Lack of progressive reduction in P3 amplitude after the first-episode of schizophrenia: A 6-year follow-up study

P3 event-related potential may track the course of neurophysiological pathology in schizophrenia. Reduction in the amplitude of the auditory P3 is a widely replicated finding, already present at the first psychotic episode, in schizophrenia. Whether a progressive deficit is present in auditory P3 in schizophrenia over the course of illness is yet to be clarified. Previous longitudinal studies did not report any change in P3 over time in schizophrenia. However, these studies have been inconclusive, because of their relatively short follow-up periods, lack of follow-up data on controls, and assessment of patients already at the chronic stages of schizophrenia. Auditory P3 potentials, elicited by an oddball paradigm, were assessed in 14 patients with first-episode schizophrenia and 22 healthy controls at baseline and at the 6-year follow-up. P3 amplitudes were smaller in patients with first-episode schizophrenia than in controls. Importantly, over the 6-year interval, the P3 amplitudes were reduced in controls, but they did not change in patients. The lack of P3 reduction over time in patients with schizophrenia might be explained by the maximal reduction in P3 already at baseline or by the alleviation of P3 reduction over time. (C) 2016 Elsevier Ireland Ltd. All rights reserved

Novelty P3 and P3b in first-episode schizophrenia and chronic schizophrenia

The objective of this study was to evaluate P3b and novelty P3 responses in patients with first-episode schizophrenia (FES) and chronic schizophrenia (CS). P3b is consistently reported to be reduced in CS. However, novelty P3 results in CS are controversial. Novelty P3 is not studied, and there are only a few P3b studies in patients with FES. Subject groups comprised 31 patients with FES and 36 younger control subjects, and 26 patients with CS and 35 older control subjects. Automatically elicited auditory novelty P3 and effortfully elicited auditory P3b potentials were assessed. P3b amplitudes were reduced in both patients with FES and CS relative to their controls. CS and FES patients did not differ in P3b amplitude. Novelty P3 amplitude was reduced in patients with CS. Novelty P3 amplitude in patients with FES did not differ from their controls. P3b amplitude reduction may be a trait marker of schizophrenia and may not progress over the course of illness, although this can only be definitively determined by longitudinal studies. Novelty P3 amplitude reduction present in patients with CS, is not found at the onset of illness. Novelty P3 seems unaffected early in the disease process. (c) 2006 Elsevier Inc. All rights reserved

P50 gating at acute and post-acute phases of first-episode schizophrenia

Deficit in P50 sensory gating has repeatedly been shown in schizophrenia. In order to determine the contribution of trait and/or state features to P50 gating deficit in schizophrenia we evaluated the P50 gating in patients with first-episode schizophrenia (FES) at acute and post-acute phases. Subject groups comprised 16 patients with FES and 24 healthy controls. Patients were tested at the acute phase of the illness and retested at the post-acute phase when their positive symptoms improved. During the testing at the acute phase five patients were neuroleptic-naive and the others were taking atypical antipsychotics which were started recently in order to control the acute excitation. Patients were receiving risperidone, olanzapine or quetiapine treatment at the post-acute phase. P50 gating was impaired in patients at the acute phase compared to controls. However, at the post-acute phase P50 gating was increased compared to the acute phase, reaching to the gating values of controls. P50 gating improvement might be emerged from atypical antipsychotic medication, although this can only be definitively determined by randomized studies including different antipsychotics. (C) 2008 Elsevier Inc. All rights reserved

Time-frequency analysis of the event-related potentials associated with the Stroop test

Multiple executive processes are suggested to be engaged at Stroop test, and time-frequency analysis is acknowledged to improve the informative utility of EEG in cognitive brain research. We aimed to investigate event-related oscillations associated with the Stroop test. EEG data was collected from 23 healthy volunteers while they performed a computer version of Stroop test. Both evoked (phase-locked) and total (phase-locked + non-phase-locked) oscillatory responses in the EEG were analyzed by wavelet transform. Data from the congruent (color-word matching) and incongruent stimuli (color-word non-matching) conditions are compared. In the incongruent condition, N450 wave was more negative and amplitude of the late slow wave was more positive. In the time-frequency plane, the fronto-central total theta amplitude (300-700 ms) was larger in the incongruent condition. The evoked delta (250-600 ms) was larger in the congruent condition particularly over parieto-occipital regions. The larger frontal theta response in the incongruent condition was associated with the detection of interference and inhibition of the response to task-irrelevant features, while the larger evoked delta in the congruent condition was suggestive of the easier decision process owing to congruency between the physical attribute and the verbal meaning of the stimuli. Furthermore, in the incongruent condition, amplitude of the occipital total alpha in the very late phase (700-900 ms) was smaller. This prolonged desynchronization in the alpha band could be reflecting augmentation of attentional filters in visual modality for the next stimulus. These multiple findings on EEG time-frequency plane provide improved description of the overlapping processes in Stroop test. (C) 2014 Elsevier B.V. All rights reserved

N2 AND P3 POTENTIALS IN EARLY-ONSET AND LATE-ONSET PATIENTS WITH OBSESSIVE-COMPULSIVE DISORDER

Background: Impaired cognitive control processes may be central in the pathogenesis of obsessive-compulsive disorder (OCD). Our objective was to evaluate cognitive control processes with event-related potentials in early-onset OCD (EO) and late-onset OCD (LO), which are suggested to have distinct characteristics. Methods: Participants were unmedicated EO (n = 26) and LO patients (n = 33) without comorbid psychopathology and healthy controls (n = 54). Go/No-go tasks with 50 and 80% Go trial probabilities were implemented to manipulate the strength of response conflict and inhibitory demands. Results: LO patients had shorter N2 latencies than controls and did not show the N2 amplitude increase seen in controls with the increase in Go trial probability as suggestive of abnormal conflict monitoring processes. Both EO and LO patients showed smaller P3 increase than controls with the increase in Go trial probability, suggesting problems in modifying attentional control with changes in task demands. P3 was more anteriorly distributed in LO patients than controls. Additionally, P3 increase, with the increase in Go trial probability, was larger in frontal and central sites than in parietal sites in controls, whereas in EO patients it was almost homogenous across anteroposterior sites. Conclusions: N2 processes were affected only in LO, whereas P3 processes were affected in both EO and LO, although, somewhat differently. P3 distributions suggest that EO and LO patients have differences concerning the contributions of frontal and parietal components of attentional networks to the execution of Go/No-go tasks. Our results imply that EO and LO are distinct subtypes affecting the cognitive control systems differently. (C) 2013 Wiley Periodicals, Inc