Repetitive head impacts and chronic traumatic encephalopathy are associated with TDP-43 inclusions and hippocampal sclerosis

IF 9.3 1区 医学 Q1 CLINICAL NEUROLOGY
Raymond Nicks, Nathan F. Clement, Victor E. Alvarez, Yorghos Tripodis, Zachery H. Baucom, Bertrand R. Huber, Jesse Mez, Michael L. Alosco, Nurgul Aytan, Jonathan D. Cherry, Kerry A. Cormier, Carol Kubilius, Rebecca Mathias, Sarah E. Svirsky, Morgan J. Pothast, Audrey M. Hildebrandt, Jaeyoon Chung, Xudong Han, John F. Crary, Ann C. McKee, Matthew P. Frosch, Thor D. Stein
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引用次数: 6

Abstract

Hippocampal sclerosis (HS) is associated with advanced age as well as transactive response DNA-binding protein with 43 kDa (TDP-43) deposits. Both hippocampal sclerosis and TDP-43 proteinopathy have also been described in chronic traumatic encephalopathy (CTE), a neurodegenerative disease linked to exposure to repetitive head impacts (RHI). However, the prevalence of HS in CTE, the pattern of TDP-43 pathology, and associations of HS and TDP-43 with RHI are unknown. A group of participants with a history of RHI and CTE at autopsy (n = 401) as well as a group with HS-aging without CTE (n = 33) was examined to determine the prevalence of HS and TDP-43 inclusions in CTE and to compare the clinical and pathological features of HS and TDP-43 inclusions in CTE to HS-aging. In CTE, HS was present in 23.4%, and TDP-43 inclusions were present in 43.3% of participants. HS in CTE occurred at a relatively young age (mean 77.0 years) and was associated with a greater number of years of RHI than CTE without HS adjusting for age (p = 0.029). In CTE, TDP-43 inclusions occurred frequently in the frontal cortex and occurred both with and without limbic TDP-43. Additionally, structural equation modeling demonstrated that RHI exposure years were associated with hippocampal TDP-43 inclusions (p < 0.001) through increased CTE stage (p < 0.001). Overall, RHI and the development of CTE pathology may contribute to TDP-43 deposition and hippocampal sclerosis.

重复性头部撞击和慢性创伤性脑病与TDP-43内含物和海马硬化有关
海马硬化症(HS)与高龄以及具有43kDa沉积物的反式反应DNA结合蛋白(TDP-43)有关。海马硬化症和TDP-43蛋白病也被描述为慢性创伤性脑病(CTE),这是一种与反复头部撞击(RHI)有关的神经退行性疾病。然而,HS在CTE中的患病率、TDP-43的病理模式以及HS和TDP-43与RHI的关系尚不清楚。尸检时有RHI和CTE病史的一组参与者(n = 401)以及没有CTE的HS老化组(n = 33),以确定CTE中HS和TDP-43内含物的患病率,并将CTE中的HS和TDP-43内含物与HS衰老的临床和病理特征进行比较。在CTE中,23.4%的参与者存在HS,43.3%的参与者存在TDP-43内含物。CTE中的HS发生在相对年轻的年龄(平均77.0岁),并且与没有根据年龄调整HS的CTE相比,与RHI的年数更多相关(p = 0.029)。在CTE中,TDP-43包涵体经常发生在额叶皮层,并且在有或没有边缘TDP-43的情况下都发生。此外,结构方程模型显示RHI暴露年份与海马TDP-43内含物有关(p <; 0.001)通过增加的CTE阶段(p <; 0.001)。总体而言,RHI和CTE病理学的发展可能有助于TDP-43沉积和海马硬化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Neuropathologica
Acta Neuropathologica 医学-病理学
CiteScore
23.70
自引率
3.90%
发文量
118
审稿时长
4-8 weeks
期刊介绍: Acta Neuropathologica publishes top-quality papers on the pathology of neurological diseases and experimental studies on molecular and cellular mechanisms using in vitro and in vivo models, ideally validated by analysis of human tissues. The journal accepts Original Papers, Review Articles, Case Reports, and Scientific Correspondence (Letters). Manuscripts must adhere to ethical standards, including review by appropriate ethics committees for human studies and compliance with principles of laboratory animal care for animal experiments. Failure to comply may result in rejection of the manuscript, and authors are responsible for ensuring accuracy and adherence to these requirements.
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