Perceived Loss of Memory Ability and Cerebral Metabolic Decline in Persons With the Apolipoprotein E-IV Genetic Risk for Alzheimer Disease
Abstract
Context Concerns about age-related memory loss are greater in persons who have the apolipoprotein E-IV (APOE4) genetic risk for Alzheimer disease, but the correlation between the degree of concerns and future cerebral metabolic decline is unknown. Objective To investigate whether the degree of self-perceived memory loss is associated with regional cerebral metabolic decline. Design Longitudinal study. Setting Aging and Memory Research Center, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles. Participants Thirty right-handed, cognitively intact, middle-aged and older adults (age range, 50-82 years) with age-associated memory complaints, 14 of whom were carriers of the apolipoprotein E-IV allele, were recruited for longitudinal study. Main outcome measures At baseline, we administered a standardized neuropsychological battery and assessed self-appraisal of memory functioning using the Memory Functioning Questionnaire, which yields 4 factor scores indicating frequency of forgetting, seriousness of forgetting, retrospective functioning, and mnemonics use. Regional cerebral glucose metabolism was determined using fluorodeoxyglucose F18-positron emission tomography at baseline and after 2 years. Results At baseline, APOE4 carriers and noncarriers did not differ significantly on objective memory measures or on Memory Functioning Questionnaire factor scores. However, the factor score for frequency of forgetting significantly correlated with g…
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Altered brain metabolism, especially increased aerobic glycolysis and impaired oxygen consumption in the brains of ApoE4 carriers, is suggested by studies from human plasma and humanized mouse models.
“Altered brain metabolism, especially increased aerobic glycolysis and impaired oxygen consumption in the brains of ApoE4 carriers, is suggested in studies from human plasma and humanized mouse models.2”
From ApoE4-dependent lysosomal cholesterol accumulation impairs mitochondrial homeostasis and oxidative phosphorylation in human astrocytes (2023) · cites this paper as [2]
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- Authors
- Ercoli, L., Siddarth, P., Huang, S.-C., Miller, K., Bookheimer, S. Y., Wright, B. C., Phelps, M. E., & Small, G.
- Affiliations
- University of California, Los Angeles (US)
- Venue
- Archives of General Psychiatry
- Publisher
- American Medical Association (AMA)
- Published
- 2006-04-01
- Volume
- 63
- Issue
- 4
- Pages
- 442
- ISSN
- 0003-990X (ISSN-L)
- OpenAlex
- W1964500623
- Cited by
- 31
- References
- 6
- Citations by year
- 2026: 1 · 2024: 1 · 2023: 1 · 2019: 5 · 2016: 2 · 2015: 1 · 2014: 1 · 2013: 2 · 2012: 2
- FWCI
- 2.03
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Archives of General Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (RG296051)
- National Institute on Aging (AG05 128, AG100784, AG112268, AG-13308, P50AG016570, AG 10123, P50AG005128, AG 16570, R01AG013308, P30AG010123)
- National Institute of Mental Health (MH52453, R01MH052453)
- National Institute of Neurological Disorders and Stroke (P01NS026630, NS31 153, R01NS031153, NS 26630)
- National Center for Research Resources (M01RR000865)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Cognitive Functions and Memory
- Keywords
- APOE ε4, Alzheimer's disease, regional cerebral glucose metabolism, metabolic decline, compensatory strategies, prodromal Alzheimer's disease, memory function
- MeSH terms
- Aged, Aged, 80 and over, Alzheimer Disease, Apolipoproteins E, Awareness, Brain, Cognition Disorders, Genotype, Glucose, Health Status, Heterozygote, Humans, Functional Laterality, Longitudinal Studies, Memory Disorders, Middle Aged, Neuropsychological Tests, Surveys and Questionnaires, Fluorodeoxyglucose F18, Genetic Predisposition to Disease, Positron-Emission Tomography, Apolipoprotein E4
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