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Cerebellar-limbic neurocircuit is the novel biosignature of physio-cognitive decline syndrome
Both physical and cognitive deficits occur in the aging process. We operationally defined the phenomenon as physio-cognitive decline syndrome (PCDS) and aimed to decipher its corresponding neuroanatomy patterns and neurocircuit. High resolution 3T brain magnetic resonance imaging (MRI) images from a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803525/ https://www.ncbi.nlm.nih.gov/pubmed/33234736 http://dx.doi.org/10.18632/aging.104135 |
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author | Liu, Li-Kuo Chou, Kun-Hsien Hsu, Chih-Chin Heather Peng, Li-Ning Lee, Wei-Ju Chen, Wei-Ta Lin, Ching-Po Chung, Chih-Ping Wang, Pei-Ning Chen, Liang-Kung |
author_facet | Liu, Li-Kuo Chou, Kun-Hsien Hsu, Chih-Chin Heather Peng, Li-Ning Lee, Wei-Ju Chen, Wei-Ta Lin, Ching-Po Chung, Chih-Ping Wang, Pei-Ning Chen, Liang-Kung |
author_sort | Liu, Li-Kuo |
collection | PubMed |
description | Both physical and cognitive deficits occur in the aging process. We operationally defined the phenomenon as physio-cognitive decline syndrome (PCDS) and aimed to decipher its corresponding neuroanatomy patterns and neurocircuit. High resolution 3T brain magnetic resonance imaging (MRI) images from a community-dwelling longitudinal aging cohort were analysed. PCDS was defined as weakness (handgrip strength) and/or slowness (gait speed) concomitant with impairment in any cognitive domain (defined by 1.5 standard deviation below age, sex-matched norms), but without dementia or disability. Among 1196 eligible ≥ 50-year-old (62±9 years, 47.6%men) subjects, 15.9% had PCDS. Compared to the other participants, individuals with PCDS had significantly lower gray-matter volume (GMV) in the bilateral amygdala and thalamus, right hippocampus, right temporo-occipital cortex, and left cerebellum VI and V regions. The regions of reduced GMV in people with PCDS were similar between the middle-aged and older adults; whereas larger clusters with more extensive GMV-depleted regions were observed in ≥65-year-olds with PCDS. Diffusion-weighted tractography showed disrupted hippocampus-amygdala-cerebellum connections in subjects with PCDS. The neuroanatomic characteristics revealed by this study provide evidence for pathophysiological processes associated with concomitant physio-cognitive decline in the elderly. This neurocircuit might constitute a target for future preventive interventions. |
format | Online Article Text |
id | pubmed-7803525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-78035252021-01-15 Cerebellar-limbic neurocircuit is the novel biosignature of physio-cognitive decline syndrome Liu, Li-Kuo Chou, Kun-Hsien Hsu, Chih-Chin Heather Peng, Li-Ning Lee, Wei-Ju Chen, Wei-Ta Lin, Ching-Po Chung, Chih-Ping Wang, Pei-Ning Chen, Liang-Kung Aging (Albany NY) Research Paper Both physical and cognitive deficits occur in the aging process. We operationally defined the phenomenon as physio-cognitive decline syndrome (PCDS) and aimed to decipher its corresponding neuroanatomy patterns and neurocircuit. High resolution 3T brain magnetic resonance imaging (MRI) images from a community-dwelling longitudinal aging cohort were analysed. PCDS was defined as weakness (handgrip strength) and/or slowness (gait speed) concomitant with impairment in any cognitive domain (defined by 1.5 standard deviation below age, sex-matched norms), but without dementia or disability. Among 1196 eligible ≥ 50-year-old (62±9 years, 47.6%men) subjects, 15.9% had PCDS. Compared to the other participants, individuals with PCDS had significantly lower gray-matter volume (GMV) in the bilateral amygdala and thalamus, right hippocampus, right temporo-occipital cortex, and left cerebellum VI and V regions. The regions of reduced GMV in people with PCDS were similar between the middle-aged and older adults; whereas larger clusters with more extensive GMV-depleted regions were observed in ≥65-year-olds with PCDS. Diffusion-weighted tractography showed disrupted hippocampus-amygdala-cerebellum connections in subjects with PCDS. The neuroanatomic characteristics revealed by this study provide evidence for pathophysiological processes associated with concomitant physio-cognitive decline in the elderly. This neurocircuit might constitute a target for future preventive interventions. Impact Journals 2020-11-25 /pmc/articles/PMC7803525/ /pubmed/33234736 http://dx.doi.org/10.18632/aging.104135 Text en Copyright: © 2020 Liu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Liu, Li-Kuo Chou, Kun-Hsien Hsu, Chih-Chin Heather Peng, Li-Ning Lee, Wei-Ju Chen, Wei-Ta Lin, Ching-Po Chung, Chih-Ping Wang, Pei-Ning Chen, Liang-Kung Cerebellar-limbic neurocircuit is the novel biosignature of physio-cognitive decline syndrome |
title | Cerebellar-limbic neurocircuit is the novel biosignature of physio-cognitive decline syndrome |
title_full | Cerebellar-limbic neurocircuit is the novel biosignature of physio-cognitive decline syndrome |
title_fullStr | Cerebellar-limbic neurocircuit is the novel biosignature of physio-cognitive decline syndrome |
title_full_unstemmed | Cerebellar-limbic neurocircuit is the novel biosignature of physio-cognitive decline syndrome |
title_short | Cerebellar-limbic neurocircuit is the novel biosignature of physio-cognitive decline syndrome |
title_sort | cerebellar-limbic neurocircuit is the novel biosignature of physio-cognitive decline syndrome |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803525/ https://www.ncbi.nlm.nih.gov/pubmed/33234736 http://dx.doi.org/10.18632/aging.104135 |
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