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载脂蛋白 E-ε4 与阿尔茨海默病和路易体痴呆症谱系中的海马体积、学习和记忆有关。

APOE-ε4 associates with hippocampal volume, learning, and memory across the spectrum of Alzheimer's disease and dementia with Lewy bodies.

机构信息

Institute of Medical Science, Faculty of Medicine, University of Toronto, Toronto, ON, Canada; LC Campbell Cognitive Neurology Research Unit, Sunnybrook Research Institute, University of Toronto, Toronto, ON, Canada.

Division of Neurology, Department of Medicine, University of Toronto, Toronto, ON, Canada; Hurvitz Brain Sciences Research Program, Sunnybrook Research Institute, University of Toronto, Toronto, ON, Canada.

出版信息

Alzheimers Dement. 2018 Sep;14(9):1137-1147. doi: 10.1016/j.jalz.2018.04.005. Epub 2018 May 18.

Abstract

INTRODUCTION

Although the apolipoprotein E ε4-allele (APOE-ε4) is a susceptibility factor for Alzheimer's disease (AD) and dementia with Lewy bodies (DLB), its relationship with imaging and cognitive measures across the AD/DLB spectrum remains unexplored.

METHODS

We studied 298 patients (AD = 250, DLB = 48; 38 autopsy-confirmed; NCT01800214) using neuropsychological testing, volumetric magnetic resonance imaging, and APOE genotyping to investigate the association of APOE-ε4 with hippocampal volume and learning/memory phenotypes, irrespective of diagnosis.

RESULTS

Across the AD/DLB spectrum: (1) hippocampal volumes were smaller with increasing APOE-ε4 dosage (no genotype × diagnosis interaction observed), (2) learning performance as assessed by total recall scores was associated with hippocampal volumes only among APOE-ε4 carriers, and (3) APOE-ε4 carriers performed worse on long-delay free word recall.

DISCUSSION

These findings provide evidence that APOE-ε4 is linked to hippocampal atrophy and learning/memory phenotypes across the AD/DLB spectrum, which could be useful as biomarkers of disease progression in therapeutic trials of mixed disease.

摘要

简介

尽管载脂蛋白 E ε4 等位基因(APOE-ε4)是阿尔茨海默病(AD)和路易体痴呆(DLB)的易感因素,但它与 AD/DLB 谱系中成像和认知测量的关系仍未得到探索。

方法

我们使用神经心理学测试、容积磁共振成像和 APOE 基因分型研究了 298 名患者(AD=250,DLB=48;38 例经尸检证实;NCT01800214),以研究 APOE-ε4 与海马体积和学习/记忆表型的关系,而不考虑诊断。

结果

在 AD/DLB 谱系中:(1)随着 APOE-ε4 剂量的增加,海马体积减小(未观察到基因型×诊断的相互作用);(2)仅在 APOE-ε4 携带者中,通过总回忆分数评估的学习表现与海马体积相关;(3)APOE-ε4 携带者在长延迟自由单词回忆方面表现更差。

讨论

这些发现提供了证据表明,APOE-ε4 与 AD/DLB 谱系中的海马萎缩和学习/记忆表型有关,这可能作为混合疾病治疗试验中疾病进展的生物标志物有用。

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