Much of Late Life Cognitive Decline Is Not due to Common Neurodegenerative Pathologies

被引:249
作者
Boyle, Patricia A. [1 ,2 ]
Wilson, Robert S. [1 ,2 ,3 ]
Yu, Lei [1 ,3 ]
Barr, Alasdair M. [4 ]
Honer, William G. [5 ]
Schneider, Julie A. [1 ,3 ]
Bennett, David A. [1 ,3 ]
机构
[1] Rush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
[2] Rush Univ, Med Ctr, Dept Behav Sci, Chicago, IL 60612 USA
[3] Rush Univ, Med Ctr, Dept Neurol Sci, Chicago, IL 60612 USA
[4] Univ British Columbia, Dept Anesthesia Pharmacol & Therapeut, Vancouver, BC V5Z 1M9, Canada
[5] Univ British Columbia, Dept Psychiat, Vancouver, BC, Canada
基金
加拿大健康研究院;
关键词
ALZHEIMER-DISEASE; DEMENTIA; NEUROPATHOLOGY; BRAIN; IMPAIRMENT; RESERVE; OLD; AGE;
D O I
10.1002/ana.23964
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
ObjectiveThe pathologic indices of Alzheimer disease, cerebrovascular disease, and Lewy body disease accumulate in the brains of older persons with and without dementia, but the extent to which they account for late life cognitive decline remains unknown. We tested the hypothesis that these pathologic indices account for the majority of late life cognitive decline. MethodsA total of 856 deceased participants from 2 longitudinal clinical-pathologic studies, Rush Memory and Aging Project and Religious Orders Study, completed a mean of 7.5 annual evaluations, including 17 cognitive tests. Neuropathologic examinations provided quantitative measures of global Alzheimer pathology, amyloid load, tangle density, macroscopic infarcts, microinfarcts, and neocortical Lewy bodies. Random coefficient models were used to examine the linear relation of pathologic indices with global cognitive decline. In subsequent analyses, random change point models were used to examine the relation of the pathologic indices with the onset of terminal decline and rates of preterminal and terminal decline (ie, nonlinear decline). ResultsCognition declined a mean of about 0.11U per year (estimate=-0.109, standard error [SE]=0.004, p<0.001), with significant individual differences in rates of decline; the variance estimate for the individual slopes was 0.013 (SE=0.112, p<0.001). In separate analyses, global Alzheimer pathology, amyloid, tangles, macroscopic infarcts, and neocortical Lewy bodies were associated with faster rates of decline and explained 22%, 6%, 34%, 2%, and 8% of the variation in decline, respectively. When analyzed simultaneously, the pathologic indices accounted for a total of 41% of the variation in decline, and the majority remained unexplained. Furthermore, in random change point models examining the influence of the pathologic indices on the onset of terminal decline and the preterminal and terminal components of the cognitive trajectory, the common pathologic indices accounted for less than a third of the variation in the onset of terminal decline and rates of preterminal and terminal decline. InterpretationThe pathologic indices of the common causes of dementia are important determinants of cognitive decline in old age and account for a large proportion of the variation in late life cognitive decline. Surprisingly, however, much of the variation in cognitive decline remains unexplained, suggesting that other important determinants of cognitive decline remain to be identified. Identification of the mechanisms that contribute to the large unexplained proportion of cognitive decline is urgently needed to prevent late life cognitive decline. Ann Neurol 2013;74:478-489
引用
收藏
页码:478 / 489
页数:12
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