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Functional correlates of response inhibition in impulse control disorders in Parkinson’s disease

Impulse control disorder is a prevalent side-effect of Parkinson’s disease (PD) medication, with a strong negative impact on the quality of life of those affected. Although impulsivity has classically been associated with response inhibition deficits, previous evidence from PD patients with impulse...

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Autores principales: Esteban-Peñalba, Teresa, Paz-Alonso, Pedro M., Navalpotro-Gómez, Irene, Rodríguez-Oroz, María C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449263/
https://www.ncbi.nlm.nih.gov/pubmed/34536820
http://dx.doi.org/10.1016/j.nicl.2021.102822
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author Esteban-Peñalba, Teresa
Paz-Alonso, Pedro M.
Navalpotro-Gómez, Irene
Rodríguez-Oroz, María C.
author_facet Esteban-Peñalba, Teresa
Paz-Alonso, Pedro M.
Navalpotro-Gómez, Irene
Rodríguez-Oroz, María C.
author_sort Esteban-Peñalba, Teresa
collection PubMed
description Impulse control disorder is a prevalent side-effect of Parkinson’s disease (PD) medication, with a strong negative impact on the quality of life of those affected. Although impulsivity has classically been associated with response inhibition deficits, previous evidence from PD patients with impulse control disorder (ICD) has not revealed behavioral dysfunction in response inhibition. In this study, 18 PD patients with ICD, 17 PD patients without this complication, and 15 healthy controls performed a version of the conditional Stop Signal Task during functional magnetic resonance imaging. Whole-brain contrasts, regions of interest, and functional connectivity analyses were conducted. Our aim was to investigate the neural underpinnings of two aspects of response inhibition: proactive inhibition, inhibition that has been prepared beforehand, and restrained inhibition, inhibition of an invalid inhibitory tendency. We observed that, in respect to the other two groups, PD patients with ICD exhibited hyperactivation of the stopping network bilaterally while performing proactive inhibition. When engaged in restrained inhibition, they showed hyperactivation of the left inferior frontal gyrus, an area linked to action monitoring. Restrained inhibition also resulted in changes to the functional co-activation between inhibitory regions and left inferior parietal cortex and right supramarginal gyrus. Our findings indicate that PD patients with ICD completed the inhibition task correctly, showing altered engagement of inhibitory and attentional areas. During proactive inhibition they showed bilateral hyperactivation of two inhibitory regions, while during restrained inhibition they showed additional involvement of attentional areas responsible for alerting and orienting.
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spelling pubmed-84492632021-09-24 Functional correlates of response inhibition in impulse control disorders in Parkinson’s disease Esteban-Peñalba, Teresa Paz-Alonso, Pedro M. Navalpotro-Gómez, Irene Rodríguez-Oroz, María C. Neuroimage Clin Regular Article Impulse control disorder is a prevalent side-effect of Parkinson’s disease (PD) medication, with a strong negative impact on the quality of life of those affected. Although impulsivity has classically been associated with response inhibition deficits, previous evidence from PD patients with impulse control disorder (ICD) has not revealed behavioral dysfunction in response inhibition. In this study, 18 PD patients with ICD, 17 PD patients without this complication, and 15 healthy controls performed a version of the conditional Stop Signal Task during functional magnetic resonance imaging. Whole-brain contrasts, regions of interest, and functional connectivity analyses were conducted. Our aim was to investigate the neural underpinnings of two aspects of response inhibition: proactive inhibition, inhibition that has been prepared beforehand, and restrained inhibition, inhibition of an invalid inhibitory tendency. We observed that, in respect to the other two groups, PD patients with ICD exhibited hyperactivation of the stopping network bilaterally while performing proactive inhibition. When engaged in restrained inhibition, they showed hyperactivation of the left inferior frontal gyrus, an area linked to action monitoring. Restrained inhibition also resulted in changes to the functional co-activation between inhibitory regions and left inferior parietal cortex and right supramarginal gyrus. Our findings indicate that PD patients with ICD completed the inhibition task correctly, showing altered engagement of inhibitory and attentional areas. During proactive inhibition they showed bilateral hyperactivation of two inhibitory regions, while during restrained inhibition they showed additional involvement of attentional areas responsible for alerting and orienting. Elsevier 2021-09-11 /pmc/articles/PMC8449263/ /pubmed/34536820 http://dx.doi.org/10.1016/j.nicl.2021.102822 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Esteban-Peñalba, Teresa
Paz-Alonso, Pedro M.
Navalpotro-Gómez, Irene
Rodríguez-Oroz, María C.
Functional correlates of response inhibition in impulse control disorders in Parkinson’s disease
title Functional correlates of response inhibition in impulse control disorders in Parkinson’s disease
title_full Functional correlates of response inhibition in impulse control disorders in Parkinson’s disease
title_fullStr Functional correlates of response inhibition in impulse control disorders in Parkinson’s disease
title_full_unstemmed Functional correlates of response inhibition in impulse control disorders in Parkinson’s disease
title_short Functional correlates of response inhibition in impulse control disorders in Parkinson’s disease
title_sort functional correlates of response inhibition in impulse control disorders in parkinson’s disease
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449263/
https://www.ncbi.nlm.nih.gov/pubmed/34536820
http://dx.doi.org/10.1016/j.nicl.2021.102822
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