首页> 外文期刊>Annals of the New York Academy of Sciences >Olfaction in Aging and Alzheimer's Disease: Event-related Potentials to a Cross-modal Odor-Recognition Memory Task Discriminate ApoE ε4~+ and ApoE ε4~- Individuals
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Olfaction in Aging and Alzheimer's Disease: Event-related Potentials to a Cross-modal Odor-Recognition Memory Task Discriminate ApoE ε4~+ and ApoE ε4~- Individuals

机译:嗅觉衰老和阿尔茨海默氏病:跨模式气味识别记忆任务的事件相关电位可以区分ApoEε4〜+和ApoEε4〜-

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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) ε4 allele. The present study investigated olfactory and cognitive processing deficits in ApoE ε4~+ individuals using a cross-modal recognition memory task and an objective electrophysio-logical measure, the event-related potential (ERP). Ten ε4~+ individuals (5 M, 5 F, mean [M] = 75.1 years) and 10 age- and gender-matched ε4~- 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 ε4~+ individuals, and intraclass correlations demonstrated differential activity between the two groups. These findings are consistent with a compensatory hypothesis, which posits that nondemented ε4~+ 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 ε4~+ and ApoE e4~- individuals and may contribute to identifying the phenotype of persons who will develop Alzheimer's disease.
机译:阿尔茨海默氏病(AD)是一种破坏性神经退行性疾病,影响超过500万美国人。目前,只有通过尸检后才能通过病理组织学确认对AD的明确和明确的诊断,这表明需要对具有AD风险的患者进行认知功能的客观测量。 AD的最重要的遗传危险因素是载脂蛋白E(ApoE)ε4等位基因。本研究使用交叉模式识别记忆任务和客观的电生理测量方法,事件相关电位(ERP),研究了ApoEε4〜+个体的嗅觉和认知加工缺陷。十个ε4〜+个体(5 M,5 F,平均[M] = 75.1岁)和10个年龄和性别匹配的ε4〜-个体(5 M,5 F,M = 71岁)依次编码一组16嗅觉刺激,并随后显示先前呈现的气味名称(目标)或不呈现(箔)。当参与者使用两键鼠标将目标与箔片区分开时,记录了19个电极的EEG活性。在ε4〜+个体中,P3潜伏期明显更长,并且类内相关性表明两组之间的活动差异。这些发现与补偿假说相符,该假说假设非痴呆的ε4〜+个体将在认知过程上投入更多的精力或参与替代策略,因此需要更大程度地激活神经组织或募集不同的神经种群。研究结果还表明,对识别记忆的跨模式ERP研究可以区分ApoEε4〜+和ApoE e4〜-个体的早期神经认知变化,并且可能有助于识别将发展为阿尔茨海默氏病的人的表型。

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