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

Abstract 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 var...

Full description

Bibliographic Details
Main Authors: Amirali Vahid, Moritz Mückschel, Andres Neuhaus, Ann-Kathrin Stock, Christian Beste
Format: Article
Language:English
Published: Nature Publishing Group 2018-11-01
Series:Scientific Reports
Subjects:
Online Access:https://doi.org/10.1038/s41598-018-34727-7
id doaj-e9de6ebc91344907a2f8bc1bdf5ba4bb
record_format Article
spelling doaj-e9de6ebc91344907a2f8bc1bdf5ba4bb2020-12-08T05:32:11ZengNature Publishing GroupScientific Reports2045-23222018-11-018111510.1038/s41598-018-34727-7Machine learning provides novel neurophysiological features that predict performance to inhibit automated responsesAmirali Vahid0Moritz Mückschel1Andres Neuhaus2Ann-Kathrin Stock3Christian Beste4Cognitive Neurophysiology, Department of Child and Adolescent Psychiatry, Faculty of Medicine of the TU DresdenCognitive Neurophysiology, Department of Child and Adolescent Psychiatry, Faculty of Medicine of the TU DresdenDepartment of Psychiatry, Charite University Hospital BerlinCognitive Neurophysiology, Department of Child and Adolescent Psychiatry, Faculty of Medicine of the TU DresdenCognitive Neurophysiology, Department of Child and Adolescent Psychiatry, Faculty of Medicine of the TU DresdenAbstract 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.https://doi.org/10.1038/s41598-018-34727-7Neurophysiological FeaturesEvent-related Potentials (ERP)Behavioral PerformanceSequential Floating Forward Selection (SFFS)NoGo Trials
collection DOAJ
language English
format Article
sources DOAJ
author Amirali Vahid
Moritz Mückschel
Andres Neuhaus
Ann-Kathrin Stock
Christian Beste
spellingShingle Amirali Vahid
Moritz Mückschel
Andres Neuhaus
Ann-Kathrin Stock
Christian Beste
Machine learning provides novel neurophysiological features that predict performance to inhibit automated responses
Scientific Reports
Neurophysiological Features
Event-related Potentials (ERP)
Behavioral Performance
Sequential Floating Forward Selection (SFFS)
NoGo Trials
author_facet Amirali Vahid
Moritz Mückschel
Andres Neuhaus
Ann-Kathrin Stock
Christian Beste
author_sort Amirali Vahid
title 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_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_sort machine learning provides novel neurophysiological features that predict performance to inhibit automated responses
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2018-11-01
description Abstract 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.
topic Neurophysiological Features
Event-related Potentials (ERP)
Behavioral Performance
Sequential Floating Forward Selection (SFFS)
NoGo Trials
url https://doi.org/10.1038/s41598-018-34727-7
work_keys_str_mv AT amiralivahid machinelearningprovidesnovelneurophysiologicalfeaturesthatpredictperformancetoinhibitautomatedresponses
AT moritzmuckschel machinelearningprovidesnovelneurophysiologicalfeaturesthatpredictperformancetoinhibitautomatedresponses
AT andresneuhaus machinelearningprovidesnovelneurophysiologicalfeaturesthatpredictperformancetoinhibitautomatedresponses
AT annkathrinstock machinelearningprovidesnovelneurophysiologicalfeaturesthatpredictperformancetoinhibitautomatedresponses
AT christianbeste machinelearningprovidesnovelneurophysiologicalfeaturesthatpredictperformancetoinhibitautomatedresponses
_version_ 1724391704976424960