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

被引:10
作者
Armstrong, Richard A. [1 ]
McKee, Ann C. [2 ,3 ,4 ]
Stein, Thor D. [4 ,5 ]
Alvarez, Victor E. [3 ,5 ]
Cairns, Nigel J. [6 ,7 ]
机构
[1] Aston Univ, Vis Sci, Birmingham B4 7ET, W Midlands, England
[2] VA Boston HealthCare Syst, Boston, MA 02130 USA
[3] Boston Univ, Sch Med, Dept Neurol, Boston, MA 02118 USA
[4] Boston Univ, Sch Med, Dept Pathol & Lab Med, Boston, MA 02118 USA
[5] Dept Vet Affairs Med Ctr, Bedford, MA 01730 USA
[6] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[7] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
关键词
Chronic traumatic encephalopathy (CTE); Alzheimer's disease neuropathologic change (ADNC); Tauopathy; Laminar distribution; LAMINAR DISTRIBUTION; TEMPORAL CORTEX; DEMENTIA; SPECTRUM;
D O I
10.1007/s10072-018-3686-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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, NTT 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.
引用
收藏
页码:529 / 533
页数:5
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