Factors predicting normalization of reproductive hormones after cessation of anabolic-androgenic steroids in men: a single center retrospective study

Author:

Grant Bonnie1ORCID,Campbell John2,Pradeep Anjali1,Burns Angela D3,Bassett Paul4,Abbara Ali1ORCID,Saket Priyadarshi2,Minhas Sukhbinder5,Dhillo Waljit S1,McVeigh James6,Bhasin Shalender7ORCID,Jayasena Channa N1ORCID

Affiliation:

1. Section of Investigative Medicine, Imperial College London, Commonwealth Building, Hammersmith Hospital , Du Cane Road, London W12 0NN , United Kingdom

2. Glasgow Alcohol & Drug Recovery Services, NHS Greater Glasgow & Clyde , Glasgow G5 8BG , United Kingdom

3. Department of Clinical Biochemistry, Queen Elizabeth University Hospital , 1345 Govan Road, Glasgow G51 4TF , United Kingdom

4. Statsconsultancy Ltd , 40 Longwood Lane, Amersham, Bucks HP7 9EN , United Kingdom

5. Department of Urology, Charing Cross Hospital , Fulham Palace Road, London W6 8RF , United Kingdom

6. Department of Sociology, Manchester Metropolitan University , 4 Rosamund Street West, Manchester M15 6LL , United Kingdom

7. Brigham and Women's Hospital , Division of Endocrinology, Diabetes and Hypertension, 221 Longwood Avenue, Boston, MA 02115 , United States

Abstract

Abstract Objective Symptomatic hypogonadism discourages men from stopping anabolic-androgenic steroids (AAS). Some men illicitly take drugs temporarily stimulating endogenous testosterone following AAS cessation (post-cycle therapy; PCT) to lessen hypogonadal symptoms. We investigated whether prior PCT use was associated with the normalization of reproductive hormones following AAS cessation. Methods Retrospective analysis of 641 men attending a clinic between 2015-2022 for a single, nonfasting, random blood test <36 months following AAS cessation, with or without PCT. Normalized reproductive hormones (ie, a combination of reference range serum luteinizing hormone, follicle-stimulating hormone, and total testosterone levels) were the surrogate marker of biochemical recovery. Results Normalization of reproductive hormones was achieved in 48.2% of men. PCT use was associated with faster biochemical recovery (13.0 (IQR8.0-19.0) weeks, PCT; 26.0 (IQR10.5-52) weeks, no-PCT; P < .001). Odds of biochemical recovery during multivariable analysis were: (1) higher with PCT (OR3.80) vs no-PCT (P = .001), in men stopping AAS ≤3 months previously; (2) reduced when 2 (OR0.55), 3 (OR0.46), or 4 (OR0.25) AAS were administered vs 1 drug (P = .009); (3) lower with AAS >6 vs ≤3 months previously (OR0.34, P = .01); (4) higher with last reported AAS >3 months (OR 5.68) vs ≤3 months (P = .001). PCT use was not associated with biochemical recovery in men stopping AAS >3 months previously. Conclusion Without evidence-based withdrawal protocols, men commonly try avoiding post-AAS hypogonadism with PCT, which is illicit, ill-defined, and not recommended. Only half of men had complete biochemical testicular recovery after stopping AAS. The surprising association of self-reported PCT use with short-term biochemical recovery from AAS-induced hypogonadism warrants further investigation.

Funder

MRC

NIHR

NIHR Biomedical Research Centre Funding Scheme

NIHR/Imperial Clinical Research Facility

NIHR Research Professorship

NIHR Post-Doctoral Fellowship

Publisher

Oxford University Press (OUP)

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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