Diagnosing and monitoring recovery of patients with mild traumatic brain injury (mTBI) is challenging because of the lack of objective, quantitative measures. Diagnosis is based on description of injuries often not witnessed, subtle neurocognitive symptoms, and neuropsychological testing. Since working memory (WM) is at the center of cognitive functions impaired in mTBI, this study was designed to define objective quantitative electroencephalographic (qEEG) measures of WM processing that may correlate with cognitive changes associated with acute mTBI. First-time mTBI patients and mild peripheral (limb) trauma controls without head injury were recruited from the emergency department. WM was assessed by a continuous performance task (N-back). EEG recordings were obtained during N-back testing on three occasions: within five days, two weeks, and one month after injury. Compared with controls, mTBI patients showed abnormal induced and evoked alpha activity including event-related desynchronization (ERD) and synchronization (ERS). For induced alpha power, TBI patients had excessive frontal ERD on their first and third visit. For evoked alpha, mTBI patients had lower parietal ERD/ERS at the second and third visits. These exploratory qEEG findings offer new and non-invasive candidate measures to characterize the evolution of injury over the first month, with potential to provide much-needed objective measures of brain dysfunction to diagnose and monitor the consequences of mTBI.

In this study, we compared the brain activation profiles obtained from resting state Magnetoencephalographic (MEG) activity in 15 dyslexic patients with the profiles of 15 normal controls, using power spectral density (PSD) analysis. We first estimated intracranial dipolar MEG sources on a dense grid on the cortical surface and then projected these sources on a standardized atlas with 68 regions of interest (ROIs). Averaging the PSD values of all sources in each ROI across all control subjects resulted in a normative database that was used to convert the PSD values of dyslexic patients into z-scores in eight distinct frequency bands. We found that dyslexic patients exhibited statistically significant overactivation in the delta band (0.1-4 Hz) in the right temporal (entorhinal and insula), left inferior frontal (Broca's area), and right inferior frontal regions. Overactivation may be interpreted as a compensatory mechanism for reading characterizing dyslexic patients. These findings suggest that resting-state MEG activation maps may be used as specific biomarkers that can help with the diagnosis of and assess the efficacy of intervention in dyslexia.

In this study we analyzed event related potentials (ERPs) obtained in an N-back working memory test that varied in difficulty from 0- to 2-back. We collected 21 channels of activity from 11 mild traumatic brain injury (mTBI) patients and 7 normal controls, on three different visits, and used the amplitude and latency of the P300 component to characterize the subjects. A preprocessing procedure based on independent component analysis was used first to identify and eliminate electrophysiological noise on a single trial basis. Then to obtain more reliable statistics, the recording electrodes were lumped into five main groups corresponding roughly to frontal, central, parietal, and left and right temporal brain regions. For each subject, the P300 amplitude and latency were measured after averaging the activity of all channels in each group. Group analyses showed that latencies in the central region were significantly shorter in controls, at every visit for the 2-back test. The lack of significant differences across the three visits for the mTBI group indicates that mTBI subjects are not improving at the rate that might have been expected, confirming previous reports that mTBI deficits may persist for years.

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In this study, we compared the brain activation profiles obtained from resting state Electroencephalographic (EEG) and Magnetoencephalographic (MEG) activity in six mild traumatic brain injury (mTBI) patients and five orthopedic controls, using power spectral density (PSD) analysis. We first estimated intracranial dipolar EEG/MEG sources on a dense grid on the cortical surface and then projected these sources on a standardized atlas with 68 regions of interest (ROIs). Averaging the PSD values of all sources in each ROI across all control subjects resulted in a normative database that was used to convert the PSD values of mTBI patients into z-scores in eight distinct frequency bands. We found that mTBI patients exhibited statistically significant overactivation in the delta, theta, and low alpha bands. Additionally, the MEG modality seemed to better characterize the group of individual subjects. These findings suggest that resting-state EEG/MEG activation maps may be used as specific biomarkers that can help with the diagnosis of and assess the efficacy of intervention in mTBI patients.