Suppr超能文献

[tau蛋白病和α-突触核蛋白病的神经病理学以及睡眠障碍的神经解剖学:应对挑战]

[Neuropathology of tauopathies and synucleinopathies, and neuroanatomy of sleep disorders: meeting the challenge].

作者信息

Hauw J-J, Hausser-Hauw C, Duyckaerts C

机构信息

Laboratoire de Neuropathologie Raymond Escourolle, Groupe Hospitalier Pitié-Salpêtrière, Paris.

出版信息

Rev Neurol (Paris). 2003 Nov;159(11 Suppl):6S59-70.

Abstract

Abnormalities of tau and alpha-synuclein have been described in a variety of neurodegenerative diseases often associated with sleep disorders. Neuropathological descriptions concerning these diseases are rapidly expanding, and they become difficult to summarise. On the other hand, the human neuroanatomy of sleep remains an ill defined issue. Main tauopathies are Alzheimer's disease, progressive supranuclear palsy, cortico-basal degeneration, argyrophilic grain disease, Pick disease and fronto-temporal degeneration with Parkinsonism associated with chromosome 17. In contrast to Alzheimer's disease, where abnormal tau containing cells are mainly neurones, in the other disorders, both neurones and glial cells are affected. The presynaptic protein alpha-synuclein is a major constituent of Lewy-type lesions in Parkinson disease and in dementia with Lewy bodies. Alpha-synuclein is also found in neurones and glia of Multi System Atrophy. This led to group these disorders into the still ill defined group of synucleinopathies. The lesions of tauopathies and synucleinopathies are presented, and their distribution in the most common disorders is described, distinguishing when possible neuronal loss and neuropathological markers. Recent data show that their extension is far larger than previously assumed and that they involve a variety of areas possibly involved in sleep regulation. Sleep disorders have been described in various tauopathies and synucleinopathies. However, no detailed clinico-pathological reports concerning the distribution of affected and spared areas in patients studied by polysomnography are available. Furthermore, the similarities of sleep disorders associated with different diseases, the interindividual variability, the frequently associated disorders, and the difficulties in quantifying neuronal loss make any clinicopathological correlation uncertain. The knowledge of sleep neuroanatomy is mainly based on animal studies. The few data concerning the structures of human brain areas involved in sleep organisation are recalled. Several systems known to be acting in sleep physiology are usually affected by tauopathies and synucleinopathies, but the pattern of their involvement in sleep pathology remains highly conjectural. The neuropathology of sleep disorders in tauopathies and synucleinopathies is a still uncultivated field.

摘要

在多种常伴有睡眠障碍的神经退行性疾病中,已发现tau蛋白和α-突触核蛋白异常。关于这些疾病的神经病理学描述正在迅速扩展,难以进行总结。另一方面,人类睡眠的神经解剖学仍是一个定义不明确的问题。主要的tau蛋白病包括阿尔茨海默病、进行性核上性麻痹、皮质基底节变性、嗜银颗粒病、匹克病以及与17号染色体相关的帕金森病伴额颞叶变性。与阿尔茨海默病不同,在阿尔茨海默病中,含有异常tau蛋白的细胞主要是神经元,而在其他疾病中,神经元和神经胶质细胞均会受到影响。突触前蛋白α-突触核蛋白是帕金森病和路易体痴呆中路易体样病变的主要成分。在多系统萎缩的神经元和神经胶质细胞中也发现了α-突触核蛋白。这导致将这些疾病归为定义仍不明确的突触核蛋白病组。本文介绍了tau蛋白病和突触核蛋白病的病变,并描述了它们在最常见疾病中的分布,尽可能区分神经元丢失和神经病理学标志物。最近的数据表明,它们的范围比以前认为的要大得多,并且涉及可能参与睡眠调节的各种区域。在各种tau蛋白病和突触核蛋白病中均有睡眠障碍的描述。然而,尚无关于通过多导睡眠图研究的患者中受累和未受累区域分布情况的详细临床病理报告。此外,不同疾病相关睡眠障碍的相似性、个体间变异性、常伴发的疾病以及量化神经元丢失的困难使得任何临床病理相关性都不确定。睡眠神经解剖学的知识主要基于动物研究。本文回顾了关于参与睡眠组织的人类脑区结构的少量数据。已知在睡眠生理学中起作用的几个系统通常会受到tau蛋白病和突触核蛋白病的影响,但其在睡眠病理学中的受累模式仍高度推测性。tau蛋白病和突触核蛋白病中睡眠障碍的神经病理学仍是一个未开垦的领域。

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