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Genetic liability in individuals at ultra-high risk of psychosis: A comparison study of 9 psychiatric traits

Individuals at ultra-high risk (UHR) of psychosis are characterised by the emergence of attenuated psychotic symptoms and deterioration in functioning. In view of the high non-psychotic comorbidity and low rates of transition to psychosis, the specificity of the UHR status has been called into quest...

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Detalles Bibliográficos
Autores principales: Lim, Keane, Lam, Max, Huang, Hailiang, Liu, Jianjun, Lee, Jimmy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710117/
https://www.ncbi.nlm.nih.gov/pubmed/33264322
http://dx.doi.org/10.1371/journal.pone.0243104
Descripción
Sumario:Individuals at ultra-high risk (UHR) of psychosis are characterised by the emergence of attenuated psychotic symptoms and deterioration in functioning. In view of the high non-psychotic comorbidity and low rates of transition to psychosis, the specificity of the UHR status has been called into question. This study aims to (i) investigate if the UHR construct is associated with the genetic liability of schizophrenia or other psychiatric conditions; (ii) examine the ability of polygenic risk scores (PRS) to discriminate healthy controls from UHR, remission and conversion status. PRS was calculated for 210 youths (n(UHR) = 102, n(Control) = 108) recruited as part of the Longitudinal Youth at Risk Study (LYRIKS) using nine psychiatric traits derived from twelve large-scale psychiatric genome-wide association studies as discovery datasets. PRS was also examined to discriminate UHR-Healthy control status, and healthy controls from UHR remission and conversion status. Result indicated that schizophrenia PRS appears to best index the genetic liability of UHR, while trend level associations were observed for depression and cross-disorder PRS. Schizophrenia PRS discriminated healthy controls from UHR (R(2) = 7.9%, p = 2.59 x 10(−3), OR = 1.82), healthy controls from non-remitters (R(2) = 8.1%, p = 4.90 x 10(−4), OR = 1.90), and converters (R(2) = 7.6%, p = 1.61 x 10(−3), OR = 1.82), with modest predictive ability. A trend gradient increase in schizophrenia PRS was observed across categories. The association between schizophrenia PRS and UHR status supports the hypothesis that the schizophrenia polygenic liability indexes the risk for developing psychosis.