Integrated Alzheimer's Disease Rating Scale: Clinically meaningful change estimates

被引:32
作者
Wessels, Alette M. [1 ]
Rentz, Dorene M. [2 ,3 ]
Case, Michael [1 ]
Lauzon, Steve [1 ]
Sims, John R. [1 ]
机构
[1] Eli Lilly & Co, 1 Lilly Corp Ctr, Indianapolis, IN 46285 USA
[2] Harvard Med Sch, Dept Neurol, Massachusetts Gen Hosp, Boston, MA 02115 USA
[3] Harvard Med Sch, Ctr Alzheimer Res & Treatment, Dept Neurol, Brigham & Womens Hosp, Boston, MA 02115 USA
关键词
Alzheimer's disease; clinical meaningfulness; cognitive/functional composite endpoint; Integrated Alzheimer's Disease Rating Scale; minimal clinically important change; minimal clinically important difference; INTERPRETING CHANGE; DEMENTIA; TRIALS; BOXES; SUM; CDR;
D O I
10.1002/trc2.12312
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: The Integrated Alzheimer's Disease Rating Scale (iADRS) has been used to detect differences in disease progression in early Alzheimer's disease (AD). The objectives of this study were to enhance understanding of iADRS point changes within the context of clinical trials, and to establish a minimal clinically important difference (MCID) on the iADRS. Methods: Data from AMARANTH and EXPEDITION3 were analyzed using various approaches, including anchor-based, distribution-based, regression analyses, and cumulative distribution function (CDF) plots. Three potential anchors were examined, including the Clinical Dementia Rating-Sum of Boxes, Mini-Mental State Examination, and Functional Activities Questionnaire. Triangulation of all results was used to determine the MCID for participants with mild cognitive impairment (MCI) due to AD and AD with mild dementia. Results: All three anchors met criteria for "sufficiently associated" (vertical bar r vertical bar = 0.4-0.7). Cumulatively, results from anchor-based and distribution-based results converged to suggest an iADRS MCID of 5 points for MCI due to AD and 9 points for AD with mild dementia. Regression analyses and CDF plots supported these values. Discussion: These findings suggest the iADRS can be used in clinical trials to detect a clinically meaningful outcome of AD progression.
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页数:9
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