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Changes in dynamic transitions between integrated and segregated states underlie visual hallucinations in Parkinson’s disease
Hallucinations are a core feature of psychosis and common in Parkinson’s. Their transient, unexpected nature suggests a change in dynamic brain states, but underlying causes are unknown. Here, we examine temporal dynamics and underlying structural connectivity in Parkinson’s-hallucinations using a c...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458713/ https://www.ncbi.nlm.nih.gov/pubmed/36075964 http://dx.doi.org/10.1038/s42003-022-03903-x |
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author | Zarkali, Angeliki Luppi, Andrea I. Stamatakis, Emmanuel A. Reeves, Suzanne McColgan, Peter Leyland, Louise-Ann Lees, Andrew J. Weil, Rimona S. |
author_facet | Zarkali, Angeliki Luppi, Andrea I. Stamatakis, Emmanuel A. Reeves, Suzanne McColgan, Peter Leyland, Louise-Ann Lees, Andrew J. Weil, Rimona S. |
author_sort | Zarkali, Angeliki |
collection | PubMed |
description | Hallucinations are a core feature of psychosis and common in Parkinson’s. Their transient, unexpected nature suggests a change in dynamic brain states, but underlying causes are unknown. Here, we examine temporal dynamics and underlying structural connectivity in Parkinson’s-hallucinations using a combination of functional and structural MRI, network control theory, neurotransmitter density and genetic analyses. We show that Parkinson’s-hallucinators spent more time in a predominantly Segregated functional state with fewer between-state transitions. The transition from integrated-to-segregated state had lower energy cost in Parkinson’s-hallucinators; and was therefore potentially preferable. The regional energy needed for this transition was correlated with regional neurotransmitter density and gene expression for serotoninergic, GABAergic, noradrenergic and cholinergic, but not dopaminergic, receptors. We show how the combination of neurochemistry and brain structure jointly shape functional brain dynamics leading to hallucinations and highlight potential therapeutic targets by linking these changes to neurotransmitter systems involved in early sensory and complex visual processing. |
format | Online Article Text |
id | pubmed-9458713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94587132022-09-10 Changes in dynamic transitions between integrated and segregated states underlie visual hallucinations in Parkinson’s disease Zarkali, Angeliki Luppi, Andrea I. Stamatakis, Emmanuel A. Reeves, Suzanne McColgan, Peter Leyland, Louise-Ann Lees, Andrew J. Weil, Rimona S. Commun Biol Article Hallucinations are a core feature of psychosis and common in Parkinson’s. Their transient, unexpected nature suggests a change in dynamic brain states, but underlying causes are unknown. Here, we examine temporal dynamics and underlying structural connectivity in Parkinson’s-hallucinations using a combination of functional and structural MRI, network control theory, neurotransmitter density and genetic analyses. We show that Parkinson’s-hallucinators spent more time in a predominantly Segregated functional state with fewer between-state transitions. The transition from integrated-to-segregated state had lower energy cost in Parkinson’s-hallucinators; and was therefore potentially preferable. The regional energy needed for this transition was correlated with regional neurotransmitter density and gene expression for serotoninergic, GABAergic, noradrenergic and cholinergic, but not dopaminergic, receptors. We show how the combination of neurochemistry and brain structure jointly shape functional brain dynamics leading to hallucinations and highlight potential therapeutic targets by linking these changes to neurotransmitter systems involved in early sensory and complex visual processing. Nature Publishing Group UK 2022-09-08 /pmc/articles/PMC9458713/ /pubmed/36075964 http://dx.doi.org/10.1038/s42003-022-03903-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zarkali, Angeliki Luppi, Andrea I. Stamatakis, Emmanuel A. Reeves, Suzanne McColgan, Peter Leyland, Louise-Ann Lees, Andrew J. Weil, Rimona S. Changes in dynamic transitions between integrated and segregated states underlie visual hallucinations in Parkinson’s disease |
title | Changes in dynamic transitions between integrated and segregated states underlie visual hallucinations in Parkinson’s disease |
title_full | Changes in dynamic transitions between integrated and segregated states underlie visual hallucinations in Parkinson’s disease |
title_fullStr | Changes in dynamic transitions between integrated and segregated states underlie visual hallucinations in Parkinson’s disease |
title_full_unstemmed | Changes in dynamic transitions between integrated and segregated states underlie visual hallucinations in Parkinson’s disease |
title_short | Changes in dynamic transitions between integrated and segregated states underlie visual hallucinations in Parkinson’s disease |
title_sort | changes in dynamic transitions between integrated and segregated states underlie visual hallucinations in parkinson’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458713/ https://www.ncbi.nlm.nih.gov/pubmed/36075964 http://dx.doi.org/10.1038/s42003-022-03903-x |
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