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Whole-brain connectivity during encoding: age-related differences and associations with cognitive and brain structural decline

There is a limited understanding of age differences in functional connectivity during memory encoding. In the present study, a sample of cognitively healthy adult participants (n = 488, 18–81 years), a subsample of whom had longitudinal cognitive and brain structural data spanning on average 8 years...

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Autores principales: Capogna, Elettra, Sneve, Markus H, Raud, Liisa, Folvik, Line, Ness, Hedda T, Walhovd, Kristine B, Fjell, Anders M, Vidal-Piñeiro, Didac
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9758575/
https://www.ncbi.nlm.nih.gov/pubmed/35193146
http://dx.doi.org/10.1093/cercor/bhac053
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author Capogna, Elettra
Sneve, Markus H
Raud, Liisa
Folvik, Line
Ness, Hedda T
Walhovd, Kristine B
Fjell, Anders M
Vidal-Piñeiro, Didac
author_facet Capogna, Elettra
Sneve, Markus H
Raud, Liisa
Folvik, Line
Ness, Hedda T
Walhovd, Kristine B
Fjell, Anders M
Vidal-Piñeiro, Didac
author_sort Capogna, Elettra
collection PubMed
description There is a limited understanding of age differences in functional connectivity during memory encoding. In the present study, a sample of cognitively healthy adult participants (n = 488, 18–81 years), a subsample of whom had longitudinal cognitive and brain structural data spanning on average 8 years back, underwent functional magnetic resonance imaging while performing an associative memory encoding task. We investigated (1) age-related differences in whole-brain connectivity during memory encoding; (2) whether encoding connectivity patterns overlapped with the activity signatures of specific cognitive processes, and (3) whether connectivity associated with memory encoding related to longitudinal brain structural and cognitive changes. Age was associated with lower intranetwork connectivity among cortical networks and higher internetwork connectivity between networks supporting higher level cognitive functions and unimodal and attentional areas during encoding. Task-connectivity between mediotemporal and posterior parietal regions—which overlapped with areas involved in mental imagery—was related to better memory performance only in older age. The connectivity patterns supporting memory performance in older age reflected preservation of thickness of the medial temporal cortex. The results are more in accordance with a maintenance rather than a compensation account.
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spelling pubmed-97585752022-12-19 Whole-brain connectivity during encoding: age-related differences and associations with cognitive and brain structural decline Capogna, Elettra Sneve, Markus H Raud, Liisa Folvik, Line Ness, Hedda T Walhovd, Kristine B Fjell, Anders M Vidal-Piñeiro, Didac Cereb Cortex Original Article There is a limited understanding of age differences in functional connectivity during memory encoding. In the present study, a sample of cognitively healthy adult participants (n = 488, 18–81 years), a subsample of whom had longitudinal cognitive and brain structural data spanning on average 8 years back, underwent functional magnetic resonance imaging while performing an associative memory encoding task. We investigated (1) age-related differences in whole-brain connectivity during memory encoding; (2) whether encoding connectivity patterns overlapped with the activity signatures of specific cognitive processes, and (3) whether connectivity associated with memory encoding related to longitudinal brain structural and cognitive changes. Age was associated with lower intranetwork connectivity among cortical networks and higher internetwork connectivity between networks supporting higher level cognitive functions and unimodal and attentional areas during encoding. Task-connectivity between mediotemporal and posterior parietal regions—which overlapped with areas involved in mental imagery—was related to better memory performance only in older age. The connectivity patterns supporting memory performance in older age reflected preservation of thickness of the medial temporal cortex. The results are more in accordance with a maintenance rather than a compensation account. Oxford University Press 2022-02-22 /pmc/articles/PMC9758575/ /pubmed/35193146 http://dx.doi.org/10.1093/cercor/bhac053 Text en © The Author(s) 2022. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permission@oup.com. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Capogna, Elettra
Sneve, Markus H
Raud, Liisa
Folvik, Line
Ness, Hedda T
Walhovd, Kristine B
Fjell, Anders M
Vidal-Piñeiro, Didac
Whole-brain connectivity during encoding: age-related differences and associations with cognitive and brain structural decline
title Whole-brain connectivity during encoding: age-related differences and associations with cognitive and brain structural decline
title_full Whole-brain connectivity during encoding: age-related differences and associations with cognitive and brain structural decline
title_fullStr Whole-brain connectivity during encoding: age-related differences and associations with cognitive and brain structural decline
title_full_unstemmed Whole-brain connectivity during encoding: age-related differences and associations with cognitive and brain structural decline
title_short Whole-brain connectivity during encoding: age-related differences and associations with cognitive and brain structural decline
title_sort whole-brain connectivity during encoding: age-related differences and associations with cognitive and brain structural decline
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9758575/
https://www.ncbi.nlm.nih.gov/pubmed/35193146
http://dx.doi.org/10.1093/cercor/bhac053
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