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Decreased grey matter in the postural control network is associated with lateral flexion of the trunk in Parkinson’s disease

BACKGROUND: Disruption of central networks, particularly of those responsible for integrating multimodal afferents in a spatial reference frame, were proposed in the pathophysiology of lateral trunk flexion in Parkinson’s disease (PD). Knowledge about the underlying neuroanatomical structures is lim...

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Autores principales: Brugger, Florian, Walch, Julia, Hägele-Link, Stefan, Abela, Eugenio, Galovic, Marian, Kägi, Georg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645287/
https://www.ncbi.nlm.nih.gov/pubmed/33395964
http://dx.doi.org/10.1016/j.nicl.2020.102469
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author Brugger, Florian
Walch, Julia
Hägele-Link, Stefan
Abela, Eugenio
Galovic, Marian
Kägi, Georg
author_facet Brugger, Florian
Walch, Julia
Hägele-Link, Stefan
Abela, Eugenio
Galovic, Marian
Kägi, Georg
author_sort Brugger, Florian
collection PubMed
description BACKGROUND: Disruption of central networks, particularly of those responsible for integrating multimodal afferents in a spatial reference frame, were proposed in the pathophysiology of lateral trunk flexion in Parkinson’s disease (PD). Knowledge about the underlying neuroanatomical structures is limited. OBJECTIVE: To investigate if decreased focal grey matter (GM) is associated with trunk flexion to the side and if the revealed GM clusters correlate with a disturbed perception of verticality in PD. METHODS: 37 PD patients with and without lateral trunk flexion were recruited. Standardized photos were taken from each patient and trunk orientation was measured by a blinded rater. Voxel-based morphometry (VBM) was used to detect associated clusters of decreased GM. The subjective visual vertical (SVV) was assessed as a marker for perception of verticality and SVV estimates were correlated with GM clusters. RESULTS: VBM revealed clusters of decreased GM in the right posterior parietal cortex and in the right thalamus were associated with lateral trunk flexion. The SVV correlated with the extent of trunk flexion, and the side of the SVV tilt correlated with the side of trunk flexion. GM values from the thalamus correlated with the SVV estimates. CONCLUSIONS: We report an association between neurodegenerative changes within the posterior parietal cortex and the thalamus and lateral trunk flexion in PD. These brain structures are part of a network proposed to be engaged in postural control and spatial self-perception. Disturbed perception of verticality points to a shifted egocentric spatial reference as an important pathophysiological feature.
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spelling pubmed-76452872020-11-13 Decreased grey matter in the postural control network is associated with lateral flexion of the trunk in Parkinson’s disease Brugger, Florian Walch, Julia Hägele-Link, Stefan Abela, Eugenio Galovic, Marian Kägi, Georg Neuroimage Clin Regular Article BACKGROUND: Disruption of central networks, particularly of those responsible for integrating multimodal afferents in a spatial reference frame, were proposed in the pathophysiology of lateral trunk flexion in Parkinson’s disease (PD). Knowledge about the underlying neuroanatomical structures is limited. OBJECTIVE: To investigate if decreased focal grey matter (GM) is associated with trunk flexion to the side and if the revealed GM clusters correlate with a disturbed perception of verticality in PD. METHODS: 37 PD patients with and without lateral trunk flexion were recruited. Standardized photos were taken from each patient and trunk orientation was measured by a blinded rater. Voxel-based morphometry (VBM) was used to detect associated clusters of decreased GM. The subjective visual vertical (SVV) was assessed as a marker for perception of verticality and SVV estimates were correlated with GM clusters. RESULTS: VBM revealed clusters of decreased GM in the right posterior parietal cortex and in the right thalamus were associated with lateral trunk flexion. The SVV correlated with the extent of trunk flexion, and the side of the SVV tilt correlated with the side of trunk flexion. GM values from the thalamus correlated with the SVV estimates. CONCLUSIONS: We report an association between neurodegenerative changes within the posterior parietal cortex and the thalamus and lateral trunk flexion in PD. These brain structures are part of a network proposed to be engaged in postural control and spatial self-perception. Disturbed perception of verticality points to a shifted egocentric spatial reference as an important pathophysiological feature. Elsevier 2020-10-15 /pmc/articles/PMC7645287/ /pubmed/33395964 http://dx.doi.org/10.1016/j.nicl.2020.102469 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
Brugger, Florian
Walch, Julia
Hägele-Link, Stefan
Abela, Eugenio
Galovic, Marian
Kägi, Georg
Decreased grey matter in the postural control network is associated with lateral flexion of the trunk in Parkinson’s disease
title Decreased grey matter in the postural control network is associated with lateral flexion of the trunk in Parkinson’s disease
title_full Decreased grey matter in the postural control network is associated with lateral flexion of the trunk in Parkinson’s disease
title_fullStr Decreased grey matter in the postural control network is associated with lateral flexion of the trunk in Parkinson’s disease
title_full_unstemmed Decreased grey matter in the postural control network is associated with lateral flexion of the trunk in Parkinson’s disease
title_short Decreased grey matter in the postural control network is associated with lateral flexion of the trunk in Parkinson’s disease
title_sort decreased grey matter in the postural control network is associated with lateral flexion of the trunk in parkinson’s disease
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645287/
https://www.ncbi.nlm.nih.gov/pubmed/33395964
http://dx.doi.org/10.1016/j.nicl.2020.102469
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