Development of a straightforward and sensitive scale for MCI and early AD clinical trials

被引:15
作者
Huang, Yifan [1 ]
Ito, Kaori [1 ]
Billing, Clare B., Jr. [1 ,2 ]
Anziano, Richard J. [1 ]
机构
[1] Pfizer Inc, Groton, CT 06340 USA
[2] SystaMed Inc, Groton, CT USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; Mild cognitive impairment; Alzheimer's Disease Assessment Scale-cognitive subscale; Composite endpoints; Clinical trials; Signal-to-noise ratio; ALZHEIMERS ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; RECOMMENDATIONS; DISEASE; COG;
D O I
10.1016/j.jalz.2014.03.008
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Although the Clinical Dementia Rating Scale-Sum of Boxes score (CDR-SB) is a widely accepted and commonly used global scale, validated clinical endpoints of cognitive changes are unavailable in the predementia stages of Alzheimer's disease (AD), and a new clinical assessment with reliability and sensitivity is needed in the mild cognitive impairment (MCI) population. Methods: Using Alzheimer's Disease Neuroimaging Initiative (ADNI)-1/GO data, signal-to-noise ratios (SNRs) were calculated to quantify the sensitivity of a measure for detecting disease progression and hypothetical treatment effects. All possible combinations of selected sensitive measures were assessed for developing composite scores. The analyses were performed in the MCI population and subpopulations enriched by apolipoprotein E4 (APOE epsilon 4), hippocampal volume, and cerebrospinal fluid beta-amyloid. Results: The best composite score was "Word Recall + Delayed Word Recall- + Orientation + CDR-SB + FAQ", more sensitive than beta-item Alzheimer's Disease Assessment Scale-cognitive subscale or CDR-SB. Conclusion: The proposed composite score derived from the existing clinical endpoints demonstrated higher sensitivity in the MCI population and is easy to implement and standardize across studies. (C) 2015 The Alzheimer's Association. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:404 / 414
页数:11
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