Annals of Neurology · 1996 · 56 citations · 21 references
MedicineGeneticsNeurologyAgingDementiaMemoryAlzheimer DiseaseCognitive AgingCognitive ImpairmentDementia DiagnosisDementia Risk FactorsNeurodegenerative DiseasesAllele FrequencyAlzheimer Disease DementiaApoe GeneticsApolipoprotein E Genotype RiskApolipoprotein E VariantsControl Group DesignMatched Control GroupPreclinical Disease Stages
Many studies have demonstrated a strong association between the presence of one or two epsilon 4 alleles and Alzheimer's disease (AD), although few data are available on the apolipoprotein E (APOE) epsilon 4 frequencies at the preclinical stages of AD. Thus, with a view to determining whether APOE genotyping could be useful in the early detection of AD, we determined the Apoe allele frequencies in patients with memory complaints without dementia (age-related memory decline, ARMD). We found an APOE epsilon 4 allele frequency of 0.315 in the ARMD group, similar to 0.293 in the AD group, in contrast to 0.057 in the control group. Significant differences (t=-2.91, df=25, p=0.008) were found between the Alzheimer's Disease Assessment Scale (ADAS) total scores in the ARMD patients with at least one epsilon 4 allele (mean=24.2) compared with the ARMD patients without the epsilon 4 allele (mean=14.7). Our results suggest that the patients with memory complaints, a high ADAS score, and the presence of one or two APOE-4 alleles could be at high risk for developing AD. Thus, we propose that genotyping in conjunction with the ADAS scale may prove useful as diagnostic markers of AD in the presymptomatic stages.
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