Testosterone for Androgen Deficiency-Like Symptoms in Men Without Pathologic Hypogonadism: A Randomized, Placebo-Controlled Cross-over With Masked Choice Extension Clinical Trial.


Journal

The journals of gerontology. Series A, Biological sciences and medical sciences
ISSN: 1758-535X
Titre abrégé: J Gerontol A Biol Sci Med Sci
Pays: United States
ID NLM: 9502837

Informations de publication

Date de publication:
16 09 2020
Historique:
received: 18 04 2019
pubmed: 20 8 2019
medline: 11 2 2021
entrez: 20 8 2019
Statut: ppublish

Résumé

Off-label testosterone prescribing for androgen deficiency (AD)-like sexual and energy symptoms of older men without pathologic hypogonadism has increased dramatically without convincing evidence of efficacy. In a randomized, double-blind, placebo-controlled study with three phases, we entered 45 men aged at least 40 years without pathologic hypogonadism but with AD-like energy and/or sexual symptoms to either daily testosterone or placebo gel treatment for 6 weeks in a cross-over study design with a third, mandatory extension phase in which participants chose which previous treatment they preferred to repeat while remaining masked to their original treatment. Primary endpoints were energy and sexual symptoms as assessed by a visual analog scale (Lead Symptom Score [LSS]). Increasing serum testosterone to the healthy young male range produced no significant benefit more than placebo for energy or sexual LSS. Covariate effects of age, body mass index, and pretreatment baseline serum testosterone on quality-of-life scales were detected. Only 1 out of 22 indices from seven quality-of-life scales was significantly improved by testosterone treatment over placebo. Participants did not choose testosterone significantly more than placebo as their preferred treatment in the third phase. Six-week testosterone treatment does not improve energy or sexual symptoms more than placebo in symptomatic men without pathologic hypogonadism.

Sections du résumé

BACKGROUND
Off-label testosterone prescribing for androgen deficiency (AD)-like sexual and energy symptoms of older men without pathologic hypogonadism has increased dramatically without convincing evidence of efficacy.
METHODS
In a randomized, double-blind, placebo-controlled study with three phases, we entered 45 men aged at least 40 years without pathologic hypogonadism but with AD-like energy and/or sexual symptoms to either daily testosterone or placebo gel treatment for 6 weeks in a cross-over study design with a third, mandatory extension phase in which participants chose which previous treatment they preferred to repeat while remaining masked to their original treatment. Primary endpoints were energy and sexual symptoms as assessed by a visual analog scale (Lead Symptom Score [LSS]).
RESULTS
Increasing serum testosterone to the healthy young male range produced no significant benefit more than placebo for energy or sexual LSS. Covariate effects of age, body mass index, and pretreatment baseline serum testosterone on quality-of-life scales were detected. Only 1 out of 22 indices from seven quality-of-life scales was significantly improved by testosterone treatment over placebo. Participants did not choose testosterone significantly more than placebo as their preferred treatment in the third phase.
CONCLUSIONS
Six-week testosterone treatment does not improve energy or sexual symptoms more than placebo in symptomatic men without pathologic hypogonadism.

Identifiants

pubmed: 31425577
pii: 5551526
doi: 10.1093/gerona/glz195
doi:

Substances chimiques

Androgens 0
Testosterone 3XMK78S47O

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1723-1731

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of The Gerontological Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Shao Feng Mok (SF)

Andrology Department, Concord Hospital, Sydney, New South Wales, Australia.
ANZAC Research Institute, University of Sydney, New South Wales, Australia.
Department of Medicine, National University Hospital, Singapore.

Carolyn Fennell (C)

Andrology Department, Concord Hospital, Sydney, New South Wales, Australia.
ANZAC Research Institute, University of Sydney, New South Wales, Australia.

Sasha Savkovic (S)

Andrology Department, Concord Hospital, Sydney, New South Wales, Australia.
ANZAC Research Institute, University of Sydney, New South Wales, Australia.

Leo Turner (L)

Andrology Department, Concord Hospital, Sydney, New South Wales, Australia.
ANZAC Research Institute, University of Sydney, New South Wales, Australia.

Veena Jayadev (V)

Andrology Department, Concord Hospital, Sydney, New South Wales, Australia.
ANZAC Research Institute, University of Sydney, New South Wales, Australia.

Ann Conway (A)

Andrology Department, Concord Hospital, Sydney, New South Wales, Australia.
ANZAC Research Institute, University of Sydney, New South Wales, Australia.

David J Handelsman (DJ)

Andrology Department, Concord Hospital, Sydney, New South Wales, Australia.
ANZAC Research Institute, University of Sydney, New South Wales, Australia.

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Classifications MeSH