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Shifts in Gait Signatures Mark the End of Lifespan in Mice, With Sex Differences in Timing

Reduced walking speed is a hallmark of functional decline in aging across species. An age-related change in walking style may represent an additional key marker signifying deterioration of the nervous system. Due to the speed dependence of gait metrics combined with slowing of gait during aging, it...

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Autores principales: Broom, Lauren, Stephen, Jessica, Nayar, Varun, VanderHorst, Veronique G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366415/
https://www.ncbi.nlm.nih.gov/pubmed/34408647
http://dx.doi.org/10.3389/fnagi.2021.716993
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author Broom, Lauren
Stephen, Jessica
Nayar, Varun
VanderHorst, Veronique G.
author_facet Broom, Lauren
Stephen, Jessica
Nayar, Varun
VanderHorst, Veronique G.
author_sort Broom, Lauren
collection PubMed
description Reduced walking speed is a hallmark of functional decline in aging across species. An age-related change in walking style may represent an additional key marker signifying deterioration of the nervous system. Due to the speed dependence of gait metrics combined with slowing of gait during aging, it has been challenging to determine whether changes in gait metrics represent a change in style. In this longitudinal study we employed gait signatures to separate changes in walking style and speed in mice. We compared gait signatures at mature adult age with middle aged, old and geriatric time points and included female and male sub-cohorts to examine sex differences in nature or timing signature shifts. To determine whether gait signature shifts occurred independently from a decline in other mobility domains we measured balance and locomotor activity. We found that walking speed declined early, whereas gait signatures shifted very late during the aging process. Shifts represented longer swing time and stride length than expected for speed, as in slow motion, and were preceded by a decline in other mobility domains. The pattern of shifts was similar between female and male cohorts, but with sex differences in timing. We conclude that changes in walking style, speed and other mobility domains represent separate age-related phenomena. These findings call for careful, sex specific selection of type and timing of outcome measures in mechanistic or interventional studies. The pattern of age-related gait signature shifts is distinct from patterns seen in neurodegenerative conditions and may be a translatable marker for the end of the lifespan.
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spelling pubmed-83664152021-08-17 Shifts in Gait Signatures Mark the End of Lifespan in Mice, With Sex Differences in Timing Broom, Lauren Stephen, Jessica Nayar, Varun VanderHorst, Veronique G. Front Aging Neurosci Neuroscience Reduced walking speed is a hallmark of functional decline in aging across species. An age-related change in walking style may represent an additional key marker signifying deterioration of the nervous system. Due to the speed dependence of gait metrics combined with slowing of gait during aging, it has been challenging to determine whether changes in gait metrics represent a change in style. In this longitudinal study we employed gait signatures to separate changes in walking style and speed in mice. We compared gait signatures at mature adult age with middle aged, old and geriatric time points and included female and male sub-cohorts to examine sex differences in nature or timing signature shifts. To determine whether gait signature shifts occurred independently from a decline in other mobility domains we measured balance and locomotor activity. We found that walking speed declined early, whereas gait signatures shifted very late during the aging process. Shifts represented longer swing time and stride length than expected for speed, as in slow motion, and were preceded by a decline in other mobility domains. The pattern of shifts was similar between female and male cohorts, but with sex differences in timing. We conclude that changes in walking style, speed and other mobility domains represent separate age-related phenomena. These findings call for careful, sex specific selection of type and timing of outcome measures in mechanistic or interventional studies. The pattern of age-related gait signature shifts is distinct from patterns seen in neurodegenerative conditions and may be a translatable marker for the end of the lifespan. Frontiers Media S.A. 2021-08-02 /pmc/articles/PMC8366415/ /pubmed/34408647 http://dx.doi.org/10.3389/fnagi.2021.716993 Text en Copyright © 2021 Broom, Stephen, Nayar and VanderHorst. https://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
Broom, Lauren
Stephen, Jessica
Nayar, Varun
VanderHorst, Veronique G.
Shifts in Gait Signatures Mark the End of Lifespan in Mice, With Sex Differences in Timing
title Shifts in Gait Signatures Mark the End of Lifespan in Mice, With Sex Differences in Timing
title_full Shifts in Gait Signatures Mark the End of Lifespan in Mice, With Sex Differences in Timing
title_fullStr Shifts in Gait Signatures Mark the End of Lifespan in Mice, With Sex Differences in Timing
title_full_unstemmed Shifts in Gait Signatures Mark the End of Lifespan in Mice, With Sex Differences in Timing
title_short Shifts in Gait Signatures Mark the End of Lifespan in Mice, With Sex Differences in Timing
title_sort shifts in gait signatures mark the end of lifespan in mice, with sex differences in timing
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366415/
https://www.ncbi.nlm.nih.gov/pubmed/34408647
http://dx.doi.org/10.3389/fnagi.2021.716993
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