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dc.contributor.authorRuiz de Azúa García, Sonia ORCID
dc.contributor.authorMatute Almau, Carlos José
dc.contributor.authorStertz, Laura
dc.contributor.authorMosquera, Fernando
dc.contributor.authorPalomino Fernández de Larrea, Aitor
dc.contributor.authorDe la Rosa, Iris
dc.contributor.authorBarbeito, Sara
dc.contributor.authorVega, Patricia
dc.contributor.authorKapczinski, Flavío
dc.contributor.authorGonzález Pinto Arrillaga, Ana María ORCID
dc.date.accessioned2013-05-28T11:48:23Z
dc.date.available2013-05-28T11:48:23Z
dc.date.issued2013
dc.identifier.citationBMC Psychiatry (13)27 : (2013)es
dc.identifier.issn1471-244X
dc.identifier.urihttp://hdl.handle.net/10810/10162
dc.description.abstractBackground: Cognitive impairments are seen in first psychotic episode (FEP) patients. The neurobiological underpinnings that might underlie these changes remain unknown. The aim of this study is to investigate whether Brain Derived Neurotrophic Factor (BDNF) levels are associated with cognitive impairment in FEP patients compared with healthy controls. Methods: 45 FEP patients and 45 healthy controls matched by age, gender and educational level were selected from the Basque Country area of Spain. Plasma BDNF levels were assessed in healthy controls and in patients. A battery of cognitive tests was applied to both groups, with the patients being assessed at 6 months after the acute episode and only in those with a clinical response to treatment. Results: Plasma BDNF levels were altered in patients compared with the control group. In FEP patients, we observed a positive association between BDNF levels at six months and five cognitive domains (learning ability,immediate and delayed memory, abstract thinking and processing speed) which persisted after controlling for medications prescribed, drug use, intelligence quotient (IQ) and negative symptoms. In the healthy control group, BDNF levels were not associated with cognitive test scores. Conclusion: Our results suggest that BDNF is associated with the cognitive impairment seen after a FEP. Further investigations of the role of this neurotrophin in the symptoms associated with psychosis onset are warranted.es
dc.language.isoenges
dc.publisherBioMed Centrales
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectpsychotic disorderes
dc.subjectbrain-derived neurotrophic factores
dc.subjectschizophreniaes
dc.subjectcognitiones
dc.titlePlasma brain-derived neurotrophic factor levels, learning capacity and cognition in patients with first episode psychosises
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2013 Ruiz de Azua et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.es
dc.relation.publisherversionhttp://www.biomedcentral.com/1471-244X/13/27es
dc.identifier.doi10.1186/1471-244X-13-27
dc.departamentoesNeurocienciases_ES
dc.departamentoeuNeurozientziakes_ES
dc.subject.categoriaPSYCHIATRY AND MENTAL HEALTH


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