El Haj Mohamad, Antoine Pascal, Amouyel Philippe, Lambert Jean-Charles, Pasquier Florence, Kapogiannis Dimitrios
Laboratoire SCALab UMR CNRS 9193, University of Lille, France.
Laboratoire SCALab UMR CNRS 9193, University of Lille, France.
Ageing Res Rev. 2016 May;27:15-22. doi: 10.1016/j.arr.2016.02.002. Epub 2016 Feb 11.
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 ε4 (APOE ε4) 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 ε4 and identified fourteen papers. Although most of these papers reported significant relationships between APOE ε4 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 ε4 on general cognitive functioning in AD. We identify several shortcoming and limitations of the research on the relationship between APOE ε4 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 ε4 (i.e., zero, one, or two ε4 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 ε4 and episodic memory decline in AD.
越来越多的研究探讨了情景记忆衰退(阿尔茨海默病(AD)的认知标志)与载脂蛋白Eε4(APOEε4)等位基因(该疾病的主要遗传风险因素)之间的关系。我们的综述试图总结并批判性地评估这一文献。我们对评估了APOEε4基因分型的AD患者情景记忆的研究进行了系统检索,共识别出14篇论文。尽管这些论文中的大多数都报告了APOEε4与AD患者情景记忆衰退之间存在显著关系,但也有一些论文并未证实这种关系。我们的综述将这一争议与关于APOEε4对AD患者一般认知功能影响的相互矛盾的文献联系起来。我们指出了关于APOEε4与AD患者情景记忆关系研究的几个缺点和局限性,比如样本量小、人群缺乏代表性、缺乏早发性与晚发性疾病的比较,以及缺乏对包含APOEε4的不同基因型(即零个、一个或两个ε4等位基因)之间的比较。所综述文献的另一个主要缺点是缺乏对情景记忆衰退的全面评估,因为情景记忆仅在编码和检索方面进行了评估,而忽略了AD中衰退的核心情景特征的评估,如情景回忆(例如,一个情景事件是如何、在哪里以及何时发生的)和记忆的主观体验(例如,情景回忆过程中的重现、情感和感受)。未来研究若考虑到这些局限性,可能会阐明APOEε4与AD患者情景记忆衰退之间关系的本质。