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Functional Connectivity Networks in Asymptomatic and Symptomatic DYT1 Carriers.
Premi, Enrico; Diano, Matteo; Gazzina, Stefano; Cauda, Franco; Gualeni, Vera; Tinazzi, Michele; Fiorio, Mirta; Liberini, Paolo; Lazzarini, Clara; Archetti, Silvana; Biasiotto, Giorgio; Turla, Marinella; Bertasi, Valeria; Cotelli, Maria; Gasparotti, Roberto; Padovani, Alessandro; Borroni, Barbara.
Afiliación
  • Premi E; Centre for Ageing Brain and Neurodegenerative Disorders, Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
  • Diano M; GCS fMRI Koelliker Hospital, Turin, Italy.
  • Gazzina S; Department of Psychology, University of Turin, Turin, Italy.
  • Cauda F; Centre for Ageing Brain and Neurodegenerative Disorders, Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
  • Gualeni V; GCS fMRI Koelliker Hospital, Turin, Italy.
  • Tinazzi M; Department of Psychology, University of Turin, Turin, Italy.
  • Fiorio M; Centre for Ageing Brain and Neurodegenerative Disorders, Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
  • Liberini P; Department of Neurological and Movement Sciences, University of Verona, Verona, Italy.
  • Lazzarini C; Department of Neurological and Movement Sciences, University of Verona, Verona, Italy.
  • Archetti S; Centre for Ageing Brain and Neurodegenerative Disorders, Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.
  • Biasiotto G; Neurophysiology Department, University Hospital "Spedali Civili,", Brescia, Italy.
  • Turla M; Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
  • Bertasi V; Biotechnology Laboratory, Department of Diagnostic, "Spedali Civili" Hospital, Brescia, Italy.
  • Cotelli M; Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
  • Gasparotti R; Biotechnology Laboratory, Department of Diagnostic, "Spedali Civili" Hospital, Brescia, Italy.
  • Padovani A; Neurology Unit, Valle Camonica Hospital, Brescia, Italy.
  • Borroni B; Neurology Unit, Valle Camonica Hospital, Brescia, Italy.
Mov Disord ; 31(11): 1739-1743, 2016 11.
Article en En | MEDLINE | ID: mdl-27453152
BACKGROUND: DYT1 mutation is characterized by focal to generalized dystonia and incomplete penetrance. To explore the complex perturbations in the different neural networks and the mutual interactions among them, we studied symptomatic and asymptomatic DTY1 mutation carriers by resting-state functional MRI. METHODS: A total of 7 symptomatic DYT1, 10 asymptomatic DYT1, and 26 healthy controls were considered. Resting-state functional MRI (Oxford Centre for Functional MRI of the Brain) [FMRIB] Software Library) (FSL) MELODIC, dual regression, (as a toolbox of FSL, with Nets is referred to "networks") (FSLNets) (http://fsl.fmrib.ox.ac.uk/fsl/fslwiki/FSLNets) was performed on 9 resting-state neural networks. RESULTS: DYT1 mutation signature (symptomatic DYT1 and asymptomatic DYT1) was characterized by increased connectivity in the dorsal attention network and in the left fronto-parietal network. Functional correlates of symptomatic DYT1 patients (symptomatic DYT1 vs healthy controls) showed increased connectivity in the sensorimotor network. DISCUSSION: This study argues that DYT1 dystonia is a network disorder, with crucial nodes in sensory-motor integration of posterior parietal structures. A better characterization of cortical networks involved in dystonia is crucial for possible neurophysiological therapeutic interventions. © 2016 International Parkinson and Movement Disorder Society.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Corteza Cerebral / Chaperonas Moleculares / Distonía Muscular Deformante / Conectoma Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Corteza Cerebral / Chaperonas Moleculares / Distonía Muscular Deformante / Conectoma Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Italia