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Dementia risk in Parkinson’s disease is associated with interhemispheric connectivity loss and determined by regional gene expression

Parkinson’s dementia is a common and devastating part of Parkinson’s disease. Whilst timing and severity vary, dementia in Parkinson’s is often preceded by visual dysfunction. White matter changes, representing axonal loss, occur early in the disease process. Clarifying which white matter connection...

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Autores principales: Zarkali, Angeliki, McColgan, Peter, Ryten, Mina, Reynolds, Regina H., Leyland, Louise-Ann, Lees, Andrew J., Rees, Geraint, Weil, Rimona S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581968/
https://www.ncbi.nlm.nih.gov/pubmed/33395965
http://dx.doi.org/10.1016/j.nicl.2020.102470
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author Zarkali, Angeliki
McColgan, Peter
Ryten, Mina
Reynolds, Regina H.
Leyland, Louise-Ann
Lees, Andrew J.
Rees, Geraint
Weil, Rimona S.
author_facet Zarkali, Angeliki
McColgan, Peter
Ryten, Mina
Reynolds, Regina H.
Leyland, Louise-Ann
Lees, Andrew J.
Rees, Geraint
Weil, Rimona S.
author_sort Zarkali, Angeliki
collection PubMed
description Parkinson’s dementia is a common and devastating part of Parkinson’s disease. Whilst timing and severity vary, dementia in Parkinson’s is often preceded by visual dysfunction. White matter changes, representing axonal loss, occur early in the disease process. Clarifying which white matter connections are affected in Parkinson’s with visual dysfunction and why specific connections are vulnerable will provide important mechanistic insights. Here, we use diffusion tractography in 100 Parkinson’s patients (33 low visual performers) and 34 controls to identify patterns of connectivity loss in Parkinson’s with visual dysfunction. We examine the relationship between regional transcription and connectivity loss, using the Allen Institute for Brain Science transcriptome atlas. We show that interhemispheric connections are preferentially affected in Parkinson’s low visual performers. Interhemispheric connection loss was associated with downweighted genes related to the smoothened signalling pathway (enriched in glutamatergic neurons) and upweighted metabolic genes. Risk genes for Parkinson’s but not Alzheimer’s or Dementia with Lewy bodies were over-represented in upweighted genes associated with interhemispheric connection loss. Our findings suggest selective vulnerability in Parkinson’s patients at highest risk of dementia (those with visual dysfunction), where differences in gene expression and metabolic dysfunction, affecting longer connections with higher metabolic burden, drive connectivity loss.
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spelling pubmed-75819682020-10-27 Dementia risk in Parkinson’s disease is associated with interhemispheric connectivity loss and determined by regional gene expression Zarkali, Angeliki McColgan, Peter Ryten, Mina Reynolds, Regina H. Leyland, Louise-Ann Lees, Andrew J. Rees, Geraint Weil, Rimona S. Neuroimage Clin Regular Article Parkinson’s dementia is a common and devastating part of Parkinson’s disease. Whilst timing and severity vary, dementia in Parkinson’s is often preceded by visual dysfunction. White matter changes, representing axonal loss, occur early in the disease process. Clarifying which white matter connections are affected in Parkinson’s with visual dysfunction and why specific connections are vulnerable will provide important mechanistic insights. Here, we use diffusion tractography in 100 Parkinson’s patients (33 low visual performers) and 34 controls to identify patterns of connectivity loss in Parkinson’s with visual dysfunction. We examine the relationship between regional transcription and connectivity loss, using the Allen Institute for Brain Science transcriptome atlas. We show that interhemispheric connections are preferentially affected in Parkinson’s low visual performers. Interhemispheric connection loss was associated with downweighted genes related to the smoothened signalling pathway (enriched in glutamatergic neurons) and upweighted metabolic genes. Risk genes for Parkinson’s but not Alzheimer’s or Dementia with Lewy bodies were over-represented in upweighted genes associated with interhemispheric connection loss. Our findings suggest selective vulnerability in Parkinson’s patients at highest risk of dementia (those with visual dysfunction), where differences in gene expression and metabolic dysfunction, affecting longer connections with higher metabolic burden, drive connectivity loss. Elsevier 2020-10-15 /pmc/articles/PMC7581968/ /pubmed/33395965 http://dx.doi.org/10.1016/j.nicl.2020.102470 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular Article
Zarkali, Angeliki
McColgan, Peter
Ryten, Mina
Reynolds, Regina H.
Leyland, Louise-Ann
Lees, Andrew J.
Rees, Geraint
Weil, Rimona S.
Dementia risk in Parkinson’s disease is associated with interhemispheric connectivity loss and determined by regional gene expression
title Dementia risk in Parkinson’s disease is associated with interhemispheric connectivity loss and determined by regional gene expression
title_full Dementia risk in Parkinson’s disease is associated with interhemispheric connectivity loss and determined by regional gene expression
title_fullStr Dementia risk in Parkinson’s disease is associated with interhemispheric connectivity loss and determined by regional gene expression
title_full_unstemmed Dementia risk in Parkinson’s disease is associated with interhemispheric connectivity loss and determined by regional gene expression
title_short Dementia risk in Parkinson’s disease is associated with interhemispheric connectivity loss and determined by regional gene expression
title_sort dementia risk in parkinson’s disease is associated with interhemispheric connectivity loss and determined by regional gene expression
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581968/
https://www.ncbi.nlm.nih.gov/pubmed/33395965
http://dx.doi.org/10.1016/j.nicl.2020.102470
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