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Minor gait impairment despite white matter damage in pure small vessel disease

OBJECTIVE: Gait impairment is common in patients with cerebral small vessel disease (SVD). However, gait studies in elderly SVD patients might be confounded by age‐related comorbidities, such as polyneuropathy or sarcopenia. We therefore studied young patients with the genetically defined SVD CADASI...

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Autores principales: Finsterwalder, Sofia, Wuehr, Max, Gesierich, Benno, Dietze, Anna, Konieczny, Marek J., Schmidt, Reinhold, Schniepp, Roman, Duering, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801180/
https://www.ncbi.nlm.nih.gov/pubmed/31524338
http://dx.doi.org/10.1002/acn3.50891
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author Finsterwalder, Sofia
Wuehr, Max
Gesierich, Benno
Dietze, Anna
Konieczny, Marek J.
Schmidt, Reinhold
Schniepp, Roman
Duering, Marco
author_facet Finsterwalder, Sofia
Wuehr, Max
Gesierich, Benno
Dietze, Anna
Konieczny, Marek J.
Schmidt, Reinhold
Schniepp, Roman
Duering, Marco
author_sort Finsterwalder, Sofia
collection PubMed
description OBJECTIVE: Gait impairment is common in patients with cerebral small vessel disease (SVD). However, gait studies in elderly SVD patients might be confounded by age‐related comorbidities, such as polyneuropathy or sarcopenia. We therefore studied young patients with the genetically defined SVD CADASIL. Our aim was to examine the effects of pure SVD on single and dual task gait, and to investigate associations of gait performance with cognitive deficits and white matter alterations. METHODS: We investigated single task walking and calculatory, semantic, or motoric dual task costs in 39 CADASIL patients (mean age 50 ± 8) using a computerized walkway. We obtained 3.0T MRI and neuropsychological data on processing speed, the main cognitive deficit in CADASIL. Spatiotemporal gait parameters were standardized based on data from 192 healthy controls. Associations between white matter integrity, assessed by diffusion tensor imaging, and gait were analyzed using both a global marker and voxel‐wise analysis. RESULTS: Compared to controls, CADASIL patients showed only mild single task gait impairment, and only in the rhythm domain. The semantic dual task additionally uncovered mild deficits in the pace domain. Processing speed was not associated with gait. White matter alterations were related to single task stride length but not to dual task performance. INTERPRETATION: Despite severe disease burden, gait performance in patients with pure small vessel disease was relatively preserved in single and dual tasks. Results suggest that age‐related pathologies other than small vessel disease might play a role for gait impairment in elderly SVD patients.
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spelling pubmed-68011802019-10-22 Minor gait impairment despite white matter damage in pure small vessel disease Finsterwalder, Sofia Wuehr, Max Gesierich, Benno Dietze, Anna Konieczny, Marek J. Schmidt, Reinhold Schniepp, Roman Duering, Marco Ann Clin Transl Neurol Research Articles OBJECTIVE: Gait impairment is common in patients with cerebral small vessel disease (SVD). However, gait studies in elderly SVD patients might be confounded by age‐related comorbidities, such as polyneuropathy or sarcopenia. We therefore studied young patients with the genetically defined SVD CADASIL. Our aim was to examine the effects of pure SVD on single and dual task gait, and to investigate associations of gait performance with cognitive deficits and white matter alterations. METHODS: We investigated single task walking and calculatory, semantic, or motoric dual task costs in 39 CADASIL patients (mean age 50 ± 8) using a computerized walkway. We obtained 3.0T MRI and neuropsychological data on processing speed, the main cognitive deficit in CADASIL. Spatiotemporal gait parameters were standardized based on data from 192 healthy controls. Associations between white matter integrity, assessed by diffusion tensor imaging, and gait were analyzed using both a global marker and voxel‐wise analysis. RESULTS: Compared to controls, CADASIL patients showed only mild single task gait impairment, and only in the rhythm domain. The semantic dual task additionally uncovered mild deficits in the pace domain. Processing speed was not associated with gait. White matter alterations were related to single task stride length but not to dual task performance. INTERPRETATION: Despite severe disease burden, gait performance in patients with pure small vessel disease was relatively preserved in single and dual tasks. Results suggest that age‐related pathologies other than small vessel disease might play a role for gait impairment in elderly SVD patients. John Wiley and Sons Inc. 2019-09-16 /pmc/articles/PMC6801180/ /pubmed/31524338 http://dx.doi.org/10.1002/acn3.50891 Text en © 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Finsterwalder, Sofia
Wuehr, Max
Gesierich, Benno
Dietze, Anna
Konieczny, Marek J.
Schmidt, Reinhold
Schniepp, Roman
Duering, Marco
Minor gait impairment despite white matter damage in pure small vessel disease
title Minor gait impairment despite white matter damage in pure small vessel disease
title_full Minor gait impairment despite white matter damage in pure small vessel disease
title_fullStr Minor gait impairment despite white matter damage in pure small vessel disease
title_full_unstemmed Minor gait impairment despite white matter damage in pure small vessel disease
title_short Minor gait impairment despite white matter damage in pure small vessel disease
title_sort minor gait impairment despite white matter damage in pure small vessel disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801180/
https://www.ncbi.nlm.nih.gov/pubmed/31524338
http://dx.doi.org/10.1002/acn3.50891
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