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血液淀粉样-β寡聚体与阿尔茨海默病的神经退行性变有关。

Blood amyloid-β oligomerization associated with neurodegeneration of Alzheimer's disease.

机构信息

Department of Neurology, Chung-Ang University College of Medicine, Seoul, Republic of Korea.

Research and Development, PeopleBio Inc., Gyeonggi-do, Republic of Korea.

出版信息

Alzheimers Res Ther. 2019 May 10;11(1):40. doi: 10.1186/s13195-019-0499-7.

DOI:10.1186/s13195-019-0499-7
PMID:31077246
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6511146/
Abstract

INTRODUCTION

Oligomeric amyloid-ß is a major toxic species associated with Alzheimer's disease pathogenesis. Methods used to measure oligomeric amyloid-β in the blood have increased in number in recent years. The Multimer Detection System-Oligomeric Amyloid-β (MDS-OAβ) is a specific method to measure oligomerization tendencies in the blood. The objective of this study was to determine the association between amyloid-ß oligomerization in the plasma and structural changes of the brain.

METHODS

We studied 162 subjects composed of 92 community-based normal healthy subjects, 17 with subjective cognitive decline, 14 with mild cognitive impairment and 39 with Alzheimer's disease dementia. All subjects underwent MDS-OAβ and three-dimensional T1 magnetic resonance imaging. To determine the structural changes of the brain that are statistically correlated with MDS-OAβ level, we used voxel-based morphometry with corrections for age and total intracranial volume covariates.

RESULTS

We found brain volume reduction in the bilateral temporal, amygdala, parahippocampal and lower parietal lobe and left cingulate and precuneus regions (family-wise error, p < 0.05). Reduction was also found in white matter in proximity to the left temporal and bilateral lower parietal lobes and posterior corpus callosum (family-wise error, p < 0.05). Brain volume increment was not observed in any regions within grey or white matter.

DISCUSSION

Findings suggest that substantial correlation exists between amyloid ß oligomerization in the blood and brain volume reduction in the form of Alzheimer's disease despite of uncertainty in the casual relationship.

摘要

简介

寡聚淀粉样蛋白-β是与阿尔茨海默病发病机制相关的主要毒性物质。近年来,用于测量血液中寡聚淀粉样蛋白-β的方法数量有所增加。多聚体检测系统-寡聚淀粉样蛋白-β(MDS-OAβ)是一种测量血液中寡聚化倾向的特异性方法。本研究的目的是确定血浆中淀粉样蛋白-β的寡聚化与大脑结构变化之间的关系。

方法

我们研究了 162 名受试者,其中包括 92 名社区正常健康受试者、17 名主观认知减退患者、14 名轻度认知障碍患者和 39 名阿尔茨海默病痴呆患者。所有受试者均接受 MDS-OAβ 和三维 T1 磁共振成像检查。为了确定与 MDS-OAβ 水平具有统计学相关性的大脑结构变化,我们使用了基于体素的形态测量学方法,并对年龄和总颅内体积协变量进行了校正。

结果

我们发现双侧颞叶、杏仁核、海马旁回和下顶叶以及左扣带回和楔前叶区域的脑容量减少(全脑错误校正,p<0.05)。还发现左侧颞叶和双侧下顶叶以及后胼胝体附近的白质减少(全脑错误校正,p<0.05)。在灰质或白质的任何区域都没有观察到脑容量增加。

讨论

研究结果表明,尽管因果关系不确定,但血液中淀粉样蛋白-β的寡聚化与大脑体积减少(以阿尔茨海默病的形式)之间存在显著相关性。

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