213,214 In addition, many recent reports have correlated degree of γ oscillation disturbance with degree of schizophrenia symptoms including the cognitive impairment classical in schizophrenia, positive symptoms (ie, hallucinations and delusions) and negative symptoms (ie, affective blunting, anhedonia, avolitional state).213,215,217 Finally, these γ disturbances are also present Inhibitors,research,lifescience,medical in first-degree relatives of schizophrenic patients without classical schizophrenia symptoms per se and therefore may be a traceable endophenotype.211,218,219 The rekindled interest in the study of γ oscillations mainly lies in the understanding

of the critical involvement of parvalbumin-immunoreactive basket interneurons in γ oscillations13 and the relatively selective degeneration of this parvalbumin class of neurons in schizophrenia.220 Schizophrenic patients also show a significant reduction in sleep spindles221,222 and θ-γ phase coupling.223 γ oscillation disturbances may Inhibitors,research,lifescience,medical also point to alterations in the glutamatergic system, given that glutamate neurons are the primary backbone of neural signaling. Indeed data have shown that glutamate-targeted treatments for schizophrenia may have efficacy in schizophrenic patients.224 While schizophrenia is perhaps the most pervasive and debilitating psychiatric disease, Inhibitors,research,lifescience,medical Inhibitors,research,lifescience,medical depression is the most prevalent, with roughly

20% lifetime incidence in Western populations and it inflicts the third largest measured disease burden of all illnesses in the world.225,226 Numerous studies have noted oscillation-related differences GSK1120212 chemical structure between depressed patients versus controls: increased Inhibitors,research,lifescience,medical α and β rhythm power, increased β asymmetric a in the frontal aspects of the hemispheres, and sensory-evoked responses.227,228 Such differences may be leveraged in

better treating this debilitating and sometimes-lethal disease. At the moment, while a variety of treatments exist for depression, the current state of the art in drug-based treatment is based on statisticallyinformed trial and error.229 This is due to the fact that there is no reliable means of determining which medication will work for which individual patient. A number of researchers have begun to Adenosine use EEG to not only point to differences between depressed patients and healthy controls, but have also begun to find correlates between brain rhythms and likelihood of response.227,228 Treatment response is predicted by a number of electrical parameters including baseline α power, α power asymmetry, frontal θ concordance measures within a few days of treatment, evoked responses to auditory stimuli and combinations of these measures. In general these parameters are able to predict responsivity at rates of approximately 60% to 80% accuracy.