Neural oscillatory responses to performance monitoring differ between high‐ and low‐impulsive individuals, but are unaffected by TMS

Higher impulsivity may arise from neurophysiological deficits of cognitive control in the prefrontal cortex. Cognitive control can be assessed by time‐frequency decompositions of electrophysiological data. We aimed to clarify neuroelectric mechanisms of performance monitoring in connection with impu...

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Published inHuman brain mapping Vol. 42; no. 8; pp. 2416 - 2433
Main Authors Barth, Beatrix, Rohe, Tim, Deppermann, Saskia, Fallgatter, Andreas Jochen, Ehlis, Ann‐Christine
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.06.2021
Subjects
Adult
Attention - physiology
Cerebral Cortex - physiology
Clustering
Cognitive ability
Double-Blind Method
EEG
Electroencephalography
Executive Function - physiology
Female
Humans
Impulsive behavior
Impulsive Behavior - physiology
Impulsivity
intertrial phase coherence
Male
Monitoring
Neurophysiology
performance monitoring
Phase coherence
Prefrontal cortex
Psychomotor Performance - physiology
Reaction time
Reaction Time - physiology
Reaction time task
single‐trial phase behavior coupling
Stimulation
Theta Rhythm - physiology
time‐frequency analysis
Transcranial Magnetic Stimulation
Young Adult
impulsivity
intertrial phase coherence
single-trial phase behavior coupling
transcranial magnetic stimulation
performance monitoring
time-frequency analysis
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Abstract Higher impulsivity may arise from neurophysiological deficits of cognitive control in the prefrontal cortex. Cognitive control can be assessed by time‐frequency decompositions of electrophysiological data. We aimed to clarify neuroelectric mechanisms of performance monitoring in connection with impulsiveness during a modified Eriksen flanker task in high‐ (n = 24) and low‐impulsive subjects (n = 21) and whether these are modulated by double‐blind, sham‐controlled intermittent theta burst stimulation (iTBS). We found a larger error‐specific peri‐response beta power decrease over fronto‐central sites in high‐impulsive compared to low‐impulsive participants, presumably indexing less effective motor execution processes. Lower parieto‐occipital theta intertrial phase coherence (ITPC) preceding correct responses predicted higher reaction time (RT) and higher RT variability, potentially reflecting efficacy of cognitive control or general attention. Single‐trial preresponse theta phase clustering was coupled to RT in correct trials (weighted ITPC), reflecting oscillatory dynamics that predict trial‐specific behavior. iTBS did not modulate behavior or EEG time‐frequency power. Performance monitoring was associated with time‐frequency patterns reflecting cognitive control (parieto‐occipital theta ITPC, theta weighted ITPC) as well as differential action planning/execution processes linked to trait impulsivity (frontal low beta power). Beyond that, results suggest no stimulation effect related to response‐locked time‐frequency dynamics with the current stimulation protocol. Neural oscillatory responses to performance monitoring differ between high‐ and low‐impulsive individuals, but are unaffected by iTBS. We aimed to clarify neuroelectric mechanisms of performance monitoring in connection with impulsiveness during a modified Eriksen flanker task in high‐ and low‐impulsive subjects. Performance monitoring was associated with time‐frequency patterns reflecting cognitive control (parieto‐occipital theta ITPC, theta weighted ITPC) as well as differential action planning/execution processes linked to trait impulsivity (frontal low beta power). Beyond that, results suggest no stimulation effect related to response‐locked time‐frequency dynamics with the current stimulation protocol.
AbstractList Higher impulsivity may arise from neurophysiological deficits of cognitive control in the prefrontal cortex. Cognitive control can be assessed by time-frequency decompositions of electrophysiological data. We aimed to clarify neuroelectric mechanisms of performance monitoring in connection with impulsiveness during a modified Eriksen flanker task in high- (n = 24) and low-impulsive subjects (n = 21) and whether these are modulated by double-blind, sham-controlled intermittent theta burst stimulation (iTBS). We found a larger error-specific peri-response beta power decrease over fronto-central sites in high-impulsive compared to low-impulsive participants, presumably indexing less effective motor execution processes. Lower parieto-occipital theta intertrial phase coherence (ITPC) preceding correct responses predicted higher reaction time (RT) and higher RT variability, potentially reflecting efficacy of cognitive control or general attention. Single-trial preresponse theta phase clustering was coupled to RT in correct trials (weighted ITPC), reflecting oscillatory dynamics that predict trial-specific behavior. iTBS did not modulate behavior or EEG time-frequency power. Performance monitoring was associated with time-frequency patterns reflecting cognitive control (parieto-occipital theta ITPC, theta weighted ITPC) as well as differential action planning/execution processes linked to trait impulsivity (frontal low beta power). Beyond that, results suggest no stimulation effect related to response-locked time-frequency dynamics with the current stimulation protocol. Neural oscillatory responses to performance monitoring differ between high- and low-impulsive individuals, but are unaffected by iTBS.
