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Apolipoprotein E and cognitive change in an elderly population
B T Hyman1, T Gomez-Isla, M Briggs
1Neurology Service, Massachusetts General Hospital, Boston, MA 02114, USA.
Annals of Neurology
|July 1, 1996
Summary
The apolipoprotein E (apoE) epsilon 4 allele slightly increases cognitive impairment risk, while apoE epsilon 2 offers protection. However, many with apoE E4/4 reach old age cognitively unimpaired, limiting genotyping
Area of Science:
- Neuroscience
- Genetics
- Epidemiology
Background:
- The apolipoprotein E (apoE) epsilon 4 allele is linked to increased Alzheimer's disease risk, while the epsilon 2 allele is underrepresented.
- Understanding the impact of apoE genotypes on cognitive function in the general elderly population is crucial for risk assessment.
Purpose of the Study:
- To investigate the association between apolipoprotein E (apoE) genotypes (epsilon 4 and epsilon 2) and the risk of cognitive impairment in older adults.
- To determine the predictive value of apoE genotyping for cognitive decline over a 4- to 7-year period.
Main Methods:
- A population-based sample of 1,899 individuals aged 65+ was studied.
- Multiple regression and logistic regression analyses were used to assess the effects of apoE genotypes on cognitive performance, specifically delayed recall.
- Cognitive impairment risk was evaluated based on apoE epsilon 4 and epsilon 2 allele presence.
Main Results:
- Both apoE epsilon 4 and apoE epsilon 2 alleles significantly predicted performance on a delayed recall task.
- The odds ratio for cognitive impairment was approximately 1.37 for apoE epsilon 4 and 0.53 for apoE epsilon 2.
- These effects were more pronounced in women, yet 85% of elderly individuals with the apoE E4/4 genotype remained cognitively unimpaired.
Conclusions:
- Apolipoprotein E (apoE) genotyping has a modest effect on predicting cognitive impairment in the general elderly population.
- Despite carrying the apoE epsilon 4 allele, many individuals maintain cognitive function into old age.
- ApoE genotyping is likely to have limited utility as a diagnostic or prognostic tool for cognitive decline.