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本文引用的文献

1
"New Old Pathologies": AD, PART, and Cerebral Age-Related TDP-43 With Sclerosis (CARTS).“新的旧病理学”:阿尔茨海默病、进行性核上性麻痹以及伴有脑硬化的年龄相关性脑TDP-43(CARTS)
J Neuropathol Exp Neurol. 2016 Jun;75(6):482-98. doi: 10.1093/jnen/nlw033. Epub 2016 May 21.
2
Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes.额颞叶变性综合征的患病率、特征及生存率
Neurology. 2016 May 3;86(18):1736-43. doi: 10.1212/WNL.0000000000002638. Epub 2016 Apr 1.
3
Hippocampal Sclerosis but Not Normal Aging or Alzheimer Disease Is Associated With TDP-43 Pathology in the Basal Forebrain of Aged Persons.海马硬化而非正常衰老或阿尔茨海默病与老年人基底前脑的TDP-43病理学相关。
J Neuropathol Exp Neurol. 2016 May;75(5):397-407. doi: 10.1093/jnen/nlw014. Epub 2016 Mar 12.
4
Brain pathologies in extreme old age.高龄阶段的脑部病变
Neurobiol Aging. 2016 Jan;37:1-11. doi: 10.1016/j.neurobiolaging.2015.10.009. Epub 2015 Oct 19.
5
TAR DNA-binding protein 43 and pathological subtype of Alzheimer's disease impact clinical features.TAR DNA结合蛋白43与阿尔茨海默病的病理亚型影响临床特征。
Ann Neurol. 2015 Nov;78(5):697-709. doi: 10.1002/ana.24493. Epub 2015 Sep 16.
6
Hippocampal Sclerosis of Aging Can Be Segmental: Two Cases and Review of the Literature.衰老性海马硬化可呈节段性:两例报告并文献复习
J Neuropathol Exp Neurol. 2015 Jul;74(7):642-52. doi: 10.1097/NEN.0000000000000204.
7
Emerging mechanisms of molecular pathology in ALS.肌萎缩侧索硬化症分子病理学的新机制
J Clin Invest. 2015 Jun;125(6):2548. doi: 10.1172/JCI82693. Epub 2015 Jun 1.
8
PART, a distinct tauopathy, different from classical sporadic Alzheimer disease.PART,一种独特的tau蛋白病,与经典的散发性阿尔茨海默病不同。
Acta Neuropathol. 2015 May;129(5):757-62. doi: 10.1007/s00401-015-1407-2. Epub 2015 Mar 17.
9
Hippocampal sclerosis and TDP-43 pathology in aging and Alzheimer disease.衰老和阿尔茨海默病中的海马硬化与TDP-43病理改变
Ann Neurol. 2015 Jun;77(6):942-52. doi: 10.1002/ana.24388. Epub 2015 Apr 22.
10
Hippocampal sclerosis in Lewy body disease is a TDP-43 proteinopathy similar to FTLD-TDP Type A.路易体病中的海马硬化是一种与A型额颞叶痴呆-TDP相似的TDP-43蛋白病。
Acta Neuropathol. 2015 Jan;129(1):53-64. doi: 10.1007/s00401-014-1358-z. Epub 2014 Nov 4.

老年患者的海马硬化:以伴有硬化的脑年龄相关性TDP-43为重点的实例与指南

Hippocampal Sclerosis in Older Patients: Practical Examples and Guidance With a Focus on Cerebral Age-Related TDP-43 With Sclerosis.

作者信息

Cykowski Matthew D, Powell Suzanne Z, Schulz Paul E, Takei Hidehiro, Rivera Andreana L, Jackson Robert E, Roman Gustavo, Jicha Gregory A, Nelson Peter T

机构信息

From the Departments of Pathology and Genomic Medicine (Drs Cykowski, Powell, Rivera, and Takei), Internal Medicine (Dr Jackson), and Neurology (Dr Roman), Houston Methodist Hospital, Houston, Texas; the Department of Neurology, University of Texas Health Science Center at Houston (Dr Schulz); the Department of Pathology, Division of Neuropathology (Dr Nelson) and Sanders-Brown Center on Aging (Drs Jicha and Nelson), University of Kentucky, Lexington.

出版信息

Arch Pathol Lab Med. 2017 Aug;141(8):1113-1126. doi: 10.5858/arpa.2016-0469-SA. Epub 2017 May 3.

DOI:10.5858/arpa.2016-0469-SA
PMID:28467211
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5922266/
Abstract

CONTEXT

  • Autopsy studies of the older population (≥65 years of age), and particularly of the "oldest-old" (≥85 years of age), have identified a significant proportion (∼20%) of cognitively impaired patients in which hippocampal sclerosis is the major substrate of an amnestic syndrome. Hippocampal sclerosis may also be comorbid with frontotemporal lobar degeneration, Alzheimer disease, and Lewy body disease. Until recently, the terms hippocampal sclerosis of aging or hippocampal sclerosis dementia were applied in this context. Recent discoveries have prompted a conceptual expansion of hippocampal sclerosis of aging because (1) cellular inclusions of TAR DNA-binding protein 43 kDa (TDP-43) are frequent; (2) TDP-43 pathology may be found outside hippocampus; and (3) brain arteriolosclerosis is a common, possibly pathogenic, component.

OBJECTIVE

  • To aid pathologists with recent recommendations for diagnoses of common neuropathologies in older persons, particularly hippocampal sclerosis, and highlight the recent shift in diagnostic terminology from HS-aging to cerebral age-related TDP-43 with sclerosis (CARTS).

DATA SOURCES

  • Peer-reviewed literature and 5 autopsy examples that illustrate common age-related neuropathologies, including CARTS, and emphasize the importance of distinguishing CARTS from late-onset frontotemporal lobar degeneration with TDP-43 pathology and from advanced Alzheimer disease with TDP-43 pathology.

CONCLUSIONS

  • In advanced old age, the substrates of cognitive impairment are often multifactorial. This article demonstrates common and frequently comorbid neuropathologic substrates of cognitive impairment in the older population, including CARTS, to aid those practicing in this area of pathology.
摘要

背景

对老年人群(≥65岁),尤其是“高龄老人”(≥85岁)的尸检研究发现,相当一部分(约20%)认知障碍患者中,海马硬化是遗忘综合征的主要病理基础。海马硬化也可能与额颞叶变性、阿尔茨海默病和路易体病合并存在。直到最近,在这种情况下还使用衰老性海马硬化或海马硬化性痴呆等术语。最近的发现促使衰老性海马硬化的概念得到扩展,因为(1)经常出现43 kDa的TAR DNA结合蛋白(TDP-43)的细胞内包涵体;(2)TDP-43病理改变可能在海马以外的部位发现;(3)脑小动脉硬化是一种常见的、可能具有致病性的成分。

目的

帮助病理学家了解老年人常见神经病理学诊断的最新建议,特别是海马硬化,并强调诊断术语从衰老性海马硬化(HS-aging)到伴有硬化的脑年龄相关TDP-43(CARTS)的近期转变。

数据来源

同行评审文献以及5个尸检实例,这些实例说明了常见的年龄相关神经病理学,包括CARTS,并强调了区分CARTS与伴有TDP-43病理改变的晚发性额颞叶变性以及与伴有TDP-43病理改变的晚期阿尔茨海默病的重要性。

结论

在高龄阶段,认知障碍的病理基础往往是多因素的。本文展示了老年人群认知障碍常见且经常合并存在的神经病理基础,包括CARTS,以帮助从事该病理学领域工作的人员。