A Combined Measure of Cognition and Function for Clinical Trials: The Integrated Alzheimer's Disease Rating Scale (iADRS).

IF 8.5 3区 医学 Q1 CLINICAL NEUROLOGY Jpad-Journal of Prevention of Alzheimers Disease Pub Date : 2015-12-01 DOI:10.14283/JPAD.2015.82
A. Wessels, E. Siemers, P. Yu, S. Andersen, K. Holdridge, J. Sims, K. Sundell, Y. Stern, D. Rentz, B. Dubois, Roy W Jones, J. Cummings, P. Aisen
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引用次数: 48

Abstract

It is generally recognized that more sensitive instruments for the earliest stages of Alzheimer's disease (AD) are needed. The integrated Alzheimer's Disease Rating Scale (iADRS) combines scores from 2 widely accepted measures, the Alzheimer's Disease Assessment Scale-Cognitive subscale (ADAS-Cog) and the Alzheimer's Disease Cooperative Study - instrumental Activities of Daily Living (ADCS-iADL). Disease progression and treatment differences as measured by the iADRS were analyzed using data from solanezumab EXPEDITION, EXPEDITION2, and EXPEDITION-EXT Studies; semagacestat IDENTITY Study; and donepezil ADCS - mild cognitive impairment (ADCS-MCI) Study. Psychometric properties of the iADRS were established through principal component analysis (PCA) and estimation of contributions of subscores and individual item scores to the iADRS total score. The iADRS performed better than most composites and scales in detecting disease progression and comparably or better than individual scales in detecting treatment differences. PCA demonstrated the iADRS can be divided into two principal components primarily representing cognitive items and instrumental ADLs. Dynamic ranges of the subscales were similar across all studies, reflecting approximately equal contributions from both subscales to the iADRS total score. In item analyses, every item contributed to the total score, with varying strength of contributions by item and across data sets. The iADRS demonstrated acceptable psychometric properties and was effective in capturing disease progression from MCI through moderate AD and treatment effects across the early disease spectrum. These findings suggest the iADRS can be used in studies of mixed populations, ensuring sensitivity to treatment effects as subjects progress during studies of putative disease-modifying agents.
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临床试验中认知和功能的综合测量:阿尔茨海默病综合评定量表(iADRS)。
人们普遍认为,需要更灵敏的仪器来检测阿尔茨海默病(AD)的早期阶段。综合阿尔茨海默病评定量表(iADRS)结合了两种广泛接受的测量方法的得分,阿尔茨海默病评估量表-认知子量表(ADAS-Cog)和阿尔茨海默病合作研究-日常生活工具活动(ADCS-iADL)。使用来自solanezumab EXPEDITION、EXPEDITION2和EXPEDITION- ext研究的数据分析了iADRS测量的疾病进展和治疗差异;semagacestat身份研究;多奈哌齐ADCS-轻度认知障碍(ADCS- mci)研究。通过主成分分析(PCA)和估计子项得分和单项得分对iADRS总分的贡献来确定iADRS的心理测量特性。iADRS在检测疾病进展方面优于大多数复合量表和量表,在检测治疗差异方面与个体量表相当或更好。主成分分析表明,iADRS可分为两个主要成分,主要代表认知项目和工具性adl。所有研究中各分量表的动态范围相似,反映了两个分量表对iADRS总分的贡献大致相等。在项目分析中,每个项目对总分都有贡献,不同项目和不同数据集的贡献强度不同。iADRS显示了可接受的心理测量特性,并且有效地捕获了从轻度认知障碍到中度AD的疾病进展以及早期疾病谱系的治疗效果。这些发现表明,iADRS可用于混合人群的研究,确保受试者在研究假定的疾病调节剂过程中对治疗效果的敏感性。
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来源期刊
自引率
7.80%
发文量
85
期刊介绍: The JPAD « Journal of Prevention of Alzheimer’Disease » will publish reviews, original research articles and short reports to improve our knowledge in the field of Alzheimer prevention including : neurosciences, biomarkers, imaging, epidemiology, public health, physical cognitive exercise, nutrition, risk and protective factors, drug development, trials design, and heath economic outcomes. JPAD will publish also the meeting abstracts from Clinical Trial on Alzheimer Disease (CTAD) and will be distributed both in paper and online version worldwide.
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