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Cognitive asymmetries associated with apolipoprotein E genotype in patients with Alzheimer's disease

Published online by Cambridge University Press:  01 July 2003

MICHAEL J. FINTON
Affiliation:
The Wallace-Kettering Neuroscience Institute, Kettering, Ohio
JOHN A. LUCAS
Affiliation:
The Wallace-Kettering Neuroscience Institute, Kettering, Ohio Mayo Clinic Jacksonville, Jacksonville, Florida
JULIE D. RIPPETH
Affiliation:
The Wallace-Kettering Neuroscience Institute, Kettering, Ohio University of California San Diego (UCSD)
DARYL L. BOHAC
Affiliation:
The Wallace-Kettering Neuroscience Institute, Kettering, Ohio University of Nebraska Medical Center, Omaha
GLENN E. SMITH
Affiliation:
The Wallace-Kettering Neuroscience Institute, Kettering, Ohio Mayo Clinic Rochester, Rochester, Minnesota
ROBERT J. IVNIK
Affiliation:
The Wallace-Kettering Neuroscience Institute, Kettering, Ohio Mayo Clinic Rochester, Rochester, Minnesota
RONALD C. PETERSEN
Affiliation:
The Wallace-Kettering Neuroscience Institute, Kettering, Ohio Mayo Clinic Rochester, Rochester, Minnesota
NEILL R. GRAFF-RADFORD
Affiliation:
The Wallace-Kettering Neuroscience Institute, Kettering, Ohio Mayo Clinic Jacksonville, Jacksonville, Florida

Abstract

The relationship between apolipoprotein E (apoE) genotype and cognitive performance was examined in 200 patients with probable Alzheimer's disease (AD). Differences between composite measures of verbal and nonverbal functioning were used to define asymmetric patterns of cognition. Patients who were homozygous for apoE ε4 demonstrated relatively worse nonverbal as compared to verbal cognitive ability. In contrast, participants who were heterozygous for apoE ε4 or who possessed no ε4 allele demonstrated relatively equivalent verbal and nonverbal cognitive abilities. Although age and dementia severity also contributed to these patterns, apoE genotype appears to have a significant unique contribution to cognitive performance in these individuals. The ε4 allele may thus be associated with a specific neurocognitive phenotype among patients with AD, with the overall pattern of cognitive asymmetry dependent upon ε4 dose. (JINS, 2003, 9, 751–759.)

Type
Research Article
Copyright
© 2003 The International Neuropsychological Society

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