Temporal Order of Alzheimer's Disease-Related Cognitive Marker Changes in BLSA and WRAP Longitudinal Studies

被引:16
作者
Bilgel, Murat [1 ]
Koscik, Rebecca L. [2 ]
An, Yang [1 ]
Prince, Jerry L. [3 ]
Resnick, Susan M. [1 ]
Johnson, Sterling C. [2 ,4 ,5 ,6 ]
Jedynak, Bruno M. [7 ]
机构
[1] NIA, Lab Behav Neurosci, Intramural Res Program, Baltimore, MD 21224 USA
[2] Univ Wisconsin, Sch Med & Publ Hlth, Wisconsin Alzheimers Inst, Madison, WI USA
[3] Johns Hopkins Univ, Dept Elect & Comp Engn, Baltimore, MD 21218 USA
[4] Wm S Middleton Vet Hosp, Geriatr Res Educ & Clin Ctr, Madison, WI USA
[5] Univ Wisconsin, Sch Med & Publ Hlth, Alzheimers Dis Res Ctr, Madison, WI USA
[6] Univ Wisconsin, Waisman Lab Brain Imaging & Behav, Madison, WI USA
[7] Portland State Univ, Dept Math & Stat, Portland, OR 97207 USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; cognition; longitudinal studies; neuropsychological tests; preclinical; NORMAL OLDER INDIVIDUALS; AMYLOID-BETA; DIGIT SPAN; WISCONSIN-REGISTRY; MEMORY DECLINE; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; PROSPECTIVE COHORT; NEURAL FUNCTION;
D O I
10.3233/JAD-170448
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Investigation of the temporal trajectories of currently used neuropsychological tests is critical to identifying earliest changing measures on the path to dementia due to Alzheimer's disease (AD). We used the Progression Score (PS) method to characterize the temporal trajectories of measures of verbal memory, executive function, attention, processing speed, language, and mental status using data spanning normal cognition, mild cognitive impairment, and AD from 1,661 participants with a total of 7,839 visits (age at last visit 77.6 SD 9.2) in the Baltimore Longitudinal Study of Aging (BLSA) and 1510 participants with a total of 3,473 visits (age at last visit 59.5 SD 7.4) in the Wisconsin Registry for Alzheimer's Prevention (WRAP). This method aligns individuals in time based on the similarity of their longitudinal measurements to reveal temporal trajectories. As a validation of our methodology, we explored the associations between the individualized cognitive progression scores (Cog-PS) computed by our method and clinical diagnosis. Digit span tests were the first to show declines in both data sets, and were detected mainly among cognitively normal individuals. These were followed by tests of verbal memory, which were in turn followed by Trail Making Tests, Boston Naming Test, and Mini-Mental State Examination. Differences in Cog-PS across the clinical diagnosis and APOE epsilon 4 groups were statistically significant, highlighting the potential use of Cog-PS as individualized indicators of disease progression. Identifying cognitive measures that are changing in preclinical AD can lead to the development of novel cognitive tests that are finely tuned to detecting earliest changes.
引用
收藏
页码:1335 / 1347
页数:13
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