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早期淀粉样蛋白病变中的白质微结构破坏

White matter microstructure disruption in early stage amyloid pathology.

作者信息

Collij Lyduine E, Ingala Silvia, Top Herwin, Wottschel Viktor, Stickney Kristine E, Tomassen Jori, Konijnenberg Elles, Ten Kate Mara, Sudre Carole, Lopes Alves Isadora, Yaqub Maqsood M, Wink Alle Meije, Van 't Ent Dennis, Scheltens Philip, van Berckel Bart N M, Visser Pieter Jelle, Barkhof Frederik, Braber Anouk Den

机构信息

Dept. of Radiology and Nuclear Medicine Amsterdam UMC, Location VUmc Amsterdam The Netherlands.

Dept. of Biological Psychology VU University Amsterdam Amsterdam The Netherlands.

出版信息

Alzheimers Dement (Amst). 2021 Apr 1;13(1):e12124. doi: 10.1002/dad2.12124. eCollection 2021.

Abstract

INTRODUCTION

Amyloid beta (Aβ) accumulation is the first pathological hallmark of Alzheimer's disease (AD), and it is associated with altered white matter (WM) microstructure. We aimed to investigate this relationship at a regional level in a cognitively unimpaired cohort.

METHODS

We included 179 individuals from the European Medical Information Framework for AD (EMIF-AD) preclinAD study, who underwent diffusion magnetic resonance (MR) to determine tract-level fractional anisotropy (FA); mean, radial, and axial diffusivity (MD/RD/AxD); and dynamic [F]flutemetamol) positron emission tomography (PET) imaging to assess amyloid burden.

RESULTS

Regression analyses showed a non-linear relationship between regional amyloid burden and WM microstructure. Low amyloid burden was associated with increased FA and decreased MD/RD/AxD, followed by decreased FA and increased MD/RD/AxD upon higher amyloid burden. The strongest association was observed between amyloid burden in the precuneus and body of the corpus callosum (CC) FA and diffusivity (MD/RD) measures. In addition, amyloid burden in the anterior cingulate cortex strongly related to AxD and RD measures in the genu CC.

DISCUSSION

Early amyloid deposition is associated with changes in WM microstructure. The non-linear relationship might reflect multiple stages of axonal damage.

摘要

引言

β淀粉样蛋白(Aβ)积累是阿尔茨海默病(AD)的首个病理特征,且与白质(WM)微观结构改变相关。我们旨在对认知未受损队列中的区域层面这种关系进行研究。

方法

我们纳入了来自欧洲AD医学信息框架(EMIF-AD)临床前AD研究的179名个体,这些个体接受了扩散磁共振(MR)检查以确定纤维束层面的分数各向异性(FA)、平均、径向和轴向扩散率(MD/RD/AxD),并进行了动态[F]氟代脱氧葡萄糖正电子发射断层扫描(PET)成像以评估淀粉样蛋白负荷。

结果

回归分析显示区域淀粉样蛋白负荷与WM微观结构之间存在非线性关系。低淀粉样蛋白负荷与FA增加及MD/RD/AxD降低相关,而在更高淀粉样蛋白负荷时则出现FA降低及MD/RD/AxD增加。在楔前叶和胼胝体(CC)体部的淀粉样蛋白负荷与FA及扩散率(MD/RD)测量值之间观察到最强的相关性。此外,前扣带回皮质的淀粉样蛋白负荷与膝部CC的AxD和RD测量值密切相关。

讨论

早期淀粉样蛋白沉积与WM微观结构变化相关。这种非线性关系可能反映了轴突损伤的多个阶段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/426d/8015832/071b02d42d53/DAD2-13-e12124-g001.jpg

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