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The default mode network is disrupted in parkinson's disease with visual hallucinations

Background: Visual hallucinations (VH) are one of the most striking nonmotor symptoms in Parkinson's disease (PD), and predict dementia and mortality. Aberrant default mode network (DMN) is associated with other psychoses. Here, we tested the hypothesis that DMN dysfunction contributes to VH in...

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Autores principales: Yao, Nailin, Shek‐Kwan Chang, Richard, Cheung, Charlton, Pang, Shirley, Lau, Kui Kai, Suckling, John, Rowe, James B., Yu, Kevin, Ka‐Fung Mak, Henry, Chua, Siew‐Eng, Ho, Shu Leong., McAlonan, Grainne M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657500/
https://www.ncbi.nlm.nih.gov/pubmed/24985056
http://dx.doi.org/10.1002/hbm.22577
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author Yao, Nailin
Shek‐Kwan Chang, Richard
Cheung, Charlton
Pang, Shirley
Lau, Kui Kai
Suckling, John
Rowe, James B.
Yu, Kevin
Ka‐Fung Mak, Henry
Chua, Siew‐Eng
Ho, Shu Leong.
McAlonan, Grainne M.
author_facet Yao, Nailin
Shek‐Kwan Chang, Richard
Cheung, Charlton
Pang, Shirley
Lau, Kui Kai
Suckling, John
Rowe, James B.
Yu, Kevin
Ka‐Fung Mak, Henry
Chua, Siew‐Eng
Ho, Shu Leong.
McAlonan, Grainne M.
author_sort Yao, Nailin
collection PubMed
description Background: Visual hallucinations (VH) are one of the most striking nonmotor symptoms in Parkinson's disease (PD), and predict dementia and mortality. Aberrant default mode network (DMN) is associated with other psychoses. Here, we tested the hypothesis that DMN dysfunction contributes to VH in PD. Methods: Resting state functional data was acquired from individuals with PD with VH (PDVH) and without VH (PDnonVH), matched for levodopa drug equivalent dose, and a healthy control group (HC). Independent component analysis was used to investigate group differences in functional connectivity within the DMN. In addition, we investigated whether the functional changes associated with hallucinations were accompanied by differences in cortical thickness. Results: There were no group differences in cortical thickness but functional coactivation within components of the DMN was significantly lower in both PDVH and PDnonVH groups compared to HC. Functional coactivation within the DMN was found to be greater in PDVH group relative to PDnonVH group. Conclusion: Our study demonstrates, for the first time that, within a functionally abnormal DMN in PD, relatively higher “connectivity” is associated with VH. We postulate that aberrant connectivity in a large scale network affects sensory information processing and perception, and contributes to “positive” symptom generation in PD. Hum Brain Mapp 35:5658–5666, 2014. © 2014 The Authors Human Brain Mapping Published by Wiley Periodicals, Inc.
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spelling pubmed-46575002015-12-02 The default mode network is disrupted in parkinson's disease with visual hallucinations Yao, Nailin Shek‐Kwan Chang, Richard Cheung, Charlton Pang, Shirley Lau, Kui Kai Suckling, John Rowe, James B. Yu, Kevin Ka‐Fung Mak, Henry Chua, Siew‐Eng Ho, Shu Leong. McAlonan, Grainne M. Hum Brain Mapp Research Articles Background: Visual hallucinations (VH) are one of the most striking nonmotor symptoms in Parkinson's disease (PD), and predict dementia and mortality. Aberrant default mode network (DMN) is associated with other psychoses. Here, we tested the hypothesis that DMN dysfunction contributes to VH in PD. Methods: Resting state functional data was acquired from individuals with PD with VH (PDVH) and without VH (PDnonVH), matched for levodopa drug equivalent dose, and a healthy control group (HC). Independent component analysis was used to investigate group differences in functional connectivity within the DMN. In addition, we investigated whether the functional changes associated with hallucinations were accompanied by differences in cortical thickness. Results: There were no group differences in cortical thickness but functional coactivation within components of the DMN was significantly lower in both PDVH and PDnonVH groups compared to HC. Functional coactivation within the DMN was found to be greater in PDVH group relative to PDnonVH group. Conclusion: Our study demonstrates, for the first time that, within a functionally abnormal DMN in PD, relatively higher “connectivity” is associated with VH. We postulate that aberrant connectivity in a large scale network affects sensory information processing and perception, and contributes to “positive” symptom generation in PD. Hum Brain Mapp 35:5658–5666, 2014. © 2014 The Authors Human Brain Mapping Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2014-07-01 /pmc/articles/PMC4657500/ /pubmed/24985056 http://dx.doi.org/10.1002/hbm.22577 Text en Copyright © 2014 The Authors Human Brain Mapping Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Yao, Nailin
Shek‐Kwan Chang, Richard
Cheung, Charlton
Pang, Shirley
Lau, Kui Kai
Suckling, John
Rowe, James B.
Yu, Kevin
Ka‐Fung Mak, Henry
Chua, Siew‐Eng
Ho, Shu Leong.
McAlonan, Grainne M.
The default mode network is disrupted in parkinson's disease with visual hallucinations
title The default mode network is disrupted in parkinson's disease with visual hallucinations
title_full The default mode network is disrupted in parkinson's disease with visual hallucinations
title_fullStr The default mode network is disrupted in parkinson's disease with visual hallucinations
title_full_unstemmed The default mode network is disrupted in parkinson's disease with visual hallucinations
title_short The default mode network is disrupted in parkinson's disease with visual hallucinations
title_sort default mode network is disrupted in parkinson's disease with visual hallucinations
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657500/
https://www.ncbi.nlm.nih.gov/pubmed/24985056
http://dx.doi.org/10.1002/hbm.22577
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