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Resting-state functional connectivity as a marker of disease progression in Parkinson's disease: A longitudinal MEG study()

The assessment of resting-state functional connectivity has become an important tool in studying brain disease mechanisms. Here we use magnetoencephalography to longitudinally evaluate functional connectivity changes in relation to clinical measures of disease progression in Parkinson's disease...

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Autores principales: Olde Dubbelink, Kim T.E., Stoffers, Diederick, Deijen, Jan Berend, Twisk, Jos W.R., Stam, Cornelis J., Hillebrand, Arjan, Berendse, Henk W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777670/
https://www.ncbi.nlm.nih.gov/pubmed/24179812
http://dx.doi.org/10.1016/j.nicl.2013.04.003
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author Olde Dubbelink, Kim T.E.
Stoffers, Diederick
Deijen, Jan Berend
Twisk, Jos W.R.
Stam, Cornelis J.
Hillebrand, Arjan
Berendse, Henk W.
author_facet Olde Dubbelink, Kim T.E.
Stoffers, Diederick
Deijen, Jan Berend
Twisk, Jos W.R.
Stam, Cornelis J.
Hillebrand, Arjan
Berendse, Henk W.
author_sort Olde Dubbelink, Kim T.E.
collection PubMed
description The assessment of resting-state functional connectivity has become an important tool in studying brain disease mechanisms. Here we use magnetoencephalography to longitudinally evaluate functional connectivity changes in relation to clinical measures of disease progression in Parkinson's disease (PD). Using a source-space based approach with detailed anatomical mapping, functional connectivity was assessed for temporal, prefrontal and high order sensory association areas known to show neuropathological changes in early clinical disease stages. At baseline, early stage, untreated PD patients (n = 12) had lower parahippocampal and temporal delta band connectivity and higher temporal alpha1 band connectivity compared to controls. Longitudinal analyses over a 4-year period in a larger patient group (n = 43) revealed decreases in alpha1 and alpha2 band connectivity for multiple seed regions that were associated with motor or cognitive deterioration. In the earliest clinical stages of PD, delta and alpha1 band resting-state functional connectivity is altered in temporal cortical regions. With disease progression, a reversal of the initial changes in alpha1 and additional decreases in alpha2 band connectivity evolving in a more widespread cortical pattern. These changes in functional connectivity appear to reflect clinically relevant phenomena and therefore hold promise as a marker of disease progression, with potential predictive value for clinical outcome.
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spelling pubmed-37776702013-10-31 Resting-state functional connectivity as a marker of disease progression in Parkinson's disease: A longitudinal MEG study() Olde Dubbelink, Kim T.E. Stoffers, Diederick Deijen, Jan Berend Twisk, Jos W.R. Stam, Cornelis J. Hillebrand, Arjan Berendse, Henk W. Neuroimage Clin Article The assessment of resting-state functional connectivity has become an important tool in studying brain disease mechanisms. Here we use magnetoencephalography to longitudinally evaluate functional connectivity changes in relation to clinical measures of disease progression in Parkinson's disease (PD). Using a source-space based approach with detailed anatomical mapping, functional connectivity was assessed for temporal, prefrontal and high order sensory association areas known to show neuropathological changes in early clinical disease stages. At baseline, early stage, untreated PD patients (n = 12) had lower parahippocampal and temporal delta band connectivity and higher temporal alpha1 band connectivity compared to controls. Longitudinal analyses over a 4-year period in a larger patient group (n = 43) revealed decreases in alpha1 and alpha2 band connectivity for multiple seed regions that were associated with motor or cognitive deterioration. In the earliest clinical stages of PD, delta and alpha1 band resting-state functional connectivity is altered in temporal cortical regions. With disease progression, a reversal of the initial changes in alpha1 and additional decreases in alpha2 band connectivity evolving in a more widespread cortical pattern. These changes in functional connectivity appear to reflect clinically relevant phenomena and therefore hold promise as a marker of disease progression, with potential predictive value for clinical outcome. Elsevier 2013-04-11 /pmc/articles/PMC3777670/ /pubmed/24179812 http://dx.doi.org/10.1016/j.nicl.2013.04.003 Text en © 2013 The Authors http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Olde Dubbelink, Kim T.E.
Stoffers, Diederick
Deijen, Jan Berend
Twisk, Jos W.R.
Stam, Cornelis J.
Hillebrand, Arjan
Berendse, Henk W.
Resting-state functional connectivity as a marker of disease progression in Parkinson's disease: A longitudinal MEG study()
title Resting-state functional connectivity as a marker of disease progression in Parkinson's disease: A longitudinal MEG study()
title_full Resting-state functional connectivity as a marker of disease progression in Parkinson's disease: A longitudinal MEG study()
title_fullStr Resting-state functional connectivity as a marker of disease progression in Parkinson's disease: A longitudinal MEG study()
title_full_unstemmed Resting-state functional connectivity as a marker of disease progression in Parkinson's disease: A longitudinal MEG study()
title_short Resting-state functional connectivity as a marker of disease progression in Parkinson's disease: A longitudinal MEG study()
title_sort resting-state functional connectivity as a marker of disease progression in parkinson's disease: a longitudinal meg study()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777670/
https://www.ncbi.nlm.nih.gov/pubmed/24179812
http://dx.doi.org/10.1016/j.nicl.2013.04.003
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