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Role of dopamine and gray matter density in aging effects and individual differences of functional connectomes

With increasing age, functional connectomes become dissimilar across normal individuals, reflecting heterogenous aging effects on functional connectivity (FC). We investigated the distribution of these effects across the connectome and their relationship with age-related differences in dopamine (DA)...

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Autores principales: Garzón, Benjamín, Lövdén, Martin, de Boer, Lieke, Axelsson, Jan, Riklund, Katrine, Bäckman, Lars, Nyberg, Lars, Guitart-Masip, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7981334/
https://www.ncbi.nlm.nih.gov/pubmed/33423111
http://dx.doi.org/10.1007/s00429-020-02205-4
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author Garzón, Benjamín
Lövdén, Martin
de Boer, Lieke
Axelsson, Jan
Riklund, Katrine
Bäckman, Lars
Nyberg, Lars
Guitart-Masip, Marc
author_facet Garzón, Benjamín
Lövdén, Martin
de Boer, Lieke
Axelsson, Jan
Riklund, Katrine
Bäckman, Lars
Nyberg, Lars
Guitart-Masip, Marc
author_sort Garzón, Benjamín
collection PubMed
description With increasing age, functional connectomes become dissimilar across normal individuals, reflecting heterogenous aging effects on functional connectivity (FC). We investigated the distribution of these effects across the connectome and their relationship with age-related differences in dopamine (DA) D1 receptor availability and gray matter density (GMD). With this aim, we determined aging effects on mean and interindividual variance of FC using fMRI in 30 younger and 30 older healthy subjects and mapped the contribution of each connection to the patterns of age-related similarity loss. Aging effects on mean FC accounted mainly for the dissimilarity between connectomes of younger and older adults, and were related, across brain regions, to aging effects on DA D1 receptor availability. Aging effects on the variance of FC indicated a global increase in variance with advancing age, explained connectome dissimilarity among older subjects and were related to aging effects on variance of GMD. The relationship between aging and the similarity of connectomes can thus be partly explained by age differences in DA modulation and gray matter structure. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00429-020-02205-4.
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spelling pubmed-79813342021-04-12 Role of dopamine and gray matter density in aging effects and individual differences of functional connectomes Garzón, Benjamín Lövdén, Martin de Boer, Lieke Axelsson, Jan Riklund, Katrine Bäckman, Lars Nyberg, Lars Guitart-Masip, Marc Brain Struct Funct Original Article With increasing age, functional connectomes become dissimilar across normal individuals, reflecting heterogenous aging effects on functional connectivity (FC). We investigated the distribution of these effects across the connectome and their relationship with age-related differences in dopamine (DA) D1 receptor availability and gray matter density (GMD). With this aim, we determined aging effects on mean and interindividual variance of FC using fMRI in 30 younger and 30 older healthy subjects and mapped the contribution of each connection to the patterns of age-related similarity loss. Aging effects on mean FC accounted mainly for the dissimilarity between connectomes of younger and older adults, and were related, across brain regions, to aging effects on DA D1 receptor availability. Aging effects on the variance of FC indicated a global increase in variance with advancing age, explained connectome dissimilarity among older subjects and were related to aging effects on variance of GMD. The relationship between aging and the similarity of connectomes can thus be partly explained by age differences in DA modulation and gray matter structure. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00429-020-02205-4. Springer Berlin Heidelberg 2021-01-09 2021 /pmc/articles/PMC7981334/ /pubmed/33423111 http://dx.doi.org/10.1007/s00429-020-02205-4 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Garzón, Benjamín
Lövdén, Martin
de Boer, Lieke
Axelsson, Jan
Riklund, Katrine
Bäckman, Lars
Nyberg, Lars
Guitart-Masip, Marc
Role of dopamine and gray matter density in aging effects and individual differences of functional connectomes
title Role of dopamine and gray matter density in aging effects and individual differences of functional connectomes
title_full Role of dopamine and gray matter density in aging effects and individual differences of functional connectomes
title_fullStr Role of dopamine and gray matter density in aging effects and individual differences of functional connectomes
title_full_unstemmed Role of dopamine and gray matter density in aging effects and individual differences of functional connectomes
title_short Role of dopamine and gray matter density in aging effects and individual differences of functional connectomes
title_sort role of dopamine and gray matter density in aging effects and individual differences of functional connectomes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7981334/
https://www.ncbi.nlm.nih.gov/pubmed/33423111
http://dx.doi.org/10.1007/s00429-020-02205-4
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