Deficits in Go and NoGo P3 potentials in patients with schizophrenia.

Cognitive control processes elicited during a cued continuous performance test were evaluated using event-related potentials in 46 patients who were within the first 5 years of diagnosis of schizophrenia, and 29 healthy controls. Patients had longer reaction times, lower hit rates, and higher false alarm rates compared with controls. Patients had an overall P3 amplitude reduction that was more prominent on NoGo compared with Go trials. This greater P3 reduction on NoGo trials was present in central and parietal regions, but was absent in the frontal region, where the P3 reduction was comparable on NoGo and Go trials. Our findings suggest that the neural activity contributing to Go and NoGo P3s are both deteriorated in schizophrenia, but those contributing to central and parietal NoGo P3s are the most severely affected ones. We conclude that the cognitive control processes engaged during execution, and particularly during inhibition of a prepared motor response were disturbed in the early course of schizophrenia. Our findings might be related to our sample being in relatively early stages of schizophrenia and/or related to the use of atypical antipsychotics by most of our patients.

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.

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.

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.

Cognitive deficits in clinical and familial high risk groups for psychosis are common as in first episode schizophrenia.

The aim of this study is to compare the neurocognitive functions in individuals with clinical or genetic risk for psychosis, in patients with first-episode schizophrenia (FES) and in healthy controls. We compared cognitive functions of 52 individuals at ultra high risk (UHR) for psychosis, 53 patients with FES, their 30 healthy siblings (familial high risk group, FHR) and controls. FES group had worse neuropsychological performance than controls in all of the domains. UHR group had worse performance in verbal learning, attention, and working memory than controls. Additionally, individuals at UHR with familial risk had worse performance on executive functions than the control group. FES group had lower global composite score than UHR group, and worse sustained attention than FHR group. FHR group had worse performance on executive functions and attention than controls. We found no difference in cognitive performances of UHR and FHR groups. Cognitive deficits in UHR and FHR groups were largely similar to those with FES. These findings support that cognitive deficits may arise before the first episode of schizophrenia.