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Memory Resilience to Alzheimer's Genetic Risk: Sex Effects in Predictor Profiles

dc.contributor.authorMcDermott, Kirstie L
dc.contributor.authorMcFall, G. Peggy
dc.contributor.authorAndrews, Shea
dc.contributor.authorAnstey, Kaarin
dc.contributor.authorDixon, Roger A.
dc.date.accessioned2021-08-06T04:43:48Z
dc.date.issued2017
dc.date.updated2020-11-23T10:48:53Z
dc.description.abstractObjectives: Apolipoprotein E (APOE) ɛ4 and Clusterin (CLU) C alleles are risk factors for Alzheimer’s disease (AD) and episodic memory (EM) decline. Memory resilience occurs when genetically at-risk adults perform at high and sustained levels. We investigated whether (a) memory resilience to AD genetic risk is predicted by biological and other risk markers and (b) the prediction profiles vary by sex and AD risk variant. Method: Using a longitudinal sample of nondemented adults (n = 642, aged 53–95) we focused on memory resilience (over 9 years) to 2 AD risk variants (APOE, CLU). Growth mixture models classified resilience. Random forest analysis, stratified by sex, tested the predictive importance of 22 nongenetic risk factors from 5 domains (n = 24–112). Results: For both sexes, younger age, higher education, stronger grip, and everyday novel cognitive activity predicted memory resilience. For women, 9 factors from functional, health, mobility, and lifestyle domains were also predictive. For men, only fewer depressive symptoms was an additional important predictor. The prediction profiles were similar for APOE and CLU. Discussion: Although several factors predicted resilience in both sexes, a greater number applied only to women. Sexspecific mechanisms and intervention targets are implied.en_AU
dc.description.sponsorshipThis work was supported by the National Institutes of Health (National Institute on Aging; grant number R01 AG008235); the Canada Research Chairs program; and the Canadian Consortium on Neurodegeneration in Aging (with funding from Canadian Institutes of Health Research and partners, including SANOFI-ADVENTIS R&D) to Roger Dixon. The National Health and Medical Research Council (Research Fellowship #1102694 and Grant #1100579) supported Kaarin Anstey’s involvement.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1873-9598en_AU
dc.identifier.urihttp://hdl.handle.net/1885/243250
dc.language.isoen_AUen_AU
dc.publisherOxford University Pressen_AU
dc.relationhttp://purl.org/au-research/grants/nhmrc/1102694en_AU
dc.relationhttp://purl.org/au-research/grants/nhmrc/1100579en_AU
dc.rights© The Author 2016. Published by Oxford University Press on behalf of The Gerontological Society of Americaen_AU
dc.sourceInternational Journal of Gerontologyen_AU
dc.subjectAlzheimer’s risk factorsen_AU
dc.subjectApolipoprotein Een_AU
dc.subjectClusterinen_AU
dc.subjectRandom forest analysisen_AU
dc.subjectVictoria Longitudinal Studyen_AU
dc.titleMemory Resilience to Alzheimer's Genetic Risk: Sex Effects in Predictor Profilesen_AU
dc.typeJournal articleen_AU
local.bibliographicCitation.issue6en_AU
local.bibliographicCitation.lastpage946en_AU
local.bibliographicCitation.startpage937en_AU
local.contributor.affiliationMcDermott, Kirstie L, University of Albertaen_AU
local.contributor.affiliationMcFall, G. Peggy, University of Albertaen_AU
local.contributor.affiliationAndrews, Shea, College of Health and Medicine, ANUen_AU
local.contributor.affiliationAnstey, Kaarin, College of Health and Medicine, ANUen_AU
local.contributor.affiliationDixon, Roger A., University of Albertaen_AU
local.contributor.authoruidAndrews, Shea, u5279955en_AU
local.contributor.authoruidAnstey, Kaarin, u4038535en_AU
local.description.embargo2099-12-31
local.description.notesImported from ARIESen_AU
local.identifier.absfor111702 - Aged Health Careen_AU
local.identifier.ariespublicationu4321547xPUB102en_AU
local.identifier.citationvolume72en_AU
local.identifier.doi10.1093/geronb/gbw161en_AU
local.identifier.scopusID2-s2.0-85031946581
local.identifier.thomsonID000412844300004
local.publisher.urlhttps://academic.oup.com/en_AU
local.type.statusPublished Versionen_AU

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