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

被引:7
作者
Colmant, Lise [1 ,2 ,3 ]
Bierbrauer, Anne [4 ,5 ]
Bellaali, Youssef [2 ]
Kunz, Lukas [6 ]
Van Dongen, Jasper [7 ]
Sleegers, Kristel [7 ]
Axmacher, Nikolai [5 ]
Lefevre, Philippe [1 ,3 ]
Hanseeuw, Bernard [1 ,2 ,8 ,9 ]
机构
[1] UCLouvain, Inst Neurosci, Ave Mounier 53-B 1 53 05, B-1200 Brussels, Belgium
[2] Clin Univ St Luc, Brussels, Belgium
[3] UCLouvain, Inst Informat & Commun Technol, Elect & Appl Math, Louvain La Neuve, Belgium
[4] Med Ctr Hamburg Eppendorf, Inst Syst Neurosci, Hamburg, Germany
[5] Ruhr Univ Bochum, Inst Cognit Neurosci, Fac Psychol, Dept Neuropsychol, Bochum, Germany
[6] Univ Hosp Bonn, Dept Epileptol, Bonn, Germany
[7] Univ Antwerp, Dept Mol Genet, VIB, Antwerp, Belgium
[8] Harvard Med Sch, Massachusetts Gen Hosp, Gordon Ctr Med Imaging, Dept Radiol, Boston, MA USA
[9] WEL Res Inst, WELBIO Dept, Wavre, Belgium
关键词
Path integration; Aging; Alzheimer's disease; APOE; Entorhinal cortex; AGE-RELATED-CHANGES; SPATIAL NAVIGATION; ENTORHINAL CORTEX; GRID CELLS; DEFICITS; REPRESENTATIONS; MEMORY; PART;
D O I
10.1016/j.neurobiolaging.2023.07.025
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
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 epsilon 4 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.(c) 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:170 / 181
页数:12
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