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Altered Structural Brain Networks in Tuberous Sclerosis Complex.
Im, Kiho; Ahtam, Banu; Haehn, Daniel; Peters, Jurriaan M; Warfield, Simon K; Sahin, Mustafa; Ellen Grant, P.
Afiliación
  • Im K; Division of Newborn Medicine Fetal Neonatal Neuroimaging and Developmental Science Center.
  • Ahtam B; Division of Newborn Medicine Fetal Neonatal Neuroimaging and Developmental Science Center.
  • Haehn D; Fetal Neonatal Neuroimaging and Developmental Science Center Department of Radiology.
  • Peters JM; Department of Neurology Computational Radiology Laboratory, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
  • Warfield SK; Department of Radiology Computational Radiology Laboratory, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
  • Sahin M; Department of Neurology.
  • Ellen Grant P; Division of Newborn Medicine Fetal Neonatal Neuroimaging and Developmental Science Center Department of Radiology Department of Radiology, Massachusetts General Hospital, Athinoula A. Martinos Center for Biomedical Imaging, Charlestown, MA 02119, USA.
Cereb Cortex ; 26(5): 2046-58, 2016 May.
Article en En | MEDLINE | ID: mdl-25750257
Tuberous sclerosis complex (TSC) is characterized by benign hamartomas in multiple organs including the brain and its clinical phenotypes may be associated with abnormal neural connections. We aimed to provide the first detailed findings on disrupted structural brain networks in TSC patients. Structural whole-brain connectivity maps were constructed using structural and diffusion MRI in 20 TSC (age range: 3-24 years) and 20 typically developing (TD; 3-23 years) subjects. We assessed global (short- and long-association and interhemispheric fibers) and regional white matter connectivity, and performed graph theoretical analysis using gyral pattern- and atlas-based node parcellations. Significantly higher mean diffusivity (MD) was shown in TSC patients than in TD controls throughout the whole brain and positively correlated with tuber load severity. A significant increase in MD was mainly influenced by an increase in radial diffusivity. Furthermore, interhemispheric connectivity was particularly reduced in TSC, which leads to increased network segregation within hemispheres. TSC patients with developmental delay (DD) showed significantly higher MD than those without DD primarily in intrahemispheric connections. Our analysis allows non-biased determination of differential white matter involvement, which may provide better measures of "lesion load" and lead to a better understanding of disease mechanisms.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esclerosis Tuberosa / Encéfalo / Neoplasias Encefálicas Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Cereb Cortex Asunto de la revista: CEREBRO Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esclerosis Tuberosa / Encéfalo / Neoplasias Encefálicas Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Cereb Cortex Asunto de la revista: CEREBRO Año: 2016 Tipo del documento: Article