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Distinct Relationship Between Cognitive Flexibility and White Matter Integrity in Individuals at Risk of Parkinson’s Disease

BACKGROUND AND OBJECTIVE: Executive dysfunction is the most common cognitive impairment in Parkinson’s disease (PD), occurring even in its early stages. In our study, we applied diffusion tensor imaging (DTI) to investigate white matter integrity and its association with a specific executive functio...

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Autores principales: Alzaid, Haidar, Ethofer, Thomas, Hobert, Markus A., Kardatzki, Bernd, Erb, Michael, Maetzler, Walter, Berg, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439016/
https://www.ncbi.nlm.nih.gov/pubmed/32903902
http://dx.doi.org/10.3389/fnagi.2020.00250
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author Alzaid, Haidar
Ethofer, Thomas
Hobert, Markus A.
Kardatzki, Bernd
Erb, Michael
Maetzler, Walter
Berg, Daniela
author_facet Alzaid, Haidar
Ethofer, Thomas
Hobert, Markus A.
Kardatzki, Bernd
Erb, Michael
Maetzler, Walter
Berg, Daniela
author_sort Alzaid, Haidar
collection PubMed
description BACKGROUND AND OBJECTIVE: Executive dysfunction is the most common cognitive impairment in Parkinson’s disease (PD), occurring even in its early stages. In our study, we applied diffusion tensor imaging (DTI) to investigate white matter integrity and its association with a specific executive function such as cognitive flexibility in individuals with risk factors for PD. METHODS: We examined 50 individuals with risk factors for developing PD and 24 healthy controls from the TREND (Tübinger Evaluation of Risk Factors for Early Detection of Neurodegeneration) study including neuropsychological evaluation and DTI. Cognitive flexibility was assessed using the trail making test (TMT). Tract based spatial statistics (TBSS) were employed to assess white matter abnormalities and their correlation with cognitive flexibility. RESULTS: TMT performance correlated with mean and axial diffusivity in several white matter regions, predominantly in the frontoparietal white matter. These effects were stronger in PD risk persons (PD-RP) than in controls as evidenced by a significant group interaction. White matter integrity and TMT performance did not significantly differ across groups. CONCLUSION: Based on our results, PD-RP do no exhibit white matter changes or impaired cognitive flexibility. However, specific executive functions in PD-RP are more related to white matter alterations than in healthy older adults.
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spelling pubmed-74390162020-09-03 Distinct Relationship Between Cognitive Flexibility and White Matter Integrity in Individuals at Risk of Parkinson’s Disease Alzaid, Haidar Ethofer, Thomas Hobert, Markus A. Kardatzki, Bernd Erb, Michael Maetzler, Walter Berg, Daniela Front Aging Neurosci Neuroscience BACKGROUND AND OBJECTIVE: Executive dysfunction is the most common cognitive impairment in Parkinson’s disease (PD), occurring even in its early stages. In our study, we applied diffusion tensor imaging (DTI) to investigate white matter integrity and its association with a specific executive function such as cognitive flexibility in individuals with risk factors for PD. METHODS: We examined 50 individuals with risk factors for developing PD and 24 healthy controls from the TREND (Tübinger Evaluation of Risk Factors for Early Detection of Neurodegeneration) study including neuropsychological evaluation and DTI. Cognitive flexibility was assessed using the trail making test (TMT). Tract based spatial statistics (TBSS) were employed to assess white matter abnormalities and their correlation with cognitive flexibility. RESULTS: TMT performance correlated with mean and axial diffusivity in several white matter regions, predominantly in the frontoparietal white matter. These effects were stronger in PD risk persons (PD-RP) than in controls as evidenced by a significant group interaction. White matter integrity and TMT performance did not significantly differ across groups. CONCLUSION: Based on our results, PD-RP do no exhibit white matter changes or impaired cognitive flexibility. However, specific executive functions in PD-RP are more related to white matter alterations than in healthy older adults. Frontiers Media S.A. 2020-08-13 /pmc/articles/PMC7439016/ /pubmed/32903902 http://dx.doi.org/10.3389/fnagi.2020.00250 Text en Copyright © 2020 Alzaid, Ethofer, Hobert, Kardatzki, Erb, Maetzler and Berg. 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(s) 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 Neuroscience
Alzaid, Haidar
Ethofer, Thomas
Hobert, Markus A.
Kardatzki, Bernd
Erb, Michael
Maetzler, Walter
Berg, Daniela
Distinct Relationship Between Cognitive Flexibility and White Matter Integrity in Individuals at Risk of Parkinson’s Disease
title Distinct Relationship Between Cognitive Flexibility and White Matter Integrity in Individuals at Risk of Parkinson’s Disease
title_full Distinct Relationship Between Cognitive Flexibility and White Matter Integrity in Individuals at Risk of Parkinson’s Disease
title_fullStr Distinct Relationship Between Cognitive Flexibility and White Matter Integrity in Individuals at Risk of Parkinson’s Disease
title_full_unstemmed Distinct Relationship Between Cognitive Flexibility and White Matter Integrity in Individuals at Risk of Parkinson’s Disease
title_short Distinct Relationship Between Cognitive Flexibility and White Matter Integrity in Individuals at Risk of Parkinson’s Disease
title_sort distinct relationship between cognitive flexibility and white matter integrity in individuals at risk of parkinson’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439016/
https://www.ncbi.nlm.nih.gov/pubmed/32903902
http://dx.doi.org/10.3389/fnagi.2020.00250
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