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Age-related changes in brain structural covariance networks

Previous neuroimaging studies have suggested that cerebral changes over normal aging are not simply characterized by regional alterations, but rather by the reorganization of cortical connectivity patterns. The investigation of structural covariance networks (SCNs) using voxel-based morphometry is a...

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Autores principales: Li, Xinwei, Pu, Fang, Fan, Yubo, Niu, Haijun, Li, Shuyu, Li, Deyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607831/
https://www.ncbi.nlm.nih.gov/pubmed/23532684
http://dx.doi.org/10.3389/fnhum.2013.00098
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author Li, Xinwei
Pu, Fang
Fan, Yubo
Niu, Haijun
Li, Shuyu
Li, Deyu
author_facet Li, Xinwei
Pu, Fang
Fan, Yubo
Niu, Haijun
Li, Shuyu
Li, Deyu
author_sort Li, Xinwei
collection PubMed
description Previous neuroimaging studies have suggested that cerebral changes over normal aging are not simply characterized by regional alterations, but rather by the reorganization of cortical connectivity patterns. The investigation of structural covariance networks (SCNs) using voxel-based morphometry is an advanced approach to examining the pattern of covariance in gray matter (GM) volumes among different regions of the human cortex. To date, how the organization of critical SCNs change during normal aging remains largely unknown. In this study, we used an SCN mapping approach to investigate eight large-scale networks in 240 healthy participants aged 18–89 years. These participants were subdivided into young (18–23 years), middle aged (30–58 years), and older (61–89 years) subjects. Eight seed regions were chosen from widely reported functional intrinsic connectivity networks. The voxels showing significant positive associations with these seed regions were used to describe the topological organization of an SCN. All of these networks exhibited non-linear patterns in their spatial extent that were associated with normal aging. These networks, except the primary motor network, had a distributed topology in young participants, a sharply localized topology in middle aged participants, and were relatively stable in older participants. The structural covariance derived using the primary motor cortex was limited to the ipsilateral motor regions in the young and older participants, but included contralateral homologous regions in the middle aged participants. In addition, there were significant between-group differences in the structural networks associated with language-related speech and semantics processing, executive control, and the default-mode network (DMN). Taken together, the results of this study demonstrate age-related changes in the topological organization of SCNs, and provide insights into normal aging of the human brain.
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spelling pubmed-36078312013-03-26 Age-related changes in brain structural covariance networks Li, Xinwei Pu, Fang Fan, Yubo Niu, Haijun Li, Shuyu Li, Deyu Front Hum Neurosci Neuroscience Previous neuroimaging studies have suggested that cerebral changes over normal aging are not simply characterized by regional alterations, but rather by the reorganization of cortical connectivity patterns. The investigation of structural covariance networks (SCNs) using voxel-based morphometry is an advanced approach to examining the pattern of covariance in gray matter (GM) volumes among different regions of the human cortex. To date, how the organization of critical SCNs change during normal aging remains largely unknown. In this study, we used an SCN mapping approach to investigate eight large-scale networks in 240 healthy participants aged 18–89 years. These participants were subdivided into young (18–23 years), middle aged (30–58 years), and older (61–89 years) subjects. Eight seed regions were chosen from widely reported functional intrinsic connectivity networks. The voxels showing significant positive associations with these seed regions were used to describe the topological organization of an SCN. All of these networks exhibited non-linear patterns in their spatial extent that were associated with normal aging. These networks, except the primary motor network, had a distributed topology in young participants, a sharply localized topology in middle aged participants, and were relatively stable in older participants. The structural covariance derived using the primary motor cortex was limited to the ipsilateral motor regions in the young and older participants, but included contralateral homologous regions in the middle aged participants. In addition, there were significant between-group differences in the structural networks associated with language-related speech and semantics processing, executive control, and the default-mode network (DMN). Taken together, the results of this study demonstrate age-related changes in the topological organization of SCNs, and provide insights into normal aging of the human brain. Frontiers Media S.A. 2013-03-26 /pmc/articles/PMC3607831/ /pubmed/23532684 http://dx.doi.org/10.3389/fnhum.2013.00098 Text en Copyright © 2013 Li, Pu, Fan, Niu, Li and Li. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Li, Xinwei
Pu, Fang
Fan, Yubo
Niu, Haijun
Li, Shuyu
Li, Deyu
Age-related changes in brain structural covariance networks
title Age-related changes in brain structural covariance networks
title_full Age-related changes in brain structural covariance networks
title_fullStr Age-related changes in brain structural covariance networks
title_full_unstemmed Age-related changes in brain structural covariance networks
title_short Age-related changes in brain structural covariance networks
title_sort age-related changes in brain structural covariance networks
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607831/
https://www.ncbi.nlm.nih.gov/pubmed/23532684
http://dx.doi.org/10.3389/fnhum.2013.00098
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