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本文引用的文献

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100 years and counting: prospects for defeating Alzheimer's disease.百年征程仍在继续:攻克阿尔茨海默病的前景
Science. 2006 Nov 3;314(5800):781-4. doi: 10.1126/science.1132813.
2
Inflammatory changes parallel the early stages of Alzheimer disease.炎症变化与阿尔茨海默病的早期阶段相似。
Neurobiol Aging. 2007 Dec;28(12):1821-33. doi: 10.1016/j.neurobiolaging.2006.08.014. Epub 2006 Oct 18.
3
A hundred years of Alzheimer's disease research.百年阿尔茨海默病研究。
Neuron. 2006 Oct 5;52(1):3-13. doi: 10.1016/j.neuron.2006.09.016.
4
Staging of Alzheimer disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistry.使用石蜡切片和免疫细胞化学对阿尔茨海默病相关神经原纤维病变进行分期。
Acta Neuropathol. 2006 Oct;112(4):389-404. doi: 10.1007/s00401-006-0127-z. Epub 2006 Aug 12.
5
Alzheimer's disease and the aging brain.阿尔茨海默病与衰老大脑。
J Geriatr Psychiatry Neurol. 2006 Sep;19(3):125-8. doi: 10.1177/0891988706291079.
6
Single cell gene expression profiling in Alzheimer's disease.阿尔茨海默病中的单细胞基因表达谱分析。
NeuroRx. 2006 Jul;3(3):302-18. doi: 10.1016/j.nurx.2006.05.007.
7
Tau protein abnormalities associated with the progression of alzheimer disease type dementia.与阿尔茨海默病型痴呆进展相关的tau蛋白异常。
Neurobiol Aging. 2007 Jan;28(1):1-7. doi: 10.1016/j.neurobiolaging.2005.11.001. Epub 2005 Dec 15.
8
Harnessing the power of gene microarrays for the study of brain aging and Alzheimer's disease: statistical reliability and functional correlation.利用基因微阵列技术研究大脑衰老和阿尔茨海默病:统计可靠性与功能相关性
Ageing Res Rev. 2005 Nov;4(4):481-512. doi: 10.1016/j.arr.2005.06.006. Epub 2005 Oct 27.
9
Alzheimer's disease: mRNA expression profiles of multiple patients show alterations of genes involved with calcium signaling.阿尔茨海默病:多名患者的mRNA表达谱显示与钙信号传导相关的基因发生改变。
Neurobiol Dis. 2006 Mar;21(3):618-25. doi: 10.1016/j.nbd.2005.09.004. Epub 2005 Oct 27.
10
Differences in apolipoprotein E3/3 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease.阿尔茨海默病中海马体载脂蛋白E3/3和E4/4等位基因特异性基因表达的差异。
Neurobiol Dis. 2006 Feb;21(2):256-75. doi: 10.1016/j.nbd.2005.07.004. Epub 2005 Sep 29.

阿尔茨海默病和痴呆症中脑区的转录易损性。

Transcriptional vulnerability of brain regions in Alzheimer's disease and dementia.

作者信息

Haroutunian Vahram, Katsel Pavel, Schmeidler James

机构信息

Department of Psychiatry, The Mount Sinai School of Medicine, New York, NY 10029, USA.

出版信息

Neurobiol Aging. 2009 Apr;30(4):561-73. doi: 10.1016/j.neurobiolaging.2007.07.021. Epub 2007 Sep 12.

DOI:10.1016/j.neurobiolaging.2007.07.021
PMID:17845826
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2746014/
Abstract

This study determined (a) the association between stages of Alzheimer's disease (AD) and overall gene expression change, and (b) brain regions of greatest vulnerability to transcriptional change as the disease progressed. Fifteen cerebrocortical sites and the hippocampus were examined in persons with either no cognitive impairment or neuropathology, or with only AD-associated lesions. Cases were stratified into groups of 7-19 based on the degree of cognitive impairment (clinical dementia rating scale, CDR); neurofibrillary tangle distribution and severity (Braak staging) or density of cerebrocortical neuritic plaque (NP; grouping by NP density). Transcriptional change was assessed by Affymetrix U133 mRNA microarray analysis. The results suggested that (a) gene expression changes in the temporal and prefrontal cortices are more closely related to disease severity than other regions examined; (b) more genes are down-regulated at any given disease severity stage than up-regulated; (c) the degree of gene expression change in a given regions depends on the disease severity classification scheme used; and (d) the classification of cases by CDR provides a more orderly gradient of gene expression change in most brain regions than Braak staging or NP grouping.

摘要

本研究确定了

(a)阿尔茨海默病(AD)各阶段与整体基因表达变化之间的关联;(b)随着疾病进展,转录变化最易发生的脑区。对15个大脑皮质部位和海马体进行了检查,这些受试者要么没有认知障碍或神经病理学改变,要么仅有与AD相关的病变。根据认知障碍程度(临床痴呆评定量表,CDR)、神经原纤维缠结分布和严重程度(Braak分期)或大脑皮质神经炎性斑块密度(NP;按NP密度分组),将病例分为7 - 19组。通过Affymetrix U133 mRNA微阵列分析评估转录变化。结果表明:(a)颞叶和前额叶皮质的基因表达变化比其他检查区域与疾病严重程度的关系更密切;(b)在任何给定的疾病严重程度阶段,下调的基因比上调的基因更多;(c)给定区域的基因表达变化程度取决于所使用的疾病严重程度分类方案;(d)与Braak分期或NP分组相比,按CDR对病例进行分类在大多数脑区提供了更有序的基因表达变化梯度。