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一种用于常染色体显性阿尔茨海默病临床试验的新型认知疾病进展模型。

A novel cognitive disease progression model for clinical trials in autosomal-dominant Alzheimer's disease.

机构信息

Division of Biostatistics, Washington University School of Medicine, St. Louis, MO, USA.

Berry Consultants, Austin, TX, USA.

出版信息

Stat Med. 2018 Sep 20;37(21):3047-3055. doi: 10.1002/sim.7811. Epub 2018 May 14.

Abstract

Clinical trial outcomes for Alzheimer's disease are typically analyzed by using the mixed model for repeated measures (MMRM) or similar models that compare an efficacy scale change from baseline between treatment arms with or without participants' disease stage as a covariate. The MMRM focuses on a single-point fixed follow-up duration regardless of the exposure for each participant. In contrast to these typical models, we have developed a novel semiparametric cognitive disease progression model (DPM) for autosomal dominant Alzheimer's disease based on the Dominantly Inherited Alzheimer Network (DIAN) observational study. This model includes 3 novel features, in which the DPM (1) aligns and compares participants by disease stage, (2) uses a proportional treatment effect similar to the concept of the Cox proportional hazard ratio, and (3) incorporates extended follow-up data from participants with different follow-up durations using all data until last participant visit. We present the DPM model developed by using the DIAN observational study data and demonstrate through simulation that the cognitive DPM used in hypothetical intervention clinical trials produces substantial gains in power compared with the MMRM.

摘要

阿尔茨海默病的临床试验结果通常采用重复测量混合模型(MMRM)或类似的模型进行分析,这些模型将治疗组与基线相比的疗效量表变化与参与者的疾病阶段作为协变量进行比较。MMRM 侧重于单一固定随访时间点,而不考虑每个参与者的暴露情况。与这些典型模型不同,我们基于常染色体显性阿尔茨海默病的 Dominantly Inherited Alzheimer Network(DIAN)观察性研究,开发了一种新的半参数认知疾病进展模型(DPM)。该模型包含 3 个新特征,其中 DPM(1)通过疾病阶段对齐和比较参与者,(2)使用类似于 Cox 比例风险比概念的比例治疗效果,(3)通过使用所有数据直到最后一个参与者就诊,纳入具有不同随访时间的参与者的扩展随访数据。我们展示了使用 DIAN 观察性研究数据开发的 DPM 模型,并通过模拟证明,与 MMRM 相比,用于假设干预临床试验的认知 DPM 可显著提高功效。

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