Cited by 141Neural and Behavioral Psychology StudiesFunctional Brain Connectivity StudiesNeurobiology of Language and Bilingualism

The DOI matches its Crossref record; 82 of the 82 references it cites were found in a registry or an index.

Common and unique neural networks for proactive and reactive response inhibition revealed by independent component analysis of functional MRI data

van Belle, Janna, Vink, Matthijs, Durston, Sarah, Zandbelt, Bram B.·2014·NeuroImage

Abstract

Response inhibition involves proactive and reactive modes. Proactive inhibition is goal-directed, triggered by warning cues, and serves to restrain actions. Reactive inhibition is stimulus-driven, triggered by salient stop-signals, and used to stop actions completely. Functional MRI studies have identified brain regions that activate during proactive and reactive inhibition. It remains unclear how these brain regions operate in functional networks, and whether proactive and reactive inhibition depend on common networks, unique networks, or a combination. To address this we analyzed a large fMRI dataset (N=65) of a stop-signal task designed to measure proactive and reactive inhibition, using independent component analysis (ICA). We found 1) three frontal networks that were associated with both proactive and reactive inhibition, 2) one network in the superior parietal lobe, which also included dorsal premotor cortex and left putamen, that was specifically associated with proactive inhibition, and 3) two right-lateralized frontal and fronto-parietal networks, including the right inferior frontal gyrus and temporoparietal junction as well as a bilateral fronto-temporal network that were uniquely associated with reactive inhibition. Overlap between networks was observed in dorsolateral prefrontal and parietal cortices. Taken together, we offer a new perspective on the neural underpinnings of inhibitory control, by showing that proactive inhibition and reactive inhibition are supported by a group of common and unique networks that appear to integrate and interact in frontoparietal areas.

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Crossref · 10.1016/j.neuroimage.2014.09.014

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  1. McKeown, 1998, Independent component analysis of fMRI data: examining the assumptions, Hum. Brain Mapp.

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Metadata

Authors
van Belle, J., Vink, M., Durston, S., & Zandbelt, B. B.
Affiliations
  • University Medical Center Utrecht (NL)
  • Vanderbilt University (US)
Venue
NeuroImage
Publisher
Elsevier BV
Published
2014-12
Volume
103
Pages
65-74
ISSN
1053-8119 (ISSN-L)
OpenAlex
W1987055966
Cited by
141
References
82
Citations by year
2026: 9 · 2025: 9 · 2024: 11 · 2023: 8 · 2022: 14 · 2021: 15 · 2020: 16 · 2019: 11 · 2018: 12 · 2017: 7 · 2016: 17 · 2015: 10 · 2014: 1
FWCI
6.51
Type
journal article
Language
en
Open access
closed
Locations
  • NeuroImage (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neurobiology of Language and Bilingualism
Keywords
response inhibition, proactive inhibition, reactive inhibition, inhibitory control, artificial neural networks, stop-signal task, frontal network, superior parietal lobule, dorsolateral prefrontal cortex, parietal cortex, right hemisphere lateralization, temporoparietal junction, inferior frontal gyrus, putamen, dorsal premotor cortex
MeSH terms
Adult, Brain, Brain Mapping, Female, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Male, Nerve Net, Reactive Inhibition

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