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Differential Age-Related Changes in Structural Covariance Networks of Human Anterior and Posterior Hippocampus

The hippocampus plays an important role in memory function relying on information interaction between distributed brain areas. The hippocampus can be divided into the anterior and posterior sections with different structure and function along its long axis. The aim of this study is to investigate th...

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Autores principales: Li, Xinwei, Li, Qiongling, Wang, Xuetong, Li, Deyu, Li, Shuyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954440/
https://www.ncbi.nlm.nih.gov/pubmed/29867561
http://dx.doi.org/10.3389/fphys.2018.00518
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author Li, Xinwei
Li, Qiongling
Wang, Xuetong
Li, Deyu
Li, Shuyu
author_facet Li, Xinwei
Li, Qiongling
Wang, Xuetong
Li, Deyu
Li, Shuyu
author_sort Li, Xinwei
collection PubMed
description The hippocampus plays an important role in memory function relying on information interaction between distributed brain areas. The hippocampus can be divided into the anterior and posterior sections with different structure and function along its long axis. The aim of this study is to investigate the effects of normal aging on the structural covariance of the anterior hippocampus (aHPC) and the posterior hippocampus (pHPC). In this study, 240 healthy subjects aged 18–89 years were selected and subdivided into young (18–23 years), middle-aged (30–58 years), and older (61–89 years) groups. The aHPC and pHPC was divided based on the location of uncal apex in the MNI space. Then, the structural covariance networks were constructed by examining their covariance in gray matter volumes with other brain regions. Finally, the influence of age on the structural covariance of these hippocampal sections was explored. We found that the aHPC and pHPC had different structural covariance patterns, but both of them were associated with the medial temporal lobe and insula. Moreover, both increased and decreased covariances were found with the aHPC but only increased covariance was found with the pHPC with age (p < 0.05, family-wise error corrected). These decreased connections occurred within the default mode network, while the increased connectivity mainly occurred in other memory systems that differ from the hippocampus. This study reveals different age-related influence on the structural networks of the aHPC and pHPC, providing an essential insight into the mechanisms of the hippocampus in normal aging.
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spelling pubmed-59544402018-06-04 Differential Age-Related Changes in Structural Covariance Networks of Human Anterior and Posterior Hippocampus Li, Xinwei Li, Qiongling Wang, Xuetong Li, Deyu Li, Shuyu Front Physiol Physiology The hippocampus plays an important role in memory function relying on information interaction between distributed brain areas. The hippocampus can be divided into the anterior and posterior sections with different structure and function along its long axis. The aim of this study is to investigate the effects of normal aging on the structural covariance of the anterior hippocampus (aHPC) and the posterior hippocampus (pHPC). In this study, 240 healthy subjects aged 18–89 years were selected and subdivided into young (18–23 years), middle-aged (30–58 years), and older (61–89 years) groups. The aHPC and pHPC was divided based on the location of uncal apex in the MNI space. Then, the structural covariance networks were constructed by examining their covariance in gray matter volumes with other brain regions. Finally, the influence of age on the structural covariance of these hippocampal sections was explored. We found that the aHPC and pHPC had different structural covariance patterns, but both of them were associated with the medial temporal lobe and insula. Moreover, both increased and decreased covariances were found with the aHPC but only increased covariance was found with the pHPC with age (p < 0.05, family-wise error corrected). These decreased connections occurred within the default mode network, while the increased connectivity mainly occurred in other memory systems that differ from the hippocampus. This study reveals different age-related influence on the structural networks of the aHPC and pHPC, providing an essential insight into the mechanisms of the hippocampus in normal aging. Frontiers Media S.A. 2018-05-09 /pmc/articles/PMC5954440/ /pubmed/29867561 http://dx.doi.org/10.3389/fphys.2018.00518 Text en Copyright © 2018 Li, Li, Wang, Li and Li. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Li, Xinwei
Li, Qiongling
Wang, Xuetong
Li, Deyu
Li, Shuyu
Differential Age-Related Changes in Structural Covariance Networks of Human Anterior and Posterior Hippocampus
title Differential Age-Related Changes in Structural Covariance Networks of Human Anterior and Posterior Hippocampus
title_full Differential Age-Related Changes in Structural Covariance Networks of Human Anterior and Posterior Hippocampus
title_fullStr Differential Age-Related Changes in Structural Covariance Networks of Human Anterior and Posterior Hippocampus
title_full_unstemmed Differential Age-Related Changes in Structural Covariance Networks of Human Anterior and Posterior Hippocampus
title_short Differential Age-Related Changes in Structural Covariance Networks of Human Anterior and Posterior Hippocampus
title_sort differential age-related changes in structural covariance networks of human anterior and posterior hippocampus
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954440/
https://www.ncbi.nlm.nih.gov/pubmed/29867561
http://dx.doi.org/10.3389/fphys.2018.00518
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