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Evaluation of the specificity of the central diagnostic criterion for chronic traumatic encephalopathy.
Lorigan, Jennifer; Kearney, Hugh; Grimes, Bryan; Heffernan, Josephine; Beausang, Alan; Cryan, Jane; Farrell, Michael A; Brett, Francesca M.
Afiliação
  • Lorigan J; Department of Neuropathology, Beaumont Hospital, Beaumont Road, Dublin 9, Ireland. jennifermlorigan@rcsi.com.
  • Kearney H; Department of Neuropathology, Beaumont Hospital, Beaumont Road, Dublin 9, Ireland.
  • Grimes B; Department of Neuropathology, Beaumont Hospital, Beaumont Road, Dublin 9, Ireland.
  • Heffernan J; Department of Neuropathology, Beaumont Hospital, Beaumont Road, Dublin 9, Ireland.
  • Beausang A; Department of Neuropathology, Beaumont Hospital, Beaumont Road, Dublin 9, Ireland.
  • Cryan J; Department of Neuropathology, Beaumont Hospital, Beaumont Road, Dublin 9, Ireland.
  • Farrell MA; Department of Neuropathology, Beaumont Hospital, Beaumont Road, Dublin 9, Ireland.
  • Brett FM; Department of Neuropathology, Beaumont Hospital, Beaumont Road, Dublin 9, Ireland.
Ir J Med Sci ; 188(3): 993-998, 2019 Aug.
Article em En | MEDLINE | ID: mdl-30506345
ABSTRACT

INTRODUCTION:

Chronic traumatic encephalopathy (CTE) is a postmortem diagnosis. Consensus postmortem, but not antemortem, diagnostic criteria have been established. A key factor in these criteria is evidence of phosphorylated-tau (p-tau) around sulcal vessels in the cortex. However, this sign has been observed anecdotally in a diverse range of neurodegenerative diseases (NDD). We therefore hypothesise that this criterion may lack specificity.

METHODS:

To test this, we assessed patients with NDD, but no documented history of brain trauma, for sulcal p-tau. Tissue was retrieved from Dublin Brain Bank (known NDD n = 17; control with no diagnosed NDD n = 6; CTE n = 1), and slides were prepared from three sites with a predilection for trauma superior frontal gyrus, temporal pole, and superior temporal gyrus. We stained the resulting anonymised slides with both hemotoxylin and eosin (H&E) and p-tau. Three neuropathologists, blinded to the clinical history and neuropathological diagnosis in each instance, evaluated each case for sulcal p-tau. We calculated the interrater agreement, using Fleiss's kappa, and the specificity of this neuropathological sign.

RESULTS:

Sulcal p-tau was highly specific to diagnosed CTE cases (specificity 0.98), with moderate interrater agreement (κ = 0.45).

CONCLUSION:

In conclusion, therefore, we observed sulcal p-tau to be a sign highly specific to CTE when compared with NDD cases in the absence of head trauma.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Proteínas tau / Encefalopatia Traumática Crônica Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Proteínas tau / Encefalopatia Traumática Crônica Idioma: En Ano de publicação: 2019 Tipo de documento: Article