Search bioRxiv⌕ Search

Biology subjects

da Cruz, J. R.

Publications and source records attributed to da Cruz, J. R..

2 recordsLinked to original sources

Higher inter-trial latency variability contributes to reduced visual EEG responses in schizophrenia

Patients with schizophrenia show strong impairments in visual backward masking, which are associated with reduced EEG N1 responses. However, it is currently unclear whether reduced N1 amplitudes in patients reflect attenuated neural responses or increased inter-trial latency variability, as both can lead to reduced trial-averaged responses. Previous studies using trial-averaged data cannot distinguish between these two possibilities. Here, we estimated inter-trial latency variability of the visual N1 component and found significantly increased variability in patients compared to controls. Inter-trial latency-variability was a strong predictor of the N1 amplitude in both groups. Importantly, after accounting for the effect of latency variability in the group comparison, patients continued to exhibit significantly reduced N1 amplitudes, although the effect size diminished from large to medium. These findings indicate that both higher latency variability and attenuated neural responses contribute to visual processing deficits in schizophrenia.

neuroscience↗

Electrophysiological correlates of visual backward masking in patients with bipolar disorder

BackgroundIn visual backward masking (VBM), a target is followed by a mask that decreases target discriminability. Schizophrenia patients (SZ) show strong and reproducible masking impairments, which are associated with reduced EEG amplitudes. Patients with bipolar disorder (BP) show masking deficits, too. Here, we investigated the neural EEG correlates of VBM in BP. Methods122 SZ, 94 unaffected controls, and 38 BP joined a standard VBM experiment. 123 SZ, 94 unaffected controls and 16 BP joined a corresponding EEG experiment, analyzed in terms of the global field power. ResultsAs in previous studies, SZ and BP show strong masking deficits. Importantly and similarly to SZ, BP show decreased global field power amplitudes at approximately 200 ms after the target onset, compared to controls. ConclusionsThese results suggest that VBM deficits are not specific for schizophrenia but for a broader range of functional psychoses. Potentially, both SZ and BP show deficient target enhancement.

neuroscience↗