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Sex differences in multilayer functional network topology over the course of aging in 37543 UK Biobank participants

Aging is a major risk factor for cardiovascular and neurodegenerative disorders, with considerable societal and economic implications. Healthy aging is accompanied by changes in functional connectivity between and within resting-state functional networks, which have been associated with cognitive de...

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Autores principales: Mijalkov, Mite, Veréb, Dániel, Jamialahmadi, Oveis, Canal-Garcia, Anna, Gómez-Ruiz, Emiliano, Vidal-Piñeiro, Didac, Romeo, Stefano, Volpe, Giovanni, Pereira, Joana B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MIT Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275214/
https://www.ncbi.nlm.nih.gov/pubmed/37334001
http://dx.doi.org/10.1162/netn_a_00286
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author Mijalkov, Mite
Veréb, Dániel
Jamialahmadi, Oveis
Canal-Garcia, Anna
Gómez-Ruiz, Emiliano
Vidal-Piñeiro, Didac
Romeo, Stefano
Volpe, Giovanni
Pereira, Joana B.
author_facet Mijalkov, Mite
Veréb, Dániel
Jamialahmadi, Oveis
Canal-Garcia, Anna
Gómez-Ruiz, Emiliano
Vidal-Piñeiro, Didac
Romeo, Stefano
Volpe, Giovanni
Pereira, Joana B.
author_sort Mijalkov, Mite
collection PubMed
description Aging is a major risk factor for cardiovascular and neurodegenerative disorders, with considerable societal and economic implications. Healthy aging is accompanied by changes in functional connectivity between and within resting-state functional networks, which have been associated with cognitive decline. However, there is no consensus on the impact of sex on these age-related functional trajectories. Here, we show that multilayer measures provide crucial information on the interaction between sex and age on network topology, allowing for better assessment of cognitive, structural, and cardiovascular risk factors that have been shown to differ between men and women, as well as providing additional insights into the genetic influences on changes in functional connectivity that occur during aging. In a large cross-sectional sample of 37,543 individuals from the UK Biobank cohort, we demonstrate that such multilayer measures that capture the relationship between positive and negative connections are more sensitive to sex-related changes in the whole-brain connectivity patterns and their topological architecture throughout aging, when compared to standard connectivity and topological measures. Our findings indicate that multilayer measures contain previously unknown information on the relationship between sex and age, which opens up new avenues for research into functional brain connectivity in aging.
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spelling pubmed-102752142023-06-17 Sex differences in multilayer functional network topology over the course of aging in 37543 UK Biobank participants Mijalkov, Mite Veréb, Dániel Jamialahmadi, Oveis Canal-Garcia, Anna Gómez-Ruiz, Emiliano Vidal-Piñeiro, Didac Romeo, Stefano Volpe, Giovanni Pereira, Joana B. Netw Neurosci Research Article Aging is a major risk factor for cardiovascular and neurodegenerative disorders, with considerable societal and economic implications. Healthy aging is accompanied by changes in functional connectivity between and within resting-state functional networks, which have been associated with cognitive decline. However, there is no consensus on the impact of sex on these age-related functional trajectories. Here, we show that multilayer measures provide crucial information on the interaction between sex and age on network topology, allowing for better assessment of cognitive, structural, and cardiovascular risk factors that have been shown to differ between men and women, as well as providing additional insights into the genetic influences on changes in functional connectivity that occur during aging. In a large cross-sectional sample of 37,543 individuals from the UK Biobank cohort, we demonstrate that such multilayer measures that capture the relationship between positive and negative connections are more sensitive to sex-related changes in the whole-brain connectivity patterns and their topological architecture throughout aging, when compared to standard connectivity and topological measures. Our findings indicate that multilayer measures contain previously unknown information on the relationship between sex and age, which opens up new avenues for research into functional brain connectivity in aging. MIT Press 2023-01-01 /pmc/articles/PMC10275214/ /pubmed/37334001 http://dx.doi.org/10.1162/netn_a_00286 Text en © 2022 Massachusetts Institute of Technology https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. For a full description of the license, please visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Mijalkov, Mite
Veréb, Dániel
Jamialahmadi, Oveis
Canal-Garcia, Anna
Gómez-Ruiz, Emiliano
Vidal-Piñeiro, Didac
Romeo, Stefano
Volpe, Giovanni
Pereira, Joana B.
Sex differences in multilayer functional network topology over the course of aging in 37543 UK Biobank participants
title Sex differences in multilayer functional network topology over the course of aging in 37543 UK Biobank participants
title_full Sex differences in multilayer functional network topology over the course of aging in 37543 UK Biobank participants
title_fullStr Sex differences in multilayer functional network topology over the course of aging in 37543 UK Biobank participants
title_full_unstemmed Sex differences in multilayer functional network topology over the course of aging in 37543 UK Biobank participants
title_short Sex differences in multilayer functional network topology over the course of aging in 37543 UK Biobank participants
title_sort sex differences in multilayer functional network topology over the course of aging in 37543 uk biobank participants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275214/
https://www.ncbi.nlm.nih.gov/pubmed/37334001
http://dx.doi.org/10.1162/netn_a_00286
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