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Automatic sensory information processing abnormalities across the illness course of schizophrenia
C Jahshan1, K S Cadenhead, A J Rissling
1Mental Illness Research, Education and Clinical Center, Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, CA, USA.
Schizophrenia patients show deficits in sensory discrimination (MMN, P3a) and attention (RON) even early in the illness. Mismatch negativity and P3a may serve as early biomarkers for psychosis risk.
Area of Science:
- Neuroscience
- Psychiatry
- Cognitive Science
Background:
- Chronic schizophrenia is associated with reduced mismatch negativity (MMN) and P3a event-related potentials, indicating sensory discrimination deficits.
- These auditory event-related potentials have not been extensively studied in the early stages of psychotic illness.
Purpose of the Study:
- To investigate mismatch negativity (MMN), P3a, and reorienting negativity (RON) across the schizophrenia spectrum.
- To examine auditory event-related potentials in individuals at risk for psychosis, recent-onset schizophrenia, chronic schizophrenia, and healthy controls.
Main Methods:
- Assessed MMN, P3a, and RON using a duration-deviant auditory oddball paradigm.
- Evaluated 118 participants across four groups: at-risk for psychosis (n=26), recent-onset patients (n=31), chronic patients (n=33), and normal controls (n=28).
Main Results:
- All patient groups exhibited frontocentral MMN and P3a deficits.
- At-risk individuals showed intermediate MMN and P3a amplitudes between controls and recent-onset patients.
- Recent-onset and chronic patients, unlike at-risk subjects, displayed reduced RON amplitudes compared to controls. Negative symptoms in at-risk individuals correlated with P3a and RON deficits.
Conclusions:
- Auditory processing abnormalities, including sensory discrimination and attention reorienting, are present early in schizophrenia.
- MMN and P3a reductions observed before psychosis onset suggest their potential as early schizophrenia biomarkers.
- Findings indicate possible progressive worsening of these deficits across illness stages.
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