Autor: |
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 |
Jazyk: |
angličtina |
Rok vydání: |
2008 |
Předmět: |
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Zdroj: |
BMC Geriatrics, Vol 8, Iss 1, p 14 (2008) |
Druh dokumentu: |
article |
ISSN: |
1471-2318 |
DOI: |
10.1186/1471-2318-8-14 |
Popis: |
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. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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