Apolipoprotein E (APOE) ε4 and episodic memory decline in Alzheimer's disease: A review

被引:61
|
作者
El Haj, Mohamad [1 ]
Antoine, Pascal [1 ]
Amouyel, Philippe [2 ]
Lambert, Jean-Charles [2 ]
Pasquier, Florence [3 ]
Kapogiannis, Dimitrios [4 ]
机构
[1] Univ Lille, Lab SCALab, UMR CNRS 9193, F-59653 Villeneuve Dascq, France
[2] Univ Lille 2, Inst Pasteur Lille, INSERM, U744, Lille, France
[3] Univ Lille Nord France, UDSL & Memory Clin, CHU, Lille, France
[4] NIA, Neurosci Lab, Baltimore, MD 21224 USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; APOE; Apolipoprotein E; Episodic memory; CATECHOL-O-METHYLTRANSFERASE; MILD COGNITIVE IMPAIRMENT; HEALTHY OLDER-ADULTS; E GENOTYPE; AUTONOETIC CONSCIOUSNESS; AUTOBIOGRAPHICAL MEMORY; VAL(66)MET POLYMORPHISM; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; AMYLOID DEPOSITION;
D O I
10.1016/j.arr.2016.02.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A growing body of research has examined the relationship between episodic memory decline, the cognitive hallmark of Alzheimer's disease (AD), and the presence of Apolipoprotein E epsilon 4 (APOE epsilon 4) allele, a major genetic risk factor for the disease. Our review attempts to summarize and critically evaluate this literature. We performed a systematic search for studies assessing episodic memory in AD patients who were genotyped for APOE epsilon 4 and identified fourteen papers. Although most of these papers reported significant relationships between APOE epsilon 4 and episodic memory decline in AD, some papers did not confirm this relationship. Our review links this controversy to the conflicting literature about the effects of APOE epsilon 4 on general cognitive functioning in AD. We identify several shortcoming and limitations of the research on the relationship between APOE epsilon 4 and episodic memory in AD, such as small sample sizes, non-representative populations, lack of comparison of early-onset vs. late-onset disease, and lack of comparison among different genotypes that include APOE epsilon 4 (i.e., zero, one, or two epsilon 4 alleles). Another major shortcoming of the reviewed literature was the lack of comprehensive evaluation of episodic memory decline, since episodic memory was solely evaluated with regard to encoding and retrieval, omitting evaluation of core episodic features that decline in AD, such as context recall (e.g., how, where, and when an episodic event has occurred) and subjective experience of remembering (e.g., reliving, emotion and feeling during episodic recollection). Future research taking these limitations into consideration could illuminate the nature of the relationship between APOE epsilon 4 and episodic memory decline in AD. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:15 / 22
页数:8
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