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Cholinergic centro-cingulate network in Parkinson disease and normal aging
Decreased cholinergic binding within the recently identified centro-cingulate brain network robustly has been shown to robustly correlate with the severity of cognitive impairment in Parkinson disease (PD). This network with key hubs within the cingulum, operculum and peri-central cortical regions a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10637805/ https://www.ncbi.nlm.nih.gov/pubmed/37899134 http://dx.doi.org/10.18632/aging.205209 |
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author | Bohnen, Nicolaas I. van der Zee, Sygrid Albin, Roger |
author_facet | Bohnen, Nicolaas I. van der Zee, Sygrid Albin, Roger |
author_sort | Bohnen, Nicolaas I. |
collection | PubMed |
description | Decreased cholinergic binding within the recently identified centro-cingulate brain network robustly has been shown to robustly correlate with the severity of cognitive impairment in Parkinson disease (PD). This network with key hubs within the cingulum, operculum and peri-central cortical regions also correlates with elements of parkinsonian motor impairments, including postural instability and gait difficulties, such as falls or freezing. MRI neuroimaging studies have shown that the anterior midcingulate cortex is a key node for cognitive aspects of movement generation, i.e., intentional motor control. Recent evidence also suggests a novel aspect of organization of primary motor cortex, describing “effector” regions for fine movement control intercalated with interlinked “inter-effector” regions devoted to whole-body control. A distinguishing feature of inter-effector regions is tight linkage to the cingular and opercular regions. Such inter-effector regions have been proposed to be part of a greater somato-cognitive action network necessary for integration of goals and movement. Recent evidence also points to vulnerabilities of cholinergic nerve terminals in the centro-cingulate network in older non-PD adults. These features of normal aging underscore that cortical cholinergic terminal losses in age-associated neurodegenerative disorders are likely not exclusively the result of disease-specific etiologies but also related to otherwise normal aging. Practical implications of this overlap are that addressing disease-specific and general aging etiologies involved in neurodegeneration, may be of benefit in age-associated neurodegenerative disorders where significant cholinergic systems degeneration is present. |
format | Online Article Text |
id | pubmed-10637805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-106378052023-11-15 Cholinergic centro-cingulate network in Parkinson disease and normal aging Bohnen, Nicolaas I. van der Zee, Sygrid Albin, Roger Aging (Albany NY) Research Perspective Decreased cholinergic binding within the recently identified centro-cingulate brain network robustly has been shown to robustly correlate with the severity of cognitive impairment in Parkinson disease (PD). This network with key hubs within the cingulum, operculum and peri-central cortical regions also correlates with elements of parkinsonian motor impairments, including postural instability and gait difficulties, such as falls or freezing. MRI neuroimaging studies have shown that the anterior midcingulate cortex is a key node for cognitive aspects of movement generation, i.e., intentional motor control. Recent evidence also suggests a novel aspect of organization of primary motor cortex, describing “effector” regions for fine movement control intercalated with interlinked “inter-effector” regions devoted to whole-body control. A distinguishing feature of inter-effector regions is tight linkage to the cingular and opercular regions. Such inter-effector regions have been proposed to be part of a greater somato-cognitive action network necessary for integration of goals and movement. Recent evidence also points to vulnerabilities of cholinergic nerve terminals in the centro-cingulate network in older non-PD adults. These features of normal aging underscore that cortical cholinergic terminal losses in age-associated neurodegenerative disorders are likely not exclusively the result of disease-specific etiologies but also related to otherwise normal aging. Practical implications of this overlap are that addressing disease-specific and general aging etiologies involved in neurodegeneration, may be of benefit in age-associated neurodegenerative disorders where significant cholinergic systems degeneration is present. Impact Journals 2023-10-27 /pmc/articles/PMC10637805/ /pubmed/37899134 http://dx.doi.org/10.18632/aging.205209 Text en Copyright: © 2023 Bohnen 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 Perspective Bohnen, Nicolaas I. van der Zee, Sygrid Albin, Roger Cholinergic centro-cingulate network in Parkinson disease and normal aging |
title | Cholinergic centro-cingulate network in Parkinson disease and normal aging |
title_full | Cholinergic centro-cingulate network in Parkinson disease and normal aging |
title_fullStr | Cholinergic centro-cingulate network in Parkinson disease and normal aging |
title_full_unstemmed | Cholinergic centro-cingulate network in Parkinson disease and normal aging |
title_short | Cholinergic centro-cingulate network in Parkinson disease and normal aging |
title_sort | cholinergic centro-cingulate network in parkinson disease and normal aging |
topic | Research Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10637805/ https://www.ncbi.nlm.nih.gov/pubmed/37899134 http://dx.doi.org/10.18632/aging.205209 |
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