Abstract

Objective: Attentional problems are amongst the most commonly reported complaints following mild traumatic brain injury (mTBI), including difficulties orienting and disengaging attention, sustaining it over time, and dividing attentional resources across multiple simultaneous demands. The objective of this study was to track, using a single novel electrophysiological task, various components associated with the deployment of visuospatial selective attention. Methods: A paradigm was designed to evoke earlier visual evoked potentials (VEPs), as well as attention-related and visuocognitive ERPs. Data from 36 individuals with mTBI (19 subacute, 17 chronic) and 22 uninjured controls are presented. Postconcussion symptoms (PCS), anxiety (BAI), depression (BDI-II) and visual attention (TEA Map Search, DKEFS Trail Making Test) were also assessed. Results: Earlier VEPs (P1, N1), as well as processes related to visuospatial orientation (N2pc) and encoding in visual short-term memory (SPCN), appear comparable in mTBI and control participants. However, there appears to be a disruption in the spatiotemporal dynamics of attention (N2pc-Ptc, P2) in subacute mTBI, which recovers within six months. This is also reflected in altered neuropsychological performance (information processing speed, attentional shifting). Furthermore, orientation of attention (P3a) and working memory processes (P3b) are also affected and remain as such in the chronic post-mTBI period, in co-occurrence with persisting postconcussion symptomatology. Conclusions: This study adds original findings indicating that such a sensitive and rigorous ERP task implemented at diagnostic and follow-up levels could allow for the identification of subtle but complex brain activation and connectivity deficits that can occur following mTBI.

Highlights

  • An increasing number of studies have shown the impact of mild traumatic brain injury on cognitive functions

  • In the case of mild traumatic brain injury (mTBI), these forces are responsible for stretching of the axons and microbleeds, which lead to a complex neurometabolic cascade [2]

  • We studied components reflecting earlier visual–attentional processing, such as the N1 [25,26], P1 [27], and P2 [28] components, which we expected would not be different between the mTBI and control groups

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Summary

Introduction

An increasing number of studies have shown the impact of mild traumatic brain injury (mTBI) on cognitive functions. The fact that mTBIs are considered a major health issue involving long-term health risks raises questions as to how their impact can be best identified and measured in order to be treated and managed optimally. In the case of mTBI, these forces are responsible for stretching of the axons and microbleeds, which lead to a complex neurometabolic cascade [2]. There is growing and reproducible evidence that following mTBI microstructural damage and neurochemical imbalances occur in a number of brain regions (e.g., frontal, temporal, motor cortex) and in white matter integrity (e.g., corpus callosum) [3,4,5,6,7,8].

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