Preclinical memory decline in cognitively normal apolipoprotein E-ε4 homozygotes

Richard J. Caselli, N. R. Graff-Radford, E. M. Reiman, A. Weaver, D. Osborne, J. Lucas, A. Uecker, S. N. Thibodeau

Research output: Contribution to journalArticlepeer-review

107 Scopus citations


Objective: To determine, in a cross-sectional evaluation of nondemented individuals, if age-related memory decline is influenced by apolipoprotein E (apoE) genotype. Background: The apoE-4 allele is an important risk factor for AD. PET in cognitively normal apoE-4 carriers (mean age, 56 years) shows reduced cerebral metabolism suggestive of very early AD that precedes clinically evident memory loss or MRI-based hippocampal atrophy. Methods: Tests of immediate and delayed recall (primary outcome measures) and other neuropsychological measures (secondary outcome measures) were given to three genetically defined groups of cognitively normal individuals (age, 49 to 69 years) including apoE-4 homozygotes (n = 25), apoE-4 heterozygotes (n = 25, all ε3/4), and apoE-4 noncarriers (n = 50). Groups were matched for age, gender, and educational background. Cross-sectional comparisons between the genetic subgroups of the relationship between age and test score were performed for each neuropsychological measure. Results: There were no intergroup differences in mean scores on any neuropsychological measure, but tests sensitive to immediate and delayed recall showed a significant negative correlation with age in the apoE-4 homozygote group relative to the noncarrier group. Conclusion: Consistent with previous neuropsychological studies of early AD, this cross-sectional study suggests that age-related memory decline occurs earlier in cognitively healthy apoE-4 homozygotes than in apoE-4 heterozygotes and noncarriers, and precedes clinically detectable AD.

Original languageEnglish (US)
Pages (from-to)201-207
Number of pages7
Issue number1
StatePublished - Jul 13 1999

ASJC Scopus subject areas

  • Clinical Neurology


Dive into the research topics of 'Preclinical memory decline in cognitively normal apolipoprotein E-ε4 homozygotes'. Together they form a unique fingerprint.

Cite this