Testosterone in advance age: a New Zealand longitudinal cohort study: Life and Living in Advanced Age (Te Puāwaitanga o Ngā Tapuwae Kia Ora Tonu).

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dc.contributor.author Connolly, Martin en
dc.contributor.author Kerse, Ngaire en
dc.contributor.author Wilkinson, Tim en
dc.contributor.author Menzies, Oliver en
dc.contributor.author Rolleston, Anna en
dc.contributor.author Chong, Yih Harng en
dc.contributor.author Broad, Joanna en
dc.contributor.author Moyes, Simon en
dc.contributor.author Jatrana, Santosh en
dc.contributor.author Teh, Ruth en
dc.date.accessioned 2018-11-19T01:44:53Z en
dc.date.issued 2017-11-12 en
dc.identifier.issn 2044-6055 en
dc.identifier.uri http://hdl.handle.net/2292/44454 en
dc.description.abstract OBJECTIVES:Serum testosterone (T) levels in men decline with age. Low T levels are associated with sarcopenia and frailty in men aged >80 years. T levels have not previously been directly associated with disability in older men. We explored associations between T levels, frailty and disability in a cohort of octogenarian men. SETTING:Data from all men from Life and Living in Advanced Age Cohort Study in New Zealand, a longitudinal cohort study in community-dwelling older adults. PARTICIPANTS:Community-dwelling (>80 years) adult men excluding those receiving T treatment or with prostatic carcinoma. OUTCOMES MEASURES:Associations between baseline total testosterone (TT) and calculated free testosterone (fT), frailty (Fried scale) and disability (Nottingham Extended Activities of Daily Living scale (NEADL)) (baseline and 24 months) were examined using multivariate regression and Wald's χ2 techniques. Subjects with the lowest quartile of baseline TT and fT values were compared with those in the upper three quartiles. RESULTS:Participants: 243 men, mean (SD) age 83.7 (2.0) years. Mean (SD) TT=17.6 (6.8) nmol/L and fT=225.3 (85.4) pmol/L. On multivariate analyses, lower TT levels were associated with frailty: β=0.41, p=0.017, coefficient of determination (R2)=0.10 and disability (NEADL) (β=-1.27, p=0.017, R2=0.11), low haemoglobin (β=-7.38, p=0.0016, R2=0.05), high fasting glucose (β=0.38, p=0.038, R2=0.04) and high C reactive protein (CRP) (β=3.57, p=0.01, R2=0.06). Low fT levels were associated with frailty (β=0.39, p=0.024, R2=0.09) but not baseline NEADL (β=-1.29, p=0.09, R2=0.09). Low fT was associated with low haemoglobin (β=-7.83, p=0.0008, R2=0.05) and high CRP (β=2.86, p=0.04, R2=0.05). Relationships between baseline TT and fT, and 24-month outcomes of disability and frailty were not significant. CONCLUSIONS:In men over 80 years, we confirm an association between T levels and baseline frailty scores. The new finding of association between T levels and disability is potentially relevant to debates on T supplementation in older men, though, as associations were not present at 24 months, further work is needed. en
dc.format.medium Electronic en
dc.language eng en
dc.relation.ispartofseries BMJ open en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://www.sherpa.ac.uk/romeo/issn/2044-6055/ en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.rights.uri http://creativecommons.org/licenses/by-nc/4.0/ en
dc.subject Humans en
dc.subject Testosterone en
dc.subject Activities of Daily Living en
dc.subject Multivariate Analysis en
dc.subject Longitudinal Studies en
dc.subject Aged, 80 and over en
dc.subject Frail Elderly en
dc.subject New Zealand en
dc.subject Male en
dc.subject Sarcopenia en
dc.subject Independent Living en
dc.subject Frailty en
dc.title Testosterone in advance age: a New Zealand longitudinal cohort study: Life and Living in Advanced Age (Te Puāwaitanga o Ngā Tapuwae Kia Ora Tonu). en
dc.type Journal Article en
dc.identifier.doi 10.1136/bmjopen-2017-016572 en
pubs.issue 11 en
pubs.begin-page e016572 en
pubs.volume 7 en
dc.rights.holder Copyright: The authors en
dc.identifier.pmid 29133315 en
pubs.publication-status Published en
dc.rights.accessrights http://purl.org/eprint/accessRights/OpenAccess en
pubs.subtype research-article en
pubs.subtype Journal Article en
pubs.elements-id 713114 en
pubs.org-id Medical and Health Sciences en
pubs.org-id Population Health en
pubs.org-id Gen.Practice& Primary Hlthcare en
pubs.org-id School of Medicine en
pubs.org-id Medicine Department en
dc.identifier.eissn 2044-6055 en
pubs.record-created-at-source-date 2017-11-15 en
pubs.dimensions-id 29133315 en


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