Beta-amyloid burden predicts poorer mnemonic discrimination in cognitively normal older adults

被引:16
作者
Webb, Christina E. [1 ]
Foster, Chris M. [1 ]
Horn, Marci M. [1 ]
Kennedy, Kristen M. [1 ]
Rodrigue, Karen M. [1 ]
机构
[1] Univ Texas Dallas, Sch Behav & Brain Sci, Ctr Vital Longev, 1600 Viceroy Dr,Suite 800, Dallas, TX 75235 USA
关键词
Beta-amyloid; Mnemonic discrimination; Memory; Cognitive aging; Preclinical Alzheimer's disease; PATTERN SEPARATION; ALZHEIMERS-DISEASE; APOLIPOPROTEIN-E; COMPLETION; TASK;
D O I
10.1016/j.neuroimage.2020.117199
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
One of the earliest indicators of Alzheimer's disease pathology is the presence of beta-amyloid (A beta) protein deposition. Significant amyloid deposition is evident even in older adults who exhibit little or no overt cognitive or memory impairment. Hippocampal-based processes that help distinguish between highly similar memory representations may be the most susceptible to early disease pathology. Amyloid associations with memory have been difficult to establish, possibly because typical memory assessments do not tax hippocampal operations sufficiently. Thus, the present study utilized a spatial mnemonic discrimination task designed to tax hippocampal pattern separation/completion processes in a sample of cognitively normal middle-aged and older adults (53-98 years old) who underwent PET F-18-Florbetapir A beta scanning. The degree of interference between studied and new information varied, allowing for an examination of mnemonic discrimination as a function of mnemonic similarity. Results indicated that greater beta-amyloid burden was associated with poorer discrimination across decreasing levels of interference, suggesting that even subtle elevation of beta-amyloid in cognitively normal adults is associated with impoverished performance on a hippocampally demanding memory task. The present study demonstrates that degree of amyloid burden negatively impacts the ability of aging adults to accurately distinguish old from increasingly distinct new information, providing novel insight into the cognitive expression of beta-amyloid neuropathology.
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页数:6
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