BMC Geriatrics (Jul 2008)

The association of <it>APOE </it>genotype and cognitive decline in interaction with risk factors in a 65–69 year old community sample

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

DOI
https://doi.org/10.1186/1471-2318-8-14
Journal volume & issue
Vol. 8, no. 1
p. 14

Abstract

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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 1 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.