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五种神经退行性疾病中β-淀粉样蛋白沉积物的皮质层状分布。

Cortical laminar distribution of β-amyloid deposits in five neurodegenerative disorders.

机构信息

Vision Sciences, Aston University, Birmingham, United Kingdom.

出版信息

Folia Neuropathol. 2020;58(1):1-9. doi: 10.5114/fn.2020.94001.

Abstract

Alzheimer's disease neuropathologic change (ADNC) in the form of β-amyloid (Aβ) deposits occurs not only in Alzheimer's disease (AD) and Down's syndrome (DS) but also as a 'co-pathology' in several disorders including dementia with Lewy bodies (DLB), corticobasal degeneration (CBD), and chronic traumatic encephalopathy (CTE). To determine whether cortical laminar degeneration, as measured by Aβ deposition, is similar in different disorders, changes in density of the diffuse, primitive, and classic morphological subtypes of Aβ deposit were studied across all cortical layers in the frontal and temporal cortex in AD, DS, DLB, CBD, and CTE using quantitative analysis and polynomial curve fitting. In AD, CTE, and DLB, the diffuse Aβ deposits were distributed most frequently in the upper cortical layers, distribution being more variable in DS and CBD. In all disorders, the primitive Aβ deposits were distributed primarily in the upper layers, but in DLB, a bimodal distribution with peaks of density in upper and lower layers was evident in some gyri. The distribution of the classic deposits varied both within and among disorders. The many similarities in laminar distribution among disorders suggest common patterns of cortical degeneration. Where differences occur, they may reflect variations in the 'prion-like' propagation of Aβ along anatomical pathways in the different disorders.

摘要

阿尔茨海默病(AD)神经病理改变(ADNC)的形式β-淀粉样蛋白(Aβ)沉积不仅发生在 AD 和唐氏综合征(DS)中,也作为几种疾病的“共病”存在,包括路易体痴呆(DLB)、皮质基底节变性(CBD)和慢性创伤性脑病(CTE)。为了确定 Aβ沉积所测量的皮质层状变性在不同疾病中是否相似,研究人员使用定量分析和多项式曲线拟合,研究了 AD、DS、DLB、CBD 和 CTE 中额颞叶皮质所有皮层层中弥漫性、原始和经典形态亚型 Aβ沉积密度的变化。在 AD、CTE 和 DLB 中,弥漫性 Aβ沉积最常分布在上皮层,DS 和 CBD 中的分布更具变异性。在所有疾病中,原始 Aβ沉积主要分布在上层,但在一些脑回中,DLB 中存在双峰分布,密度峰值在上层和下层。经典沉积的分布在疾病内和疾病间均存在差异。疾病间层状分布的许多相似性表明存在共同的皮质退化模式。出现差异的地方,可能反映了 Aβ 在不同疾病中沿解剖途径“类朊病毒样”传播的差异。

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