Cargando…

Machine learning provides novel neurophysiological features that predict performance to inhibit automated responses

Neurophysiological features like event-related potentials (ERPs) have long been used to identify different cognitive sub-processes that may contribute to task performance. It has however remained unclear whether “classical” ERPs are truly the best reflection or even causal to observable variations i...

Descripción completa

Detalles Bibliográficos
Autores principales: Vahid, Amirali, Mückschel, Moritz, Neuhaus, Andres, Stock, Ann-Kathrin, Beste, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215005/
https://www.ncbi.nlm.nih.gov/pubmed/30390016
http://dx.doi.org/10.1038/s41598-018-34727-7
_version_ 1783368057284984832
author Vahid, Amirali
Mückschel, Moritz
Neuhaus, Andres
Stock, Ann-Kathrin
Beste, Christian
author_facet Vahid, Amirali
Mückschel, Moritz
Neuhaus, Andres
Stock, Ann-Kathrin
Beste, Christian
author_sort Vahid, Amirali
collection PubMed
description Neurophysiological features like event-related potentials (ERPs) have long been used to identify different cognitive sub-processes that may contribute to task performance. It has however remained unclear whether “classical” ERPs are truly the best reflection or even causal to observable variations in behavior. Here, we used a data-driven strategy to extract features from neurophysiological data of n = 240 healthy young individuals who performed a Go/Nogo task and used machine learning methods in combination with source localization to identify the best predictors of inter-individual performance variations. Both Nogo-N2 and Nogo-P3 yielded predictions close to chance level, but a feature in between those two processes, associated with motor cortex activity (BA4), predicted group membership with up to ~68%. We further found two Nogo-associated features in the theta and alpha bands, that predicted behavioral performance with up to ~78%. Notably, the theta band feature contributed most to the prediction and occurred at the same time as the predictive ERP feature. Our approach provides a rigorous test for established neurophysiological correlates of response inhibition and suggests that other processes, which occur in between the Nogo-N2 and P3, might be of equal, if not even greater, importance.
format Online
Article
Text
id pubmed-6215005
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-62150052018-11-06 Machine learning provides novel neurophysiological features that predict performance to inhibit automated responses Vahid, Amirali Mückschel, Moritz Neuhaus, Andres Stock, Ann-Kathrin Beste, Christian Sci Rep Article Neurophysiological features like event-related potentials (ERPs) have long been used to identify different cognitive sub-processes that may contribute to task performance. It has however remained unclear whether “classical” ERPs are truly the best reflection or even causal to observable variations in behavior. Here, we used a data-driven strategy to extract features from neurophysiological data of n = 240 healthy young individuals who performed a Go/Nogo task and used machine learning methods in combination with source localization to identify the best predictors of inter-individual performance variations. Both Nogo-N2 and Nogo-P3 yielded predictions close to chance level, but a feature in between those two processes, associated with motor cortex activity (BA4), predicted group membership with up to ~68%. We further found two Nogo-associated features in the theta and alpha bands, that predicted behavioral performance with up to ~78%. Notably, the theta band feature contributed most to the prediction and occurred at the same time as the predictive ERP feature. Our approach provides a rigorous test for established neurophysiological correlates of response inhibition and suggests that other processes, which occur in between the Nogo-N2 and P3, might be of equal, if not even greater, importance. Nature Publishing Group UK 2018-11-02 /pmc/articles/PMC6215005/ /pubmed/30390016 http://dx.doi.org/10.1038/s41598-018-34727-7 Text en © The Author(s) 2018 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
Vahid, Amirali
Mückschel, Moritz
Neuhaus, Andres
Stock, Ann-Kathrin
Beste, Christian
Machine learning provides novel neurophysiological features that predict performance to inhibit automated responses
title Machine learning provides novel neurophysiological features that predict performance to inhibit automated responses
title_full Machine learning provides novel neurophysiological features that predict performance to inhibit automated responses
title_fullStr Machine learning provides novel neurophysiological features that predict performance to inhibit automated responses
title_full_unstemmed Machine learning provides novel neurophysiological features that predict performance to inhibit automated responses
title_short Machine learning provides novel neurophysiological features that predict performance to inhibit automated responses
title_sort machine learning provides novel neurophysiological features that predict performance to inhibit automated responses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215005/
https://www.ncbi.nlm.nih.gov/pubmed/30390016
http://dx.doi.org/10.1038/s41598-018-34727-7
work_keys_str_mv AT vahidamirali machinelearningprovidesnovelneurophysiologicalfeaturesthatpredictperformancetoinhibitautomatedresponses
AT muckschelmoritz machinelearningprovidesnovelneurophysiologicalfeaturesthatpredictperformancetoinhibitautomatedresponses
AT neuhausandres machinelearningprovidesnovelneurophysiologicalfeaturesthatpredictperformancetoinhibitautomatedresponses
AT stockannkathrin machinelearningprovidesnovelneurophysiologicalfeaturesthatpredictperformancetoinhibitautomatedresponses
AT bestechristian machinelearningprovidesnovelneurophysiologicalfeaturesthatpredictperformancetoinhibitautomatedresponses