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. 2019 Mar;40(3):529-533.
doi: 10.1007/s10072-018-3686-6. Epub 2018 Dec 18.

Cortical degeneration in chronic traumatic encephalopathy and Alzheimer's disease neuropathologic change

Affiliations

Cortical degeneration in chronic traumatic encephalopathy and Alzheimer's disease neuropathologic change

Richard A Armstrong et al. Neurol Sci. 2019 Mar.

Abstract

Objectives: An observational study to compare the laminar distributions in frontal and temporal cortex of the tau-immunoreactive pathologies in chronic traumatic encephalopathy (CTE) and Alzheimer's disease neuropathologic change (ADNC).

Patients: Post-mortem material of (1) four cases of CTE without ADNC, (2) seven cases of CTE with ADNC (CTE/ADNC), and (3) seven cases of ADNC alone.

Results: In CTE and CTE/ADNC, neurofibrillary tangles (NFT), neuropil threads (NT), and dot-like grains (DLG) were distributed either in upper cortex or across all layers. Low densities of astrocytic tangles (AT) and abnormally enlarged neurons (EN) were not localized to any specific layer. Surviving neurons exhibited peaks of density in both upper and lower cortex, and vacuole density was greatest in superficial layers. In ADNC, neuritic plaques (NP) were more frequent, AT rare, NFT and NT were more widely distributed, NT affected lower layers more frequently, and surviving neurons were less frequently bimodal than in CTE and CTE/ADNC.

Conclusion: Tau pathology in CTE and CTE/ADNC consistently affected the upper cortex but was more widely distributed in ADNC. The presence of CTE may encourage the development of ADNC pathology later in the course of the disease.

Keywords: Alzheimer’s disease neuropathologic change (ADNC); Chronic traumatic encephalopathy (CTE); Laminar distribution; Tauopathy.

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Conflict of interest statement

These studies were approved by the local Institute Review Board of Boston University and were carried out according to the 1995 Declaration of Helsinki (as modified in Edinburgh, 2000).

Figures

Fig. 1
Fig. 1
Quantitative analysis of the laminar distribution of the tau-immunoreactive pathology at the temporal pole (TP) in a case of chronic traumatic encephalopathy (CTE) with Alzheimer disease neuropathologic change (ADNC). Curves of best fit: NFT: third-order polynomial (r = 0.70, P < 0.01), NT: third-order polynomial (r = 0.63, P < 0.01), DLG: fourth-order polynomial (r = 0.75, P < 0.01)

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