Recovery of male reproductive endocrine function after ceasing prolonged testosterone undecanoate injections

Author:

Handelsman David J12ORCID,Desai Reena12,Conway Ann J12,Shankara-Narayana Nandini12,Stuckey Bronwyn G A3,Inder Warrick J4,Grossmann Mathis5ORCID,Yeap Bu Beng67,Jesudason David8,Ly Lam P12,Bracken Karen9,Wittert Gary Allen8

Affiliation:

1. 1ANZAC Research Institute, University of Sydney, Sydney, New South Wales, Australia

2. 2Department of Andrology, Concord Hospital, Concord, Australia

3. 3Department of Endocrinology and Diabetes, Keogh Institute for Medical Research, Sir Charles Gairdner Hospital and University of Western Australia, Western Australia, Australia

4. 4Princess Alexandra Hospital and the University of Queensland, Queensland, Australia

5. 5The Austin Hospital and University of Melbourne, Victoria, Australia

6. 6Medical School, University of Western Australia, Perth, Western Australia, Australia

7. 7Department of Endocrinology and Diabetes, Fiona Stanley Hospital, Perth, Western Australia, Australia

8. 8Freemasons Centre for Male Health and Wellbeing, University of Adelaide, Adelaide, South Australia, Australia

9. 9NHMRC Clinical Trials Centre, University of Sydney, Sydney, New South Wales, Australia

Abstract

Context The time course of male reproductive hormone recovery after stopping injectable testosterone undecanoate (TU) treatment is not known. Objective The aim of this study was to investigate the rate, extent, and determinants of reproductive hormone recovery over 12 months after stopping TU injections. Materials and Methods Men (n = 303) with glucose intolerance but without pathologic hypogonadism who completed a 2-year placebo (P)-controlled randomized clinical trial of TU treatment were recruited for further 12 months while remaining blinded to treatment. Sex steroids (testosterone (T), dihydrotestosterone, oestradiol, oestrone) by liquid chromatography-mass sprectometry, luteinizing hormone (LH), follicle-stimulating hormone (FSH) and sex hormone-binding globulin (SHBG) by immunoassays and sexual function questionnaires (Psychosexual Diary Questionnaire, International Index of Erectile Function, and short form survey (SF-12)) were measured at entry (3 months after the last injection) and 6, 12, 18, 24, 40, and 52 weeks later. Results In the nested cohort of TU-treated men, serum T was initially higher but declined at 12 weeks remaining stable thereafter with serum T and SHBG at 11 and 13%, respectively, lower than P-treated men. Similarly, both questionnaires showed initial carry-over higher scores in T-treated men but after 18 weeks showed no difference between T- and P-treated men. Initially, fully suppressed serum LH and FSH recovered slowly towards the participant’s own pre-treatment baseline over 12 months since the last injection. Conclusions After stopping 2 years of 1000 mg injectable TU treatment, full reproductive hormone recovery is slow and progressive over 15 months since the last testosterone injection but may take longer than 12 months to be complete. Persistent proportionate reduction in serum SHBG and T reflects lasting exogenous T effects on hepatic SHBG secretion rather than androgen deficiency.

Publisher

Oxford University Press (OUP)

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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