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Cognitive performance and leukocyte telomere length in two narrow age-range cohorts: a population study

dc.contributor.authorMather, Karen A
dc.contributor.authorJorm, Anthony F
dc.contributor.authorMilburn, Peter J
dc.contributor.authorEasteal, Simon
dc.contributor.authorChristensen, Helen
dc.contributor.authorAnstey, Kaarin
dc.date.accessioned2016-01-05T03:35:23Z
dc.date.available2016-01-05T03:35:23Z
dc.date.issued2010-09-16
dc.date.updated2016-02-24T10:27:10Z
dc.description.abstractBACKGROUND Cognitive function and telomere length both decline with age. A correlation between these two measures would suggest that they may be influenced by the same underlying age-related biological process. Several studies suggest telomere length may be positively correlated with cognitive performance but the evidence is equivocal. In this report, the relationships between telomere length and cognitive performance at Wave 2 and cognitive change from Wave 1 to Wave 2 are assessed in two narrow age-range population cohorts. METHODS We tested the hypothesis that leukocyte telomere length correlates positively with cognitive performance and cognitive decline in two community cohorts of middle-aged (n = 351, 44-49 years) and older (n = 295, 64-70 years) adults, who participated in two waves of a longitudinal study undertaken in the Canberra-Queanbeyan region of Australia. Telomere length was estimated at Wave 2. Cognitive performance was measured using the Symbol Digit Modalities Test, the immediate recall test of the California Verbal Learning Test, reaction time (simple & choice) and the Trails Test Part B. RESULTS Cross-sectionally at Wave 2, telomere length correlated with Symbol Digit Modalities Test scores (men) and simple reaction time (women) for the older cohort only, although the latter finding was in the opposite direction to that hypothesised. Telomere length measured at Wave 2 was not associated with cognitive change from Wave 1 to Wave 2 for either cohort, except for two associations of small magnitude (immediate recall in the older cohort, choice reaction time in older women), which were also in the contrary direction to that predicted. CONCLUSIONS These results do not give strong support to the hypothesis that leukocyte telomere length is associated with either levels of cognitive performance or age-related cognitive change.
dc.description.sponsorshipThis work was supported by an Australian National Health and Medical Research Council Program Grant 179805 and an R.M. Gibson Grant from the Australian Association of Gerontology. A.F. Jorm, K.J. Anstey and H. Christensen are funded by NHMRC Fellowships.en_AU
dc.identifier.issn1471-2318en_AU
dc.identifier.urihttp://hdl.handle.net/1885/95244
dc.publisherBioMed Central
dc.relationhttp://purl.org/au-research/grants/nhmrc/179805
dc.rights© Mather et al. 2010 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.sourceBMC Geriatrics
dc.subjectadult
dc.subjectage factors
dc.subjectaged
dc.subjectaging
dc.subjectcognition
dc.subjectcognition disorders
dc.subjectcohort studies
dc.subjectcross-sectional studies
dc.subjectfemale
dc.subjecthumans
dc.subjectleukocytes
dc.subjectlongitudinal studies
dc.subjectmale
dc.subjectmiddle aged
dc.subjectpsychomotor performance
dc.subjecttelomere
dc.subjectpopulation surveillance
dc.titleCognitive performance and leukocyte telomere length in two narrow age-range cohorts: a population study
dc.typeJournal article
local.bibliographicCitation.issue1en_AU
local.bibliographicCitation.startpage62en_AU
local.contributor.affiliationMather, Karen, College of Medicine, Biology and Environment, CMBE Research School of Population Health, National Institute for Mental Health Research, The Australian National Universityen_AU
local.contributor.affiliationJorm, Anthony F., University of Melbourne, Australiaen_AU
local.contributor.affiliationAnstey, Kaarin, College of Medicine, Biology and Environment, CMBE Research School of Population Health, National Institute for Mental Health Research, The Australian National Universityen_AU
local.contributor.affiliationMilburn, Peter J., College of Medicine, Biology and Environment, CMBE John Curtin School of Medical Research, Genome Sciences, The Australian National Universityen_AU
local.contributor.affiliationEasteal, Simon, College of Medicine, Biology and Environment, CMBE John Curtin School of Medical Research, Genome Sciences, The Australian National Universityen_AU
local.contributor.affiliationChristensen, Helen, College of Medicine, Biology and Environment, CMBE Research School of Population Health, National Institute for Mental Health Research, The Australian National Universityen_AU
local.contributor.authoruidu3937176en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor170100en_AU
local.identifier.ariespublicationu4020362xPUB191en_AU
local.identifier.citationvolume10en_AU
local.identifier.doi10.1186/1471-2318-10-62en_AU
local.identifier.essn1471-2318en_AU
local.identifier.scopusID2-s2.0-77956578925
local.identifier.thomsonID000208731600062
local.publisher.urlhttp://www.biomedcentral.com/en_AU
local.type.statusPublished Versionen_AU

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