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dc.contributor.authorMuntané, Gerardes_ES
dc.contributor.authorVázquez Bourgon, Javier es_ES
dc.contributor.authorSada, Esteres_ES
dc.contributor.authorMartorell, Lourdeses_ES
dc.contributor.authorPapiol, Sergies_ES
dc.contributor.authorBosch, Elenaes_ES
dc.contributor.authorNavarro, Arcadies_ES
dc.contributor.authorCrespo Facorro, Benedicto es_ES
dc.contributor.authorVilella, Elisabetes_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-06-16T14:18:09Z
dc.date.issued2023es_ES
dc.identifier.issn0924-9338es_ES
dc.identifier.issn1778-3585es_ES
dc.identifier.urihttps://hdl.handle.net/10902/29333
dc.description.abstractBackground. Individuals with a first episode of psychosis (FEP) show rapid weight gain during the first months of treatment, which is associated with a reduction in general physical health. Although genetics is assumed to be a significant contributor to weight gain, its exact role is unknown. Methods. We assembled a population-based FEP cohort of 381 individuals that was split into a Training (n=224) set and a Validation (n=157) set to calculate the polygenic risk score (PRS) in a two-step process. In parallel, we obtained reference genome-wide association studies for body mass index (BMI) and schizophrenia (SCZ) to examine the pleiotropic landscape between the two traits. BMI PRSs were added to linear models that included sociodemographic and clinical variables to predict BMI increase (ΔBMI) in the Validation set. Results. The results confirmed considerable shared genetic susceptibility for the two traits involving 449 near-independent genomic loci. The inclusion of BMI PRSs significantly improved the prediction of ΔBMI at 12 months after the onset of antipsychotic treatment by 49.4% compared to a clinical model. In addition, we demonstrated that the PRS containing pleiotropic information between BMI and SCZ predicted ΔBMI better at 3 (12.2%) and 12 months (53.2%). Conclusions. We prove for the first time that genetic factors play a key role in determining ΔBMI during the FEP. This finding has important clinical implications for the early identification of individuals most vulnerable to weight gain and highlights the importance of examining genetic pleiotropy in the context of medically important comorbidities for predicting future outcomes.es_ES
dc.description.sponsorshipFinancial Support. This work was supported by the Catalan Agency of Research and Universities (AGAUR, 2017SGR-00444, PI: E.V.). G.M. is supported by Instituto de Salud Carlos III (PI18/00514 and PI21/00612). The Santander (PAFIP) cohort was funded by the following grants: Instituto de Salud Carlos III (FIS00/3095, PI020499, PI050427, PI060507), Plan Nacional de Drogas Research (2005-Orden sco/3246/2004), SENY Fundatio Research (2005-0308007), Fundacion Marques de Valdecilla (A/02/07, API07/011), and MINECO/FEDER (SAF2016-76046-R, SAF2013-46292-R). J.V.-B. is supported by funding from Instituto de Investigación Valdecilla (INT/A21/10, INT/ A20/04). A.N. is supported by funding from AEI-PGC2018-BI00 (FEDER/ UE) (MINECO/FEDER, UE),“Unidad de Excelencia María de Maeztu,”funded by the AEI (CEX2018-000792-M), Secretaria d’Universitats i Recerca, and the CERCA Program of the Departament d’Economia i Coneixement de la Generalitat de Catalunya (GRC 2017 SGR 880).es_ES
dc.format.extent9 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceEuropean Psychiatry, 2023, 66(1), e28, 1-9es_ES
dc.titlePolygenic risk scores enhance prediction of body mass index increase in individuals with a first episode of psychosises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1192/j.eurpsy.2023.9es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1192/j.eurpsy.2023.9es_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International