Show simple item record

Article

dc.creatorPardiñas, Antonio F.es
dc.creatorSmart, Sophie E.es
dc.creatorWillcocks, Isabella R.es
dc.creatorHolmans, Peter A.es
dc.creatorDennison, Charlotte Aes
dc.creatorLynham, Amy Jes
dc.creatorCrespo Facorro, Benedictoes
dc.date.accessioned2022-11-22T16:09:52Z
dc.date.available2022-11-22T16:09:52Z
dc.date.issued2022
dc.identifier.issn2168-622xes
dc.identifier.issn2168-6238es
dc.identifier.urihttps://hdl.handle.net/11441/139692
dc.description.abstractImportance About 20% to 30% of people with schizophrenia have psychotic symptoms that do not respond adequately to first-line antipsychotic treatment. This clinical presentation, chronic and highly disabling, is known as treatment-resistant schizophrenia (TRS). The causes of treatment resistance and their relationships with causes underlying schizophrenia are largely unknown. Adequately powered genetic studies of TRS are scarce because of the difficulty in collecting data from well-characterized TRS cohorts. Objective To examine the genetic architecture of TRS through the reassessment of genetic data from schizophrenia studies and its validation in carefully ascertained clinical samples. Conclusions and Relevance In this GWAS, common genetic variants were differentially associated with TRS, and these associations may have been obscured through the amalgamation of large GWAS samples in previous studies of broadly defined schizophrenia. Findings of this study suggest the validity of meta-analytic approaches for studies on patient outcomes, including treatment resistance. Design, Setting, and Participants Two case-control genome-wide association studies (GWASs) of schizophrenia were performed in which the case samples were defined as individuals with TRS (n = 10 501) and individuals with non-TRS (n = 20 325). The differences in effect sizes for allelic associations were then determined between both studies, the reasoning being such differences reflect treatment resistance instead of schizophrenia. Genotype data were retrieved from the CLOZUK and Psychiatric Genomics Consortium (PGC) schizophrenia studies. The output was validated using polygenic risk score (PRS) profiling of 2 independent schizophrenia cohorts with TRS and non-TRS: a prevalence sample with 817 individuals (Cardiff Cognition in Schizophrenia [CardiffCOGS]) and an incidence sample with 563 individuals (Genetics Workstream of the Schizophrenia Treatment Resistance and Therapeutic Advances [STRATA-G]). Main Outcomes and Measures GWAS of treatment resistance in schizophrenia. The results of the GWAS were compared with complex polygenic traits through a genetic correlation approach and were used for PRS analysis on the independent validation cohorts using the same TRS definition. Results The study included a total of 85 490 participants (48 635 [56.9%] male) in its GWAS stage and 1380 participants (859 [62.2%] male) in its PRS validation stage. Treatment resistance in schizophrenia emerged as a polygenic trait with detectable heritability (1% to 4%), and several traits related to intelligence and cognition were found to be genetically correlated with it (genetic correlation, 0.41-0.69). PRS analysis in the CardiffCOGS prevalence sample showed a positive association between TRS and a history of taking clozapine (r2 = 2.03%; P = .001), which was replicated in the STRATA-G incidence sample (r2 = 1.09%; P = .04).es
dc.format.extent10es
dc.language.isoenges
dc.publisherAmerican Medical Associationes
dc.rightsAtribución 4.0 Internacional*
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectSchizophreniaes
dc.subjectInteraction Testinges
dc.subjectScoring to Estimatees
dc.subjectGenetic Variantses
dc.titleInteraction testing and polygenic risk scoring to estimate the association of common genetic variants with treatment resistance in schizophreniaes
dc.typeinfo:eu-repo/semantics/articlees
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Psiquiatríaes
dc.relation.publisherversionhttps://jamanetwork.com/journals/jamapsychiatry/fullarticle/2787666es
dc.identifier.doi10.1001/jamapsychiatry.2021.3799es
dc.journaltitleJama Psychiatryes
dc.publication.volumen79es
dc.publication.issue3es
dc.publication.initialPage260es
dc.publication.endPage269es

FilesSizeFormatViewDescription
379.pdf1.010MbIcon   [PDF] View/Open  

This item appears in the following collection(s)

Show simple item record

Atribución 4.0 Internacional
Except where otherwise noted, this item's license is described as: Atribución 4.0 Internacional