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Thalamic functional connectivity and its association with behavioral performance in older age

INTRODUCTION: Despite the thalamus’ dense connectivity with both cortical and subcortical structures, few studies have specifically investigated how thalamic connectivity changes with age and how such changes are associated with behavior. This study investigated the effect of age on thalamo‐cortical...

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Autores principales: Goldstone, Aimée, Mayhew, Stephen D., Hale, Joanne R., Wilson, Rebecca S., Bagshaw, Andrew P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893345/
https://www.ncbi.nlm.nih.gov/pubmed/29670825
http://dx.doi.org/10.1002/brb3.943
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author Goldstone, Aimée
Mayhew, Stephen D.
Hale, Joanne R.
Wilson, Rebecca S.
Bagshaw, Andrew P.
author_facet Goldstone, Aimée
Mayhew, Stephen D.
Hale, Joanne R.
Wilson, Rebecca S.
Bagshaw, Andrew P.
author_sort Goldstone, Aimée
collection PubMed
description INTRODUCTION: Despite the thalamus’ dense connectivity with both cortical and subcortical structures, few studies have specifically investigated how thalamic connectivity changes with age and how such changes are associated with behavior. This study investigated the effect of age on thalamo‐cortical and thalamo‐hippocampal functional connectivity (FC) and the association between thalamic FC and visual–spatial memory and reaction time (RT) performance in older adults. METHODS: Resting‐state functional magnetic resonance images were obtained from younger (n = 20) and older (n = 20) adults. A seed‐based approach was used to assess the FC between the thalamus and (1) sensory resting‐state networks; (2) the hippocampus. Participants also completed visual–spatial memory and RT tasks, from the Cambridge Neuropsychological Test Automated Battery (CANTAB). RESULTS: Older adults exhibited a loss of specificity in the FC between sensory thalamic subregions and corresponding sensory cortex. Greater thalamo‐motor FC in older adults was associated with faster RTs. Furthermore, older adults exhibited greater thalamo‐hippocampal FC compared to younger adults, which was greatest for those with the poorest visual–spatial memory performance. CONCLUSION: Although older adults exhibited poorer visual–spatial memory and slower reaction times compared to younger adults, “good” and “poorer” older performers exhibited different patterns of thalamo‐cortical and thalamo‐hippocampal FC. These results highlight the potential role of thalamic connectivity in supporting reaction times and memory in aging. Furthermore, these results highlight the importance of including the thalamus in studies of aging to fully understand how brain changes with age may be associated with behavior.
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spelling pubmed-58933452018-04-18 Thalamic functional connectivity and its association with behavioral performance in older age Goldstone, Aimée Mayhew, Stephen D. Hale, Joanne R. Wilson, Rebecca S. Bagshaw, Andrew P. Brain Behav Original Research INTRODUCTION: Despite the thalamus’ dense connectivity with both cortical and subcortical structures, few studies have specifically investigated how thalamic connectivity changes with age and how such changes are associated with behavior. This study investigated the effect of age on thalamo‐cortical and thalamo‐hippocampal functional connectivity (FC) and the association between thalamic FC and visual–spatial memory and reaction time (RT) performance in older adults. METHODS: Resting‐state functional magnetic resonance images were obtained from younger (n = 20) and older (n = 20) adults. A seed‐based approach was used to assess the FC between the thalamus and (1) sensory resting‐state networks; (2) the hippocampus. Participants also completed visual–spatial memory and RT tasks, from the Cambridge Neuropsychological Test Automated Battery (CANTAB). RESULTS: Older adults exhibited a loss of specificity in the FC between sensory thalamic subregions and corresponding sensory cortex. Greater thalamo‐motor FC in older adults was associated with faster RTs. Furthermore, older adults exhibited greater thalamo‐hippocampal FC compared to younger adults, which was greatest for those with the poorest visual–spatial memory performance. CONCLUSION: Although older adults exhibited poorer visual–spatial memory and slower reaction times compared to younger adults, “good” and “poorer” older performers exhibited different patterns of thalamo‐cortical and thalamo‐hippocampal FC. These results highlight the potential role of thalamic connectivity in supporting reaction times and memory in aging. Furthermore, these results highlight the importance of including the thalamus in studies of aging to fully understand how brain changes with age may be associated with behavior. John Wiley and Sons Inc. 2018-02-27 /pmc/articles/PMC5893345/ /pubmed/29670825 http://dx.doi.org/10.1002/brb3.943 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. 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 Original Research
Goldstone, Aimée
Mayhew, Stephen D.
Hale, Joanne R.
Wilson, Rebecca S.
Bagshaw, Andrew P.
Thalamic functional connectivity and its association with behavioral performance in older age
title Thalamic functional connectivity and its association with behavioral performance in older age
title_full Thalamic functional connectivity and its association with behavioral performance in older age
title_fullStr Thalamic functional connectivity and its association with behavioral performance in older age
title_full_unstemmed Thalamic functional connectivity and its association with behavioral performance in older age
title_short Thalamic functional connectivity and its association with behavioral performance in older age
title_sort thalamic functional connectivity and its association with behavioral performance in older age
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893345/
https://www.ncbi.nlm.nih.gov/pubmed/29670825
http://dx.doi.org/10.1002/brb3.943
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