Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33606
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dc.contributor.authorHandelsman, David J-
dc.contributor.authorGrossmann, Mathis-
dc.contributor.authorYeap, Bu B-
dc.contributor.authorStuckey, Bronwyn Ga-
dc.contributor.authorShankara-Narayana, Nandini-
dc.contributor.authorConway, Ann J-
dc.contributor.authorInder, Warrick J-
dc.contributor.authorMcLachlan, Robert I-
dc.contributor.authorAllan, Carolyn-
dc.contributor.authorJenkins, Alicia J-
dc.contributor.authorJesudason, David-
dc.contributor.authorBracken, Karen-
dc.contributor.authorWittert, Gary A-
dc.date2023-
dc.date.accessioned2023-08-30T07:48:10Z-
dc.date.available2023-08-30T07:48:10Z-
dc.date.issued2023-12-21-
dc.identifier.citationThe Journal of Clinical Endocrinology and Metabolism 2023-12-21; 109(1)en_US
dc.identifier.issn1945-7197-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33606-
dc.description.abstractThe T4DM study randomized 1007 men with impaired glucose tolerance or newly diagnosed diabetes to testosterone undecanoate (TU, 1000 mg) or matching placebo (P) injections every 12 weeks for 24 months with a lifestyle program with T treatment reducing diabetes diagnosis by 40%. A follow-up email survey after a median of 5.1 years since last injection obtained 599 (59%) completed surveys (316 T, 283 P) with participants in follow-up survey like non-participants in 23 anthropometric and demographic variables. Randomization to TU associated with stronger belief in study benefits during (64% vs 49%, p < 0.001) but no longer after the study (44% vs 40%, p = 0.07) and high interest in future studies. At T4DM entry, 25% had sleep apnea with new diagnosis more frequent on TU (3.0% vs 0.4%, p = 0.03) during, but not after, the study. Post-study resuming prescribed testosterone treatment was more frequent among TU treated men (6% vs 2.8%, p = 0.03). Five years after cessation of TU treatment there was no difference in self-reported rates of new diagnosis of diabetes, prostate or cardiovascular disease nor change in weight maintenance or weight loss behaviours. We conclude that randomized T treatment for 24 months in men with impaired glucose tolerance or new diabetes but without pathological hypogonadism was associated with higher levels of self-reported benefits and diagnosis of sleep apnea during, but not after, the study as well as more frequent prescribed post-study testosterone treatment consistent with androgen dependence in some men receiving prolonged injectable TU.en_US
dc.language.isoeng-
dc.subjectandrogen dependenceen_US
dc.subjectcardiovascular diseaseen_US
dc.subjectdiabetesen_US
dc.subjectprostate diseaseen_US
dc.subjecttestosteroneen_US
dc.titleLong-Term Outcomes of Testosterone Treatment in Men: A T4DM Post-Randomisation Observational Follow-Up Study.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleThe Journal of Clinical Endocrinology and Metabolismen_US
dc.identifier.affiliationANZAC Research Institute, University of Sydney and Department of Andrology, Concord Hospital, NSW 2139, Australia.en_US
dc.identifier.affiliationMedicine (University of Melbourne)en_US
dc.identifier.affiliationMedical School, University of Western Australia, Perth, WA 6009.;Department of Endocrinology and Diabetes, Fiona Stanley Hospital, Perth, WA 6150, Australia.en_US
dc.identifier.affiliationKeogh Institute for Medical Research, and Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Medical School, University of Western Australia.en_US
dc.identifier.affiliationEndocrinologyen_US
dc.identifier.affiliationANZAC Research Institute, University of Sydney and Department of Andrology, Concord Hospital, NSW 2139, Australia.en_US
dc.identifier.affiliationDepartment of Diabetes and Endocrinology, Princess Alexandra Hospital, and PA-Southside Clinical Unit, Medical School, the University of Queensland, Woolloongabba, QLD 4102  Australia.en_US
dc.identifier.affiliationHudson Institute of Medical Research and Monash University, Clayton, VIC, Australia.en_US
dc.identifier.affiliationBaker Heart and Diabetes Institute, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationDepartment of Endocrinology, The Queen Elizabeth Hospital, Adelaide, SA, Australia.en_US
dc.identifier.affiliationKolling Institute, University of Sydney, Sydney, NSW 2064, Australia.en_US
dc.identifier.affiliationFreemasons Centre for Male Health and Wellbeing, South Australian Health and Medical Research Institute and University of Adelaide, Adelaide, SA 506.en_US
dc.identifier.doi10.1210/clinem/dgad485en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-4200-7476en_US
dc.identifier.orcid0000-0001-8261-3457en_US
dc.identifier.orcid0000-0002-7612-5892en_US
dc.identifier.orcid0000-0001-6818-6065en_US
dc.identifier.pubmedid37623257-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptEndocrinology-
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