PMID- 24012459 OWN - NLM STAT- MEDLINE DCOM- 20140620 LR - 20220311 IS - 1573-2509 (Electronic) IS - 0920-9964 (Print) IS - 0920-9964 (Linking) VI - 150 IP - 2-3 DP - 2013 Nov TI - Social cognition as a mediator between neurocognition and functional outcome in individuals at clinical high risk for psychosis. PG - 542-6 LID - S0920-9964(13)00451-9 [pii] LID - 10.1016/j.schres.2013.08.015 [doi] AB - In schizophrenia, neurocognition, social cognition and functional outcome are all inter-related, with social cognition mediating the impact that impaired neurocognition has on functional outcome. Less clear is the nature of the relationship between neurocognition, social cognition and functional outcome in individuals at clinical high risk (CHR) for psychosis. 137 CHR participants completed a neurocognitive test battery, a battery of social cognition tasks and the Social Functioning Scale. Confirmatory factor analysis showed that all social cognition tasks were reliable and valid measures of the latent variable. The path from neurocognition to functioning was statistically significant (standardized coefficient beta=0.22, p<0.01). The path from social cognition to functioning was also statistically significant (beta=0.27, p<0.05). In the mediation model the bootstrapping estimate revealed a nonsignificant indirect effect that was the association of social cognition with neurocognition and with functional outcome (beta=0.20, 95% CI=-0.07 to 0.52, p=0.11). However, social cognition was significantly associated with neurocognition (beta=0.80, p<0.001) and the path from neurocognition to functioning was no longer significant as soon as the mediator (social cognition) was entered into the mediation model (beta=0.02, p=0.92). All of the model fit indices were very good. Unlike what has been observed with psychotic patients, social cognition does not seem to mediate the pathway from neurocognition to functional outcome when assessed with a measure of social attainment in individuals at CHR for psychosis. CI - (c) 2013. FAU - Barbato, Mariapaola AU - Barbato M AD - Hotchkiss Brain Institute, Department of Psychiatry, University of Calgary, Alberta, Canada. Electronic address: mbarbato@ucalgary.ca. FAU - Liu, Lu AU - Liu L FAU - Penn, David L AU - Penn DL FAU - Keefe, Richard S E AU - Keefe RS FAU - Perkins, Diana O AU - Perkins DO FAU - Woods, Scott W AU - Woods SW FAU - Addington, Jean AU - Addington J LA - eng GR - U01 MH066069/MH/NIMH NIH HHS/United States GR - U01 MH066160/MH/NIMH NIH HHS/United States GR - U01MH066160/MH/NIMH NIH HHS/United States GR - U01 MH066134/MH/NIMH NIH HHS/United States GR - U01MH06634-02/MH/NIMH NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20130905 PL - Netherlands TA - Schizophr Res JT - Schizophrenia research JID - 8804207 SB - IM MH - Adolescent MH - Cognition Disorders/*etiology MH - Factor Analysis, Statistical MH - Female MH - Humans MH - Male MH - Neuropsychological Tests MH - Psychiatric Status Rating Scales MH - Psychotic Disorders/*complications/*psychology MH - *Social Behavior MH - Statistics as Topic MH - Young Adult PMC - PMC3839963 MID - NIHMS518384 OTO - NOTNLM OT - Clinical high risk OT - Functional outcome OT - Mediation OT - Neurocognition OT - Schizophrenia OT - Social cognition COIS- Conflict of interest There are no conflicts of interest for any of the authors with respect to the data in this paper or for the study. EDAT- 2013/09/10 06:00 MHDA- 2014/06/21 06:00 PMCR- 2014/11/01 CRDT- 2013/09/10 06:00 PHST- 2013/05/23 00:00 [received] PHST- 2013/08/08 00:00 [revised] PHST- 2013/08/12 00:00 [accepted] PHST- 2013/09/10 06:00 [entrez] PHST- 2013/09/10 06:00 [pubmed] PHST- 2014/06/21 06:00 [medline] PHST- 2014/11/01 00:00 [pmc-release] AID - S0920-9964(13)00451-9 [pii] AID - 10.1016/j.schres.2013.08.015 [doi] PST - ppublish SO - Schizophr Res. 2013 Nov;150(2-3):542-6. doi: 10.1016/j.schres.2013.08.015. Epub 2013 Sep 5.