Current concepts and molecular pathology of neurodegenerative diseases.

IF 3.6 3区 医学 Q1 PATHOLOGY Pathology Pub Date : 2024-11-14 DOI:10.1016/j.pathol.2024.10.006
Shelley L Forrest, Gabor G Kovacs
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Abstract

Neurodegenerative diseases are a pathologically, clinically and genetically diverse group of diseases characterised by selective dysfunction, loss of synaptic connectivity and neurodegeneration, ​and are associated with the deposition of misfolded proteins in neurons and/or glia. Molecular studies have highlighted the role of conformationally altered proteins in the pathogenesis of neurodegenerative diseases and have paved the way for developing disease-specific biomarkers that capture and differentiate the main type/s of protein abnormality responsible for neurodegenerative diseases, some of which are currently used in clinical practice. These proteins follow sequential patterns of anatomical involvement and disease spread in the brain and may also be detected in peripheral organs. Recent studies suggest that glia are likely to have an important role in pathological spread throughout the brain and even follow distinct progression patterns from neurons. In addition to morphological and molecular approaches to the classification of these disorders, a further new stratification level incorporates the structure of protein filaments detected by cryogenic electron microscopy. Rather than occurring in isolation, combined deposition of tau, amyloid-β, α-synuclein and TDP-43 are frequently observed in neurodegenerative diseases and in the ageing brain. These can be overlooked, and their clinicopathological relevance is difficult to interpret. This review provides an overview of disease pathogenesis and diagnostic implications, recent molecular and ultrastructural classification of neurodegenerative diseases, how to approach ageing-related and mixed pathologies, ​and the importance of the protein-based classification system for practising neuropathologists and clinicians. This review also informs general pathologists about the relevance of ongoing full body autopsy studies to understand the spectrum and pathogenesis of neurodegenerative diseases.

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神经退行性疾病是一组在病理、临床和遗传上多种多样的疾病,其特征是选择性功能障碍、突触连接丧失和神经退行性变,并与神经元和/或神经胶质细胞中错误折叠蛋白的沉积有关。分子研究强调了构象改变的蛋白质在神经退行性疾病发病机制中的作用,并为开发疾病特异性生物标志物铺平了道路,这些生物标志物可捕捉和区分导致神经退行性疾病的主要蛋白质异常类型,其中一些目前已用于临床实践。这些蛋白质在大脑中按照解剖学受累和疾病扩散的顺序排列,也可在外周器官中检测到。最近的研究表明,神经胶质细胞可能在整个大脑的病理扩散中扮演重要角色,甚至遵循与神经元不同的进展模式。除了用形态学和分子方法对这些疾病进行分类外,还有一种新的分层方法,即用低温电子显微镜检测蛋白丝的结构。在神经退行性疾病和老化的大脑中,经常可以观察到 tau、淀粉样蛋白-β、α-突触核蛋白和 TDP-43 的联合沉积,而不是单独出现。这些蛋白可能被忽视,其临床病理学相关性也难以解释。本综述概述了疾病的发病机制和诊断意义、神经退行性疾病的最新分子和超微结构分类、如何处理与衰老相关的病变和混合病变,以及基于蛋白质的分类系统对神经病理学家和临床医生的重要性。这篇综述还向普通病理学家介绍了正在进行的全身尸检研究对了解神经退行性疾病谱和发病机制的意义。
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来源期刊
Pathology
Pathology 医学-病理学
CiteScore
6.50
自引率
2.20%
发文量
459
审稿时长
54 days
期刊介绍: Published by Elsevier from 2016 Pathology is the official journal of the Royal College of Pathologists of Australasia (RCPA). It is committed to publishing peer-reviewed, original articles related to the science of pathology in its broadest sense, including anatomical pathology, chemical pathology and biochemistry, cytopathology, experimental pathology, forensic pathology and morbid anatomy, genetics, haematology, immunology and immunopathology, microbiology and molecular pathology.
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