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Deviations in Hippocampal Subregion in Older Adults With Cognitive Frailty
BACKGROUND: Cognitive frailty is a particular state of cognitive vulnerability toward dementia with neuropathological hallmarks. The hippocampus is a complex, heterogeneous structure closely relates to the cognitive impairment in elderly which is composed of 12 subregions. Atrophy of these subregion...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838368/ https://www.ncbi.nlm.nih.gov/pubmed/33519422 http://dx.doi.org/10.3389/fnagi.2020.615852 |
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author | Wan, Mingyue Ye, Yu Lin, Huiying Xu, Ying Liang, Shengxiang Xia, Rui He, Jianquan Qiu, Pingting Huang, Chengwu Tao, Jing Chen, Lidian Zheng, Guohua |
author_facet | Wan, Mingyue Ye, Yu Lin, Huiying Xu, Ying Liang, Shengxiang Xia, Rui He, Jianquan Qiu, Pingting Huang, Chengwu Tao, Jing Chen, Lidian Zheng, Guohua |
author_sort | Wan, Mingyue |
collection | PubMed |
description | BACKGROUND: Cognitive frailty is a particular state of cognitive vulnerability toward dementia with neuropathological hallmarks. The hippocampus is a complex, heterogeneous structure closely relates to the cognitive impairment in elderly which is composed of 12 subregions. Atrophy of these subregions has been implicated in a variety of neurodegenerative diseases. The aim of this study was to explore the changes in hippocampal subregions in older adults with cognitive frailty and the relationship between subregions and cognitive impairment as well as physical frailty. METHODS: Twenty-six older adults with cognitive frailty and 26 matched healthy controls were included in this study. Cognitive function was evaluated by the Montreal Cognitive Assessment (MoCA) scale (Fuzhou version) and Wechsler Memory Scale-Revised Chinese version (WMS-RC), while physical frailty was tested with the Chinese version of the Edmonton Frailty Scale (EFS) and grip strength. The volume of the hippocampal subregions was measured with structural brain magnetic resonance imaging. Partial correlation analysis was carried out between the volumes of hippocampal subregions and MoCA scores, Wechsler’s Memory Quotient and physical frailty indexes. RESULTS: A significant volume decrease was found in six hippocampal subregions, including the bilateral presubiculum, the left parasubiculum, molecular layer of the hippocampus proper (molecular layer of the HP), and hippocampal amygdala transition area (HATA), and the right cornu ammonis subfield 1 (CA1) area, in older adults with cognitive frailty, while the proportion of brain parenchyma and total number of white matter fibers were lower than those in the healthy controls. Positive correlations were found between Wechsler’s Memory Quotient and the size of the left molecular layer of the HP and HATA and the right presubiculum. The sizes of the left presubiculum, molecular of the layer HP, and HATA and right CA1 and presubiculum were found to be positively correlated with MoCA score. The sizes of the left parasubiculum, molecular layer of the HP and HATA were found to be negatively correlated with the physical frailty index. CONCLUSION: Significant volume decrease occurs in hippocampal subregions of older adults with cognitive frailty, and these changes are correlated with cognitive impairment and physical frailty. Therefore, the atrophy of hippocampal subregions could participate in the pathological progression of cognitive frailty. |
format | Online Article Text |
id | pubmed-7838368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78383682021-01-28 Deviations in Hippocampal Subregion in Older Adults With Cognitive Frailty Wan, Mingyue Ye, Yu Lin, Huiying Xu, Ying Liang, Shengxiang Xia, Rui He, Jianquan Qiu, Pingting Huang, Chengwu Tao, Jing Chen, Lidian Zheng, Guohua Front Aging Neurosci Neuroscience BACKGROUND: Cognitive frailty is a particular state of cognitive vulnerability toward dementia with neuropathological hallmarks. The hippocampus is a complex, heterogeneous structure closely relates to the cognitive impairment in elderly which is composed of 12 subregions. Atrophy of these subregions has been implicated in a variety of neurodegenerative diseases. The aim of this study was to explore the changes in hippocampal subregions in older adults with cognitive frailty and the relationship between subregions and cognitive impairment as well as physical frailty. METHODS: Twenty-six older adults with cognitive frailty and 26 matched healthy controls were included in this study. Cognitive function was evaluated by the Montreal Cognitive Assessment (MoCA) scale (Fuzhou version) and Wechsler Memory Scale-Revised Chinese version (WMS-RC), while physical frailty was tested with the Chinese version of the Edmonton Frailty Scale (EFS) and grip strength. The volume of the hippocampal subregions was measured with structural brain magnetic resonance imaging. Partial correlation analysis was carried out between the volumes of hippocampal subregions and MoCA scores, Wechsler’s Memory Quotient and physical frailty indexes. RESULTS: A significant volume decrease was found in six hippocampal subregions, including the bilateral presubiculum, the left parasubiculum, molecular layer of the hippocampus proper (molecular layer of the HP), and hippocampal amygdala transition area (HATA), and the right cornu ammonis subfield 1 (CA1) area, in older adults with cognitive frailty, while the proportion of brain parenchyma and total number of white matter fibers were lower than those in the healthy controls. Positive correlations were found between Wechsler’s Memory Quotient and the size of the left molecular layer of the HP and HATA and the right presubiculum. The sizes of the left presubiculum, molecular of the layer HP, and HATA and right CA1 and presubiculum were found to be positively correlated with MoCA score. The sizes of the left parasubiculum, molecular layer of the HP and HATA were found to be negatively correlated with the physical frailty index. CONCLUSION: Significant volume decrease occurs in hippocampal subregions of older adults with cognitive frailty, and these changes are correlated with cognitive impairment and physical frailty. Therefore, the atrophy of hippocampal subregions could participate in the pathological progression of cognitive frailty. Frontiers Media S.A. 2021-01-13 /pmc/articles/PMC7838368/ /pubmed/33519422 http://dx.doi.org/10.3389/fnagi.2020.615852 Text en Copyright © 2021 Wan, Ye, Lin, Xu, Liang, Xia, He, Qiu, Huang, Tao, Chen and Zheng. 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(s) 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 | Neuroscience Wan, Mingyue Ye, Yu Lin, Huiying Xu, Ying Liang, Shengxiang Xia, Rui He, Jianquan Qiu, Pingting Huang, Chengwu Tao, Jing Chen, Lidian Zheng, Guohua Deviations in Hippocampal Subregion in Older Adults With Cognitive Frailty |
title | Deviations in Hippocampal Subregion in Older Adults With Cognitive Frailty |
title_full | Deviations in Hippocampal Subregion in Older Adults With Cognitive Frailty |
title_fullStr | Deviations in Hippocampal Subregion in Older Adults With Cognitive Frailty |
title_full_unstemmed | Deviations in Hippocampal Subregion in Older Adults With Cognitive Frailty |
title_short | Deviations in Hippocampal Subregion in Older Adults With Cognitive Frailty |
title_sort | deviations in hippocampal subregion in older adults with cognitive frailty |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838368/ https://www.ncbi.nlm.nih.gov/pubmed/33519422 http://dx.doi.org/10.3389/fnagi.2020.615852 |
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