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Cortical thickness is related to working memory performance after non-invasive brain stimulation

Non-invasive brain stimulation (NIBS) probing the dorsolateral prefrontal cortex (DLPFC) has been shown to have little effect on working memory. The variability of NIBS responses might be explained by inter-subject brain anatomical variability. We investigated whether baseline cortical brain thickne...

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Autores principales: Razza, L.B., Vanderhasselt, M.A., Luethi, M.S., Repple, J., Busatto, G., Buchpiguel, C.A., Brunoni, A.R., da Silva, P.H.R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10591489/
https://www.ncbi.nlm.nih.gov/pubmed/37878887
http://dx.doi.org/10.1590/1414-431X2023e12945
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author Razza, L.B.
Vanderhasselt, M.A.
Luethi, M.S.
Repple, J.
Busatto, G.
Buchpiguel, C.A.
Brunoni, A.R.
da Silva, P.H.R.
author_facet Razza, L.B.
Vanderhasselt, M.A.
Luethi, M.S.
Repple, J.
Busatto, G.
Buchpiguel, C.A.
Brunoni, A.R.
da Silva, P.H.R.
author_sort Razza, L.B.
collection PubMed
description Non-invasive brain stimulation (NIBS) probing the dorsolateral prefrontal cortex (DLPFC) has been shown to have little effect on working memory. The variability of NIBS responses might be explained by inter-subject brain anatomical variability. We investigated whether baseline cortical brain thickness of regions of interest was associated with working memory performance after NIBS by performing a secondary analysis of previously published research. Structural magnetic resonance imaging data were analyzed from healthy subjects who received transcranial direct current stimulation (tDCS), intermittent theta-burst stimulation (iTBS), and placebo. Twenty-two participants were randomly assigned to receive all the interventions in a random order. The working memory task was conducted after the end of each NIBS session. Regions of interest were the bilateral DLPFC, medial prefrontal cortex, and posterior cingulate cortex. Overall, 66 NIBS sessions were performed. Findings revealed a negative significant association between cortical thickness of the bilateral dorsolateral prefrontal cortex and reaction time for both tDCS (left: P=0.045, right: P=0.037) and iTBS (left: P=0.007, right: P=0.007) compared to placebo. A significant positive association was found for iTBS and posterior cingulate cortex (P=0.03). No association was found for accuracy. Our findings provide the first evidence that individual cortical thickness of healthy subjects might be associated with working memory performance following different NIBS interventions. Therefore, cortical thickness could explain - to some extent - the heterogeneous effects of NIBS probing the DLPFC.
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spelling pubmed-105914892023-10-24 Cortical thickness is related to working memory performance after non-invasive brain stimulation Razza, L.B. Vanderhasselt, M.A. Luethi, M.S. Repple, J. Busatto, G. Buchpiguel, C.A. Brunoni, A.R. da Silva, P.H.R. Braz J Med Biol Res Research Article Non-invasive brain stimulation (NIBS) probing the dorsolateral prefrontal cortex (DLPFC) has been shown to have little effect on working memory. The variability of NIBS responses might be explained by inter-subject brain anatomical variability. We investigated whether baseline cortical brain thickness of regions of interest was associated with working memory performance after NIBS by performing a secondary analysis of previously published research. Structural magnetic resonance imaging data were analyzed from healthy subjects who received transcranial direct current stimulation (tDCS), intermittent theta-burst stimulation (iTBS), and placebo. Twenty-two participants were randomly assigned to receive all the interventions in a random order. The working memory task was conducted after the end of each NIBS session. Regions of interest were the bilateral DLPFC, medial prefrontal cortex, and posterior cingulate cortex. Overall, 66 NIBS sessions were performed. Findings revealed a negative significant association between cortical thickness of the bilateral dorsolateral prefrontal cortex and reaction time for both tDCS (left: P=0.045, right: P=0.037) and iTBS (left: P=0.007, right: P=0.007) compared to placebo. A significant positive association was found for iTBS and posterior cingulate cortex (P=0.03). No association was found for accuracy. Our findings provide the first evidence that individual cortical thickness of healthy subjects might be associated with working memory performance following different NIBS interventions. Therefore, cortical thickness could explain - to some extent - the heterogeneous effects of NIBS probing the DLPFC. Associação Brasileira de Divulgação Científica 2023-10-20 /pmc/articles/PMC10591489/ /pubmed/37878887 http://dx.doi.org/10.1590/1414-431X2023e12945 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Razza, L.B.
Vanderhasselt, M.A.
Luethi, M.S.
Repple, J.
Busatto, G.
Buchpiguel, C.A.
Brunoni, A.R.
da Silva, P.H.R.
Cortical thickness is related to working memory performance after non-invasive brain stimulation
title Cortical thickness is related to working memory performance after non-invasive brain stimulation
title_full Cortical thickness is related to working memory performance after non-invasive brain stimulation
title_fullStr Cortical thickness is related to working memory performance after non-invasive brain stimulation
title_full_unstemmed Cortical thickness is related to working memory performance after non-invasive brain stimulation
title_short Cortical thickness is related to working memory performance after non-invasive brain stimulation
title_sort cortical thickness is related to working memory performance after non-invasive brain stimulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10591489/
https://www.ncbi.nlm.nih.gov/pubmed/37878887
http://dx.doi.org/10.1590/1414-431X2023e12945
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