4.6 Article

Neurophysiological correlates of dysregulated emotional arousal in severe traumatic brain injury

Journal

CLINICAL NEUROPHYSIOLOGY
Volume 126, Issue 2, Pages 314-324

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.clinph.2014.05.033

Keywords

Emotional arousal; Severe traumatic brain injury; EEG alpha power; Skin conductance level; Insula; Amygdala

Funding

  1. Australian Research Council (ARC Discovery Project ) [ID1094183]
  2. Australian National Health and Medical Research Council (NHMRC) Postdoctoral Fellowship [APP1013796]
  3. NHMRC Career Development Fellowship [APP1022684]

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Objective: This study aimed to elucidate relationships between dysregulated emotional arousal after severe traumatic brain injury (TBI), alpha power and skin conductance levels (SCL), and brain atrophy. Methods: Nineteen adults with severe TBI and 19 age-, education-, and gender-matched controls (all p's > 0.05) participated. Magnetic resonance imaging (MRI) scan established bilateral insulae and amygdale volumes. Mean EEG alpha power and SCLs were recorded simultaneously across four, 2 min conditions: eyes-closed pre-task baseline, view neutral face, happy face and angry face. Results: Scalp-wide alpha suppression occurred from pre-task baseline to the face-viewing conditions (p <.001), but was diminished in TBI (p =.04). TBI participants exhibited marginally significantly lower SCL (p =.051), and elevated alpha power hemispherically, contrasting with controls' midline dominance (p <.01). Significant atrophy was observed in most structures in TBI participants (p's = .004-0.04). Larger left insula, left amygdala and right amygdala correlated positively with alpha power and alpha suppression, and SCLs; all structures uniquely contributed to variance in arousal. Conclusions: Findings suggest that alpha power provides a sensitive measure of dysregulated emotional arousal post-TBI. Atrophy in pertinent brain structures may contribute to these disturbances. Significance: These findings have potential implications for the assessment and remediation of TBI-related arousal deficits, by directing more targeted remediation, and better assessing post-TBI recovery. Crown Copyright (C) 2014 Published by Elsevier Ireland Ltd. on behalf of International Federation of Clinical Neurophysiology. All rights reserved.

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