Suppr超能文献

早期阿尔茨海默病中海马体积丢失与载脂蛋白E基因型及生物标志物关系的磁共振成像研究

MRI of hippocampal volume loss in early Alzheimer's disease in relation to ApoE genotype and biomarkers.

作者信息

Schuff N, Woerner N, Boreta L, Kornfield T, Shaw L M, Trojanowski J Q, Thompson P M, Jack C R, Weiner M W

机构信息

Department of Veterans Affairs Medical Center, San Francisco, CA, USA.

出版信息

Brain. 2009 Apr;132(Pt 4):1067-77. doi: 10.1093/brain/awp007. Epub 2009 Feb 27.

Abstract

Hippocampal volume change over time, measured with MRI, has huge potential as a marker for Alzheimer's disease. The objectives of this study were: (i) to test if constant and accelerated hippocampal loss can be detected in Alzheimer's disease, mild cognitive impairment and normal ageing over short periods, e.g. 6-12 months, with MRI in the large multicentre setting of the Alzheimer's Disease Neuroimaging Initiative (ADNI); (ii) to determine the extent to which the polymorphism of the apolipoprotein E (ApoE) gene modulates hippocampal change; and (iii) to determine if rates of hippocampal loss correlate with cerebrospinal fluid (CSF) biomarkers of Alzheimer's disease, such as the beta-amyloid (Abeta(1-42)) and tau proteins (tau). The MRI multicentre study included 112 cognitive normal elderly individuals, 226 mild cognitive impairment and 96 Alzheimer's disease patients who all had at least three successive MRI scans, involving 47 different imaging centres. The mild cognitive impairment and Alzheimer's disease groups showed hippocampal volume loss over 6 months and accelerated loss over 1 year. Moreover, increased rates of hippocampal loss were associated with presence of the ApoE allele epsilon4 gene in Alzheimer's disease and lower CSF Abeta(1-42) in mild cognitive impairment, irrespective of ApoE genotype, whereas relations with tau were only trends. The power to measure hippocampal change was improved by exploiting correlations statistically between successive MRI observations. The demonstration of considerable hippocampal loss in mild cognitive impairment and Alzheimer's disease patients over only 6 months and accelerated loss over 12 months illustrates the power of MRI to track morphological brain changes over time in a large multisite setting. Furthermore, the relations between faster hippocampal loss in the presence of ApoE allele epsilon4 and decreased CSF Abeta(1-42) supports the concept that increased hippocampal loss is an indicator of Alzheimer's disease pathology and a potential marker for the efficacy of therapeutic interventions in Alzheimer's disease.

摘要

通过磁共振成像(MRI)测量的海马体体积随时间的变化,作为阿尔茨海默病的标志物具有巨大潜力。本研究的目的是:(i)在阿尔茨海默病神经成像计划(ADNI)的大型多中心研究中,用MRI检测在短时间内(如6 - 12个月),阿尔茨海默病、轻度认知障碍和正常衰老中是否能检测到海马体的持续和加速萎缩;(ii)确定载脂蛋白E(ApoE)基因多态性对海马体变化的调节程度;(iii)确定海马体萎缩率是否与阿尔茨海默病的脑脊液(CSF)生物标志物相关,如β - 淀粉样蛋白(Abeta(1 - 42))和tau蛋白(tau)。这项MRI多中心研究纳入了112名认知正常的老年人、226名轻度认知障碍患者和96名阿尔茨海默病患者,他们均至少接受了三次连续的MRI扫描,涉及47个不同的成像中心。轻度认知障碍和阿尔茨海默病组在6个月内出现海马体体积减少,在1年内出现加速减少。此外,无论ApoE基因型如何,阿尔茨海默病中海马体萎缩率增加与ApoE ε4等位基因的存在有关,轻度认知障碍中与脑脊液Abeta(1 - 42)降低有关,而与tau的关系仅为趋势。通过利用连续MRI观察之间的统计相关性,提高了测量海马体变化的能力。仅在6个月内轻度认知障碍和阿尔茨海默病患者就出现了明显的海马体萎缩,12个月内出现加速萎缩,这说明了MRI在大型多中心环境中追踪大脑形态随时间变化的能力。此外,ApoE ε4等位基因存在时海马体萎缩加快与脑脊液Abeta(1 - 42)降低之间的关系支持了这样的概念,即海马体萎缩增加是阿尔茨海默病病理学的一个指标,也是阿尔茨海默病治疗干预疗效的一个潜在标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0398/2668943/1d9df94feea1/awp007f1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验