Higher impulsivity may arise from neurophysiological deficits of cognitive control in the prefrontal cortex. Cognitive control can be assessed by time-frequency decompositions of electrophysiological data. We aimed to clarify neuroelectric mechanisms of performance monitoring in connection with impulsiveness during a modified Eriksen flanker task in high- (n = 24) and low-impulsive subjects (n = 21) and whether these are modulated by double-blind, sham-controlled intermittent theta burst stimulation (iTBS). We found a larger error-specific peri-response beta power decrease over fronto-central sites in high-impulsive compared to low-impulsive participants, presumably indexing less effective motor execution processes. Lower parieto-occipital theta intertrial phase coherence (ITPC) preceding correct responses predicted higher reaction time (RT) and higher RT variability, potentially reflecting efficacy of cognitive control or general attention. Single-trial preresponse theta phase clustering was coupled to RT in correct trials (weighted ITPC), reflecting oscillatory dynamics that predict trial-specific behavior. iTBS did not modulate behavior or EEG time-frequency power. Performance monitoring was associated with time-frequency patterns reflecting cognitive control (parieto-occipital theta ITPC, theta weighted ITPC) as well as differential action planning/execution processes linked to trait impulsivity (frontal low beta power). Beyond that, results suggest no stimulation effect related to response-locked time-frequency dynamics with the current stimulation protocol. Neural oscillatory responses to performance monitoring differ between high- and low-impulsive individuals, but are unaffected by iTBS.Higher impulsivity may arise from neurophysiological deficits of cognitive control in the prefrontal cortex. Cognitive control can be assessed by time-frequency decompositions of electrophysiological data. We aimed to clarify neuroelectric mechanisms of performance monitoring in connection with impulsiveness during a modified Eriksen flanker task in high- (n = 24) and low-impulsive subjects (n = 21) and whether these are modulated by double-blind, sham-controlled intermittent theta burst stimulation (iTBS). We found a larger error-specific peri-response beta power decrease over fronto-central sites in high-impulsive compared to low-impulsive participants, presumably indexing less effective motor execution processes. Lower parieto-occipital theta intertrial phase coherence (ITPC) preceding correct responses predicted higher reaction time (RT) and higher RT variability, potentially reflecting efficacy of cognitive control or general attention. Single-trial preresponse theta phase clustering was coupled to RT in correct trials (weighted ITPC), reflecting oscillatory dynamics that predict trial-specific behavior. iTBS did not modulate behavior or EEG time-frequency power. Performance monitoring was associated with time-frequency patterns reflecting cognitive control (parieto-occipital theta ITPC, theta weighted ITPC) as well as differential action planning/execution processes linked to trait impulsivity (frontal low beta power). Beyond that, results suggest no stimulation effect related to response-locked time-frequency dynamics with the current stimulation protocol. Neural oscillatory responses to performance monitoring differ between high- and low-impulsive individuals, but are unaffected by iTBS.
