PMID- 25720419 OWN - NLM STAT- MEDLINE DCOM- 20150611 LR - 20220129 IS - 1423-033X (Electronic) IS - 0254-4962 (Linking) VI - 48 IP - 2 DP - 2015 TI - First-rank symptoms and premorbid adjustment in young individuals at increased risk of developing psychosis. PG - 120-6 AB - BACKGROUND: Individuals at clinical high risk (CHR) for psychosis represent a heterogeneous group with a high rate of comorbid psychiatric disorders. There is little information on whether certain qualitative aspects of psychotic symptoms among CHR individuals may be predictive of future psychosis. This study focused on describing the prevalence of first-rank symptoms (FRS) among a sample of CHR individuals and its association with future transition to psychosis and, from a neurodevelopmental perspective, the level of adjustment of individuals at CHR during their childhood was also analysed. SAMPLING AND METHODS: Participants comprised 60 individuals at CHR (according to the Comprehensive Assessment of At-Risk Mental States, CAARMS) at the time of their referral to an early intervention service and 60 healthy volunteers (HVs). All subjects were assessed by senior research clinicians using the Mini International Neuropsychiatric Interview (MINI), and the Positive and Negative Syndrome Scale (PANSS). FRS were defined according to Kurt Schneider's original classification, and information was collected from PANSS, CAARMS and clinical reports. Early premorbid functioning was measured using the Premorbid Adjustment Scale (PAS). We grouped individuals by number and type of FRS and analysed transitions to full-blown psychosis over a 2-year follow-up period. We also correlated the general social and functional adjustment of these individuals during their childhood (6-11 years of age) with the future development of mental states at CHR and FRS. RESULTS: Over 69% of CHR individuals had more than one DSM-IV psychiatric diagnosis, mainly within the affective and anxiety diagnostic spectra. At least one FRS was present in 43.3% of CHR individuals, and 21.6% of these had more than one. Auditory hallucinations and passivity experiences were the most commonly reported. Only 10% of individuals at CHR made a transition to first-episode psychosis (FEP) over 2 years and, except for passivity experiences, the presence of one or more FRS was not significantly associated with the transition to FEP. CHR individuals, especially those with FRS, had poorer premorbid functioning and adjustment as children across educational, social and peer relationship domains than HVs. However, this was not associated with FEP 2 years later. CONCLUSIONS: FRS might not be indicators of psychosis alone but of different psychiatric disorders. In line with the neurodevelopmental model of psychosis, individuals at CHR might be exhibiting several vulnerability traits and manifestations of abnormal developmental processes that might predict a future psychiatric disorder and/or long-term impairment. FAU - Morcillo, C AU - Morcillo C FAU - Stochl, J AU - Stochl J FAU - Russo, D A AU - Russo DA FAU - Zambrana, A AU - Zambrana A FAU - Ratnayake, N AU - Ratnayake N FAU - Jones, P B AU - Jones PB FAU - Perez, J AU - Perez J LA - eng GR - G0001354/MRC_/Medical Research Council/United Kingdom GR - RP-PG-0606-1335/DH_/Department of Health/United Kingdom PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - Switzerland TA - Psychopathology JT - Psychopathology JID - 8401537 SB - IM MH - *Adaptation, Psychological MH - Adolescent MH - Adult MH - Anxiety/psychology MH - Anxiety Disorders/psychology MH - Diagnostic and Statistical Manual of Mental Disorders MH - Female MH - Humans MH - Incidence MH - Male MH - Mental Health Services MH - Prevalence MH - Psychotic Disorders/*epidemiology/prevention & control/*psychology MH - Risk Assessment MH - Risk Factors MH - *Social Adjustment MH - United Kingdom MH - Young Adult EDAT- 2015/02/28 06:00 MHDA- 2015/06/13 06:00 CRDT- 2015/02/28 06:00 PHST- 2014/07/22 00:00 [received] PHST- 2014/11/10 00:00 [accepted] PHST- 2015/02/28 06:00 [entrez] PHST- 2015/02/28 06:00 [pubmed] PHST- 2015/06/13 06:00 [medline] AID - 000369859 [pii] AID - 10.1159/000369859 [doi] PST - ppublish SO - Psychopathology. 2015;48(2):120-6. doi: 10.1159/000369859.