Estimating the Temporal Evolution of Alzheimer's Disease Pathology with Autopsy Data

被引:4
|
作者
Royall, Donald R. [1 ,2 ,3 ,4 ]
Palmer, Raymond F. [3 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Dept Psychiat, San Antonio, TX 78284 USA
[2] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, San Antonio, TX 78284 USA
[3] Univ Texas Hlth Sci Ctr San Antonio, Dept Family & Community Med, San Antonio, TX 78284 USA
[4] S Texas Vet Hlth Syst, Audie L Murphy Div GRECC, San Antonio, TX USA
关键词
Alzheimer's disease; longitudinal; neuropathology; old age; NEUROFIBRILLARY TANGLES; COGNITIVE IMPAIRMENT; SENILE PLAQUES; MISSING DATA; DEMENTIA; MODERATORS; MEDIATORS; SEVERITY; WORK;
D O I
10.3233/JAD-2012-120430
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The temporal growth of Alzheimer's disease (AD) neuropathology cannot be easily determined because autopsy data are available only after death. We combined autopsy data from 471 participants in the Honolulu-Asia Aging Study (HAAS) into latent factor measures of neurofibrillary tangle and neuritic plaque counts. These were associated with intercept and slope parameters from a latent growth curve (LGC) model of 9-year change in cognitive test performance in 3244 autopsied and non-autopsied HAAS participants. Change in cognition fully mediated the association between baseline cognitive performance and AD lesions counts. The mediation effect of cognitive change on both AD lesion models effectively dates them within the period of cognitive surveillance. Additional analyses could lead to an improved understanding of lesion propagation in AD.
引用
收藏
页码:23 / 32
页数:10
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