Higher impulsivity may arise from neurophysiological deficits of cognitive control in the prefrontal cortex. Cognitive control can be assessed by time‐frequency decompositions of electrophysiological data. We aimed to clarify neuroelectric mechanisms of performance monitoring in connection with impulsiveness during a modified Eriksen flanker task in high‐ ( n = 24) and low‐impulsive subjects ( n = 21) and whether these are modulated by double‐blind, sham‐controlled intermittent theta burst stimulation (iTBS). We found a larger error‐specific peri‐response beta power decrease over fronto‐central sites in high‐impulsive compared to low‐impulsive participants, presumably indexing less effective motor execution processes. Lower parieto‐occipital theta intertrial phase coherence (ITPC) preceding correct responses predicted higher reaction time (RT) and higher RT variability, potentially reflecting efficacy of cognitive control or general attention. Single‐trial preresponse theta phase clustering was coupled to RT in correct trials (weighted ITPC), reflecting oscillatory dynamics that predict trial‐specific behavior. iTBS did not modulate behavior or EEG time‐frequency power. Performance monitoring was associated with time‐frequency patterns reflecting cognitive control (parieto‐occipital theta ITPC, theta weighted ITPC) as well as differential action planning/execution processes linked to trait impulsivity (frontal low beta power). Beyond that, results suggest no stimulation effect related to response‐locked time‐frequency dynamics with the current stimulation protocol. Neural oscillatory responses to performance monitoring differ between high‐ and low‐impulsive individuals, but are unaffected by iTBS.
Higher impulsivity may arise from neurophysiological deficits of cognitive control in the prefrontal cortex. Cognitive control can be assessed by time‐frequency decompositions of electrophysiological data. We aimed to clarify neuroelectric mechanisms of performance monitoring in connection with impulsiveness during a modified Eriksen flanker task in high‐ ( n = 24) and low‐impulsive subjects ( n = 21) and whether these are modulated by double‐blind, sham‐controlled intermittent theta burst stimulation (iTBS). We found a larger error‐specific peri‐response beta power decrease over fronto‐central sites in high‐impulsive compared to low‐impulsive participants, presumably indexing less effective motor execution processes. Lower parieto‐occipital theta intertrial phase coherence (ITPC) preceding correct responses predicted higher reaction time (RT) and higher RT variability, potentially reflecting efficacy of cognitive control or general attention. Single‐trial preresponse theta phase clustering was coupled to RT in correct trials (weighted ITPC), reflecting oscillatory dynamics that predict trial‐specific behavior. iTBS did not modulate behavior or EEG time‐frequency power. Performance monitoring was associated with time‐frequency patterns reflecting cognitive control (parieto‐occipital theta ITPC, theta weighted ITPC) as well as differential action planning/execution processes linked to trait impulsivity (frontal low beta power). Beyond that, results suggest no stimulation effect related to response‐locked time‐frequency dynamics with the current stimulation protocol. Neural oscillatory responses to performance monitoring differ between high‐ and low‐impulsive individuals, but are unaffected by iTBS. We aimed to clarify neuroelectric mechanisms of performance monitoring in connection with impulsiveness during a modified Eriksen flanker task in high‐ and low‐impulsive subjects. Performance monitoring was associated with time‐frequency patterns reflecting cognitive control (parieto‐occipital theta ITPC, theta weighted ITPC) as well as differential action planning/execution processes linked to trait impulsivity (frontal low beta power). Beyond that, results suggest no stimulation effect related to response‐locked time‐frequency dynamics with the current stimulation protocol.
Higher impulsivity may arise from neurophysiological deficits of cognitive control in the prefrontal cortex. Cognitive control can be assessed by time‐frequency decompositions of electrophysiological data. We aimed to clarify neuroelectric mechanisms of performance monitoring in connection with impulsiveness during a modified Eriksen flanker task in high‐ (n = 24) and low‐impulsive subjects (n = 21) and whether these are modulated by double‐blind, sham‐controlled intermittent theta burst stimulation (iTBS). We found a larger error‐specific peri‐response beta power decrease over fronto‐central sites in high‐impulsive compared to low‐impulsive participants, presumably indexing less effective motor execution processes. Lower parieto‐occipital theta intertrial phase coherence (ITPC) preceding correct responses predicted higher reaction time (RT) and higher RT variability, potentially reflecting efficacy of cognitive control or general attention. Single‐trial preresponse theta phase clustering was coupled to RT in correct trials (weighted ITPC), reflecting oscillatory dynamics that predict trial‐specific behavior. iTBS did not modulate behavior or EEG time‐frequency power. Performance monitoring was associated with time‐frequency patterns reflecting cognitive control (parieto‐occipital theta ITPC, theta weighted ITPC) as well as differential action planning/execution processes linked to trait impulsivity (frontal low beta power). Beyond that, results suggest no stimulation effect related to response‐locked time‐frequency dynamics with the current stimulation protocol. Neural oscillatory responses to performance monitoring differ between high‐ and low‐impulsive individuals, but are unaffected by iTBS. We aimed to clarify neuroelectric mechanisms of performance monitoring in connection with impulsiveness during a modified Eriksen flanker task in high‐ and low‐impulsive subjects. Performance monitoring was associated with time‐frequency patterns reflecting cognitive control (parieto‐occipital theta ITPC, theta weighted ITPC) as well as differential action planning/execution processes linked to trait impulsivity (frontal low beta power). Beyond that, results suggest no stimulation effect related to response‐locked time‐frequency dynamics with the current stimulation protocol.
