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The association between stress and mood across the adult lifespan on default mode network

Aging of brain structure and function is a complex process characterized by high inter- and intra-individual variability. Such variability may arise from the interaction of multiple factors, including exposure to stressful experience and mood variation, across the lifespan. Using a multimodal neuroi...

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Autores principales: Soares, José Miguel, Marques, Paulo, Magalhães, Ricardo, Santos, Nadine Correia, Sousa, Nuno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225218/
https://www.ncbi.nlm.nih.gov/pubmed/26971253
http://dx.doi.org/10.1007/s00429-016-1203-3
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author Soares, José Miguel
Marques, Paulo
Magalhães, Ricardo
Santos, Nadine Correia
Sousa, Nuno
author_facet Soares, José Miguel
Marques, Paulo
Magalhães, Ricardo
Santos, Nadine Correia
Sousa, Nuno
author_sort Soares, José Miguel
collection PubMed
description Aging of brain structure and function is a complex process characterized by high inter- and intra-individual variability. Such variability may arise from the interaction of multiple factors, including exposure to stressful experience and mood variation, across the lifespan. Using a multimodal neuroimaging and neurocognitive approach, we investigated the association of stress, mood and their interaction, in the structure and function of the default mode network (DMN), both during rest and task-induced deactivation, throughout the adult lifespan. Data confirmed a decreased functional connectivity (FC) and task-induced deactivation of the DMN during the aging process and in subjects with lower mood; on the contrary, an increased FC was observed in subjects with higher perceived stress. Surprisingly, the association of aging with DMN was altered by stress and mood in specific regions. An increased difficulty to deactivate the DMN was noted in older participants with lower mood, contrasting with an increased deactivation in individuals presenting high stress, independently of their mood levels, with aging. Interestingly, this constant interaction across aging was globally most significant in the combination of high stress levels with a more depressed mood state, both during resting state and task-induced deactivations. The present results contribute to characterize the spectrum of FC and deactivation patterns of the DMN, highlighting the crucial association of stress and mood levels, during the adult aging process. These combinatorial approaches may help to understand the heterogeneity of the aging process in brain structure and function and several states that may lead to neuropsychiatric disorders.
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spelling pubmed-52252182017-01-24 The association between stress and mood across the adult lifespan on default mode network Soares, José Miguel Marques, Paulo Magalhães, Ricardo Santos, Nadine Correia Sousa, Nuno Brain Struct Funct Original Article Aging of brain structure and function is a complex process characterized by high inter- and intra-individual variability. Such variability may arise from the interaction of multiple factors, including exposure to stressful experience and mood variation, across the lifespan. Using a multimodal neuroimaging and neurocognitive approach, we investigated the association of stress, mood and their interaction, in the structure and function of the default mode network (DMN), both during rest and task-induced deactivation, throughout the adult lifespan. Data confirmed a decreased functional connectivity (FC) and task-induced deactivation of the DMN during the aging process and in subjects with lower mood; on the contrary, an increased FC was observed in subjects with higher perceived stress. Surprisingly, the association of aging with DMN was altered by stress and mood in specific regions. An increased difficulty to deactivate the DMN was noted in older participants with lower mood, contrasting with an increased deactivation in individuals presenting high stress, independently of their mood levels, with aging. Interestingly, this constant interaction across aging was globally most significant in the combination of high stress levels with a more depressed mood state, both during resting state and task-induced deactivations. The present results contribute to characterize the spectrum of FC and deactivation patterns of the DMN, highlighting the crucial association of stress and mood levels, during the adult aging process. These combinatorial approaches may help to understand the heterogeneity of the aging process in brain structure and function and several states that may lead to neuropsychiatric disorders. Springer Berlin Heidelberg 2016-03-12 2017 /pmc/articles/PMC5225218/ /pubmed/26971253 http://dx.doi.org/10.1007/s00429-016-1203-3 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Soares, José Miguel
Marques, Paulo
Magalhães, Ricardo
Santos, Nadine Correia
Sousa, Nuno
The association between stress and mood across the adult lifespan on default mode network
title The association between stress and mood across the adult lifespan on default mode network
title_full The association between stress and mood across the adult lifespan on default mode network
title_fullStr The association between stress and mood across the adult lifespan on default mode network
title_full_unstemmed The association between stress and mood across the adult lifespan on default mode network
title_short The association between stress and mood across the adult lifespan on default mode network
title_sort association between stress and mood across the adult lifespan on default mode network
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225218/
https://www.ncbi.nlm.nih.gov/pubmed/26971253
http://dx.doi.org/10.1007/s00429-016-1203-3
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