Haroutunian Vahram, Katsel Pavel, Schmeidler James
Department of Psychiatry, The Mount Sinai School of Medicine, New York, NY 10029, USA.
Neurobiol Aging. 2009 Apr;30(4):561-73. doi: 10.1016/j.neurobiolaging.2007.07.021. Epub 2007 Sep 12.
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.
(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。