A functional magnetic resonance imaging study of pathophysiological changes responsible for mirror movements in Parkinson's disease.

Mirror movements correspond to involuntary movements observed in the limb contralateral to the one performing voluntary movement. They can be observed in Parkinson's disease (PD) but their pathophysiology remains unclear. The present study aims at identifying their neural correlates in PD using...

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Autores principales: Alice Poisson, Bénédicte Ballanger, Elise Metereau, Jérome Redouté, Danielle Ibarolla, Jean-Christophe Comte, Hélène Gervais Bernard, Marie Vidailhet, Emmanuel Broussolle, Stéphane Thobois
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Publicado: Public Library of Science (PLoS) 2013
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Acceso en línea:https://doaj.org/article/3f9d1d2145164185a47560b08087c831
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spelling oai:doaj.org-article:3f9d1d2145164185a47560b08087c8312021-11-18T07:40:09ZA functional magnetic resonance imaging study of pathophysiological changes responsible for mirror movements in Parkinson's disease.1932-620310.1371/journal.pone.0066910https://doaj.org/article/3f9d1d2145164185a47560b08087c8312013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23825583/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Mirror movements correspond to involuntary movements observed in the limb contralateral to the one performing voluntary movement. They can be observed in Parkinson's disease (PD) but their pathophysiology remains unclear. The present study aims at identifying their neural correlates in PD using functional magnetic resonance imaging. Ten control subjects and 14-off drug patients with asymmetrical right-sided PD were included (8 with left-sided mirror movements during right-hand movements, and 6 without mirror movements). Between-group comparisons of BOLD signal were performed during right-hand movements and at rest (p<0.005 uncorrected). The comparison between PD patients with and without mirror movements showed that mirror movements were associated with an overactivation of the insula, precuneus/posterior cingulate cortex bilaterally and of the left inferior frontal cortex and with a deactivation of the right dorsolateral prefrontal cortex, medial prefrontal cortex, and pre-supplementary motor area and occipital cortex. These data suggest that mirror movements in Parkinson's disease are promoted by: 1- a deactivation of the non-mirroring inhibitory network (dorsolateral prefrontal cortex, pre-supplementary motor area); 2- an overactivation of prokinetic areas (notably the insula). The concomitant overactivation of a proactive inhibitory network (including the posterior cingulate cortex and precuneus) could reflect a compensatory inhibition of mirror movements.Alice PoissonBénédicte BallangerElise MetereauJérome RedoutéDanielle IbarollaJean-Christophe ComteHélène Gervais BernardMarie VidailhetEmmanuel BroussolleStéphane ThoboisPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 6, p e66910 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Alice Poisson
Bénédicte Ballanger
Elise Metereau
Jérome Redouté
Danielle Ibarolla
Jean-Christophe Comte
Hélène Gervais Bernard
Marie Vidailhet
Emmanuel Broussolle
Stéphane Thobois
A functional magnetic resonance imaging study of pathophysiological changes responsible for mirror movements in Parkinson's disease.
description Mirror movements correspond to involuntary movements observed in the limb contralateral to the one performing voluntary movement. They can be observed in Parkinson's disease (PD) but their pathophysiology remains unclear. The present study aims at identifying their neural correlates in PD using functional magnetic resonance imaging. Ten control subjects and 14-off drug patients with asymmetrical right-sided PD were included (8 with left-sided mirror movements during right-hand movements, and 6 without mirror movements). Between-group comparisons of BOLD signal were performed during right-hand movements and at rest (p<0.005 uncorrected). The comparison between PD patients with and without mirror movements showed that mirror movements were associated with an overactivation of the insula, precuneus/posterior cingulate cortex bilaterally and of the left inferior frontal cortex and with a deactivation of the right dorsolateral prefrontal cortex, medial prefrontal cortex, and pre-supplementary motor area and occipital cortex. These data suggest that mirror movements in Parkinson's disease are promoted by: 1- a deactivation of the non-mirroring inhibitory network (dorsolateral prefrontal cortex, pre-supplementary motor area); 2- an overactivation of prokinetic areas (notably the insula). The concomitant overactivation of a proactive inhibitory network (including the posterior cingulate cortex and precuneus) could reflect a compensatory inhibition of mirror movements.
format article
author Alice Poisson
Bénédicte Ballanger
Elise Metereau
Jérome Redouté
Danielle Ibarolla
Jean-Christophe Comte
Hélène Gervais Bernard
Marie Vidailhet
Emmanuel Broussolle
Stéphane Thobois
author_facet Alice Poisson
Bénédicte Ballanger
Elise Metereau
Jérome Redouté
Danielle Ibarolla
Jean-Christophe Comte
Hélène Gervais Bernard
Marie Vidailhet
Emmanuel Broussolle
Stéphane Thobois
author_sort Alice Poisson
title A functional magnetic resonance imaging study of pathophysiological changes responsible for mirror movements in Parkinson's disease.
title_short A functional magnetic resonance imaging study of pathophysiological changes responsible for mirror movements in Parkinson's disease.
title_full A functional magnetic resonance imaging study of pathophysiological changes responsible for mirror movements in Parkinson's disease.
title_fullStr A functional magnetic resonance imaging study of pathophysiological changes responsible for mirror movements in Parkinson's disease.
title_full_unstemmed A functional magnetic resonance imaging study of pathophysiological changes responsible for mirror movements in Parkinson's disease.
title_sort functional magnetic resonance imaging study of pathophysiological changes responsible for mirror movements in parkinson's disease.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/3f9d1d2145164185a47560b08087c831
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