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Decline in verbal memory during preclinical Alzheimer's disease: Examination of the effect of APOE genotype

Published online by Cambridge University Press:  13 November 2002

KELLY L. LANGE
Affiliation:
Joint Doctoral Program in Clinical Psychology, San Diego State University/University of California, San Diego
MARK W. BONDI
Affiliation:
Department of Psychiatry, University of California, San Diego Psychology Service, VA San Diego Healthcare System
DAVID P. SALMON
Affiliation:
Department of Neurosciences, University of California, San Diego
DOUGLAS GALASKO
Affiliation:
Department of Neurosciences, University of California, San Diego Neurology Service, VA San Diego Healthcare System
DEAN C. DELIS
Affiliation:
Department of Psychiatry, University of California, San Diego Psychology Service, VA San Diego Healthcare System
RONALD G. THOMAS
Affiliation:
Department of Family and Preventive Medicine, University of California, San Diego
LEON J. THAL
Affiliation:
Department of Neurosciences, University of California, San Diego Neurology Service, VA San Diego Healthcare System

Abstract

A subtle decline in episodic memory often occurs prior to the emergence of the full dementia syndrome in nondemented older adults who develop Alzheimer's disease (AD). The APOE-ε4 genotype may engender a more virulent form of AD that hastens this decline. To examine this possibility, we compared the rate of decline in episodic memory during the preclinical phase of AD in individuals with or without at least one APOE ε4 allele. Nondemented normal control (NC; n = 84) participants, nondemented older adults who subsequently developed dementia within 1 or 2 years (i.e., preclinical AD; n = 20), and patients with mild AD (n = 53) were examined with 2 commonly employed tests of episodic memory, the Logical Memory subtest of the Wechsler Memory Scale–Revised and the California Verbal Learning Test. Results revealed a precipitous decline in verbal memory abilities 1 to 2 years prior to the onset of the dementia syndrome, but there was little effect of APOE genotype on the rate of this memory decline. The presence of an APOE-ε4 allele, however, did have a differential effect on the sensitivity of the 2 types of memory tests for tracking progression and made an independent contribution to the prediction of conversion to AD. (JINS, 2002, 8, 943–955.)

Type
Research Article
Copyright
© 2002 The International Neuropsychological Society

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