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Brain Magnetic Susceptibility is Associated With Slower Gait in Community-Dwelling Older Adults

Age-related slowing of gait is exceedingly common and a robust predictor of various adverse health outcomes in older age. Prior neuroimaging studies have documented diverse non-specific structural brain abnormalities which are related to slow gait; however, the extent to which quantitative susceptib...

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Autores principales: Poole, Victoria, Dawe, Robert, Luergans, Sue, Bennett, David, Buchman, Aron, Arfanakis, Konstantinos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8681799/
http://dx.doi.org/10.1093/geroni/igab046.3177
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author Poole, Victoria
Dawe, Robert
Luergans, Sue
Bennett, David
Buchman, Aron
Arfanakis, Konstantinos
author_facet Poole, Victoria
Dawe, Robert
Luergans, Sue
Bennett, David
Buchman, Aron
Arfanakis, Konstantinos
author_sort Poole, Victoria
collection PubMed
description Age-related slowing of gait is exceedingly common and a robust predictor of various adverse health outcomes in older age. Prior neuroimaging studies have documented diverse non-specific structural brain abnormalities which are related to slow gait; however, the extent to which quantitative susceptibility mapping (QSM), which measures regional magnetic susceptibility in the brain, associates with gait speed remains unexplored. In the current study, 415 non-demented community-dwelling older adults (91 males; 81+/- 7 years) underwent an MRI (Siemens 3T TIM Trio) and in-home motor assessment. Gait speed was measured and averaged across 2 timed 8-ft walks. MR-acquired QSM data were pre-processed, registered to ICBM template, and spatially smoothed with a 5mm FWHM Gaussian kernel. When these maps entered group-level GLMs, voxel-wise associations with gait speed were of interest, after adjusting for demographics. We observed very strong negative associations between gait speed and magnetic susceptibility, such that those with slower gait had higher susceptibility in bilateral inferior frontal, superior temporal, and angular gyri (corrected p<.0005). Robust associations were also observed in the middle frontal, precentral, and postcentral gyri of the right hemisphere. These novel findings suggest that reduced myelination or increased iron accumulation in these brain regions may contribute to impaired gait. Future work will need to determine to what extent these cross-sectional QSM metrics are independent predictors of incident adverse health outcomes when controlling for other common brain imaging abnormalities observed in older adults.
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spelling pubmed-86817992021-12-20 Brain Magnetic Susceptibility is Associated With Slower Gait in Community-Dwelling Older Adults Poole, Victoria Dawe, Robert Luergans, Sue Bennett, David Buchman, Aron Arfanakis, Konstantinos Innov Aging Abstracts Age-related slowing of gait is exceedingly common and a robust predictor of various adverse health outcomes in older age. Prior neuroimaging studies have documented diverse non-specific structural brain abnormalities which are related to slow gait; however, the extent to which quantitative susceptibility mapping (QSM), which measures regional magnetic susceptibility in the brain, associates with gait speed remains unexplored. In the current study, 415 non-demented community-dwelling older adults (91 males; 81+/- 7 years) underwent an MRI (Siemens 3T TIM Trio) and in-home motor assessment. Gait speed was measured and averaged across 2 timed 8-ft walks. MR-acquired QSM data were pre-processed, registered to ICBM template, and spatially smoothed with a 5mm FWHM Gaussian kernel. When these maps entered group-level GLMs, voxel-wise associations with gait speed were of interest, after adjusting for demographics. We observed very strong negative associations between gait speed and magnetic susceptibility, such that those with slower gait had higher susceptibility in bilateral inferior frontal, superior temporal, and angular gyri (corrected p<.0005). Robust associations were also observed in the middle frontal, precentral, and postcentral gyri of the right hemisphere. These novel findings suggest that reduced myelination or increased iron accumulation in these brain regions may contribute to impaired gait. Future work will need to determine to what extent these cross-sectional QSM metrics are independent predictors of incident adverse health outcomes when controlling for other common brain imaging abnormalities observed in older adults. Oxford University Press 2021-12-17 /pmc/articles/PMC8681799/ http://dx.doi.org/10.1093/geroni/igab046.3177 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of The Gerontological Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Poole, Victoria
Dawe, Robert
Luergans, Sue
Bennett, David
Buchman, Aron
Arfanakis, Konstantinos
Brain Magnetic Susceptibility is Associated With Slower Gait in Community-Dwelling Older Adults
title Brain Magnetic Susceptibility is Associated With Slower Gait in Community-Dwelling Older Adults
title_full Brain Magnetic Susceptibility is Associated With Slower Gait in Community-Dwelling Older Adults
title_fullStr Brain Magnetic Susceptibility is Associated With Slower Gait in Community-Dwelling Older Adults
title_full_unstemmed Brain Magnetic Susceptibility is Associated With Slower Gait in Community-Dwelling Older Adults
title_short Brain Magnetic Susceptibility is Associated With Slower Gait in Community-Dwelling Older Adults
title_sort brain magnetic susceptibility is associated with slower gait in community-dwelling older adults
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8681799/
http://dx.doi.org/10.1093/geroni/igab046.3177
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