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dc.contributor.authorSevilla-Ramos, Manuel
dc.contributor.authorLadera Fernández, Valentina 
dc.contributor.authorGarcía García, Ricardo Sebastián 
dc.contributor.authorMurillo García, Nancy
dc.contributor.authorAyesa Arriola, Rosa
dc.date.accessioned2025-10-06T08:34:26Z
dc.date.available2025-10-06T08:34:26Z
dc.date.issued2025
dc.identifier.citationSevilla-Ramos, M., Ladera, V., García-García, R., Murillo-García, N., & Ayesa-Arriola, R. (2025). Motor dexterity in schizophrenia spectrum disorders: Familiality and association with polygenic risk scores. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 111406.es_ES
dc.identifier.issn0278-5846
dc.identifier.urihttp://hdl.handle.net/10366/167301
dc.description.abstract[EN]Objective: Motor dexterity (MD), a potential endophenotype for schizophrenia spectrum disorders, might exhibit familiality, showing greater similarity among biological relatives. Moreover, MD deficits in first-episode psychosis (FEP) patients may be related to their increased genetic liability for schizophrenia (SCZ). We examined MD familiality and its association with genetic risk for SCZ. We controlled disorder severity by analysing FEP patients with SCZ and other psychosis (OP) separately. Methods: Cross-sectional family study including 133 FEP patients and 244 of their first-degree relatives and 202 healthy controls. We used the grooved pegboard test to assess MD and estimated polygenic scores for SCZ (PGS-SCZ) in the participants. Statistical analysis included linear mixed models and intraclass correlation coefficient (ICC) Results: MD has low familiality (ICC = 0.10) in the whole sample of FEP patients and their relatives. In SCZ families, there was a trend toward MD familiality (p = 0.063). In OP families, MD was familial only in unaffected relatives (ICC = 0.33). FEP patients showed the highest PGS-SCZ, followed by parents, siblings, and healthy controls. No significant association was found between PGS-SCZ and MD. Conclusions: MD shows low familiality in FEP patients. Further research is needed to assess differences by severity of the disorder. Genetic risk for SCZ is not directly linked to MD but may influence it indirectly through neurodevelopment. PGS-SCZ was not associated with MD deficits in FEP patients, possibly reflecting the limited capacity of this tool to capture shared genetic liability between these traits. Environmental factors, in conjunction with genetic predisposition, may significantly contribute to MD development.es_ES
dc.format.mimetypeapplication/pdf
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.subjectMotor dexterityes_ES
dc.subjectFirst episode psychosises_ES
dc.subjectFamilialityes_ES
dc.subjectGenetices_ES
dc.subjectEndophenotypees_ES
dc.titleMotor dexterity in schizophrenia spectrum disorders: Familiality and association with polygenic risk scoreses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://www.sciencedirect.com/science/article/pii/S0278584625001605es_ES
dc.subject.unesco61 Psicologíaes_ES
dc.identifier.doi10.1016/j.pnpbp.2025.111406
dc.relation.projectIDThe PAFIP cohort projects were supported by the Carlos III Health Institute [grant numbers PI14/00639 , PI14/00918 , PI17/00221 , PI20/00066 , and PI23/00076 ]. Additionally, Dr. Rosa Ayesa-Arriola was financed by a Miguel Servet contract from the Carlos III Health Institute [grant number CP18/00003 ] and a Consolidator Grant from the Ministerio de Ciencia e Innovaci\u00F3n [grant number CNS2022-136110 ]. Financiadores Instituto de Salud Carlos III Spain PI14/00639 Instituto de Salud Carlos III Spain Ministerio de Ciencia e Innovación Spain CNS2022-136110 Ministerio de Ciencia e Innovación Spaines_ES
dc.rights.accessRightsinfo:eu-repo/semantics/embargoedAccesses_ES
dc.journal.titleProgress in Neuro-Psychopharmacology and Biological Psychiatryes_ES
dc.volume.number139es_ES
dc.page.initial111406es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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