Murphy Claire, Solomon Ethan S, Haase Lori, Wang Miran, Morgan Charlie D
San Diego State University, San Diego, California 92120-4913, USA.
Ann N Y Acad Sci. 2009 Jul;1170:647-57. doi: 10.1111/j.1749-6632.2009.04486.x.
Alzheimer's disease (AD) is a devastating neurodegenerative condition that affects more than 5 million Americans. Currently, a definitive and unequivocal diagnosis of AD can only be confirmed histopathogically via postmortem autopsy, demonstrating the need for objective measures of cognitive functioning for those at risk for AD. The single most important genetic risk factor of AD is the apolipoprotein E (ApoE) epsilon4 allele. The present study investigated olfactory and cognitive processing deficits in ApoE epsilon4(+) individuals using a cross-modal recognition memory task and an objective electrophysiological measure, the event-related potential (ERP). Ten epsilon4(+) individuals (5 M, 5 F, mean [M]= 75.1 years) and 10 age- and gender-matched epsilon4(-) individuals (5 M, 5 F, M = 71 years) sequentially encoded a set of 16 olfactory stimuli and were subsequently shown names of odors previously presented (targets) or not (foils). EEG activity was recorded from 19 electrodes as participants distinguished targets from foils using a two-button mouse. P3 latencies were significantly longer in epsilon4(+) individuals, and intraclass correlations demonstrated differential activity between the two groups. These findings are consistent with a compensatory hypothesis, which posits that nondemented epsilon4(+) individuals will expend greater effort in cognitive processing or engage in alternative strategies and therefore require greater activation of neural tissue or recruitment of different neural populations. The findings also suggest that cross-modal ERP studies of recognition memory discriminate early neurocognitive changes in ApoE epsilon4(+) and ApoE epsilon4(-) individuals and may contribute to identifying the phenotype of persons who will develop Alzheimer's disease.
阿尔茨海默病(AD)是一种毁灭性的神经退行性疾病,影响着超过500万美国人。目前,AD的明确诊断只能通过死后尸检进行组织病理学确认,这表明需要对有AD风险的人进行认知功能的客观测量。AD最重要的单一遗传风险因素是载脂蛋白E(ApoE)ε4等位基因。本研究使用跨模态识别记忆任务和客观的电生理测量方法——事件相关电位(ERP),调查了ApoE ε4(+)个体的嗅觉和认知加工缺陷。10名ε4(+)个体(5名男性,5名女性,平均年龄[M]=75.1岁)和10名年龄及性别匹配的ε4(-)个体(5名男性,5名女性,平均年龄M=71岁)依次对一组16种嗅觉刺激进行编码,随后向他们展示之前呈现过的气味名称(目标)或未呈现过的气味名称(干扰项)。当参与者使用双按钮鼠标区分目标和干扰项时,从19个电极记录脑电图活动。ε4(+)个体的P3潜伏期明显更长,组内相关分析显示两组之间存在差异活动。这些发现与一种代偿假说一致,该假说认为,未患痴呆的ε4(+)个体在认知加工中会付出更大努力或采用替代策略,因此需要更大程度地激活神经组织或招募不同的神经群体。研究结果还表明,识别记忆的跨模态ERP研究能够区分ApoE ε4(+)和ApoE ε4(-)个体早期的神经认知变化,可能有助于识别将患阿尔茨海默病的人的表型。