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The association of APOE genotype and cognitive decline in interaction with risk factors in a 65-69 year old community sample

  • Helen Christensen
  • , Philip J. Batterham
  • , Andrew J. Mackinnon
  • , Anthony F. Jorm
  • , Holly A. Mack
  • , Karen A. Mather
  • , Kaarin J. Anstey
  • , Perminder S. Sachdev
  • , Simon Easteal

Research output: Contribution to journalArticlepeer-review

54 Citations (Scopus)

Abstract

Background: While the evidence of an association between the apolipoprotein E (APOE) *E4 allele and Alzheimer's disease is very strong, the effect of the *E4 allele on cognitive decline in the general population is more equivocal. A cross-sectional study on the lifespan effects of the *E4 allele failed to find any effect of the *E4 allele on cognitive performance at ages 20-24, 40-44 or 60-64 years. Methods: In this four year follow-up study, we reexamine the effect of *E4 in the sample of 2,021 individuals, now aged 65-69 years. Results: Performance on the Mini-Mental State Examination (MMSE) was significantly poorer for *E4 homozygotes than heterozygotes or non-carriers. The effects of the *E4 genotype on cognitive decline over four years were found on the MMSE and Symbol-Digit Modalities test but only when controlling for risk factors such as head injury and education. Analyses were repeated with the exclusion of participants diagnosed with a mild cognitive disorder, with little change. Conclusion: It is possible that *E4 carriers become vulnerable to greater cognitive decline in the presence of other risk factors at 65-69 years of age.
Original languageEnglish
Article number14
Number of pages10
JournalBMC Geriatrics
Volume8
DOIs
Publication statusPublished - 2008

Open Access - Access Right Statement

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Keywords

  • Alzheimer's disease
  • aging
  • apolipoprotein E

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