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阿尔茨海默病及其他神经退行性痴呆合并症:临床与神经病理学概述。

Alzheimer's disease and other neurodegenerative dementias in comorbidity: A clinical and neuropathological overview.

机构信息

Department of Pathology and Molecular Medicine, Third Faculty of Medicine, Charles University, Thomayer Hospital, Prague, Czech Republic; Department of Pathology, First Faculty of Medicine, Charles University, General University Hospital, Prague, Czech Republic.

Department of Neurology and Centre of Clinical Neuroscience, First Faculty of Medicine, Charles University, General University Hospital, Prague, Czech Republic.

出版信息

Clin Biochem. 2019 Nov;73:26-31. doi: 10.1016/j.clinbiochem.2019.08.005. Epub 2019 Aug 7.

Abstract

Neuropathological diagnostic criteria of neurodegenerative disorders are based on the presence of specific inclusions in a specific area of brain tissue that correlate with clinical manifestations. Concomitant neurodegenerative disorders correspond to a combination of two (or more) different fully developed diseases in the same patient. Concomitant neurodegenerative pathology represents the presence of definite neurodegeneration and deposits of pathological proteins specific for another disease, which is not, however, fully developed. Very frequent overlaps include Alzheimer's disease and alpha-synuclein inclusions. Nevertheless, careful neuropathological investigations reveal an increasing frequency of different co-pathologies in examined brains. In Alzheimer's disease, protein TDP-43 may co-aggregate, but it is not clear whether this is atypical isolated Alzheimer's disease or overlap of Alzheimer's disease with early frontotemporal lobar degeneration. Comorbidities of Alzheimer's disease and tauopathies are relatively rare. A combination of vascular pathology with primary neurodegeneration (mostly Alzheimer's disease or dementia with Lewy bodies) is historically called mixed dementia. Overlap of different neuropathologically confirmed neurodegenerations could lead to atypical and unusual clinical presentations and may be responsible for faster disease progression. Several CSF biomarkers have been evaluated for their utility in diagnostic processes in different neurodegenerative dementias; however, evidence regarding their role in neurodegenerative overlaps is still limited.

摘要

神经退行性疾病的神经病理学诊断标准基于在脑组织的特定区域存在特定包含物,这些包含物与临床表现相关。同时发生的神经退行性疾病对应于同一患者中两种(或更多种)完全不同的疾病的组合。同时发生的神经退行性病变代表明确的神经退行性变和另一种疾病的病理性蛋白沉积的存在,但该疾病尚未完全发展。非常常见的重叠包括阿尔茨海默病和α-突触核蛋白包涵体。然而,仔细的神经病理学研究揭示了在检查的大脑中不同共病的频率不断增加。在阿尔茨海默病中,蛋白 TDP-43 可能会共同聚集,但尚不清楚这是不典型的孤立性阿尔茨海默病还是阿尔茨海默病与早期额颞叶变性的重叠。阿尔茨海默病和 tau 病的合并症相对较少。血管病理学与原发性神经退行性变(主要是阿尔茨海默病或路易体痴呆)的组合在历史上称为混合性痴呆。不同神经病理学证实的神经退行性变的重叠可能导致非典型和不寻常的临床表现,并可能导致疾病更快进展。已经评估了几种 CSF 生物标志物在不同神经退行性痴呆症的诊断过程中的效用;然而,关于它们在神经退行性重叠中的作用的证据仍然有限。

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