Novel Statistically-Derived Composite Measures for Assessing the Efficacy of Disease-Modifying Therapies in Prodromal Alzheimer's Disease Trials: An AIBL Study

被引:25
作者
Burnham, Samantha C. [1 ]
Raghavan, Nandini [2 ]
Wilson, William [3 ]
Baker, David [4 ]
Ropacki, Michael T. [5 ]
Novak, Gerald [2 ]
Ames, David [6 ,7 ]
Ellis, Kathryn [6 ]
Martins, Ralph N. [8 ,9 ]
Maruff, Paul [10 ]
Masters, Colin L. [11 ]
Romano, Gary [2 ]
Rowe, Christopher C. [12 ,13 ,14 ]
Savage, Greg [15 ,16 ]
Macaulay, S. Lance [17 ]
Narayan, Vaibhav A. [2 ]
机构
[1] CSIRO Digital Prod Flagship, Floreat, WA, Australia
[2] Janssen Res & Dev, Raritan, NJ USA
[3] CSIRO Digital Prod Flagship, N Ryde, NSW, Australia
[4] Janssen Res & Dev, Titusville, NJ USA
[5] Janssen Res & Dev, Fremont, CA USA
[6] Univ Melbourne, Dept Psychiat, Acad Unit Psychiat Old Age, Parkville, Vic 3052, Australia
[7] Natl Ageing Res Inst, Parkville, Vic, Australia
[8] Edith Cowan Univ, Sch Med Sci, Ctr Excellence Alzheimers Dis Res & Care, Joondalup, WA, Australia
[9] Hollywood Private Hosp, Sir James McCusker Alzheimers Dis Res Unit, Perth, WA, Australia
[10] Cogstate, Melbourne, Vic, Australia
[11] Univ Melbourne, MHRI, Parkville, Vic 3052, Australia
[12] Austin Hlth, Dept Nucl Med, Heidelberg, Vic, Australia
[13] Austin Hlth, Ctr PET, Heidelberg, Vic, Australia
[14] Univ Melbourne, Austin Hlth, Dept Med, Heidelberg, Vic, Australia
[15] Macquarie Univ, ARC Ctr Excellence Cognit & Its Disorders, Sydney, NSW 2109, Australia
[16] Macquarie Univ, Dept Psychol, Sydney, NSW 2109, Australia
[17] CSIRO Food & Nutr Flagship, Melbourne, Vic, Australia
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
Alzheimer's disease; clinical marker; clinical trial; mild cognitive impairment; prodromal stage; MILD COGNITIVE IMPAIRMENT; CLINICAL CHARACTERIZATION; OLDER-ADULTS; SCALE; MCI; ASSOCIATION; DIAGNOSIS;
D O I
10.3233/JAD-143015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: There is a growing consensus that disease-modifying therapies must be given at the prodromal or preclinical stages of Alzheimer's disease (AD) to be effective. A major unmet need is to develop and validate sensitive measures to track disease progression in these populations. Objective: To generate novel statistically-derived composites from standard scores, which have increased sensitivity in the assessment of change from baseline in prodromal AD. Methods: An empirically based method was employed to generate domain specific, global, and cognitive-functional novel composites. The novel composites were compared and contrasted with each other, as well as standard scores for their ability to track change from baseline. The longitudinal characteristics and power to detect decline of the measures were evaluated. Data from participants in the Australian Imaging, Biomarkers and Lifestyle (AIBL) Study characterized as mild cognitively impaired with high neocortical amyloid-beta burden were utilized for the study. Results: The best performing standard scores were CDR Sum-of-Boxes and MMSE. The statistically-derived novel composites performed better than the standard scores from which they were derived. The domain-specific composites generally did not perform as well as the global composites or the cognitive-functional composites. Conclusion: A systematic method was employed to generate novel statistically-derived composite measures from standard scores. Composites comprised of measures including function and multiple cognitive domains appeared to best capture change from baseline. These composites may be useful to assess progression or lack thereof in prodromal AD. However, the results should be replicated and validated using an independent clinical sample before implementation in a clinical trial.
引用
收藏
页码:1079 / 1089
页数:11
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