Audience Academic
Author Barth, Beatrix
Rohe, Tim
Fallgatter, Andreas Jochen
Ehlis, Ann‐Christine
Deppermann, Saskia
AuthorAffiliation 3 LEAD Graduate School & Research Network University of Tuebingen Tuebingen Germany
1 Psychophysiology and Optical Imaging, Department of Psychiatry and Psychotherapy University of Tuebingen Tuebingen Germany
2 Department of Psychology Friedrich‐Alexander University Erlangen‐Nuernberg Erlangen Germany
4 Werner Reichardt Centre for Integrative Neuroscience (CIN) University of Tuebingen Tuebingen Germany
AuthorAffiliation_xml – name: 2 Department of Psychology Friedrich‐Alexander University Erlangen‐Nuernberg Erlangen Germany
– name: 3 LEAD Graduate School & Research Network University of Tuebingen Tuebingen Germany
– name: 4 Werner Reichardt Centre for Integrative Neuroscience (CIN) University of Tuebingen Tuebingen Germany
– name: 1 Psychophysiology and Optical Imaging, Department of Psychiatry and Psychotherapy University of Tuebingen Tuebingen Germany
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  orcidid: 0000-0002-3792-3357
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Issue 8
Keywords impulsivity
intertrial phase coherence
single-trial phase behavior coupling
transcranial magnetic stimulation
performance monitoring
time-frequency analysis
Language English
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2021 The Authors. Human Brain Mapping published by Wiley Periodicals LLC.
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Funding information Deutsche Forschungsgemeinschaft, Grant/Award Number: RO 5587/1‐1; IZKF Tübingen, Grant/Award Number: 2115‐0‐0
ORCID 0000-0002-3792-3357
OpenAccessLink https://proxy.k.utb.cz/login?url=https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fhbm.25376
PMID 33605509
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PublicationDate June 1, 2021
PublicationDateYYYYMMDD 2021-06-01
PublicationDate_xml – month: 06
  year: 2021
  text: June 1, 2021
  day: 01
PublicationDecade 2020
PublicationPlace Hoboken, USA
PublicationPlace_xml – name: Hoboken, USA
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PublicationTitle Human brain mapping
PublicationTitleAlternate Hum Brain Mapp
PublicationYear 2021
Publisher John Wiley & Sons, Inc
Publisher_xml – name: John Wiley & Sons, Inc
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Snippet Higher impulsivity may arise from neurophysiological deficits of cognitive control in the prefrontal cortex. Cognitive control can be assessed by...
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SubjectTerms Adult
Attention - physiology
Cerebral Cortex - physiology
Clustering
Cognitive ability
Double-Blind Method
EEG
Electroencephalography
Executive Function - physiology
Female
Humans
Impulsive behavior
Impulsive Behavior - physiology
Impulsivity
intertrial phase coherence
Male
Monitoring
Neurophysiology
performance monitoring
Phase coherence
Prefrontal cortex
Psychomotor Performance - physiology
Reaction time
Reaction Time - physiology
Reaction time task
single‐trial phase behavior coupling
Stimulation
Theta Rhythm - physiology
time‐frequency analysis
Transcranial Magnetic Stimulation
Young Adult
Title Neural oscillatory responses to performance monitoring differ between high‐ and low‐impulsive individuals, but are unaffected by TMS
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fhbm.25376
https://www.ncbi.nlm.nih.gov/pubmed/33605509
https://www.proquest.com/docview/2520688695
https://www.proquest.com/docview/2491948161
https://pubmed.ncbi.nlm.nih.gov/PMC8090766
Volume 42
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