Attenuated mismatch negativity in patients with first-episode antipsychotic-naive schizophrenia using a source-resolved method

• Published in: NeuroImage clinical Vol. 22; p. 101760
• Main Authors: Randau, M, Oranje, B, Miyakoshi, M, Makeig, S, Fagerlund, B, Glenthøj, B, Bak, N
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier 01.01.2019
• Subjects: Adult; Electroencephalography - methods; Event-Related Potentials, P300 - physiology; Evoked Potentials - physiology; Evoked Potentials, Auditory - physiology; Female; Humans; Male; Regular; Schizophrenia - physiopathology; Signal Processing, Computer-Assisted; Young Adult; Schizophrenia; Mismatch negativity; First episode; EEG; ICA
• ISSN: 2213-1582; 2213-1582
• DOI: 10.1016/j.nicl.2019.101760

Mismatch negativity (MMN) is a measure of pre-attentive auditory information processing related to change detection. Traditional scalp-level EEG methods consistently find attenuated MMN in patients with chronic but not first-episode schizophrenia. In the current paper, we use a source-resolved method to assess MMN and hypothesize that more subtle changes can be identified with this analysis method. Fifty-six first-episode antipsychotic-naïve schizophrenia (FEANS) patients (31 males, 25 females, mean age 24.6) and 64 matched controls (37 males, 27 females, mean age 24.8) were assessed for duration-, frequency- and combined-type MMN and P3a as well as 4 clinical, 3 cognitive and 3 psychopathological measures. To evaluate and correlate MMN at source-level, independent component analysis (ICA) was applied to the continuous EEG data to derive equivalent current dipoles which were clustered into 19 clusters based on cortical location. No scalp channel group MMN or P3a amplitude differences were found. Of the localized clusters, several were in or near brain areas previously suggested to be involved in the MMN response, including frontal and anterior cingulate cortices and superior temporal and inferior frontal gyri. For duration deviants, MMN was attenuated at the right superior temporal gyrus in patients compared to healthy controls (p = 0.01), as was P3a at the superior frontal cortex (p = 0.01). No individual patient correlations with clinical, cognitive, or psychopathological measures survived correction for multiple comparisons. Attenuated source-localized MMN and P3a peak contributions can be identified in FEANS patients using a method based on independent component analysis (ICA). This indicates that deficits in pre-attentive auditory information processing are present at this early stage of schizophrenia and are not the result of disease chronicity or medication. This is to our knowledge the first study on FEANS patients using this more detailed method.