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Frontoparietal connectivity correlates with working memory performance in multiple sclerosis
Working Memory (WM) impairment is the most common cognitive deficit of patients with Multiple Sclerosis (MS). However, evidence of its neurobiological mechanisms is scarce. Here we recorded electroencephalographic activity of twenty patients with relapsing-remitting MS and minimal cognitive deficit,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7283327/ https://www.ncbi.nlm.nih.gov/pubmed/32518271 http://dx.doi.org/10.1038/s41598-020-66279-0 |
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author | Figueroa-Vargas, Alejandra Cárcamo, Claudia Henríquez-Ch, Rodrigo Zamorano, Francisco Ciampi, Ethel Uribe-San-Martin, Reinaldo Vásquez, Macarena Aboitiz, Francisco Billeke, Pablo |
author_facet | Figueroa-Vargas, Alejandra Cárcamo, Claudia Henríquez-Ch, Rodrigo Zamorano, Francisco Ciampi, Ethel Uribe-San-Martin, Reinaldo Vásquez, Macarena Aboitiz, Francisco Billeke, Pablo |
author_sort | Figueroa-Vargas, Alejandra |
collection | PubMed |
description | Working Memory (WM) impairment is the most common cognitive deficit of patients with Multiple Sclerosis (MS). However, evidence of its neurobiological mechanisms is scarce. Here we recorded electroencephalographic activity of twenty patients with relapsing-remitting MS and minimal cognitive deficit, and 20 healthy control (HC) subjects while they solved a WM task. In spite of similar performance, the HC group demonstrated both a correlation between temporoparietal theta activity and memory load, and a correlation between medial frontal theta activity and successful memory performances. MS patients did not show theses correlations leading significant differences between groups. Moreover, cortical connectivity analyses using granger causality and phase-amplitude coupling between theta and gamma revealed that HC group, but not MS group, presented a load-modulated progression of the frontal-to-parietal connectivity. This connectivity correlated with working memory capacity in MS groups. This early alterations in the oscillatory dynamics underlaying working memory could be useful for plan therapeutic interventions. |
format | Online Article Text |
id | pubmed-7283327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72833272020-06-15 Frontoparietal connectivity correlates with working memory performance in multiple sclerosis Figueroa-Vargas, Alejandra Cárcamo, Claudia Henríquez-Ch, Rodrigo Zamorano, Francisco Ciampi, Ethel Uribe-San-Martin, Reinaldo Vásquez, Macarena Aboitiz, Francisco Billeke, Pablo Sci Rep Article Working Memory (WM) impairment is the most common cognitive deficit of patients with Multiple Sclerosis (MS). However, evidence of its neurobiological mechanisms is scarce. Here we recorded electroencephalographic activity of twenty patients with relapsing-remitting MS and minimal cognitive deficit, and 20 healthy control (HC) subjects while they solved a WM task. In spite of similar performance, the HC group demonstrated both a correlation between temporoparietal theta activity and memory load, and a correlation between medial frontal theta activity and successful memory performances. MS patients did not show theses correlations leading significant differences between groups. Moreover, cortical connectivity analyses using granger causality and phase-amplitude coupling between theta and gamma revealed that HC group, but not MS group, presented a load-modulated progression of the frontal-to-parietal connectivity. This connectivity correlated with working memory capacity in MS groups. This early alterations in the oscillatory dynamics underlaying working memory could be useful for plan therapeutic interventions. Nature Publishing Group UK 2020-06-09 /pmc/articles/PMC7283327/ /pubmed/32518271 http://dx.doi.org/10.1038/s41598-020-66279-0 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Figueroa-Vargas, Alejandra Cárcamo, Claudia Henríquez-Ch, Rodrigo Zamorano, Francisco Ciampi, Ethel Uribe-San-Martin, Reinaldo Vásquez, Macarena Aboitiz, Francisco Billeke, Pablo Frontoparietal connectivity correlates with working memory performance in multiple sclerosis |
title | Frontoparietal connectivity correlates with working memory performance in multiple sclerosis |
title_full | Frontoparietal connectivity correlates with working memory performance in multiple sclerosis |
title_fullStr | Frontoparietal connectivity correlates with working memory performance in multiple sclerosis |
title_full_unstemmed | Frontoparietal connectivity correlates with working memory performance in multiple sclerosis |
title_short | Frontoparietal connectivity correlates with working memory performance in multiple sclerosis |
title_sort | frontoparietal connectivity correlates with working memory performance in multiple sclerosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7283327/ https://www.ncbi.nlm.nih.gov/pubmed/32518271 http://dx.doi.org/10.1038/s41598-020-66279-0 |
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