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Updated: Jun 26, 2025

Measurement of Fronto-limbic Activity Using an Emotional Oddball Task in Children with Familial High Risk for Schizophrenia
Published on: December 2, 2015
Mismatch Negativity in Schizophrenia, Unaffected First-degree Relatives, and Healthy Controls
Anushree Bose1, Sri Mahavir Agarwal1, Hema Nawani1
1WISER Neuromodulation Program, Department of Psychiatry, National Institute of Mental Health and Neurosciences, Bangalore, India.
Background:
Mismatch negativity (MMN) amplitude is attenuated in schizophrenia patients (SZ). However, variability in illness course among SZ samples and types of deviant stimuli used in MMN paradigms have contributed to inconsistent findings across studies. Though MMN is suggested to be impaired in schizotypy, the potential link between the two is yet to be systematically examined in unaffected first-degree relatives of schizophrenia patients (FDR).
Methods:
The SZ sample had twenty-two drug-naïve or drug-free patients (dSZ) and thirty chronic/medicated patients (cSZ). dSZ and cSZ patients were compared with thirty-six unaffected FDR and thirty-two healthy controls (HC) using a two-tone passive auditory oddball MMN paradigm in an event-related potential experiment with two conditions (presented as separate blocks)-duration-deviant (duration-MMN) and frequency-deviant (frequency-MMN). Schizotypy scores and MMN indices were examined for correlation in FDR.
Results:
Duration-MMN amplitude was significantly attenuated in both dSZ and cSZ compared to other groups. dSZ and cSZ did not differ on MMN indices. Psychopathology scores and features of illness (illness duration, medication dosage, etc.) did not correlate with MMN indices. In FDR, Schizotypal trait measures did not correlate with MMN indices.
Conclusions:
Duration-MMN emerged as a more robust indicator of prediction error signalling deficit in SZ. Frequency-MMN amplitude did not significantly differ among the groups, and MMN indices did not correlate with state and trait measures of schizophrenia-related psychopathology. These findings reiterates that auditory sensory processing captured by MMN is likely reflective of dynamic cognitive functions at the point of testing, and is unlikely to be an expression of enduring symptomatology.
Insights
Duration-Mismatch negativity (MMN) is a robust indicator of prediction error signaling deficits in schizophrenia patients. Auditory sensory processing captured by MMN reflects dynamic cognitive functions, not enduring symptoms.
Area of Science:
- Neuroscience
- Psychiatry
- Cognitive Science
Background:
- Mismatch negativity (MMN) amplitude is attenuated in schizophrenia (SZ).
- Inconsistent findings exist regarding MMN in SZ due to sample variability and stimulus types.
- MMN's link to schizotypy is underexplored in unaffected first-degree relatives (FDR) of SZ patients.
Purpose of the Study:
- To systematically examine MMN in drug-naïve SZ (dSZ), chronic SZ (cSZ), FDR, and healthy controls (HC).
- To investigate the correlation between schizotypy scores and MMN indices in FDR.
- To determine if duration-MMN or frequency-MMN is a more robust indicator of SZ-related deficits.
Main Methods:
- Utilized a two-tone passive auditory oddball MMN paradigm with duration-deviant and frequency-deviant conditions.
- Compared MMN indices between dSZ (n=22), cSZ (n=30), FDR (n=36), and HC (n=32).
- Correlated schizotypy scores with MMN indices in the FDR group.
Main Results:
- Duration-MMN amplitude was significantly attenuated in both dSZ and cSZ groups compared to controls.
- No significant differences in MMN indices were found between dSZ and cSZ.
- MMN indices did not correlate with psychopathology scores or illness features in SZ patients.
- Schizotypal trait measures did not correlate with MMN indices in FDR.
Conclusions:
- Duration-MMN is a more sensitive marker for prediction error signaling deficits in schizophrenia.
- Frequency-MMN amplitude did not differ significantly across groups.
- MMN indices do not correlate with enduring schizophrenia-related psychopathology, suggesting MMN reflects transient cognitive states.
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