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Cognitive motor impairments and brain structure in schizophrenia spectrum disorder patients with a history of catatonia.
Dean, Derek J; Woodward, Neil; Walther, Sebastian; McHugo, Maureen; Armstrong, Kristan; Heckers, Stephan.
Afiliação
  • Dean DJ; Department of Psychology, Vanderbilt University, Nashville, TN, USA. Electronic address: derek.dean@vanderbilt.edu.
  • Woodward N; Department of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Walther S; Translational Research Center, University Hospital of Psychiatry, University of Bern, Bern, Switzerland.
  • McHugo M; Department of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Armstrong K; Department of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Heckers S; Department of Psychiatry and Behavioral Sciences, Vanderbilt University Medical Center, Nashville, TN, USA.
Schizophr Res ; 222: 335-341, 2020 Aug.
Article em En | MEDLINE | ID: mdl-32423702
There is growing interest in understanding the behavioral and neural mechanisms of catatonia. Here, we examine cognition and brain structure in schizophrenia spectrum disorder (SSD) patients with a history of catatonia. A total of 172 subjects were selected from a data repository; these included SSD patients with (n = 43) and without (n = 43) a history of catatonia and healthy control subjects (n = 86). Cognitive functioning was assessed using the Screen for Cognitive Impairment in Psychiatry (SCIP) and brain structure was assessed using voxel-based morphometry (VBM) in the CAT12 toolbox. SSD patients with a history of catatonia showed worse performance on tests of verbal fluency and processing speed compared to SSD patients without such a history, even after controlling for current antipsychotic and benzodiazepine use. No differences were found between patients with and without a history of catatonia in terms of brain structure. Both patient groups combined showed significantly smaller grey matter volumes compared to healthy control subjects in brain regions consistent with prior studies, including the anterior cingulate, insular, temporal, and medial frontal cortices. The results highlight a cognitive-motor impairment in SSD patients with a history of catatonia. Challenges and limitations of examining brain structure in patients with a history of catatonia are discussed.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquizofrenia / Catatonia / Disfunção Cognitiva / Transtornos Motores Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquizofrenia / Catatonia / Disfunção Cognitiva / Transtornos Motores Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article