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Does possession of apolipoprotein E ε4 benefit cognitive function in healthy young adults?

dc.contributor.authorBunce, David
dc.contributor.authorChristensen, Helen
dc.contributor.authorEasteal, Simon
dc.contributor.authorBurns, Richard
dc.contributor.authorAnstey, Kaarin
dc.date.accessioned2015-12-10T22:14:19Z
dc.date.issued2011
dc.date.updated2016-02-24T10:27:15Z
dc.description.abstractThere is considerable evidence that the apolipoprotein E (APOE) e{open}4 allele is associated with cognitive deficits in older persons, and is a risk factor for dementia. However, it has recently been suggested that possession of the e{open}4 allele may benefit cognition in early adulthood. We tested this possibility in 5445 community-dwelling persons aged 20-24, 40-44, and 60-64 years using a comprehensive battery of cognitive measures. As the APOE e{open}2 allele may offer protection against cognitive deficits, in order to robustly test the hypothesis, we removed persons carrying this allele from the analyses. Older persons with possible dementia were also removed. We found no evidence of higher cognitive performance in young e{open}4 carriers, or cognitive deficits in older e{open}4 carriers. This did not change when a range of health variables were taken into account. We conclude that it is premature to suppose e{open}4-related benefits to cognition in healthy young adulthood and findings consistent with this hypothesis may have been related to methodological issues, or the pathology of the sample investigated.
dc.identifier.issn0028-3932
dc.identifier.urihttp://hdl.handle.net/1885/50240
dc.publisherPergamon Press
dc.sourceNeuropsychologia
dc.subjectKeywords: apolipoprotein E epsilon4; apolipoprotein E4; genomic DNA; unclassified drug; adult; adulthood; age distribution; allele; article; cognition; cognitive defect; community living; controlled study; female; human; human experiment; male; mental performance; Age; Antagonistic pleiotropy; APOE; Cognitive function
dc.titleDoes possession of apolipoprotein E ε4 benefit cognitive function in healthy young adults?
dc.typeJournal article
local.bibliographicCitation.issue7
local.bibliographicCitation.lastpage1697
local.bibliographicCitation.startpage1693
local.contributor.affiliationBunce, David, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationAnstey, Kaarin, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationBurns, Richard, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationChristensen, Helen, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationEasteal, Simon, College of Medicine, Biology and Environment, ANU
local.contributor.authoruidBunce, David, u4713234
local.contributor.authoruidAnstey, Kaarin, u4038535
local.contributor.authoruidBurns, Richard, u4009270
local.contributor.authoruidChristensen, Helen, u8804902
local.contributor.authoruidEasteal, Simon, u8200596
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor170100 - PSYCHOLOGY
local.identifier.absseo920112 - Neurodegenerative Disorders Related to Ageing
local.identifier.ariespublicationu4020362xPUB200
local.identifier.citationvolume49
local.identifier.doi10.1016/j.neuropsychologia.2011.02.042
local.identifier.scopusID2-s2.0-79956137927
local.identifier.thomsonID000292009400006
local.type.statusPublished Version

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