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dc.contributor.authorWinter-van Rossum, Ingees_ES
dc.contributor.authorSlot, Margot I. E.es_ES
dc.contributor.authorVan Hell, Hendrika H.es_ES
dc.contributor.authorBossong, Matthijs G.es_ES
dc.contributor.authorBerger, Gregores_ES
dc.contributor.authorAschauer, Haraldes_ES
dc.contributor.authorMaat, Arijaes_ES
dc.contributor.authorWalitza, Susannees_ES
dc.contributor.authorLavan, Orlyes_ES
dc.contributor.authorBaeza, Inmaculadaes_ES
dc.contributor.authorDolz, Montserrates_ES
dc.contributor.authorMonducci, Elenaes_ES
dc.contributor.authorNasro, Paolo Fiories_ES
dc.contributor.authorKroken, Rune Andreases_ES
dc.contributor.authorLawrie, Stephenes_ES
dc.contributor.authorMartínez Díez-Caneja, Covadongaes_ES
dc.contributor.authorRenner, Tobiases_ES
dc.contributor.authorSchlögelhofer, Monikaes_ES
dc.contributor.authorOtero Cuesta, María Soraya es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-01-24T11:56:18Z
dc.date.available2025-01-24T11:56:18Z
dc.date.issued2024es_ES
dc.identifier.issn0586-7614es_ES
dc.identifier.issn1745-1701es_ES
dc.identifier.urihttps://hdl.handle.net/10902/35162
dc.description.abstractBackground and Hypotheses: In the past 2 decades, substantial effort has been put into research on therapeutic options for people at ultra-high risk (UHR) for developing a first episode of psychosis (FEP), focusing on omega-3 polyunsaturated fatty acids (PUFAs) in preventing transition to psychosis. Despite an initial positive finding, subsequent studies failed to find a beneficial effect. The current study aimed to further investigate the effect of omega-3 PUFAs in UHR, to determine whether this line of research is worth pursuing. Study Design: A double-blind, randomized, placebo-controlled study testing the efficacy of 6-month treatment with omega-3 PUFAs in 135 subjects at UHR for FEP, aged 13 to 20 years on the prevention of a transition to psychosis, followed up for 18 months post-treatment. The trial was conducted at 16 general hospitals and psychiatric specialty centers located in 8 European countries and Israel. Study Results: There was no beneficial effect of treatment with omega-3 PUFAs compared to placebo; the rate of transition over 2 years did not differ between treatment arms nor was there a difference in change in symptom severity after 6-month treatment. Dropout rates and serious adverse events were similar across the groups. Conclusions: This is the third study that fails to replicate the original finding on the protective effect of omega-3 PUFAs in UHR subjects for transition to psychosis. The accumulating evidence therefore suggests that omega-3 PUFAs do not reduce transition rates to psychosis in those at increased risk at 2 years follow-up.es_ES
dc.description.sponsorshipThis work as supported by the Stanley Medical Research Institute (study code 14T-002) and Burgerstein Vitamine. Neither Stanley Medical Research Institute or Burgerstein Vitamine had any input into the trial design or data analyses. The study was overseen by a Data Safety Monitoring Board (DSMB), an independent board of experts responsible for protecting participant safety and data quality. We are grateful for the involvement and contribution of the DSMB, consisting of the following members: prof. dr. Tyrone Cannon (chair), prof. dr. Pál Czobor and prof. dr. Carmine Pariante. We are grateful for the consultancy by dr. Gregor Berger.
dc.format.extent10 p.es_ES
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.rights© The Author(s) 2024. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https:// creativecommons.org/licenses/by-nc-nd/4.0/)*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceSchizophrenia Bulletin, 2024, 186, 1-10es_ES
dc.subject.otherPsychosis prevention
dc.subject.otherTreatment
dc.subject.otherNutrition
dc.titleEffectiveness of Omega-3 fatty acids versus placebo in subjects at ultra-high risk for psychosis: the PURPOSE randomized clinical triales_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionttps://doi.org/10.1093/schbul/sbae186es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1093/schbul/sbae186es_ES
dc.type.versionpublishedVersiones_ES


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© The Author(s) 2024. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https:// creativecommons.org/licenses/by-nc-nd/4.0/)Excepto si se señala otra cosa, la licencia del ítem se describe como © The Author(s) 2024. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https:// creativecommons.org/licenses/by-nc-nd/4.0/)