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阿尔茨海默病,包括局灶性表现。

Alzheimer's Disease Including Focal Presentations.

作者信息

Villain Nicolas, Dubois Bruno

机构信息

Alzheimer Precision Medicine, Sorbonne Université, Paris, France.

Department of Neurology, Institute of Memory and Alzheimer's Disease, Assistance Publique - Hopitaux de Paris, Pitié-Salpêtrière Hospital, Paris, France.

出版信息

Semin Neurol. 2019 Apr;39(2):213-226. doi: 10.1055/s-0039-1681041. Epub 2019 Mar 29.

Abstract

Alzheimer's disease (AD) is the commonest neurodegenerative disease and the most frequent cause of dementia. It affects 30 million people worldwide. Current research criteria focus on biomarkers' status for amyloid and tau using positron emission tomography and cerebrospinal fluid analysis, independent of clinical status. Current epidemiological data, which mostly rely on biomarker-undetermined AD cases, have highlighted ApoE4 and age as the main risk factors. Rare autosomal dominant mutations also account for a small fraction of early-onset AD. The main clinical phenotype at presentation is the amnestic phenotype targeting episodic memory. This is followed by rarer phenotypes such as posterior cortical atrophy, logopenic variant of primary progressive aphasia, frontal variant AD, corticobasal syndrome, and other even rarer presentations mimicking language variants of frontotemporal dementia. Main differential diagnoses include hippocampal sclerosis with TDP-43, primary age-related tauopathy, argyrophilic grain disease, frontotemporal lobar degeneration, Lewy body disease, chronic traumatic encephalopathy as well as nondegenerative disorders such as cerebrovascular disease, chronic alcohol consumption, limbic encephalitis, medial temporal lobe epilepsy, and others. Co-occurrence of AD pathology with other neurodegenerative and vascular diseases is common and increases with age. This presents a challenge in current clinical practice due to a lack of reliable biomarkers for non-AD neurodegenerative diseases.

摘要

阿尔茨海默病(AD)是最常见的神经退行性疾病,也是痴呆最常见的病因。全球有3000万人受其影响。当前的研究标准聚焦于使用正电子发射断层扫描和脑脊液分析来检测淀粉样蛋白和tau蛋白的生物标志物状态,而不考虑临床状态。目前的流行病学数据大多依赖生物标志物未确定的AD病例,这些数据凸显了载脂蛋白E4(ApoE4)和年龄是主要风险因素。罕见的常染色体显性突变也占早发性AD的一小部分。发病时的主要临床表型是以情景记忆为目标的遗忘型表型。其次是较罕见的表型,如后部皮质萎缩、原发性进行性失语的语法缺失型变体、额叶变体AD、皮质基底节综合征,以及其他模仿额颞叶痴呆语言变体的更罕见表现。主要鉴别诊断包括伴有TDP - 43的海马硬化、原发性年龄相关tau病、嗜银颗粒病、额颞叶变性、路易体病、慢性创伤性脑病,以及非退行性疾病,如脑血管疾病、长期酗酒、边缘性脑炎、内侧颞叶癫痫等。AD病理与其他神经退行性和血管疾病的共现很常见,且随年龄增长而增加。由于缺乏针对非AD神经退行性疾病的可靠生物标志物,这给当前临床实践带来了挑战。

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