PMID- 36183600 OWN - NLM STAT- MEDLINE DCOM- 20221018 LR - 20231220 IS - 1879-1379 (Electronic) IS - 0022-3956 (Print) IS - 0022-3956 (Linking) VI - 155 DP - 2022 Nov TI - Relationships between rest-activity rhythms, sleep, and clinical symptoms in individuals at clinical high risk for psychosis and healthy comparison subjects. PG - 465-470 LID - S0022-3956(22)00499-X [pii] LID - 10.1016/j.jpsychires.2022.09.009 [doi] AB - Sleep-wake disturbances in individuals at clinical high risk (CHR) of psychosis may relate to increased symptom severity and contribute to disease progression. Here, we examined differences in rest-activity rhythms (RAR) measures, derived from actigraphy, and objective sleep outcomes, derived from electroencephalography (EEG), between 12 CHR and 16 healthy comparison (HC) individuals. Further, we examined the relationships between RAR disturbances, objective sleep outcomes and clinical psychosis symptoms (i.e., negative, positive, disorganized, general symptoms). Sleep-wake behaviors were monitored via actigraphy for 3-7 days (CHR: 5.7 +/- 1.7 days; HC: 6.3 +/- 1.2 days) prior to participants spending a night in the sleep laboratory, which was monitored with EEG. Separate regressions were used to examine the effect of clinical group on RAR measures and objective sleep outcomes after controlling for age and gender. CHR participants were found to be less active, specifically during the evening (17:00-20:00; beta = 1.145, SE = 0.362, p = .004) and nighttime (21:00-24:00; beta = 1.152, SE = 0.326, p = .002) relative to HC. Further, CHR participants had more fragmented sleep (wake after sleep onset: beta = 0.888, SE = 0.395, p = .034) and more hyperarousal during sleep (NREM gamma activity: beta = 1.087, SE = 0.348, p = .005), but these sleep disturbances were not related to reduced activity or clinical symptoms, whereas lower nighttime activity was related to more disorganized symptoms (rho = -.640, p = .025). Thus, increasing activity through behavioral interventions may have additional beneficial effects on CHR clinical symptoms. CI - Copyright (c) 2022 Elsevier Ltd. All rights reserved. FAU - LaGoy, Alice D AU - LaGoy AD AD - Department of Psychiatry, University of Pittsburgh School of Medicine, 3811 O'Hara Street, Pittsburgh, PA, 15213, USA; Department of Sports Medicine and Nutrition, University of Pittsburgh, 3600 Atwood Street, Pittsburgh, PA, 15260, USA. FAU - Mayeli, Ahmad AU - Mayeli A AD - Department of Psychiatry, University of Pittsburgh School of Medicine, 3811 O'Hara Street, Pittsburgh, PA, 15213, USA. FAU - Smagula, Stephen F AU - Smagula SF AD - Department of Psychiatry, University of Pittsburgh School of Medicine, 3811 O'Hara Street, Pittsburgh, PA, 15213, USA. FAU - Ferrarelli, Fabio AU - Ferrarelli F AD - Department of Psychiatry, University of Pittsburgh School of Medicine, 3811 O'Hara Street, Pittsburgh, PA, 15213, USA. Electronic address: ferrarellif@upmc.edu. LA - eng GR - R01 MH113827/MH/NIMH NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20220919 PL - England TA - J Psychiatr Res JT - Journal of psychiatric research JID - 0376331 SB - IM MH - Actigraphy MH - Humans MH - *Psychotic Disorders/complications/diagnosis MH - Rest MH - Sleep MH - *Sleep Wake Disorders/diagnosis/etiology PMC - PMC10729940 MID - NIHMS1950193 OTO - NOTNLM OT - Actigraphy OT - At-risk OT - EEG OT - Sleep disturbance COIS- Declaration of competing interest The authors have no conflicts of interest to report. EDAT- 2022/10/03 06:00 MHDA- 2022/10/19 06:00 PMCR- 2023/12/19 CRDT- 2022/10/02 18:18 PHST- 2022/04/08 00:00 [received] PHST- 2022/08/11 00:00 [revised] PHST- 2022/09/12 00:00 [accepted] PHST- 2022/10/03 06:00 [pubmed] PHST- 2022/10/19 06:00 [medline] PHST- 2022/10/02 18:18 [entrez] PHST- 2023/12/19 00:00 [pmc-release] AID - S0022-3956(22)00499-X [pii] AID - 10.1016/j.jpsychires.2022.09.009 [doi] PST - ppublish SO - J Psychiatr Res. 2022 Nov;155:465-470. doi: 10.1016/j.jpsychires.2022.09.009. Epub 2022 Sep 19.