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Endocrine Abstracts (2023) 95 OC5.2 | DOI: 10.1530/endoabs.95.OC5.2

BSPED2023 Oral Communications Oral Communications 5 (9 abstracts)

Gonadotropin treatment for the induction or completion of puberty for males with hypogonadotropic hypogonadism; Two Centre Experience

Dr Kyla Ng Yin 1 , Professor Leo Dunkel 1 , Dr Claire Hughes 2 , Dr Tony Hulse 3 , Dr Evelien Gevers 1,2 , Mr Lee Martin 2 , Dr Rathi Prasad 1,2 , Dr Ruben Willemsen 1,2 , Professor Gary Butler 4,5 & Dr Sasha Howard 1,2


1Centre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom. 2Department of Paediatric Endocrinology, Royal London Children’s Hospital, Barts Health NHS Trust, London, United Kingdom. 3Evelina Children’s Hospital, London, United Kingdom. 4Department of Paediatric and Adolescent Endocrinology, University College London Hospital NHS Foundation Trust, London, United Kingdom. 5UCL GOS Institute of Child Health, University College London, London, United Kingdom


Background: Hypogonadotropic hypogonadism (HH) is a key cause of absent, partial, or arrested puberty. Individuals with HH experience central disorders of the hypothalamic-pituitary-gonadal (HPG) axis, with deficiency in gonadotropin-releasing hormone (GnRH). This leads to inadequate pituitary gonadotropins (luteinising hormone (LH) and follicle-stimulating hormone (FSH)), resulting in immature gonadal development. It has substantial consequences including infertility and reduced quality of life. The mainstay of current therapy is testosterone which facilitates secondary sexual characteristics; however, spermatogenesis is only possible with gonadotropins.

Objective: To evaluate the efficacy of gonadotropin treatment to induce puberty in males with HH as per the local guidelines available on the BSPED website1. To investigate the outcomes of treatment, using pre-treatment with recombinant (r) FSH for individuals with severe HH, followed by combined rFSH and human chorionic gonadotropin (hCG), and hCG +/- rFSH for patients with partial HH (defined by baseline TV >6ml).

Design: Retrospective analysis conducted on medical records of males diagnosed with HH who received gonadotropin treatment in two large tertiary hospitals (Royal London Hospital and University College London Hospital) from 2011 to 2023.

Outcome Measures: Primary outcome assessed was testicular volume (TV). Secondary outcomes include semen analysis.

Results: A total of 23 males with HH were included, of which 5 have Kallmann syndrome and 2 have HH post-craniopharyngioma. Mean age at start of gonadotropin treatment was 16.89 (± 2.39) years old. 16 patients received pre-treatment with FSH and subsequent hCG/rFSH, and 7 patients received treatment with hCG/rFSH started simultaneously. Mean TV increased from 3.14ml (± 1.74) to 11.63ml (± 5.21) in the group treated with pre-FSH and increased from 7.33ml (± 2.75) to 14.13ml (± 3.71) in the group treated with hCG/FSH. 11 out of 15 males who completed therapy successfully banked sperm. Therapy was well tolerated with only 1 patient choosing to discontinue treatment.

Conclusions: Gonadotropin treatment was effective in inducing or completing puberty in males with HH. Our clinical practice suggests that pre-FSH treatment is a viable option for individuals with TV <6ml, resulting in significant increase in TV. Further prospective studies are warranted to validate these findings and establish standardised treatment guidelines.

1 BSPED, 2021. https://www.bsped.org.uk/media/1989/protocol-for-induction-of-puberty-with-gonadotropins-in-males-with-gnrh-or-gonadotropin-deficiency_bsped_website-002.pdf

Volume 95

50th Annual Meeting of the British Society for Paediatric Endocrinology and Diabetes

Manchester, UK
08 Nov 2023 - 10 Nov 2023

British Society for Paediatric Endocrinology and Diabetes 

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