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Functional and Brain Activation Changes Following Specialized Upper-Limb Exercise in Parkinson’s Disease
For the management of Parkinson’s disease (PD), the concept of forced exercise (FE) has drawn interest. In PD subjects, the FE executed with lower limbs has been shown to lessen symptoms and to promote brain adaptive changes. Our study is aimed to investigate the effect of an upper-limb exercise, co...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6843060/ https://www.ncbi.nlm.nih.gov/pubmed/31749690 http://dx.doi.org/10.3389/fnhum.2019.00350 |
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author | Messa, Luca Valerio Ginanneschi, Federica Momi, Davide Monti, Lucia Battisti, Carla Cioncoloni, David Pucci, Barbara Santarnecchi, Emiliano Rossi, Alessandro |
author_facet | Messa, Luca Valerio Ginanneschi, Federica Momi, Davide Monti, Lucia Battisti, Carla Cioncoloni, David Pucci, Barbara Santarnecchi, Emiliano Rossi, Alessandro |
author_sort | Messa, Luca Valerio |
collection | PubMed |
description | For the management of Parkinson’s disease (PD), the concept of forced exercise (FE) has drawn interest. In PD subjects, the FE executed with lower limbs has been shown to lessen symptoms and to promote brain adaptive changes. Our study is aimed to investigate the effect of an upper-limb exercise, conceptually comparable with the FE, in PD. Upper-limb exercise was achieved in a sitting position by using a specially designed device (Angel’s Wings(®)). Clinical data, computerized dynamic posturography, magnetic resonance imaging (MRI) (resting-state MRI and arterial spin labeling), and neuropsychological tests were used before and after 2 months’ exercise training. We found a significant long-lasting improvement in Unified Parkinson Disease Rating Scale (UPDRS)-III and cognitive scales, along with improvement in balance and postural control (better alignment of the gravity center and improvement in weight symmetry and in anticipatory motor strategies). Computerized dynamic posturography pointed out an enhanced central ability to integrate the vestibular signals with afferents from other sensory systems. Neuroimaging analyses after 2 months’ exercise training showed, with respect to pretraining condition, many changes. An increase of the cerebral blood flow was evident in the left primary motor cortex (M1), left supplementary motor cortical area, and left cerebellar cortex. The bilateral globus pallidus showed an increased functional connectivity to the right central operculum, right posterior cingulate gyrus, and left sensorimotor cortex. Seed-to-voxel analysis demonstrated a functional connectivity between M1 and the left superior frontal gyrus. Left crus II showed strengthened connections with the left pre-rolandic area, left post-rolandic area, and left supramarginal area. These findings likely reflect compensatory mechanisms to the neuropathological hallmark of PD. Overall, our results show that this upper-limb exercise model, conceptually comparable with the FE already tested in the lower limbs, leads to a global improvement (involving non-exercised limbs) likely consistent with the functional changes observed in the central nervous system. |
format | Online Article Text |
id | pubmed-6843060 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68430602019-11-20 Functional and Brain Activation Changes Following Specialized Upper-Limb Exercise in Parkinson’s Disease Messa, Luca Valerio Ginanneschi, Federica Momi, Davide Monti, Lucia Battisti, Carla Cioncoloni, David Pucci, Barbara Santarnecchi, Emiliano Rossi, Alessandro Front Hum Neurosci Neuroscience For the management of Parkinson’s disease (PD), the concept of forced exercise (FE) has drawn interest. In PD subjects, the FE executed with lower limbs has been shown to lessen symptoms and to promote brain adaptive changes. Our study is aimed to investigate the effect of an upper-limb exercise, conceptually comparable with the FE, in PD. Upper-limb exercise was achieved in a sitting position by using a specially designed device (Angel’s Wings(®)). Clinical data, computerized dynamic posturography, magnetic resonance imaging (MRI) (resting-state MRI and arterial spin labeling), and neuropsychological tests were used before and after 2 months’ exercise training. We found a significant long-lasting improvement in Unified Parkinson Disease Rating Scale (UPDRS)-III and cognitive scales, along with improvement in balance and postural control (better alignment of the gravity center and improvement in weight symmetry and in anticipatory motor strategies). Computerized dynamic posturography pointed out an enhanced central ability to integrate the vestibular signals with afferents from other sensory systems. Neuroimaging analyses after 2 months’ exercise training showed, with respect to pretraining condition, many changes. An increase of the cerebral blood flow was evident in the left primary motor cortex (M1), left supplementary motor cortical area, and left cerebellar cortex. The bilateral globus pallidus showed an increased functional connectivity to the right central operculum, right posterior cingulate gyrus, and left sensorimotor cortex. Seed-to-voxel analysis demonstrated a functional connectivity between M1 and the left superior frontal gyrus. Left crus II showed strengthened connections with the left pre-rolandic area, left post-rolandic area, and left supramarginal area. These findings likely reflect compensatory mechanisms to the neuropathological hallmark of PD. Overall, our results show that this upper-limb exercise model, conceptually comparable with the FE already tested in the lower limbs, leads to a global improvement (involving non-exercised limbs) likely consistent with the functional changes observed in the central nervous system. Frontiers Media S.A. 2019-10-15 /pmc/articles/PMC6843060/ /pubmed/31749690 http://dx.doi.org/10.3389/fnhum.2019.00350 Text en Copyright © 2019 Messa, Ginanneschi, Momi, Monti, Battisti, Cioncoloni, Pucci, Santarnecchi and Rossi. 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 Messa, Luca Valerio Ginanneschi, Federica Momi, Davide Monti, Lucia Battisti, Carla Cioncoloni, David Pucci, Barbara Santarnecchi, Emiliano Rossi, Alessandro Functional and Brain Activation Changes Following Specialized Upper-Limb Exercise in Parkinson’s Disease |
title | Functional and Brain Activation Changes Following Specialized Upper-Limb Exercise in Parkinson’s Disease |
title_full | Functional and Brain Activation Changes Following Specialized Upper-Limb Exercise in Parkinson’s Disease |
title_fullStr | Functional and Brain Activation Changes Following Specialized Upper-Limb Exercise in Parkinson’s Disease |
title_full_unstemmed | Functional and Brain Activation Changes Following Specialized Upper-Limb Exercise in Parkinson’s Disease |
title_short | Functional and Brain Activation Changes Following Specialized Upper-Limb Exercise in Parkinson’s Disease |
title_sort | functional and brain activation changes following specialized upper-limb exercise in parkinson’s disease |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6843060/ https://www.ncbi.nlm.nih.gov/pubmed/31749690 http://dx.doi.org/10.3389/fnhum.2019.00350 |
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