“…Individual differences in both theta- and delta-band PLI showed significant associations with task performance, including accuracy, reaction time, and, most notably, inter-trial reaction time variability (RTV), consistent with other relevant studies (Bender et al, 2015; Papenberg et al, 2013). Specifically, weaker inter-trial phase clustering as indicated by lower PLI values predicted greater RTV ( r = −0.46, p < 0.001).…”
Phase synchronization of neuronal oscillations is a fundamental mechanism underlying cognitive processing and behavior, including context-dependent response production and inhibition. Abnormalities in neural synchrony can lead to abnormal information processing and contribute to cognitive and behavioral deficits in neuropsychiatric disorders. However, little is known about genetic and environmental contributions to individual differences in cortical oscillatory dynamics underlying response inhibition. This study examined heritability of event-related phase synchronization of brain oscillations in 302 young female twins including 94 MZ and 57 DZ pairs performing a cued Go/No-Go version of the Continuous Performance Test (CPT). We used the Phase Locking Index (PLI) to assess inter-trial phase clustering (synchrony) in several frequency bands in two time intervals after stimulus onset (0–300 and 301–600 ms). Response inhibition (i.e., successful response suppression in No-Go trials) was characterized by a transient increase in phase synchronization of delta- and theta-band oscillations in the fronto-central midline region. Genetic analysis showed significant heritability of the phase locking measures related to response inhibition, with 30 to 49% of inter-individual variability being accounted for by genetic factors. This is the first study providing evidence for heritability of task-related neural synchrony. The present results suggest that PLI can serve as an indicator of genetically transmitted individual differences in neural substrates of response inhibition.
“…Individual differences in both theta- and delta-band PLI showed significant associations with task performance, including accuracy, reaction time, and, most notably, inter-trial reaction time variability (RTV), consistent with other relevant studies (Bender et al, 2015; Papenberg et al, 2013). Specifically, weaker inter-trial phase clustering as indicated by lower PLI values predicted greater RTV ( r = −0.46, p < 0.001).…”
Phase synchronization of neuronal oscillations is a fundamental mechanism underlying cognitive processing and behavior, including context-dependent response production and inhibition. Abnormalities in neural synchrony can lead to abnormal information processing and contribute to cognitive and behavioral deficits in neuropsychiatric disorders. However, little is known about genetic and environmental contributions to individual differences in cortical oscillatory dynamics underlying response inhibition. This study examined heritability of event-related phase synchronization of brain oscillations in 302 young female twins including 94 MZ and 57 DZ pairs performing a cued Go/No-Go version of the Continuous Performance Test (CPT). We used the Phase Locking Index (PLI) to assess inter-trial phase clustering (synchrony) in several frequency bands in two time intervals after stimulus onset (0–300 and 301–600 ms). Response inhibition (i.e., successful response suppression in No-Go trials) was characterized by a transient increase in phase synchronization of delta- and theta-band oscillations in the fronto-central midline region. Genetic analysis showed significant heritability of the phase locking measures related to response inhibition, with 30 to 49% of inter-individual variability being accounted for by genetic factors. This is the first study providing evidence for heritability of task-related neural synchrony. The present results suggest that PLI can serve as an indicator of genetically transmitted individual differences in neural substrates of response inhibition.
“…The results from Magnuson et al [] show reduced neural responses to the inhibitory control task in the ASD group. This finding, paired with increased behavioral and stimulus‐evoked neural variability in these children identified in the current study, warrants further investigation on the issue of whether reports of decreased brain activation from averaged ERP analyses might be the consequence of increased neural variability [Bender et al, ; Ouyang, Sommer, & Zhou, ]. More specifically, the study by Magnuson et al [] reported reduced N200 component amplitude in children with ASD as compared to TD children.…”
“…Analyses of P3b and lateralized readiness potential (LRP) latency distributions to infrequent or unexpected (‘oddball’) stimuli suggest that reaction time variability in ADHD may be in large part due to processing differences related to response emission rather than to stimulus interpretation (Saville et al., ). Furthermore, the heterogeneity in the spatial distribution and low amplitude of the P3 were the strongest predictors of RTV (Bender et al., ).…”
Background
Electroencephalography (EEG) and related measures have a long and productive history in child psychopathology research and are currently experiencing a renaissance in interest, particularly for use as putative biomarkers.
Method and Scope
First, the recent history leading to the use of EEG measures as endophenotypes and biomarkers for disease and treatment response are reviewed. Two key controversies within the area of non-invasive human electrophysiology research are discussed, and problems that currently either function as barriers or provide gateways to progress. First, the differences between the main types of EEG measurements (event related potentials, quantitative EEG, and time-frequency measures) and how they can contribute collectively to better understanding of cortical dynamics underlying cognition and behavior are highlighted. Second, we focus on the ongoing shift in analytic focus to specific cortical sources and source networks whose dynamics are relevant to the clinical and experimental focus of the study, and the effective increase in source signal-to-noise ratio (SNR) that may be obtained in the process.
Conclusions
Understanding of these issues informs any discussion of current trends in EEG research. We highlight possible ways to evolve our understanding of brain dynamics beyond the apparent contradictions in understanding and modeling EEG activity highlighted by these controversies. Finally, we summarize some promising future directions of EEG biomarker research in child psychopathology.
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