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Attenuated resting-state functional connectivity in patients with childhood- and adult-onset schizophrenia.
Watsky, Rebecca E; Gotts, Stephen J; Berman, Rebecca A; McAdams, Harrison M; Zhou, Xueping; Greenstein, Dede; Lalonde, Francois M; Gochman, Peter; Clasen, Liv S; Shora, Lorie; Ordóñez, Anna E; Gogtay, Nitin; Martin, Alex; Barch, Deanna M; Rapoport, Judith L; Liu, Siyuan.
Afiliação
  • Watsky RE; Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • Gotts SJ; Laboratory of Brain and Cognition, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • Berman RA; Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • McAdams HM; Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • Zhou X; Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • Greenstein D; Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • Lalonde FM; Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • Gochman P; Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • Clasen LS; Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • Shora L; Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • Ordóñez AE; Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • Gogtay N; Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • Martin A; Laboratory of Brain and Cognition, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • Barch DM; Departments of Psychology, Psychiatry and Radiology, Washington University in St. Louis, One Brookings Drive, St. Louis, MO 63130, USA.
  • Rapoport JL; Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA.
  • Liu S; Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Building 10, Bethesda, MD 20892, USA. Electronic address: siyuan.liu@nih.gov.
Schizophr Res ; 197: 219-225, 2018 07.
Article em En | MEDLINE | ID: mdl-29310911
BACKGROUND: Childhood-onset schizophrenia (COS) is a rare, severe form of the adult-onset disorder (AOS). Our previous resting-state fMRI study identified attenuated functional connectivity in COS compared with controls. Here, we ask whether COS and AOS patients and their siblings exhibit similar abnormalities of functional connectivity. METHODS: A whole-brain, data-driven approach was used to assess resting-state functional connectivity differences in COS (patients/siblings/controls, n: 26/28/33) and AOS (n: 19/28/30). There were no significant differences in age, sex, or head motion across groups in each dataset and as designed, the COS dataset has a significantly lower age than the AOS. RESULTS: Both COS and AOS patients showed decreased functional connectivity relative to controls among a wide set of brain regions (P<0.05, corrected), but their siblings did not. Decreased connectivity in COS and AOS patients showed no amplitude differences and was not modulated by age-at-onset or medication doses. Cluster analysis revealed that these regions fell into two large-scale networks: one sensorimotor network and one centered on default-mode network regions, but including higher-order cognitive areas only in COS. Decreased connectivity between these two networks was notable (P<0.05, corrected) for both patient groups. CONCLUSIONS: A shared pattern of attenuated functional connectivity was found in COS and AOS, supporting the continuity of childhood-onset and adult-onset schizophrenia. Connections were altered between sensorimotor areas and default-mode areas in both COS and AOS, suggesting potential abnormalities in processes of self-monitoring and sensory prediction. The absence of substantial dysconnectivity in siblings indicates that attenuation is state-related.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esquizofrenia / Córtex Cerebral / Conectoma / Rede Nervosa Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Revista: Schizophr Res Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esquizofrenia / Córtex Cerebral / Conectoma / Rede Nervosa Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Revista: Schizophr Res Ano de publicação: 2018 Tipo de documento: Article