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Gait initiation in progressive supranuclear palsy: brain metabolic correlates
The initiation of gait is a highly challenging task for the balance control system, and can be used to investigate the neural control of upright posture maintenance during whole-body movement. Gait initiation is a centrally-mediated motion achieved in a principled, controlled manner, including predi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689404/ https://www.ncbi.nlm.nih.gov/pubmed/33353609 http://dx.doi.org/10.1016/j.nicl.2020.102408 |
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author | Palmisano, Chiara Todisco, Massimiliano Marotta, Giorgio Volkmann, Jens Pacchetti, Claudio Frigo, Carlo A. Pezzoli, Gianni Isaias, Ioannis U. |
author_facet | Palmisano, Chiara Todisco, Massimiliano Marotta, Giorgio Volkmann, Jens Pacchetti, Claudio Frigo, Carlo A. Pezzoli, Gianni Isaias, Ioannis U. |
author_sort | Palmisano, Chiara |
collection | PubMed |
description | The initiation of gait is a highly challenging task for the balance control system, and can be used to investigate the neural control of upright posture maintenance during whole-body movement. Gait initiation is a centrally-mediated motion achieved in a principled, controlled manner, including predictive mechanisms (anticipatory postural adjustments, APA) that destabilize the antigravitary postural set of body segments for the execution of functionally-optimized stepping. Progressive supranuclear palsy (PSP) is a neurodegenerative disease characterized by early impairment of balance and frequent falls. The neural correlates of postural imbalance and falls in PSP are largely unknown. We biomechanically assessed the APA at gait initiation (imbalance, unloading, and stepping phases) of 26 patients with PSP and 14 age-matched healthy controls. Fourteen of 26 enrolled patients were able to perform valid gait initiation trials. The influence of anthropometric and base-of-support measurements on the biomechanical outcome variables was assessed and removed. Biomechanical data were correlated with clinical findings and, in 11 patients, with brain metabolic abnormalities measured using positron emission tomography and 2-deoxy-2-[18F]fluoro-D-glucose. Patients with PSP showed impaired modulation of the center of pressure displacement for a proper setting of the center of mass momentum and subsequent efficient stepping. Biomechanical measurements correlated with “Limb motor” and “Gait and midline” subscores of the Progressive Supranuclear Palsy Rating Scale. Decreased regional glucose uptake in the caudate nucleus correlated with impaired APA programming. Hypometabolism of the caudate nucleus, supplementary motor area, cingulate cortex, thalamus, and midbrain was associated with specific biomechanical resultants of APA. Our findings show that postural instability at gait initiation in patients with PSP correlates with deficient APA production, and is associated with multiple and distinctive dysfunctioning of different areas of the supraspinal locomotor network. Objective biomechanical measures can help to understand fall-related pathophysiological mechanisms and to better monitor disease progression and new interventions. |
format | Online Article Text |
id | pubmed-7689404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-76894042020-12-07 Gait initiation in progressive supranuclear palsy: brain metabolic correlates Palmisano, Chiara Todisco, Massimiliano Marotta, Giorgio Volkmann, Jens Pacchetti, Claudio Frigo, Carlo A. Pezzoli, Gianni Isaias, Ioannis U. Neuroimage Clin Regular Article The initiation of gait is a highly challenging task for the balance control system, and can be used to investigate the neural control of upright posture maintenance during whole-body movement. Gait initiation is a centrally-mediated motion achieved in a principled, controlled manner, including predictive mechanisms (anticipatory postural adjustments, APA) that destabilize the antigravitary postural set of body segments for the execution of functionally-optimized stepping. Progressive supranuclear palsy (PSP) is a neurodegenerative disease characterized by early impairment of balance and frequent falls. The neural correlates of postural imbalance and falls in PSP are largely unknown. We biomechanically assessed the APA at gait initiation (imbalance, unloading, and stepping phases) of 26 patients with PSP and 14 age-matched healthy controls. Fourteen of 26 enrolled patients were able to perform valid gait initiation trials. The influence of anthropometric and base-of-support measurements on the biomechanical outcome variables was assessed and removed. Biomechanical data were correlated with clinical findings and, in 11 patients, with brain metabolic abnormalities measured using positron emission tomography and 2-deoxy-2-[18F]fluoro-D-glucose. Patients with PSP showed impaired modulation of the center of pressure displacement for a proper setting of the center of mass momentum and subsequent efficient stepping. Biomechanical measurements correlated with “Limb motor” and “Gait and midline” subscores of the Progressive Supranuclear Palsy Rating Scale. Decreased regional glucose uptake in the caudate nucleus correlated with impaired APA programming. Hypometabolism of the caudate nucleus, supplementary motor area, cingulate cortex, thalamus, and midbrain was associated with specific biomechanical resultants of APA. Our findings show that postural instability at gait initiation in patients with PSP correlates with deficient APA production, and is associated with multiple and distinctive dysfunctioning of different areas of the supraspinal locomotor network. Objective biomechanical measures can help to understand fall-related pathophysiological mechanisms and to better monitor disease progression and new interventions. Elsevier 2020-09-02 /pmc/articles/PMC7689404/ /pubmed/33353609 http://dx.doi.org/10.1016/j.nicl.2020.102408 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article Palmisano, Chiara Todisco, Massimiliano Marotta, Giorgio Volkmann, Jens Pacchetti, Claudio Frigo, Carlo A. Pezzoli, Gianni Isaias, Ioannis U. Gait initiation in progressive supranuclear palsy: brain metabolic correlates |
title | Gait initiation in progressive supranuclear palsy: brain metabolic correlates |
title_full | Gait initiation in progressive supranuclear palsy: brain metabolic correlates |
title_fullStr | Gait initiation in progressive supranuclear palsy: brain metabolic correlates |
title_full_unstemmed | Gait initiation in progressive supranuclear palsy: brain metabolic correlates |
title_short | Gait initiation in progressive supranuclear palsy: brain metabolic correlates |
title_sort | gait initiation in progressive supranuclear palsy: brain metabolic correlates |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689404/ https://www.ncbi.nlm.nih.gov/pubmed/33353609 http://dx.doi.org/10.1016/j.nicl.2020.102408 |
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