The Effect of Apolipoprotein E ε4 (APOE ε4) on Visuospatial Working Memory in Healthy Elderly and Amnestic Mild Cognitive Impairment Patients: An Event-Related Potentials Study

被引:13
|
作者
Gu, Li-Hua [1 ]
Chen, Jiu [1 ]
Gao, Li-Juan [1 ]
Shu, Hao [1 ]
Wang, Zan [1 ]
Liu, Duan [1 ]
Yan, Yan-Na [2 ]
Li, Shi-Jiang [3 ]
Zhang, Zhi-Jun [1 ,2 ]
机构
[1] Southeast Univ, Sch Med, Affiliated ZhongDa Hosp, Dept Neurol, Nanjing, Jiangsu, Peoples R China
[2] Xinxiang Med Univ, Dept Psychol, Xinxiang, Peoples R China
[3] Med Coll Wisconsin, Dept Biophys, Milwaukee, WI 53226 USA
来源
基金
中国国家自然科学基金;
关键词
apolipoprotein E; event-related potential; amnestic mild cognitive impairment; visuospatial working memory; P300; MEDIAL TEMPORAL-LOBE; MAJOR DEPRESSIVE DISORDER; ALZHEIMERS-DISEASE; OLDER-ADULTS; BRAIN ACTIVATION; FMRI EVIDENCE; TERM-MEMORY; P300; RISK; ATTENTION;
D O I
10.3389/fnagi.2017.00145
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
Background: Apolipoprotein E ( APOE) epsilon 4 is the only established risk gene for late-onset, sporadic Alzheimer's disease (AD). Previous studies have provided inconsistent evidence for the effect of APOE epsilon 4 status on the visuospatial working memory (VSWM). Objective: The aim was to investigate the effect of APOE epsilon 4 on VSWM with an event-related potential (ERP) study in healthy controls (HC) and amnestic mild cognitive impairment (aMCI) patients. Methods: The study recorded 39 aMCI patients (27 APOE epsilon 4 non-carriers and 12 APOE epsilon 4 carriers) and their 43 matched controls (25 APOE epsilon 4 non-carriers and 18 APOE epsilon 4 carriers) with an 64-channel electroencephalogram. Participants performed an N-back task, a VSWM paradigm that manipulated the number of items to be stored in memory. Results: The present study detected reduced accuracy and delayed mean correct response time (RT) in aMCI patients compared to HC. P300, a positive component that peaks between 300 and 500 ms, was elicited by the VSWM task. In addition, aMCI patients showed decreased P300 amplitude at the central-parietal (CP1, CPz, and CP2) and parietal (P1, Pz, and P2) electrodes in 0- and 1-back task compared to HC. In both HC and aMCI patients, APOE epsilon 4 carriers showed reduced P300 amplitude with respect to non-carriers, whereas no significant differences in accuracy or RT were detected between APOE epsilon 4 carriers and non-carriers. Additionally, standardized low-resolution brain electromagnetic tomography analysis (s-LORETA) showed enhanced brain activation in the right parahippocampal gyrus (PHG) during P300 time range in APOE epsilon 4 carriers with respect to non-carriers in aMCI patients. Conclusion: It demonstrated that P300 amplitude could predict VSWM deficits in aMCI patients and contribute to early detection of VSWM deficits in APOE epsilon 4 carriers.
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页数:13
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