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Dopaminergic modulation of performance monitoring in Parkinson’s disease: An event-related potential study
Monitoring one’s actions is essential for goal-directed performance. In the event-related potential (ERP), errors are followed by fronto-centrally distributed negativities. These error(-related) negativity (N(e)/ERN) amplitudes are often found to be attenuated in patients with Parkinson’s disease (P...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259704/ https://www.ncbi.nlm.nih.gov/pubmed/28117420 http://dx.doi.org/10.1038/srep41222 |
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author | Seer, Caroline Lange, Florian Loens, Sebastian Wegner, Florian Schrader, Christoph Dressler, Dirk Dengler, Reinhard Kopp, Bruno |
author_facet | Seer, Caroline Lange, Florian Loens, Sebastian Wegner, Florian Schrader, Christoph Dressler, Dirk Dengler, Reinhard Kopp, Bruno |
author_sort | Seer, Caroline |
collection | PubMed |
description | Monitoring one’s actions is essential for goal-directed performance. In the event-related potential (ERP), errors are followed by fronto-centrally distributed negativities. These error(-related) negativity (N(e)/ERN) amplitudes are often found to be attenuated in patients with Parkinson’s disease (PD) compared to healthy controls (HC). Although N(e)/ERN has been proposed to be related to dopaminergic neuronal activity, previous research did not find evidence for effects of dopaminergic medication on N(e)/ERN amplitudes in PD. We examined 13 PD patients “on” and “off” dopaminergic medication. Their response-locked ERP amplitudes (obtained on correct [N(c)/CRN] and error [N(e)/ERN] trials of a flanker task) were compared to those of 13 HC who were tested twice as well, without receiving dopaminergic medication. While PD patients committed more errors than HC, error rates were not significantly modulated by dopaminergic medication. PD patients showed reduced N(e)/ERN amplitudes relative to HC; however, this attenuation of response-locked ERP amplitudes was not specific to errors in this study. PD-related attenuation of response-locked ERP amplitudes was most pronounced when PD patients were on medication. These results suggest overdosing of dopaminergic pathways that are relatively spared in PD, but that are related to the generation of the N(e)/ERN, notably pathways targeted on the medial prefrontal cortex. |
format | Online Article Text |
id | pubmed-5259704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52597042017-01-24 Dopaminergic modulation of performance monitoring in Parkinson’s disease: An event-related potential study Seer, Caroline Lange, Florian Loens, Sebastian Wegner, Florian Schrader, Christoph Dressler, Dirk Dengler, Reinhard Kopp, Bruno Sci Rep Article Monitoring one’s actions is essential for goal-directed performance. In the event-related potential (ERP), errors are followed by fronto-centrally distributed negativities. These error(-related) negativity (N(e)/ERN) amplitudes are often found to be attenuated in patients with Parkinson’s disease (PD) compared to healthy controls (HC). Although N(e)/ERN has been proposed to be related to dopaminergic neuronal activity, previous research did not find evidence for effects of dopaminergic medication on N(e)/ERN amplitudes in PD. We examined 13 PD patients “on” and “off” dopaminergic medication. Their response-locked ERP amplitudes (obtained on correct [N(c)/CRN] and error [N(e)/ERN] trials of a flanker task) were compared to those of 13 HC who were tested twice as well, without receiving dopaminergic medication. While PD patients committed more errors than HC, error rates were not significantly modulated by dopaminergic medication. PD patients showed reduced N(e)/ERN amplitudes relative to HC; however, this attenuation of response-locked ERP amplitudes was not specific to errors in this study. PD-related attenuation of response-locked ERP amplitudes was most pronounced when PD patients were on medication. These results suggest overdosing of dopaminergic pathways that are relatively spared in PD, but that are related to the generation of the N(e)/ERN, notably pathways targeted on the medial prefrontal cortex. Nature Publishing Group 2017-01-24 /pmc/articles/PMC5259704/ /pubmed/28117420 http://dx.doi.org/10.1038/srep41222 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Seer, Caroline Lange, Florian Loens, Sebastian Wegner, Florian Schrader, Christoph Dressler, Dirk Dengler, Reinhard Kopp, Bruno Dopaminergic modulation of performance monitoring in Parkinson’s disease: An event-related potential study |
title | Dopaminergic modulation of performance monitoring in Parkinson’s disease: An event-related potential study |
title_full | Dopaminergic modulation of performance monitoring in Parkinson’s disease: An event-related potential study |
title_fullStr | Dopaminergic modulation of performance monitoring in Parkinson’s disease: An event-related potential study |
title_full_unstemmed | Dopaminergic modulation of performance monitoring in Parkinson’s disease: An event-related potential study |
title_short | Dopaminergic modulation of performance monitoring in Parkinson’s disease: An event-related potential study |
title_sort | dopaminergic modulation of performance monitoring in parkinson’s disease: an event-related potential study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259704/ https://www.ncbi.nlm.nih.gov/pubmed/28117420 http://dx.doi.org/10.1038/srep41222 |
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