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Quantitative Gait Analysis in Patients with Huntington’s Disease

OBJECTIVE: Gait disturbance is the main factor contributing to a negative impact on quality of life in patients with Huntington’s disease (HD). Understanding gait features in patients with HD is essential for planning a successful gait strategy. The aim of this study was to investigate temporospatia...

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Autores principales: Pyo, Seon Jong, Kim, Hanjun, Kim, Il Soo, Park, Young-Min, Kim, Mi-Jung, Lee, Hye Mi, Koh, Seong-Beom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Movement Disorder Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615174/
https://www.ncbi.nlm.nih.gov/pubmed/28851209
http://dx.doi.org/10.14802/jmd.17041
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author Pyo, Seon Jong
Kim, Hanjun
Kim, Il Soo
Park, Young-Min
Kim, Mi-Jung
Lee, Hye Mi
Koh, Seong-Beom
author_facet Pyo, Seon Jong
Kim, Hanjun
Kim, Il Soo
Park, Young-Min
Kim, Mi-Jung
Lee, Hye Mi
Koh, Seong-Beom
author_sort Pyo, Seon Jong
collection PubMed
description OBJECTIVE: Gait disturbance is the main factor contributing to a negative impact on quality of life in patients with Huntington’s disease (HD). Understanding gait features in patients with HD is essential for planning a successful gait strategy. The aim of this study was to investigate temporospatial gait parameters in patients with HD compared with healthy controls. METHODS: We investigated 7 patients with HD. Diagnosis was confirmed by genetic analysis, and patients were evaluated with the Unified Huntington’s Disease Rating Scale (UHDRS). Gait features were assessed with a gait analyzer. We compared the results of patients with HD to those of 7 age- and sex-matched normal controls. RESULTS: Step length and stride length were decreased and base of support was increased in the HD group compared to the control group. In addition, coefficients of variability for step and stride length were increased in the HD group. The HD group showed slower walking velocity, an increased stance/swing phase in the gait cycle and a decreased proportion of single support time compared to the control group. Cadence did not differ significantly between groups. Among the UHDRS subscores, total motor score and total behavior score were positively correlated with step length, and total behavior score was positively correlated with walking velocity in patients with HD. CONCLUSION: Increased variability in step and stride length, slower walking velocity, increased stance phase, and decreased swing phase and single support time with preserved cadence suggest that HD gait patterns are slow, ataxic and ineffective. This study suggests that quantitative gait analysis is needed to assess gait problems in HD.
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spelling pubmed-56151742017-09-28 Quantitative Gait Analysis in Patients with Huntington’s Disease Pyo, Seon Jong Kim, Hanjun Kim, Il Soo Park, Young-Min Kim, Mi-Jung Lee, Hye Mi Koh, Seong-Beom J Mov Disord Original Article OBJECTIVE: Gait disturbance is the main factor contributing to a negative impact on quality of life in patients with Huntington’s disease (HD). Understanding gait features in patients with HD is essential for planning a successful gait strategy. The aim of this study was to investigate temporospatial gait parameters in patients with HD compared with healthy controls. METHODS: We investigated 7 patients with HD. Diagnosis was confirmed by genetic analysis, and patients were evaluated with the Unified Huntington’s Disease Rating Scale (UHDRS). Gait features were assessed with a gait analyzer. We compared the results of patients with HD to those of 7 age- and sex-matched normal controls. RESULTS: Step length and stride length were decreased and base of support was increased in the HD group compared to the control group. In addition, coefficients of variability for step and stride length were increased in the HD group. The HD group showed slower walking velocity, an increased stance/swing phase in the gait cycle and a decreased proportion of single support time compared to the control group. Cadence did not differ significantly between groups. Among the UHDRS subscores, total motor score and total behavior score were positively correlated with step length, and total behavior score was positively correlated with walking velocity in patients with HD. CONCLUSION: Increased variability in step and stride length, slower walking velocity, increased stance phase, and decreased swing phase and single support time with preserved cadence suggest that HD gait patterns are slow, ataxic and ineffective. This study suggests that quantitative gait analysis is needed to assess gait problems in HD. The Korean Movement Disorder Society 2017-09 2017-08-31 /pmc/articles/PMC5615174/ /pubmed/28851209 http://dx.doi.org/10.14802/jmd.17041 Text en Copyright © 2017 The Korean Movement Disorder Society This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Pyo, Seon Jong
Kim, Hanjun
Kim, Il Soo
Park, Young-Min
Kim, Mi-Jung
Lee, Hye Mi
Koh, Seong-Beom
Quantitative Gait Analysis in Patients with Huntington’s Disease
title Quantitative Gait Analysis in Patients with Huntington’s Disease
title_full Quantitative Gait Analysis in Patients with Huntington’s Disease
title_fullStr Quantitative Gait Analysis in Patients with Huntington’s Disease
title_full_unstemmed Quantitative Gait Analysis in Patients with Huntington’s Disease
title_short Quantitative Gait Analysis in Patients with Huntington’s Disease
title_sort quantitative gait analysis in patients with huntington’s disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615174/
https://www.ncbi.nlm.nih.gov/pubmed/28851209
http://dx.doi.org/10.14802/jmd.17041
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