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Cognitive Profiles and Hub Vulnerability in Parkinson's Disease

The clinicopathological correlations between aspects of cognition, disease severity and imaging in Parkinson's Disease (PD) have been unclear. We studied cognitive profiles, demographics, and functional connectivity patterns derived from resting-state fMRI data (rsFC) in 31 PD subjects from the...

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Autores principales: Lin, Sue-Jin, Baumeister, Tobias R., Garg, Saurabh, McKeown, Martin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019441/
https://www.ncbi.nlm.nih.gov/pubmed/29973913
http://dx.doi.org/10.3389/fneur.2018.00482
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author Lin, Sue-Jin
Baumeister, Tobias R.
Garg, Saurabh
McKeown, Martin J.
author_facet Lin, Sue-Jin
Baumeister, Tobias R.
Garg, Saurabh
McKeown, Martin J.
author_sort Lin, Sue-Jin
collection PubMed
description The clinicopathological correlations between aspects of cognition, disease severity and imaging in Parkinson's Disease (PD) have been unclear. We studied cognitive profiles, demographics, and functional connectivity patterns derived from resting-state fMRI data (rsFC) in 31 PD subjects from the Parkinson's Progression Markers Initiative (PPMI) database. We also examined rsFC from 19 healthy subjects (HS) from the Pacific Parkinson's Research Centre. Graph theoretical measures were used to summarize the rsFC patterns. Canonical correlation analysis (CCA) was used to relate separate cognitive profiles in PD that were associated with disease severity and demographic measures as well as rsFC network measures. The CCA model relating cognition to demographics suggested female gender and education supported cognitive function in PD, age and depression scores were anti-correlated with overall cognition, and UPDRS had little influence on cognition. Alone, rsFC global network measures did not significantly differ between PD and controls, yet some nodal network measures, such as network segregation, were distinguishable between PD and HS in cortical “hub” regions. The CCA model relating cognition to rsFC global network values, which was not related to the other CCA model relating cognition to demographic information, suggested modularity, rich club coefficient, and transitivity was also broadly related to cognition in PD. Our results suggest that education, aging, comorbidity, and gender impact cognition more than overall disease severity in PD. Cortical “hub” regions are vulnerable in PD, and impairments of processing speed, attention, scanning abilities, and executive skills are related to enhanced functional segregation seen in PD.
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spelling pubmed-60194412018-07-04 Cognitive Profiles and Hub Vulnerability in Parkinson's Disease Lin, Sue-Jin Baumeister, Tobias R. Garg, Saurabh McKeown, Martin J. Front Neurol Neurology The clinicopathological correlations between aspects of cognition, disease severity and imaging in Parkinson's Disease (PD) have been unclear. We studied cognitive profiles, demographics, and functional connectivity patterns derived from resting-state fMRI data (rsFC) in 31 PD subjects from the Parkinson's Progression Markers Initiative (PPMI) database. We also examined rsFC from 19 healthy subjects (HS) from the Pacific Parkinson's Research Centre. Graph theoretical measures were used to summarize the rsFC patterns. Canonical correlation analysis (CCA) was used to relate separate cognitive profiles in PD that were associated with disease severity and demographic measures as well as rsFC network measures. The CCA model relating cognition to demographics suggested female gender and education supported cognitive function in PD, age and depression scores were anti-correlated with overall cognition, and UPDRS had little influence on cognition. Alone, rsFC global network measures did not significantly differ between PD and controls, yet some nodal network measures, such as network segregation, were distinguishable between PD and HS in cortical “hub” regions. The CCA model relating cognition to rsFC global network values, which was not related to the other CCA model relating cognition to demographic information, suggested modularity, rich club coefficient, and transitivity was also broadly related to cognition in PD. Our results suggest that education, aging, comorbidity, and gender impact cognition more than overall disease severity in PD. Cortical “hub” regions are vulnerable in PD, and impairments of processing speed, attention, scanning abilities, and executive skills are related to enhanced functional segregation seen in PD. Frontiers Media S.A. 2018-06-20 /pmc/articles/PMC6019441/ /pubmed/29973913 http://dx.doi.org/10.3389/fneur.2018.00482 Text en Copyright © 2018 Lin, Baumeister, Garg and McKeown. http://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 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 Neurology
Lin, Sue-Jin
Baumeister, Tobias R.
Garg, Saurabh
McKeown, Martin J.
Cognitive Profiles and Hub Vulnerability in Parkinson's Disease
title Cognitive Profiles and Hub Vulnerability in Parkinson's Disease
title_full Cognitive Profiles and Hub Vulnerability in Parkinson's Disease
title_fullStr Cognitive Profiles and Hub Vulnerability in Parkinson's Disease
title_full_unstemmed Cognitive Profiles and Hub Vulnerability in Parkinson's Disease
title_short Cognitive Profiles and Hub Vulnerability in Parkinson's Disease
title_sort cognitive profiles and hub vulnerability in parkinson's disease
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019441/
https://www.ncbi.nlm.nih.gov/pubmed/29973913
http://dx.doi.org/10.3389/fneur.2018.00482
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