Key result
Ultra-high-risk individuals showed reduced late-latency gamma-band ASSRs compared to controls, while first-episode schizophrenia patients had reductions in both, correlating with symptoms (|rs|>0.70).
Why the study?
Does the time course of gamma-band auditory steady-state responses differ between ultra-high-risk individuals, first-episode schizophrenia patients, and healthy controls?
Cross-Sectional (n=49)
Does the time course of gamma-band auditory steady-state responses differ between ultra-high-risk individuals, first-episode schizophrenia patients, and healthy controls?
Late-latency ASSR alteration may serve as a biomarker for early detection of psychosis, while early-latency ASSR abnormality may develop through the onset of psychosis.
Reduced late-latency gamma ASSR in UHR may flag impending psychosis; leaves open its value as a conversion biomarker pending longitudinal validation.
Alterations in gamma-band auditory steady-state response (ASSR) are the most robust finding of abnormal neural oscillations in patients with first-episode (FES) and chronic schizophrenia. Gamma-band ASSRs may indicate GABAergic interneuron dysfunction. Nevertheless, it is unknown whether abnormal gamma-band ASSRs are present before the onset of psychosis. Subjects were 15 ultra-high-risk (UHR) individuals, 13 FES patients, and 21 healthy control (HC) subjects. We performed electroencephalogram recordings and measured ASSRs in each group as they were presented with click trains at 20, 30, and 40 Hz. We then conducted time-frequency analyses and calculated intertrial phase coherence and event-related spectral perturbation. The time course of gamma-band ASSRs showed significantly different features among groups. Compared with the HC group, the UHR group was characterized by intact early-latency (0-100 ms) and reduced late-latency (300-500 ms) ASSRs. In contrast, both early- and late-latency ASSRs were significantly reduced in the FES group. Gamma-band ASSRs were correlated with clinical symptoms and attentional functioning in FES (|rs| > 0.70). These results suggest differential alterations of gamma-band ASSRs between UHR and FES groups. The late-latency ASSR alteration may represent a biomarker for early detection of psychosis, while the early-latency ASSR abnormality may develop through the onset of psychosis.
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Tada et al. (2014) conducted a cross-sectional in Ultra-high-risk for psychosis and first-episode schizophrenia (n=49). Ultra-high-risk and first-episode schizophrenia status vs. Healthy controls was evaluated on Gamma-band auditory steady-state response (ASSR) early-latency (0-100 ms) and late-latency (300-500 ms) features. Ultra-high-risk individuals showed reduced late-latency gamma-band ASSRs compared to controls, while first-episode schizophrenia patients had reductions in both, correlating with symptoms (|rs|>0.70).
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