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High Degree of Heterogeneity in Alzheimer's Disease Progression Patterns

机译:阿尔茨海默氏病进展模式中的高度异质性

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摘要

There have been several reports on the varying rates of progression among Alzheimer's Disease (AD) patients; however, there has been no quantitative study of the amount of heterogeneity in AD. Obtaining a reliable quantitative measure of AD progression rates and their variances among the patients for each stage of AD is essential for evaluating results of any clinical study. The Global Deterioration Scale (GDS) and Functional Assessment Staging procedure (FAST) characterize seven stages in the course of AD from normal aging to severe dementia. Each GDS/FAST stage has a published mean duration, but the variance is unknown. We use statistical analysis to reconstruct GDS/FAST stage durations in a cohort of 648 AD patients with an average follow-up time of 4.78 years. Calculations for GDS/FAST stages 4–6 reveal that the standard deviations for stage durations are comparable with their mean values, indicating the presence of large variations in the AD progression among patients. Such amount of heterogeneity in the course of progression of AD is consistent with the existence of several sub-groups of AD patients, which differ by their patterns of decline.
机译:关于阿尔茨海默氏病(AD)患者进展速度的变化已有几篇报道。但是,还没有定量研究AD异质性的数量。获得AD各个阶段患者AD进展率及其差异的可靠定量方法对于评估任何临床研究结果至关重要。总体恶化量表(GDS)和功能评估分期程序(FAST)表征了AD从正常衰老到严重痴呆的七个阶段。每个GDS / FAST阶段都有公开的平均持续时间,但是方差未知。我们使用统计分析重建了648名AD患者的GDS / FAST分期,平均随访时间为4.78年。 GDS / FAST 4-6期的计算表明,阶段持续时间的标准差与其平均值可比,表明患者的AD进展存在较大差异。在AD进展过程中的这种异质性量与AD患者的几个亚组的存在是一致的,其亚群的下降模式不同。

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