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Chronic Traumatic Encephalopathy in a Routine Neuropathology Service in Australia.

Authors :
Suter CM
Affleck AJ
Lee M
Davies D
Burns AL
Sy J
I'Ons B
Buckland ME
Source :
Journal of neuropathology and experimental neurology [J Neuropathol Exp Neurol] 2022 Sep 19; Vol. 81 (10), pp. 790-795.
Publication Year :
2022

Abstract

Chronic traumatic encephalopathy (CTE) is a neuropathological diagnosis defined by a unique pattern of hyperphosphorylated tau (p-tau) accumulation that begins in neocortical regions of the brain. It is associated with a range of neuropsychological symptoms, but a definitive diagnosis can only be made by postmortem brain examination. In 2018, we instituted CTE screening for all autopsy brains as part of our routine departmental protocol by performing p-tau immunohistochemistry on a restricted set of 3 neocortical blocks (frontal, temporal, and parietal). This strategy allowed us to identify 4 cases of low-stage CTE from 180 consecutive autopsies. Two of the 4 cases had a documented history of brain injury; for the remaining 2 cases, there was a long history of treatment-resistant tonic/clonic epilepsy suggesting that undocumented brain injuries may have occurred. Our experience indicates that 3-block CTE screening is useful in identifying CTE in routine practice. The results of this study further support the association between prior head injuries and CTE and demonstrate that, albeit uncommon, CTE does occur in the general population. Our findings suggest that p-tau screening should be routinely pursued in brain autopsy, particularly where there is a documented or likely history of traumatic brain injury.<br /> (© The Author(s) 2022. Published by Oxford University Press on behalf of American Association of Neuropathologists, Inc. All rights reserved. For permissions, please email: journals.permissions@oup.com.)

Details

Language :
English
ISSN :
1554-6578
Volume :
81
Issue :
10
Database :
MEDLINE
Journal :
Journal of neuropathology and experimental neurology
Publication Type :
Academic Journal
Accession number :
35947764
Full Text :
https://doi.org/10.1093/jnen/nlac071