1. Context-specific memory and apolipoprotein E (ApoE) epsilon 4: cognitive evidence from the NIMH prospective study of risk for Alzheimer's disease
- Author
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Nadeem Mirza, Robert M. Cohen, Gary Linker, Judy Bergeson, Francois Lalonde, Virginia M. Rosen, James A. Levy, Karen Putnam, and Trey Sunderland
- Subjects
Oncology ,Apolipoprotein E ,Adult ,Male ,Risk ,medicine.medical_specialty ,Genotype ,Context-dependent memory ,Apolipoprotein E4 ,Neuropsychological Tests ,Apolipoproteins E ,Gene Frequency ,Alzheimer Disease ,Memory ,Internal medicine ,medicine ,Humans ,Prospective Studies ,Alleles ,National Institute of Mental Health (U.S.) ,Aged ,Aged, 80 and over ,Recall ,business.industry ,General Neuroscience ,Neuropsychology ,Wechsler Scales ,Wechsler Adult Intelligence Scale ,Cognition ,Middle Aged ,Verbal Learning ,Entorhinal cortex ,United States ,Cognitive test ,Psychiatry and Mental health ,Clinical Psychology ,Linear Models ,Female ,Neurology (clinical) ,business ,Mental Status Schedule - Abstract
The aim of the study was to determine whether the epsilon 4 allele of the apolipoprotein E (ApoE) gene was associated primarily with context-specific memory among individuals at genetic risk for developing Alzheimer's disease. The effect of ApoE status on comprehensive neuropsychological results was examined in 176 healthy adults during baseline cognitive testing in the NIMH Prospective Study of Biomarkers for Older Controls at Risk for Alzheimer's Disease (NIMH Prospective BIOCARD Study). The presence of the epsilon 4 allele was associated with significantly lower total scores on the Logical Memory II subtest of the Wechsler Memory Scale-Revised and percent of information retained after delay. Further analysis indicated the prose recall and retention effect was partially explained by a small subgroup of epsilon 4 homozygotes, suggesting a gradually progressive process that may be presaged with specific cognitive measures. The current results may represent an epsilon 4-associated breakdown between gist-related information and context-bound veridical recall. This relative disconnection may be understood in light of putative epsilon 4-related preclinical accumulation of Alzheimer pathology (tangles and plaques) in the entorhinal cortex (EC) and among frontal networks, as well as the possibility of less-efficient compensatory strategies.
- Published
- 2002