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临床试验的神经影像学结果。

Neuroimaging outcomes for clinical trials.

作者信息

Frisoni G B, Caroli A

机构信息

G.B. Frisoni, IRCCS Centro San Giovanni di Dio Fatebenefratelli, Brescia, Italy.

出版信息

J Nutr Health Aging. 2007 Jul-Aug;11(4):348-52.

Abstract

A wide range of drugs is currently under development for treating Alzheimer's Disease (AD). Clinical trials traditionally use rating scales, such as neuropsychological tests and disability scales, as outcome measures. However, their intrinsic measurement variability, the slow disease progression, and the low effectiveness of the drugs developed so far have led to trial designs with hundreds of subjects per treatment arm. Furthermore, a key issue is to establish what effect are these compounds having on the biological progression of the disease, beyond delaying symptomatic progression. The development of imaging markers, either structural, functional, or amyloid, with proven sensitivity to disease progression has recently paved the way for their use as outcome measures in clinical trials. The use of imaging measures has the double advantage of decreasing the number of subjects per treatment arm whilst also providing a direct measure of the degree of disease modification induced by the "active" molecules. The reviewed techniques, except for the most recent amyloid imaging, are those applied to prospective studies investigating changes of imaging markers over time.

摘要

目前正在研发多种治疗阿尔茨海默病(AD)的药物。传统上,临床试验使用评分量表,如神经心理学测试和残疾量表,作为疗效指标。然而,其固有的测量变异性、疾病进展缓慢以及迄今为止所开发药物的低效性,导致每个治疗组的试验设计都需要数百名受试者。此外,一个关键问题是要确定这些化合物除了延缓症状进展之外,对疾病的生物学进展有何影响。具有已证实的对疾病进展敏感性的成像标志物,无论是结构、功能还是淀粉样蛋白方面的,最近为其在临床试验中用作疗效指标铺平了道路。使用成像测量具有双重优势,既能减少每个治疗组的受试者数量,又能直接测量“活性”分子诱导的疾病修饰程度。除了最新的淀粉样蛋白成像外,所综述的技术是应用于前瞻性研究以调查成像标志物随时间变化的技术。

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