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Subcortical and cortical morphological anomalies as an endophenotype in obsessive-compulsive disorder.
Shaw, P; Sharp, W; Sudre, G; Wharton, A; Greenstein, D; Raznahan, A; Evans, A; Chakravarty, M M; Lerch, J P; Rapoport, J.
Afiliação
  • Shaw P; 1] Section on Neurobehavioral Clinical Research, Social and Behavioral Research Branch, National Human Genome Research Institute,Bethesda, MD, USA [2] Intramural Program of the National Institute of Mental Health, Bethesda, MD, USA.
  • Sharp W; Intramural Program of the National Institute of Mental Health, Bethesda, MD, USA.
  • Sudre G; Section on Neurobehavioral Clinical Research, Social and Behavioral Research Branch, National Human Genome Research Institute,Bethesda, MD, USA.
  • Wharton A; Section on Neurobehavioral Clinical Research, Social and Behavioral Research Branch, National Human Genome Research Institute,Bethesda, MD, USA.
  • Greenstein D; Intramural Program of the National Institute of Mental Health, Bethesda, MD, USA.
  • Raznahan A; Intramural Program of the National Institute of Mental Health, Bethesda, MD, USA.
  • Evans A; Brain Imaging Centre, Montreal Neuroimaging Institute and Hospital, McGill University, Montreal, QC, Canada.
  • Chakravarty MM; 1] Kimel Family Imaging-Genetics Research Laboratory, Research Imaging Centre, Centre for Addiction and Mental Health, Toronto, ON, Canada [2] Department of Psychiatry and Institute for Biomaterials and Biomedical Engineering, University of Toronto, Toronto, ON, Canada.
  • Lerch JP; 1] Program in Neuroscience and Mental Health, The Hospital for Sick Children, Toronto, ON, Canada [2] Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
  • Rapoport J; Intramural Program of the National Institute of Mental Health, Bethesda, MD, USA.
Mol Psychiatry ; 20(2): 224-31, 2015 Feb.
Article em En | MEDLINE | ID: mdl-24514568
ABSTRACT
Endophentoypes, quantifiable traits lying on the causal chain between a clinical phenotype and etiology, can be used to accelerate genomic discovery in obsessive-compulsive disorder (OCD). Here we identify the neuroanatomic changes that are shared by 22 OCD adult and adolescent patients and 25 of their unaffected siblings who are at genetic risk for the disorder. Comparisons were made against 47 age and sex matched healthy controls. We defined the surface morphology of the striatum, globus pallidus and thalamus, and thickness of the cerebral cortex. Patients with OCD show significant surface expansion compared with healthy controls, following adjustment for multiple comparisons, in interconnected regions of the caudate, thalamus and right orbitofrontal cortex. Their unaffected siblings show similar, significant expansion, most marked in the ventromedial caudate bilaterally, the right pulvinar thalamic nucleus and the right orbitofrontal cortex. These regions define a network that has been consistently implicated in OCD. In addition, both patients with OCD and unaffected siblings showed similar increased thickness of the right precuneus, which receives rich input from the thalamic pulvinar nuclei and the left medial temporal cortex. Anatomic change within the orbitofrontostriatal and posterior brain circuitry thus emerges as a promising endophenotype for OCD.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article