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White matter hyperintensities associated with impulse control disorders in Parkinson’s Disease

Impulse control disorders (ICDs) in Parkinson's disease (PD) are increasingly recognized as clinically significant non-motor features that potentially impair the quality of life. White matter hyperintensities (WMHs), detected by magnetic resonance imaging, are frequently observed in PD and can...

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Autores principales: Hernadi, Gabriella, Perlaki, Gabor, Kovacs, Marton, Pinter, David, Orsi, Gergely, Janszky, Jozsef, Kovacs, Norbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313834/
https://www.ncbi.nlm.nih.gov/pubmed/37391475
http://dx.doi.org/10.1038/s41598-023-37054-8
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author Hernadi, Gabriella
Perlaki, Gabor
Kovacs, Marton
Pinter, David
Orsi, Gergely
Janszky, Jozsef
Kovacs, Norbert
author_facet Hernadi, Gabriella
Perlaki, Gabor
Kovacs, Marton
Pinter, David
Orsi, Gergely
Janszky, Jozsef
Kovacs, Norbert
author_sort Hernadi, Gabriella
collection PubMed
description Impulse control disorders (ICDs) in Parkinson's disease (PD) are increasingly recognized as clinically significant non-motor features that potentially impair the quality of life. White matter hyperintensities (WMHs), detected by magnetic resonance imaging, are frequently observed in PD and can be associated with both motor- and certain non-motor symptoms. Given the limited number of non-motor features studied in this context, our aim was to reveal the potential association between the severity of WMHs and ICDs in PD. Fluid-attenuated inversion recovery magnetic resonance images were retrospectively evaluated in 70 patients with PD (48 males; 59.3 ± 10.1 years). The severity of WMHs was assessed by Fazekas scores and by the volume and number of supratentorial WMHs. ICDs were evaluated using the modified Minnesota Impulsive Disorders Interview. Significant interaction between age and the severity of WMHs was present for ICDs. In our younger patients (< 60.5 years), severity of WMHs was positively associated with ICDs (p = 0.004, p = 0.021, p < 0.001 and p < 0.001, respectively for periventricular white matter and total Fazekas scores and the volume and number of WMHs). Our study supports the hypothesis that WMHs of presumed vascular origin may contribute to ICDs in PD. Future prospective studies are needed to assess the prognostic relevance of this finding.
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spelling pubmed-103138342023-07-02 White matter hyperintensities associated with impulse control disorders in Parkinson’s Disease Hernadi, Gabriella Perlaki, Gabor Kovacs, Marton Pinter, David Orsi, Gergely Janszky, Jozsef Kovacs, Norbert Sci Rep Article Impulse control disorders (ICDs) in Parkinson's disease (PD) are increasingly recognized as clinically significant non-motor features that potentially impair the quality of life. White matter hyperintensities (WMHs), detected by magnetic resonance imaging, are frequently observed in PD and can be associated with both motor- and certain non-motor symptoms. Given the limited number of non-motor features studied in this context, our aim was to reveal the potential association between the severity of WMHs and ICDs in PD. Fluid-attenuated inversion recovery magnetic resonance images were retrospectively evaluated in 70 patients with PD (48 males; 59.3 ± 10.1 years). The severity of WMHs was assessed by Fazekas scores and by the volume and number of supratentorial WMHs. ICDs were evaluated using the modified Minnesota Impulsive Disorders Interview. Significant interaction between age and the severity of WMHs was present for ICDs. In our younger patients (< 60.5 years), severity of WMHs was positively associated with ICDs (p = 0.004, p = 0.021, p < 0.001 and p < 0.001, respectively for periventricular white matter and total Fazekas scores and the volume and number of WMHs). Our study supports the hypothesis that WMHs of presumed vascular origin may contribute to ICDs in PD. Future prospective studies are needed to assess the prognostic relevance of this finding. Nature Publishing Group UK 2023-06-30 /pmc/articles/PMC10313834/ /pubmed/37391475 http://dx.doi.org/10.1038/s41598-023-37054-8 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hernadi, Gabriella
Perlaki, Gabor
Kovacs, Marton
Pinter, David
Orsi, Gergely
Janszky, Jozsef
Kovacs, Norbert
White matter hyperintensities associated with impulse control disorders in Parkinson’s Disease
title White matter hyperintensities associated with impulse control disorders in Parkinson’s Disease
title_full White matter hyperintensities associated with impulse control disorders in Parkinson’s Disease
title_fullStr White matter hyperintensities associated with impulse control disorders in Parkinson’s Disease
title_full_unstemmed White matter hyperintensities associated with impulse control disorders in Parkinson’s Disease
title_short White matter hyperintensities associated with impulse control disorders in Parkinson’s Disease
title_sort white matter hyperintensities associated with impulse control disorders in parkinson’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313834/
https://www.ncbi.nlm.nih.gov/pubmed/37391475
http://dx.doi.org/10.1038/s41598-023-37054-8
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