The 40-Hz ASSR spectral power and phase-locking deficits are robust in schizophrenia, which suggests that these measures could be useful probes for assessing circuit dysfunctions in the disorder. Moreover, these findings should motivate large-scale studies of the longitudinal expression in patients with schizophrenia and at-risk populations, to further validate the 40-Hz ASSR as a potential biomarker.

No abstract

Auditory deviance detection occurs around 150 ms after the onset of a deviant sound. Recent studies in animals and humans have described change-related processes occurring during the first 50 ms after sound onset. However, it still remains an open question whether these early and late processes of deviance detection are organized hierarchically in the human auditory cortex. We applied a beamforming source reconstruction approach in order to estimate brain sources associated with 2 temporally distinct markers of deviance detection. Results showed that rare frequency changes elicit an enhancement of the Nbm component of the middle latency response (MLR) peaking at 43 ms, in addition to the magnetic mismatch negativity (MMNm) peaking at 115 ms. Sources of MMNm, located in the right superior temporal gyrus, were lateral and posterior to the deviance-related MLR activity being generated in the right primary auditory cortex. Source reconstruction analyses revealed that detection of changes in the acoustic environment is a process accomplished in 2 different time ranges, by spatially separated auditory regions. Paralleling animal studies, our findings suggest that primary and secondary areas are involved in successive stages of deviance detection and support the existence of a hierarchical network devoted to auditory change detection.

No abstract

Mismatch negativity (MMN) is a neurophysiological measure of auditory novelty detection that could serve as a translational biomarker of psychiatric disorders, such as schizophrenia. However, the replicability of its magnetoencephalographic (MEG) counterpart (MMNm) has been insufficiently addressed. In the current study, test-retest reliability of the MMNm response to both duration and omission deviants was evaluated over two MEG sessions in 16 healthy adults. MMNm amplitudes and latencies were obtained at both sensor- and source-level using a cortically-constrained minimum-norm approach. Intraclass correlations (ICC) were derived to assess stability of MEG responses over time. In addition, signal-to-noise ratios (SNR) and within-subject statistics were obtained in order to determine MMNm detectability in individual participants. ICC revealed robust values at both sensor- and source-level for both duration and omission MMNm amplitudes (ICC = 0.81-0.90), in particular in the right hemisphere, while moderate to strong values were obtained for duration MMNm and omission MMNm peak latencies (ICC = 0.74-0.88). Duration MMNm was robustly identified in individual participants with high SNR, whereas omission MMNm responses were only observed in half of the participants. Our data indicate that MMNm to unexpected duration changes and omitted sounds are highly reproducible, providing support for the use of MEG-parameters in basic and clinical research.