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解析散发性阿尔茨海默病的衰老和遗传风险对路径整合的解离效应。

Dissociating effects of aging and genetic risk of sporadic Alzheimer's disease on path integration.

作者信息

Colmant Lise, Bierbrauer Anne, Bellaali Youssef, Kunz Lukas, Van Dongen Jasper, Sleegers Kristel, Axmacher Nikolai, Lefèvre Philippe, Hanseeuw Bernard

机构信息

Institute of Neuroscience, UCLouvain, Brussels, Belgium; Cliniques Universitaires Saint-Luc, Brussels, Belgium; Institute of Information and Communication Technologies, Electronics and Applied Mathematics, UCLouvain, Louvain-la-Neuve, Belgium.

Institute for Systems Neuroscience, Medical Center Hamburg-Eppendorf, Hamburg, Germany; Department of Neuropsychology, Institute of Cognitive Neuroscience, Faculty of Psychology, Ruhr University Bochum, Germany.

出版信息

Neurobiol Aging. 2023 Nov;131:170-181. doi: 10.1016/j.neurobiolaging.2023.07.025. Epub 2023 Jul 29.

Abstract

Path integration is a spatial navigation ability that requires the integration of information derived from self-motion cues and stable landmarks, when available, to return to a previous location. Path integration declines with age and Alzheimer's disease (AD). Here, we sought to separate the effects of age and AD risk on path integration, with and without a landmark. Overall, 279 people participated, aged between 18 and 80 years old. Advanced age impaired the appropriate use of a landmark. Older participants furthermore remembered the location of the goal relative to their starting location and reproduced this initial view without considering that they had moved in the environment. This lack of adaptative behavior was not associated with AD risk. In contrast, participants at genetic risk of AD (apolipoprotein E ε4 carriers) exhibited a pure path integration deficit, corresponding to difficulty in performing path integration in the absence of a landmark. Our results show that advanced-age impacts landmark-supported path integration, and that this age effect is dissociable from the effects of AD risk impacting pure path integration.

摘要

路径整合是一种空间导航能力,它需要整合来自自我运动线索和稳定地标(如有)的信息,以便返回先前的位置。路径整合能力会随着年龄增长和患阿尔茨海默病(AD)而下降。在这里,我们试图区分年龄和AD风险对有无地标的路径整合的影响。总共有279人参与,年龄在18岁至80岁之间。高龄会妨碍对地标进行适当利用。此外,年龄较大的参与者记住了目标相对于起始位置的位置,并在不考虑自己已在环境中移动的情况下重现了最初的视图。这种缺乏适应性行为与AD风险无关。相比之下,有AD遗传风险的参与者(载脂蛋白E ε4携带者)表现出单纯的路径整合缺陷,即在没有地标的情况下进行路径整合存在困难。我们的结果表明,高龄会影响有地标支持的路径整合,并且这种年龄效应与影响单纯路径整合的AD风险效应是可分离的。

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