Canonical correlation analysis (CCA) is applied to analyze the frequency components of steady-state visual evoked potentials (SSVEP) in electroencephalogram (EEG). The essence of this method is to extract a narrowband frequency component of SSVEP in EEG. A recognition approach is proposed based on the extracted frequency features for an SSVEP-based brain computer interface (BCI). Recognition Results of the approach were higher than those using a widely used FFT (fast Fourier transform)-based spectrum estimation method.
See Mormann and Andrzejak (doi:) for a scientific commentary on this article. Seizures are thought to arise from an identifiable pre-ictal state. Brinkmann et al. report the results of an online, open-access seizure forecasting competition using intracranial EEG recordings from canines with naturally occurring epilepsy and human patients undergoing presurgical monitoring. The winning algorithms forecast seizures at rates significantly greater than chance.
Antidepressants are widely prescribed, but their efficacy relative to placebo is modest, in part because the clinical diagnosis of major depression encompasses biologically heterogeneous conditions. Here, we sought to identify a neurobiological signature of response to antidepressant treatment as compared to placebo. We designed a latent-space machine learning algorithm tailored for resting-state electroencephalography (rsEEG) and applied it to data from the largest imaging-coupled, placebo-controlled antidepressant study (n=309). Symptom improvement was robustly predicted in a manner both specific for the antidepressant sertraline (versus placebo) and generalizable across different study sites and EEG equipment. This sertraline-predictive EEG signature generalized to two depression samples, wherein it reflected general antidepressant medication responsivity, and related differentially to repetitive transcranial magnetic stimulation (rTMS) treatment outcome. Furthermore, we found that the sertraline rsEEG signature indexed prefrontal neural responsivity, as measured by concurrent TMS/EEG. Our findings advance the neurobiological understanding of antidepressant treatment through an EEG-tailored computational model and provide a clinical avenue for personalized treatment of depression.
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