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dc.contributor.authorTatay-Manteiga, Amparopt_BR
dc.contributor.authorGhisays, Patricia Correapt_BR
dc.contributor.authorCauli, Omarpt_BR
dc.contributor.authorKapczinski, Flávio Pereirapt_BR
dc.contributor.authorTabarés-Seisdedos, Rafaelpt_BR
dc.contributor.authorMartínez, Vicent Balanzápt_BR
dc.date.accessioned2019-09-14T03:54:08Zpt_BR
dc.date.issued2018pt_BR
dc.identifier.issn1664-0640pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/199335pt_BR
dc.description.abstractIntroduction: Bipolar disorder (BD) is associated with significant neurocognitive and functional impairment, which may progress across stages. The ‘latent stage’ of BD remains understudied. This cross-sectional study assessed staging, neurocognition and social functioning among BD patients and their healthy siblings. Methods: Four groups were included: euthymic type I BD patients in the early (n = 25) and late (n = 23) stages, their healthy siblings (latent stage; n = 23) and healthy controls (n = 21). All 92 subjects underwent a comprehensive neuropsychological battery of processing speed, verbal learning/memory, visual memory, working memory, verbal fluency, executive cognition, and motor speed. Social functioning was assessed using the FAST scale. Results: Siblings' social functioning was identical to that of controls, and significantly better than both early- (p < 0.005) and late- (p < 0.001) stage patients. Although all patients were strictly euthymic, those at late stages had a significantly worse social functioning than early-stage patients (p < 0.001). Compared to controls, increasingly greater neurocognitive dysfunction was observed across stages of BD (F = 1.59; p = 0.005). Healthy siblings' performance lied between those of controls and patients, with deficits in tasks of processing speed, executive attention, verbal memory/learning, and visual memory. Both early- and late-stage patients had a more severe and widespread dysfunction than siblings, with no significant differences between them. Conclusions: Genetic vulnerability to BD-I seems to be associated with neurocognitive impairments, whereas social dysfunction would be the result of the clinical phenotype. Staging models of BD should take into account these divergent findings in the latent stage.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofFrontiers in psychiatry. Lausanne. Vol. 9, (Dec. 2018), 709, 10 p.pt_BR
dc.rightsOpen Accessen
dc.subjectTranstorno bipolarpt_BR
dc.subjectBipolar disorderen
dc.subjectCogniçãopt_BR
dc.subjectClinical stagingen
dc.subjectFunctioningen
dc.subjectMemóriapt_BR
dc.subjectIrmãospt_BR
dc.subjectNeurocognitionen
dc.subjectFenótipopt_BR
dc.subjectSiblingsen
dc.subjectProgressão da doençapt_BR
dc.subjectFirst-degree relativesen
dc.titleStaging, neurocognition and social functioning in bipolar disorderpt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001102051pt_BR
dc.type.originEstrangeiropt_BR


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