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PMID: 15699382 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

fMRI evidence of compensatory mechanisms in older adults at genetic risk for Alzheimer disease.

Neurology ·Vol. 64 ·No. 3 ·2005-02-08 ·Pages 501-8

Bondi MW, Houston WS, Eyler LT, Brown GG

Abstract

To determine whether APOE genotype influences brain response and whether nonverbal stimuli generate findings comparable with those of previous studies that used verbal stimuli. The relationship between APOE genotype and blood oxygenation level dependent (BOLD) brain response was examined during a picture-encoding task in nondemented older adults. Twenty nondemented participants with normal episodic memory function were divided into two groups based on the presence (n = 10) or absence (n = 10) of the APOE epsilon4 allele. Picture learning was completed during functional MRI in a blocked design alternating between experimental (novel pictures) and control (repeated picture) conditions. Nondemented older adults with an APOE epsilon4 allele showed greater magnitude and extent of BOLD brain response during learning of new pictures relative to their matched epsilon3 counterparts. Different patterns and directions of association between hippocampal activity and learning and memory performance were also demonstrated. The results suggest that brain response differences are not due to poorer general memory abilities, differential atrophy, or brain response during control conditions, but instead appear to be directly influenced by APOE genotype. Results are consistent with a compensatory hypothesis wherein older adults at genetic risk for Alzheimer disease by virtue of the APOE epsilon4 allele appear to require additional cognitive effort to achieve comparable performance levels on tests of episodic memory encoding.

MeSH Terms
Adaptation, Psychological/physiology Aged Aged, 80 and over Alleles Alzheimer Disease/diagnosis,genetics,physiopathology,psychology Apolipoprotein E4 Apolipoproteins E/genetics Cerebral Cortex/blood supply,physiology Cerebrovascular Circulation Cognition Disease Progression Early Diagnosis Female Genetic Predisposition to Disease Genotype Hippocampus/blood supply,physiology Humans Learning/physiology Magnetic Resonance Imaging Male Memory Memory Disorders/etiology,physiopathology,psychology Neuropsychological Tests Photic Stimulation Prognosis Reference Values
Chemicals
Apolipoprotein E4 Apolipoproteins E
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Bondi Mark W
University of California San Diego and VA San Diego Healthcare System, 3350 La Jolla Village Drive, San Diego, CA 92161, USA. [email protected]
Houston Wes S
Eyler Lisa T
Brown Gregory G
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Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
1526-632X
Published
2005-02-08
Pages
501-8
Language
English
Region
United States
NLM ID
0401060
PMCID
PMC1761695
Subset
IM
Grants
NIA NIH HHS · P50 AG005131 · United States
NIA NIH HHS · R01 AG012674 · United States
NIA NIH HHS · R01 AG12674 · United States
Corrections
CommentIn
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