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脑淀粉样血管病是一种由新型早老素1突变导致的阿尔茨海默病致病性病变。

Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation.

作者信息

Dermaut B, Kumar-Singh S, De Jonghe C, Cruts M, Löfgren A, Lübke U, Cras P, Dom R, De Deyn P P, Martin J J, Van Broeckhoven C

机构信息

Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, University of Antwerp, Antwerpen, Belgium.

出版信息

Brain. 2001 Dec;124(Pt 12):2383-92. doi: 10.1093/brain/124.12.2383.

Abstract

The dense-cored plaques are considered the pathogenic type of amyloid deposition in Alzheimer's disease brains because of their predominant association with dystrophic neurites. Nevertheless, in > 90% of cases of Alzheimer's disease amyloid is also deposited in cerebral blood vessel walls (congophilic amyloid angiopathy; CAA) but its role in Alzheimer's disease pathogenesis remains enigmatic. Here, we report a family (family GB) in which early-onset Alzheimer's disease was caused by a novel presenilin 1 mutation (L282V). This was unusually severe CAA reminiscent of the Flemish amyloid precursor protein (A692G) mutation we reported previously, which causes Alzheimer's disease and/or cerebral haemorrhages. In family GB, however, the disease presented as typical progressive Alzheimer's disease in the absence of strokes or stroke-like episodes. Similarly, neuroimaging studies and neuropathological examination favoured a degenerative over a vascular dementia. Interestingly, an immunohistochemical study revealed that, similar to causing dense-cored amyloid plaques, CAA also appeared capable of instigating a strong local dystrophic and inflammatory reaction. This was suggested by the observed neuronal loss, the presence of tau- and ubiquitin-positive neurites, micro- and astrogliosis, and complement activation. Together, these data suggest that, like the dense-cored neuritic plaques, CAA might represent a pathogenic lesion that contributes significantly to the progressive neurodegeneration that occurs in Alzheimer's disease.

摘要

致密核心斑块被认为是阿尔茨海默病大脑中淀粉样蛋白沉积的致病类型,因为它们主要与营养不良性神经突相关。然而,在超过90%的阿尔茨海默病病例中,淀粉样蛋白也沉积在脑血管壁(嗜刚果红性淀粉样血管病;CAA),但其在阿尔茨海默病发病机制中的作用仍然不明。在此,我们报告一个家族(GB家族),其中早发性阿尔茨海默病由一种新的早老素1突变(L282V)引起。这是异常严重的CAA,让人联想到我们之前报道的佛兰芒淀粉样前体蛋白(A692G)突变,该突变会导致阿尔茨海默病和/或脑出血。然而,在GB家族中,该疾病表现为典型的进行性阿尔茨海默病,无中风或类中风发作。同样,神经影像学研究和神经病理学检查倾向于诊断为退行性而非血管性痴呆。有趣的是,一项免疫组织化学研究显示,与导致致密核心淀粉样斑块一样,CAA似乎也能够引发强烈的局部营养不良和炎症反应。这一点从观察到的神经元丢失、tau和泛素阳性神经突的存在、微胶质细胞增生和星形胶质细胞增生以及补体激活得到提示。总之,这些数据表明,与致密核心神经炎性斑块一样,CAA可能代表一种致病病变,对阿尔茨海默病中发生的进行性神经退行性变有显著贡献。

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