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Characterising cognitive heterogeneity in individuals at clinical high-risk for psychosis: a cluster analysis with clinical and functional outcome prediction.
Haining, Kate; Gajwani, Ruchika; Gross, Joachim; Gumley, Andrew I; Ince, Robin A A; Lawrie, Stephen M; Schultze-Lutter, Frauke; Schwannauer, Matthias; Uhlhaas, Peter J.
Afiliação
  • Haining K; Institute of Neuroscience and Psychology, University of Glasgow, Glasgow, UK.
  • Gajwani R; Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
  • Gross J; Institute of Neuroscience and Psychology, University of Glasgow, Glasgow, UK.
  • Gumley AI; Institute for Biomagnetism and Biosignalanalysis, University of Münster, Münster, Germany.
  • Ince RAA; Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
  • Lawrie SM; Institute of Neuroscience and Psychology, University of Glasgow, Glasgow, UK.
  • Schultze-Lutter F; Department of Psychiatry, University of Edinburgh, Edinburgh, UK.
  • Schwannauer M; Department of Psychiatry and Psychotherapy, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
  • Uhlhaas PJ; Department of Psychology and Mental Health, Faculty of Psychology, Airlangga University, Surabaya, Indonesia.
Eur Arch Psychiatry Clin Neurosci ; 272(3): 437-448, 2022 Apr.
Article em En | MEDLINE | ID: mdl-34401957
ABSTRACT
Schizophrenia is characterised by cognitive impairments that are already present during early stages, including in the clinical high-risk for psychosis (CHR-P) state and first-episode psychosis (FEP). Moreover, data suggest the presence of distinct cognitive subtypes during early-stage psychosis, with evidence for spared vs. impaired cognitive profiles that may be differentially associated with symptomatic and functional outcomes. Using cluster analysis, we sought to determine whether cognitive subgroups were associated with clinical and functional outcomes in CHR-P individuals. Data were available for 146 CHR-P participants of whom 122 completed a 6- and/or 12-month follow-up; 15 FEP participants; 47 participants not fulfilling CHR-P criteria (CHR-Ns); and 53 healthy controls (HCs). We performed hierarchical cluster analysis on principal components derived from neurocognitive and social cognitive measures. Within the CHR-P group, clusters were compared on clinical and functional variables and examined for associations with global functioning, persistent attenuated psychotic symptoms and transition to psychosis. Two discrete cognitive subgroups emerged across all

participants:

45.9% of CHR-P individuals were cognitively impaired compared to 93.3% of FEP, 29.8% of CHR-N and 30.2% of HC participants. Cognitively impaired CHR-P participants also had significantly poorer functioning at baseline and follow-up than their cognitively spared counterparts. Specifically, cluster membership predicted functional but not clinical outcome. Our findings support the existence of distinct cognitive subgroups in CHR-P individuals that are associated with functional outcomes, with implications for early intervention and the understanding of underlying developmental processes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Esquizofrenia / Disfunção Cognitiva Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Eur Arch Psychiatry Clin Neurosci Assunto da revista: NEUROLOGIA / PSIQUIATRIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Esquizofrenia / Disfunção Cognitiva Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Eur Arch Psychiatry Clin Neurosci Assunto da revista: NEUROLOGIA / PSIQUIATRIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido