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Three dimensional evaluation of cerebrovascular density and branching in chronic traumatic encephalopathy.
Rosen, Grace; Kirsch, Daniel; Horowitz, Sarah; Cherry, Jonathan D; Nicks, Raymond; Kelley, Hunter; Uretsky, Madeline; Dell'Aquila, Kevin; Mathias, Rebecca; Cormier, Kerry A; Kubilus, Caroline A; Mez, Jesse; Tripodis, Yorghos; Stein, Thor D; Alvarez, Victor E; Alosco, Michael L; McKee, Ann C; Huber, Bertrand R.
Afiliação
  • Rosen G; VA Boston Healthcare System, US Department of Veterans Affairs, 150 S Huntington Avenue, Boston, MA, 02130, USA.
  • Kirsch D; National Center for PTSD, US Department of Veterans Affairs, Boston, MA, USA.
  • Horowitz S; Department of Pathology and Laboratory Medicine, Boston University Chobanian & Avedisian School of Medicine, Boston, USA.
  • Cherry JD; VA Boston Healthcare System, US Department of Veterans Affairs, 150 S Huntington Avenue, Boston, MA, 02130, USA.
  • Nicks R; National Center for PTSD, US Department of Veterans Affairs, Boston, MA, USA.
  • Kelley H; Department of Pathology and Laboratory Medicine, Boston University Chobanian & Avedisian School of Medicine, Boston, USA.
  • Uretsky M; Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, USA.
  • Dell'Aquila K; Boston University Alzheimer's Disease Research Center and Boston University CTE Center, Boston, USA.
  • Mathias R; Boston University Alzheimer's Disease Research Center and Boston University CTE Center, Boston, USA.
  • Cormier KA; Boston University Alzheimer's Disease Research Center and Boston University CTE Center, Boston, USA.
  • Kubilus CA; Boston University Alzheimer's Disease Research Center and Boston University CTE Center, Boston, USA.
  • Mez J; Boston University Alzheimer's Disease Research Center and Boston University CTE Center, Boston, USA.
  • Tripodis Y; VA Boston Healthcare System, US Department of Veterans Affairs, 150 S Huntington Avenue, Boston, MA, 02130, USA.
  • Stein TD; Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, USA.
  • Alvarez VE; VA Boston Healthcare System, US Department of Veterans Affairs, 150 S Huntington Avenue, Boston, MA, 02130, USA.
  • Alosco ML; Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, USA.
  • McKee AC; Boston University Alzheimer's Disease Research Center and Boston University CTE Center, Boston, USA.
  • Huber BR; VA Bedford Healthcare System, US Department of Veterans Affairs, Bedford, MA, USA.
Acta Neuropathol Commun ; 11(1): 123, 2023 07 25.
Article em En | MEDLINE | ID: mdl-37491342
ABSTRACT
Chronic traumatic encephalopathy (CTE) is a neurodegenerative disease associated with exposure to repetitive head impacts (RHI) and characterized by perivascular accumulations of hyperphosphorylated tau protein (p-tau) at the depths of the cortical sulci. Studies of living athletes exposed to RHI, including concussive and nonconcussive impacts, have shown increased blood-brain barrier permeability, reduced cerebral blood flow, and alterations in vasoreactivity. Blood-brain barrier abnormalities have also been reported in individuals neuropathologically diagnosed with CTE. To further investigate the three-dimensional microvascular changes in individuals diagnosed with CTE and controls, we used SHIELD tissue processing and passive delipidation to optically clear and label blocks of postmortem human dorsolateral frontal cortex. We used fluorescent confocal microscopy to quantitate vascular branch density and fraction volume. We compared the findings in 41 male brain donors, age at death 31-89 years, mean age 64 years, including 12 donors with low CTE (McKee stage I-II), 13 with high CTE (McKee stage III-IV) to 16 age- and sex-matched non-CTE controls (7 with RHI exposure and 9 with no RHI exposure). The density of vessel branches in the gray matter sulcus was significantly greater in CTE cases than in controls. The ratios of sulcus versus gyrus vessel branch density and fraction volume were also greater in CTE than in controls and significantly above one for the CTE group. Hyperphosphorylated tau pathology density correlated with gray matter sulcus fraction volume. These findings point towards increased vascular coverage and branching in the dorsolateral frontal cortex (DLF) sulci in CTE, that correlates with p-tau pathology.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Neurodegenerativas / Encefalopatia Traumática Crônica Limite: Adult / Aged / Aged80 / Humans / Male / Middle aged Idioma: En Revista: Acta Neuropathol Commun Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Neurodegenerativas / Encefalopatia Traumática Crônica Limite: Adult / Aged / Aged80 / Humans / Male / Middle aged Idioma: En Revista: Acta Neuropathol Commun Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos