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An Examination of Brain Abnormalities and Mobility in Individuals with Mild Cognitive Impairment and Alzheimer's Disease

Background: Mobility changes are concerning for elderly patients with cognitive decline. Given frail older individuals' vulnerability to injury, it is critical to identify contributors to limited mobility. Objective: To examine whether structural brain abnormalities, including reduced gray matt...

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Autores principales: Fischer, Barbara L., Bacher, Rhonda, Bendlin, Barbara B., Birdsill, Alex C., Ly, Martina, Hoscheidt, Siobhan M., Chappell, Richard J., Mahoney, Jane E., Gleason, Carey E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380746/
https://www.ncbi.nlm.nih.gov/pubmed/28424612
http://dx.doi.org/10.3389/fnagi.2017.00086
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author Fischer, Barbara L.
Bacher, Rhonda
Bendlin, Barbara B.
Birdsill, Alex C.
Ly, Martina
Hoscheidt, Siobhan M.
Chappell, Richard J.
Mahoney, Jane E.
Gleason, Carey E.
author_facet Fischer, Barbara L.
Bacher, Rhonda
Bendlin, Barbara B.
Birdsill, Alex C.
Ly, Martina
Hoscheidt, Siobhan M.
Chappell, Richard J.
Mahoney, Jane E.
Gleason, Carey E.
author_sort Fischer, Barbara L.
collection PubMed
description Background: Mobility changes are concerning for elderly patients with cognitive decline. Given frail older individuals' vulnerability to injury, it is critical to identify contributors to limited mobility. Objective: To examine whether structural brain abnormalities, including reduced gray matter volume and white matter hyperintensities, would be associated with limited mobility among individuals with cognitive impairment, and to determine whether cognitive impairment would mediate this relationship. Methods: Thirty-four elderly individuals with mild cognitive impairment (MCI) and Alzheimer's disease underwent neuropsychological evaluation, mobility assessment, and structural brain neuroimaging. Linear regression was conducted with predictors including gray matter volume in six regions of interest (ROI) and white matter hyperintensity (WMH) burden, with mobility measures as outcomes. Results: Lower gray matter volume in caudate nucleus was associated with slower speed on a functional mobility task. Higher cerebellar volume was also associated with slower functional mobility. White matter hyperintensity burden was not significantly associated with mobility. Conclusion: Our findings provide evidence for associations between subcortical gray matter volume and speed on a functional mobility task among cognitively impaired individuals.
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spelling pubmed-53807462017-04-19 An Examination of Brain Abnormalities and Mobility in Individuals with Mild Cognitive Impairment and Alzheimer's Disease Fischer, Barbara L. Bacher, Rhonda Bendlin, Barbara B. Birdsill, Alex C. Ly, Martina Hoscheidt, Siobhan M. Chappell, Richard J. Mahoney, Jane E. Gleason, Carey E. Front Aging Neurosci Neuroscience Background: Mobility changes are concerning for elderly patients with cognitive decline. Given frail older individuals' vulnerability to injury, it is critical to identify contributors to limited mobility. Objective: To examine whether structural brain abnormalities, including reduced gray matter volume and white matter hyperintensities, would be associated with limited mobility among individuals with cognitive impairment, and to determine whether cognitive impairment would mediate this relationship. Methods: Thirty-four elderly individuals with mild cognitive impairment (MCI) and Alzheimer's disease underwent neuropsychological evaluation, mobility assessment, and structural brain neuroimaging. Linear regression was conducted with predictors including gray matter volume in six regions of interest (ROI) and white matter hyperintensity (WMH) burden, with mobility measures as outcomes. Results: Lower gray matter volume in caudate nucleus was associated with slower speed on a functional mobility task. Higher cerebellar volume was also associated with slower functional mobility. White matter hyperintensity burden was not significantly associated with mobility. Conclusion: Our findings provide evidence for associations between subcortical gray matter volume and speed on a functional mobility task among cognitively impaired individuals. Frontiers Media S.A. 2017-04-05 /pmc/articles/PMC5380746/ /pubmed/28424612 http://dx.doi.org/10.3389/fnagi.2017.00086 Text en Copyright © 2017 Fischer, Bacher, Bendlin, Birdsill, Ly, Hoscheidt, Chappell, Mahoney and Gleason. 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) or licensor 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
Fischer, Barbara L.
Bacher, Rhonda
Bendlin, Barbara B.
Birdsill, Alex C.
Ly, Martina
Hoscheidt, Siobhan M.
Chappell, Richard J.
Mahoney, Jane E.
Gleason, Carey E.
An Examination of Brain Abnormalities and Mobility in Individuals with Mild Cognitive Impairment and Alzheimer's Disease
title An Examination of Brain Abnormalities and Mobility in Individuals with Mild Cognitive Impairment and Alzheimer's Disease
title_full An Examination of Brain Abnormalities and Mobility in Individuals with Mild Cognitive Impairment and Alzheimer's Disease
title_fullStr An Examination of Brain Abnormalities and Mobility in Individuals with Mild Cognitive Impairment and Alzheimer's Disease
title_full_unstemmed An Examination of Brain Abnormalities and Mobility in Individuals with Mild Cognitive Impairment and Alzheimer's Disease
title_short An Examination of Brain Abnormalities and Mobility in Individuals with Mild Cognitive Impairment and Alzheimer's Disease
title_sort examination of brain abnormalities and mobility in individuals with mild cognitive impairment and alzheimer's disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380746/
https://www.ncbi.nlm.nih.gov/pubmed/28424612
http://dx.doi.org/10.3389/fnagi.2017.00086
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