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. 2009 Jul:1170:647-57.
doi: 10.1111/j.1749-6632.2009.04486.x.

Olfaction in aging and Alzheimer's disease: event-related potentials to a cross-modal odor-recognition memory task discriminate ApoE epsilon4+ and ApoE epsilon 4- 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 epsilon4+ and ApoE epsilon 4- individuals

Claire Murphy et al. Ann N Y Acad Sci. 2009 Jul.

Abstract

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.

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Figures

Figure 1
Figure 1
P3 latency for ApoE ε4+ and ε4− participants.
Figure 2
Figure 2
Intra-Class correlations for electrode sites for the four response types for ε4+ and ε4− individuals. Blue indicates the greatest differences between groups and red the highest correlations between groups.
Figure 2
Figure 2
Intra-Class correlations for electrode sites for the four response types for ε4+ and ε4− individuals. Blue indicates the greatest differences between groups and red the highest correlations between groups.
Figure 3
Figure 3
P3 amplitude for the four response types for ε4+ and ε4− individuals. Warmer colors indicate greater amplitude.
Figure 3
Figure 3
P3 amplitude for the four response types for ε4+ and ε4− individuals. Warmer colors indicate greater amplitude.

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