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Abstract
Electroencephalography in patients with a first episode of psychosis (FEP) may contribute to the diagnosis and treatment response prediction. Findings in the literature vary due to small sample sizes, medication effects, and variable illness duration. We studied macroscale resting-state EEG characteristics of antipsychotic naïve patients with FEP. We tested (1) for differences between FEP patients and controls, (2) if EEG could be used to classify patients as FEP, and (3) if EEG could be used to predict treatment response to antipsychotic medication. In total, we studied EEG recordings of 62 antipsychotic-naïve patients with FEP and 106 healthy controls. Spectral power, phase-based and amplitude-based functional connectivity, and macroscale network characteristics were analyzed, resulting in 60 EEG variables across four frequency bands. Positive and Negative Symptom Scale (PANSS) were assessed at baseline and 4–6 weeks follow-up after treatment with amisulpride or aripiprazole. Mann-Whitney U tests, a random forest (RF) classifier and RF regression were used for statistical analysis. Our study found that at baseline, FEP patients did not differ from controls in any of the EEG characteristics. A random forest classifier showed chance-level discrimination between patients and controls. The random forest regression explained 23% variance in positive symptom reduction after treatment in the patient group. In conclusion, in this largest antipsychotic- naïve EEG sample to date in FEP patients, we found no differences in macroscale EEG characteristics between patients with FEP and healthy controls. However, these EEG characteristics did show predictive value for positive symptom reduction following treatment with antipsychotic medication.
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1 University Medical Center Utrecht, Department of Psychiatry, Utrecht, The Netherlands (GRID:grid.7692.a) (ISNI:0000000090126352)
2 Copenhagen University Hospital, Mental Health Center Glostrup, Center for Neuropsychiatric Schizophrenia Research (CNSR) and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS), Glostrup, Denmark (GRID:grid.411719.b) (ISNI:0000 0004 0630 0311)
3 University Medical Center Utrecht, and Utrecht University, Department of Child Neurology, UMC Utrecht Brain Center, Utrecht, The Netherlands (GRID:grid.5477.1) (ISNI:0000000120346234)
4 Vrije Universiteit Amsterdam, Amsterdam UMC, Department of Clinical Neurophysiology and MEG Center, Department of Neurology, Amsterdam Neuroscience, Amsterdam, The Netherlands (GRID:grid.12380.38) (ISNI:0000 0004 1754 9227)
5 Copenhagen University Hospital, Mental Health Center Glostrup, Center for Neuropsychiatric Schizophrenia Research (CNSR) and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS), Glostrup, Denmark (GRID:grid.411719.b) (ISNI:0000 0004 0630 0311); University of Copenhagen, Department of Clinical Medicine, Faculty of Health and Medical Sciences, Copenhagen, Denmark (GRID:grid.5254.6) (ISNI:0000 0001 0674 042X)
6 University Medical Center Utrecht, Department of Psychiatry, Utrecht, The Netherlands (GRID:grid.7692.a) (ISNI:0000000090126352); Utrecht University, Department of Intensive Care Medicine and University Medical Center Utrecht Brain Center, Utrecht, The Netherlands (GRID:grid.5477.1) (ISNI:0000000120346234)