braking force and its correlation with gait stability in Alzheimer disease (AD). Methods: A total of 32 AD patients and 32 healthy controls (HCs) were enrolled in this study. Ga...

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Autores principales: Cheng, Qianqian, Wu, Mengxuan, Wu, Yuemin, Hu, Yaoyao, Kwapong, William Robert, Shi, Xiang, Fan, Yinying, Yu, Xin, He, Jincai, Wang, Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7516124/
https://www.ncbi.nlm.nih.gov/pubmed/33024432
http://dx.doi.org/10.3389/fnagi.2020.554168
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author Cheng, Qianqian
Wu, Mengxuan
Wu, Yuemin
Hu, Yaoyao
Kwapong, William Robert
Shi, Xiang
Fan, Yinying
Yu, Xin
He, Jincai
Wang, Zhen
author_facet Cheng, Qianqian
Wu, Mengxuan
Wu, Yuemin
Hu, Yaoyao
Kwapong, William Robert
Shi, Xiang
Fan, Yinying
Yu, Xin
He, Jincai
Wang, Zhen
author_sort Cheng, Qianqian
collection PubMed
description Background: Braking force is a gait marker associated with gait stability. This study aimed to determine the alteration of braking force and its correlation with gait stability in Alzheimer disease (AD). Methods: A total of 32 AD patients and 32 healthy controls (HCs) were enrolled in this study. Gait parameters (braking force, gait variability, and fall risk) in the walking tests of Free walk, Barrier, and Count backward were measured by JiBuEn(®) gait analysis system. Gait variability was calculated by the coefficient of variation (COV) of stride time, stance time, and swing time. Results: The braking force of AD was significantly weaker than HCs in three walking tests (P < 0.001, P < 0.001, P = 0.007). Gait variability of AD showed significant elevation than HCs in the walking of Count backward (COV(stride): P = 0.013; COV(swing): P = 0.006). Fall risk of AD was significantly higher than HCs in three walking tests (P = 0.001, P = 0.001, P = 0.001). Braking force was negatively associated with fall risks in three walking tests (P < 0.001, P < 0.001, P < 0.001). There were significant negative correlations between braking force and gait variability in the walking of Free walk (COV(stride): P = 0.018; COV(swing): P = 0.013) and Barrier (COV(stride): P = 0.002; COV(swing): P = 0.001), but not Count backward (COV(stride): P = 0.888; COV(swing): P = 0.555). Conclusion: Braking force was weaker in AD compared to HCs, reflecting the worse gait stability of AD. Our study suggests that weakening of braking force may be a new gait marker to indicate cognitive and motor impairment and predict fall risk in AD.
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spelling pubmed-75161242020-10-05 Weaker Braking Force, A New Marker of Worse Gait Stability in Alzheimer Disease Cheng, Qianqian Wu, Mengxuan Wu, Yuemin Hu, Yaoyao Kwapong, William Robert Shi, Xiang Fan, Yinying Yu, Xin He, Jincai Wang, Zhen Front Aging Neurosci Neuroscience Background: Braking force is a gait marker associated with gait stability. This study aimed to determine the alteration of braking force and its correlation with gait stability in Alzheimer disease (AD). Methods: A total of 32 AD patients and 32 healthy controls (HCs) were enrolled in this study. Gait parameters (braking force, gait variability, and fall risk) in the walking tests of Free walk, Barrier, and Count backward were measured by JiBuEn(®) gait analysis system. Gait variability was calculated by the coefficient of variation (COV) of stride time, stance time, and swing time. Results: The braking force of AD was significantly weaker than HCs in three walking tests (P < 0.001, P < 0.001, P = 0.007). Gait variability of AD showed significant elevation than HCs in the walking of Count backward (COV(stride): P = 0.013; COV(swing): P = 0.006). Fall risk of AD was significantly higher than HCs in three walking tests (P = 0.001, P = 0.001, P = 0.001). Braking force was negatively associated with fall risks in three walking tests (P < 0.001, P < 0.001, P < 0.001). There were significant negative correlations between braking force and gait variability in the walking of Free walk (COV(stride): P = 0.018; COV(swing): P = 0.013) and Barrier (COV(stride): P = 0.002; COV(swing): P = 0.001), but not Count backward (COV(stride): P = 0.888; COV(swing): P = 0.555). Conclusion: Braking force was weaker in AD compared to HCs, reflecting the worse gait stability of AD. Our study suggests that weakening of braking force may be a new gait marker to indicate cognitive and motor impairment and predict fall risk in AD. Frontiers Media S.A. 2020-09-11 /pmc/articles/PMC7516124/ /pubmed/33024432 http://dx.doi.org/10.3389/fnagi.2020.554168 Text en Copyright © 2020 Cheng, Wu, Wu, Hu, Kwapong, Shi, Fan, Yu, He and Wang. 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 Neuroscience
Cheng, Qianqian
Wu, Mengxuan
Wu, Yuemin
Hu, Yaoyao
Kwapong, William Robert
Shi, Xiang
Fan, Yinying
Yu, Xin
He, Jincai
Wang, Zhen
Weaker Braking Force, A New Marker of Worse Gait Stability in Alzheimer Disease
title Weaker Braking Force, A New Marker of Worse Gait Stability in Alzheimer Disease
title_full Weaker Braking Force, A New Marker of Worse Gait Stability in Alzheimer Disease
title_fullStr Weaker Braking Force, A New Marker of Worse Gait Stability in Alzheimer Disease
title_full_unstemmed Weaker Braking Force, A New Marker of Worse Gait Stability in Alzheimer Disease
title_short Weaker Braking Force, A New Marker of Worse Gait Stability in Alzheimer Disease
title_sort weaker braking force, a new marker of worse gait stability in alzheimer disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7516124/
https://www.ncbi.nlm.nih.gov/pubmed/33024432
http://dx.doi.org/10.3389/fnagi.2020.554168
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