The specificity of the auditory P300 responses and its association with clinical outcomes in youth with psychosis risk syndrome.

BACKGROUND

Schizophrenia often occurs in youth, and psychosis risk syndrome (PRS) occurs before the onset of psychosis. Assessing the neuropsychological abnormalities of PRS individuals can help in early identification and active intervention of mental illness. Auditory P300 amplitude defect is an important manifestation of attention processing abnormality in PRS, but it is still unclear whether there are abnormalities in the attention processing of rhythmic compound tone stimuli in PRS individuals, and whether the P300 amplitude induced by these stimuli is specific to PRS individuals and related to their clinical outcomes.

METHODS

In total, 226 participants, including 122 patients with PRS, 51 patients with emotional disorders (ED), and 53 healthy controls (HC) were assessed. Baseline electroencephalography was recorded during the compound tone oddball task. The event-related potentials (ERPs) induced by rhythmic compound tone stimuli of two frequencies (20-Hz, 40-Hz) were measured. Almost all patients with PRS were followed up for 12 months and reclassified into four groups: PRS-conversion, PRS-symptomatic, PRS-emotional disorder, and PRS-complete remission. The differences in baseline ERPs were compared among the clinical outcome groups.

RESULTS

Regardless of the stimulation frequency, the average P300 amplitude were significantly higher in patients with PRS than in those with ED ( = 0.003,  = 0.48) and in HC ( = 0.002,  = 0.44) group. The average P300 amplitude of PRS-conversion group was significantly higher than that of the PRS-complete remission ( = 0.016,  = 0.72) and HC group ( = 0.001,  = 0.76), and the average P300 amplitude of PRS-symptomatic group was significantly higher than that of the HC group ( = 0.006,  = 0.48). Regardless of the groups (PRS, ED, HC) or the PRS clinical outcome groups, the average P300 amplitude induced by 20-Hz tone stimulation was significantly higher than that induced by 40-Hz stimulation (s < 0.001, Ƞ = 0.074-0.082). The average reaction times of PRS was significantly faster than that of ED ( = 0.01,  = 0.38), and the average reaction times of the participants to 20-Hz target stimulation was significantly faster than that to 40-Hz target stimulation ( < 0.001,  = 0.21).

CONCLUSION

The auditory P300 amplitude induced by rhythmic compound tone stimuli is a specific electrophysiological manifestation of PRS, and the auditory P300 amplitude induced by compound tone stimuli shows promise as a putative prognostic biomarker for PRS clinical outcomes, including conversion to psychosis and clinical complete remission.