Progression of Alzheimer's disease as measured by Clinical Dementia Rating Sum of Boxes scores

被引:94
作者
Williams, Monique M. [1 ,2 ,3 ]
Storandt, Martha [1 ,4 ]
Roe, Catherine M. [1 ,5 ]
Morris, John C. [1 ,5 ,6 ,7 ,8 ]
机构
[1] Washington Univ, Charles F & Joanne Knight Alzheimers Dis Res Ctr, St Louis, MO 63130 USA
[2] Washington Univ, Dept Med, St Louis, MO USA
[3] Washington Univ, Dept Psychiat, St Louis, MO USA
[4] Washington Univ, Dept Psychol, St Louis, MO 63130 USA
[5] Washington Univ, Dept Neurol, St Louis, MO USA
[6] Washington Univ, Dept Pathol & Immunol, St Louis, MO USA
[7] Washington Univ, Program Phys Therapy, St Louis, MO USA
[8] Washington Univ, Program Occupat Therapy, St Louis, MO USA
关键词
Alzheimer's disease; Assessment of dementia; Clinical Dementia Rating; Clinical Dementia Rating Sum of Boxes; Cohort studies;
D O I
10.1016/j.jalz.2012.01.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: This study examined rates of dementia progression as ascertained by the Clinical Dementia Rating Sum of Boxes (CDR-SB) for symptomatic Alzheimer's disease (sAD), and assessed participant characteristics as predictors of CDR-SB progression. Methods: Participants (n = 792) were enrolled in longitudinal studies at an Alzheimer's Disease Research Center, received a diagnosis of sAD with a global CDR of 0.5 (n = 466) or 1 (n = 326), and had at least one follow-up assessment. Progression in CDR-SB over time as a function of baseline global CDR was examined. Results: A longitudinal increase (P <.0001) in CDR-SB was observed. The annual rate of change in CDR-SB scores was 1.43 (standard error [SE] = 0.05) in the CDR 0.5 sample and 1.91 (SE = 0.07) in the CDR 1 sample. For participants followed from the beginning of the CDR stage, time to progression to a higher global CDR was longer for individuals who were CDR 0.5 (3.75 years; 95% confidence interval [CI]: 3.18-4.33) than those who were CDR 1 at baseline (2.98 years; 95% CI: 2.75-3.22). In the total CDR 0.5 sample, the significant predictors of progression to the next global CDR stage (P < .01) were age at first sAD diagnosis and apolipoprotein E4 genotype. Conclusions: The study findings are relevant to sAD clinical trial design and accurate, reliable ascertainment of the effect of disease-modifying treatments. (C) 2013 The Alzheimer's Association. All rights reserved.
引用
收藏
页码:S39 / S44
页数:6
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