Reconsidering electrophysiological markers of response inhibition in light of trigger failures in the stop-signal task

被引:23
|
作者
Skippen, P. [1 ,2 ]
Fulham, W. R. [1 ,2 ]
Michie, P. T. [1 ,2 ]
Matzke, D. [3 ]
Heathcote, A. [4 ]
Karayanidis, F. [1 ,2 ,5 ]
机构
[1] Univ Newcastle, Sch Psychol, Funct Neuroimaging Lab, Newcastle, NSW, Australia
[2] Univ Newcastle, Prior Res Ctr Brain & Mental Hlth, Newcastle, NSW, Australia
[3] Univ Amsterdam, Dept Psychol, Psychol Methods, Amsterdam, Netherlands
[4] Univ Tasmania, Sch Psychol, Hobart, Tas, Australia
[5] Univ Newcastle, Prior Res Ctr Stroke & Brain Injury, Newcastle, NSW, Australia
基金
澳大利亚研究理事会;
关键词
Bayesian model; ERP; N100; P300; response inhibition; stop-signal task; trigger failure; INFERIOR FRONTAL GYRUS; COGNITIVE CONTROL; N2/P3; COMPLEX; RACE MODEL; ATTENTION; PROBABILITY; LAPLACIAN; CORTEX; BRAIN; TIME;
D O I
10.1111/psyp.13619
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
This study investigates the neural correlates underpinning response inhibition using a parametric ex-Gaussian model of stop-signal task performance, fit with hierarchical Bayesian methods, in a large healthy sample (N = 156). The parametric model accounted for both stop-signal reaction time (SSRT) and trigger failure (i.e., failures to initiate the inhibition process). The returned SSRT estimate (SSRTEXG3) was attenuated by approximate to 65 ms compared to traditional nonparametric SSRT estimates (SSRTint). The amplitude and latency of the N1 and P3 event-related potential components were derived for both stop-success and stop-failure trials and compared to behavioral estimates derived from traditional (SSRTint) and parametric (SSRTEXG3, trigger failure) models. Both the fronto-central N1 and P3 peaked earlier and were larger for stop-success than stop-failure trials. For stop-failure trials only, N1 peak latency correlated with both SSRT estimates as well as trigger failure and temporally coincided with SSRTEXG3, but not SSRTint. In contrast, P3 peak and onset latency were not associated with any behavioral estimates of inhibition for either trial type. While the N1 peaked earlier for stop-success than stop-failure trials, this effect was not found in poor task performers (i.e., high trigger failure/slow SSRT). These findings are consistent with attentional modulation of both the speed and reliability of the inhibition process, but not for poor performers. Together with the absence of any P3 onset latency effect, our findings suggest that attentional mechanisms are important in supporting speeded and reliable inhibition processes required in the stop-signal task.
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页数:18
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