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Pedunculopontine Nucleus Dysconnectivity Correlates With Gait Impairment in Parkinson’s Disease: An Exploratory Study

BACKGROUND: Gait impairment is a debilitating and progressive feature of Parkinson’s disease (PD). Increasing evidence suggests that gait control is partly mediated by cholinergic signaling from the pedunculopontine nucleus (PPN). OBJECTIVE: We investigated whether PPN structural connectivity correl...

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Autores principales: Joza, Stephen, Camicioli, Richard, Martin, W. R. Wayne, Wieler, Marguerite, Gee, Myrlene, Ba, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304714/
https://www.ncbi.nlm.nih.gov/pubmed/35875799
http://dx.doi.org/10.3389/fnagi.2022.874692
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author Joza, Stephen
Camicioli, Richard
Martin, W. R. Wayne
Wieler, Marguerite
Gee, Myrlene
Ba, Fang
author_facet Joza, Stephen
Camicioli, Richard
Martin, W. R. Wayne
Wieler, Marguerite
Gee, Myrlene
Ba, Fang
author_sort Joza, Stephen
collection PubMed
description BACKGROUND: Gait impairment is a debilitating and progressive feature of Parkinson’s disease (PD). Increasing evidence suggests that gait control is partly mediated by cholinergic signaling from the pedunculopontine nucleus (PPN). OBJECTIVE: We investigated whether PPN structural connectivity correlated with quantitative gait measures in PD. METHODS: Twenty PD patients and 15 controls underwent diffusion tensor imaging to quantify structural connectivity of the PPN. Whole brain analysis using tract-based spatial statistics and probabilistic tractography were performed using the PPN as a seed region of interest for cortical and subcortical target structures. Gait metrics were recorded in subjects’ medication ON and OFF states, and were used to determine if specific features of gait dysfunction in PD were related to PPN structural connectivity. RESULTS: Tract-based spatial statistics revealed reduced structural connectivity involving the corpus callosum and right superior corona radiata, but did not correlate with gait measures. Abnormalities in PPN structural connectivity in PD were lateralized to the right hemisphere, with pathways involving the right caudate nucleus, amygdala, pre-supplementary motor area, and primary somatosensory cortex. Altered connectivity of the right PPN-caudate nucleus was associated with worsened cadence, stride time, and velocity while in the ON state; altered connectivity of the right PPN-amygdala was associated with reduced stride length in the OFF state. CONCLUSION: Our exploratory analysis detects a potential correlation between gait dysfunction in PD and a characteristic pattern of connectivity deficits in the PPN network involving the right caudate nucleus and amygdala, which may be investigated in future larger studies.
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spelling pubmed-93047142022-07-23 Pedunculopontine Nucleus Dysconnectivity Correlates With Gait Impairment in Parkinson’s Disease: An Exploratory Study Joza, Stephen Camicioli, Richard Martin, W. R. Wayne Wieler, Marguerite Gee, Myrlene Ba, Fang Front Aging Neurosci Aging Neuroscience BACKGROUND: Gait impairment is a debilitating and progressive feature of Parkinson’s disease (PD). Increasing evidence suggests that gait control is partly mediated by cholinergic signaling from the pedunculopontine nucleus (PPN). OBJECTIVE: We investigated whether PPN structural connectivity correlated with quantitative gait measures in PD. METHODS: Twenty PD patients and 15 controls underwent diffusion tensor imaging to quantify structural connectivity of the PPN. Whole brain analysis using tract-based spatial statistics and probabilistic tractography were performed using the PPN as a seed region of interest for cortical and subcortical target structures. Gait metrics were recorded in subjects’ medication ON and OFF states, and were used to determine if specific features of gait dysfunction in PD were related to PPN structural connectivity. RESULTS: Tract-based spatial statistics revealed reduced structural connectivity involving the corpus callosum and right superior corona radiata, but did not correlate with gait measures. Abnormalities in PPN structural connectivity in PD were lateralized to the right hemisphere, with pathways involving the right caudate nucleus, amygdala, pre-supplementary motor area, and primary somatosensory cortex. Altered connectivity of the right PPN-caudate nucleus was associated with worsened cadence, stride time, and velocity while in the ON state; altered connectivity of the right PPN-amygdala was associated with reduced stride length in the OFF state. CONCLUSION: Our exploratory analysis detects a potential correlation between gait dysfunction in PD and a characteristic pattern of connectivity deficits in the PPN network involving the right caudate nucleus and amygdala, which may be investigated in future larger studies. Frontiers Media S.A. 2022-07-08 /pmc/articles/PMC9304714/ /pubmed/35875799 http://dx.doi.org/10.3389/fnagi.2022.874692 Text en Copyright © 2022 Joza, Camicioli, Martin, Wieler, Gee and Ba. https://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 Aging Neuroscience
Joza, Stephen
Camicioli, Richard
Martin, W. R. Wayne
Wieler, Marguerite
Gee, Myrlene
Ba, Fang
Pedunculopontine Nucleus Dysconnectivity Correlates With Gait Impairment in Parkinson’s Disease: An Exploratory Study
title Pedunculopontine Nucleus Dysconnectivity Correlates With Gait Impairment in Parkinson’s Disease: An Exploratory Study
title_full Pedunculopontine Nucleus Dysconnectivity Correlates With Gait Impairment in Parkinson’s Disease: An Exploratory Study
title_fullStr Pedunculopontine Nucleus Dysconnectivity Correlates With Gait Impairment in Parkinson’s Disease: An Exploratory Study
title_full_unstemmed Pedunculopontine Nucleus Dysconnectivity Correlates With Gait Impairment in Parkinson’s Disease: An Exploratory Study
title_short Pedunculopontine Nucleus Dysconnectivity Correlates With Gait Impairment in Parkinson’s Disease: An Exploratory Study
title_sort pedunculopontine nucleus dysconnectivity correlates with gait impairment in parkinson’s disease: an exploratory study
topic Aging Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304714/
https://www.ncbi.nlm.nih.gov/pubmed/35875799
http://dx.doi.org/10.3389/fnagi.2022.874692
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