Suppr超能文献

中国队列中的原发性年龄相关性tau蛋白病

Primary age-related tauopathy in a Chinese cohort.

作者信息

Wang Xin, Zhang Lei, Lu Hui, Wu Juan-Li, Liang Hua-Zheng, Liu Chong, Tao Qing-Qing, Wu Zhi-Ying, Zhu Ke-Qing

机构信息

China Brain Bank and Department of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, and Department of Neurobiology, School of Medicine, Zhejiang University, Hangzhou 310058, China.

Department of Pathology, School of Medicine, Zhejiang University, Hangzhou 310058, China.

出版信息

J Zhejiang Univ Sci B. 2020;21(3):256-262. doi: 10.1631/jzus.B1900262.

Abstract

Primary age-related tauopathy (PART) is characterized by the presence of tau neurofibrillary tangles (NFTs) which are typically observed in Alzheimer's disease (AD) brains, with few or without β-amyloid (Aβ) plaques. The diagnosis of PART can be categorized into "definite" or "possible" depending on the amount of Aβ plaques. Definite PART is diagnosed when NFTs are observed and the Braak stage is ≤IV, with Thal Aβ Phase 0 (Crary et al., 2014). According to the neuropathological diagnostic criteria, we reported that PART was frequently observed in the Chinese population according to our findings from specimens in our brain bank, with 47% of brain bank subjects meeting the criteria for PART. There is no consensus on the nature of PART. It remains to be elucidated whether PART is an early form of AD or a novel tauopathy (Duyckaerts et al., 2015; Jellinger et al., 2015).

摘要

原发性年龄相关性tau蛋白病(PART)的特征是存在tau神经原纤维缠结(NFTs),这在阿尔茨海默病(AD)脑内通常可以观察到,而β-淀粉样蛋白(Aβ)斑块很少或没有。PART的诊断可根据Aβ斑块的数量分为“确诊”或“可能”。当观察到NFTs且Braak分期≤IV期,Thal Aβ分期为0期时,可诊断为确诊PART(Crary等人,2014年)。根据神经病理学诊断标准,根据我们脑库标本的研究结果,我们报告在中国人群中经常观察到PART,脑库中47%的受试者符合PART标准。关于PART的性质尚无共识。PART是AD的早期形式还是一种新型tau蛋白病仍有待阐明(Duyckaerts等人,2015年;Jellinger等人,2015年)。

相似文献

1
Primary age-related tauopathy in a Chinese cohort.中国队列中的原发性年龄相关性tau蛋白病
J Zhejiang Univ Sci B. 2020;21(3):256-262. doi: 10.1631/jzus.B1900262.
2
Phosphorylated TDP-43 Staging of Primary Age-Related Tauopathy.磷酸化 TDP-43 对原发性年龄相关性 tau 病的分期。
Neurosci Bull. 2019 Apr;35(2):183-192. doi: 10.1007/s12264-018-0300-0. Epub 2018 Oct 31.
7
Altered Proteins in the Aging Brain.衰老大脑中的蛋白质变化
J Neuropathol Exp Neurol. 2016 Apr;75(4):316-25. doi: 10.1093/jnen/nlw002. Epub 2016 Mar 15.
8
Tauopathy: A common mechanism for neurodegeneration and brain aging.tau 病:神经退行性变和大脑老化的常见机制。
Mech Ageing Dev. 2019 Mar;178:72-79. doi: 10.1016/j.mad.2019.01.007. Epub 2019 Jan 19.

引用本文的文献

本文引用的文献

6
Phosphorylated TDP-43 Staging of Primary Age-Related Tauopathy.磷酸化 TDP-43 对原发性年龄相关性 tau 病的分期。
Neurosci Bull. 2019 Apr;35(2):183-192. doi: 10.1007/s12264-018-0300-0. Epub 2018 Oct 31.
7
Early Alzheimer-type lesions in cognitively normal subjects.认知正常个体的早期阿尔茨海默病样病变。
Neurobiol Aging. 2018 Feb;62:34-44. doi: 10.1016/j.neurobiolaging.2017.10.002. Epub 2017 Oct 13.
10
Altered Proteins in the Aging Brain.衰老大脑中的蛋白质变化
J Neuropathol Exp Neurol. 2016 Apr;75(4):316-25. doi: 10.1093/jnen/nlw002. Epub 2016 Mar 15.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验