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The apolipoprotein E epsilon 2 allele and decline in episodic memory
R S Wilson1, J L Bienias, E Berry-Kravis
1Rush Alzheimer's Disease Center and Rush Institute for Healthy Aging, Department of Neurological Sciences, Rush-Presbyterian-St Luke's Medical Center, Chicago, USA. rwilson@rush.edu
Journal of Neurology, Neurosurgery, and Psychiatry
|November 20, 2002
Summary
The apolipoprotein E (apoE) epsilon 2 allele may protect against episodic memory decline in older adults. This contrasts with the epsilon 4 allele, which is linked to faster cognitive decline.
Area of Science:
- Neuroscience
- Genetics
- Cognitive Aging
Background:
- The apolipoprotein E (apoE) epsilon 4 allele is associated with cognitive decline, particularly in episodic memory.
- The impact of the apoE epsilon 2 allele on cognitive function has been less clear.
Purpose of the Study:
- To investigate the effect of apoE genotype on cognitive change over time in older adults.
- To determine if the apoE epsilon 2 allele influences the rate of decline in various cognitive domains.
Main Methods:
- Longitudinal study of 669 cognitively healthy older adults (Religious Orders Study) over eight years.
- Cognitive function assessed annually, with summary measures for episodic memory, semantic memory, working memory, perceptual speed, and visuospatial ability.
- Growth curve models analyzed cognitive change in relation to apoE genotype (epsilon 2, epsilon 3/3 reference, epsilon 4).
Main Results:
- Significant differences in episodic memory change rates among apoE subgroups.
- The apoE epsilon 2 subgroup showed an average annual increase in episodic memory, while epsilon 3/3 and epsilon 4 subgroups declined.
- The apoE epsilon 4 subgroup exhibited faster decline in semantic memory and perceptual speed compared to epsilon 3/3.
Conclusions:
- Presence of one or more apoE epsilon 2 alleles is linked to slower decline in episodic memory in older individuals.
- The apoE epsilon 2 allele does not appear to affect the rate of decline in other cognitive domains.
- Findings highlight differential effects of apoE alleles on cognitive aging trajectories.