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Differential Vulnerability of Hippocampal Subfields in Primary Age-Related Tauopathy and Chronic Traumatic Encephalopathy.
Farrell, Kurt; Iida, Megan A; Cherry, Jonathan D; Casella, Alicia; Stein, Thor D; Bieniek, Kevin F; Walker, Jamie M; Richardson, Timothy E; White, Charles L; Alvarez, Victor E; Huber, Bertrand R; Dickson, Dennis W; Insausti, Ricardo; Dams-O'Connor, Kristen; McKee, Ann C; Crary, John F.
Afiliação
  • Farrell K; Departments of Pathology, Artificial Intelligence & Human Health, Nash Family Department of Neuroscience, Ronald M. Loeb Center for Alzheimer's Disease, Friedman Brain Institute, Neuropathology Brain Bank & Research CoRE, Icahn School of Medicine at Mount Sinai, New York, New York, U
  • Iida MA; Departments of Pathology, Artificial Intelligence & Human Health, Nash Family Department of Neuroscience, Ronald M. Loeb Center for Alzheimer's Disease, Friedman Brain Institute, Neuropathology Brain Bank & Research CoRE, Icahn School of Medicine at Mount Sinai, New York, New York, U
  • Cherry JD; Department of Pathology, Alzheimer's Disease and CTE Center, Boston University School of Medicine, Boston, Massachusetts, USA.
  • Casella A; Department of Veterans Affairs Medical Center, Bedford, Massachusetts, USA.
  • Stein TD; VA Boston Healthcare System, Boston, Massachusetts, USA.
  • Bieniek KF; Departments of Pathology, Artificial Intelligence & Human Health, Nash Family Department of Neuroscience, Ronald M. Loeb Center for Alzheimer's Disease, Friedman Brain Institute, Neuropathology Brain Bank & Research CoRE, Icahn School of Medicine at Mount Sinai, New York, New York, U
  • Walker JM; Department of Pathology, Alzheimer's Disease and CTE Center, Boston University School of Medicine, Boston, Massachusetts, USA.
  • Richardson TE; Department of Veterans Affairs Medical Center, Bedford, Massachusetts, USA.
  • White CL; VA Boston Healthcare System, Boston, Massachusetts, USA.
  • Alvarez VE; Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health Science Center, San Antonio, Texas, USA.
  • Huber BR; Department of Pathology, University of Texas Health Science Center, San Antonio, Texas, USA.
  • Dickson DW; Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health Science Center, San Antonio, Texas, USA.
  • Insausti R; Department of Pathology, University of Texas Health Science Center, San Antonio, Texas, USA.
  • Dams-O'Connor K; Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health Science Center, San Antonio, Texas, USA.
  • McKee AC; Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
  • Crary JF; Department of Pathology, Alzheimer's Disease and CTE Center, Boston University School of Medicine, Boston, Massachusetts, USA.
J Neuropathol Exp Neurol ; 81(10): 781-789, 2022 09 19.
Article em En | MEDLINE | ID: mdl-36004533
ABSTRACT
Chronic traumatic encephalopathy (CTE) is a tauopathy associated with repetitive mild head impacts characterized by perivascular hyperphosphorylated tau (p-tau) in neurofibrillary tangles (NFTs) and neurites in the depths of the neocortical sulci. In moderate to advanced CTE, NFTs accumulate in the hippocampus, potentially overlapping neuroanatomically with primary age-related tauopathy (PART), an age-related tauopathy characterized by Alzheimer disease-like tau pathology in the hippocampus devoid of amyloid plaques. We measured p-tau burden using positive-pixel counts on immunohistochemically stained and neuroanatomically segmented hippocampal tissue. Subjects with CTE had a higher total p-tau burden than PART subjects in all sectors (p = 0.005). Within groups, PART had significantly higher total p-tau burden in CA1/subiculum compared to CA3 (p = 0.02) and CA4 (p = 0.01) and total p-tau burden in CA2 trended higher than CA4 (p = 0.06). In CTE, total p-tau burden in CA1/subiculum was significantly higher than in the dentate gyrus; and CA2 also trended higher than dentate gyrus (p = 0.01, p = 0.06). When controlling for p-tau burden across the entire hippocampus, CA3 and CA4 had significantly higher p-tau burden in CTE than PART (p < 0.0001). These data demonstrate differences in hippocampal p-tau burden and regional distribution in CTE compared to PART that might be helpful in differential diagnosis and reveal insights into disease pathogenesis.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tauopatias / Encefalopatia Traumática Crônica Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tauopatias / Encefalopatia Traumática Crônica Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article