Effect of oxandrolone and timing of pubertal induction on final height in Turner syndrome: final analysis of the UK randomised placebo-controlled trial.


Journal

Archives of disease in childhood
ISSN: 1468-2044
Titre abrégé: Arch Dis Child
Pays: England
ID NLM: 0372434

Informations de publication

Date de publication:
01 2021
Historique:
pubmed: 22 12 2019
medline: 4 2 2021
entrez: 22 12 2019
Statut: ppublish

Résumé

The UK Turner syndrome (TS) study examined the effect on final height of oxandrolone 0.05 mg/kg/day (maximum dose 2.5 mg) versus placebo from 9 years of age; and delaying ethinylestradiol induction of puberty by 2 years from 12 (E12) to 14 (E14) years in growth hormone-treated girls with TS. The study ran from 1999 to 2013. By 2011, eighty-two of 92 participants had reached final height and an interim analysis using the Super-Imposition by Translation And Rotation model showed significant increases in final height with both oxandrolone and E14. The analysis has been repeated now that all 92 patients have reached final height. Oxandrolone still significantly increased final height by 4.1 cm (95% CI 1.6 to 6.6, n=92) compared with 4.6 cm previously. However, the E14 effect was no longer significant at 2.7 cm (95% CI -0.8 to 6.1, n=56) compared with 3.8 cm previously.

Identifiants

pubmed: 31862699
pii: archdischild-2019-317695
doi: 10.1136/archdischild-2019-317695
doi:

Substances chimiques

Anabolic Agents 0
Oxandrolone 7H6TM3CT4L

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

74-76

Subventions

Organisme : Medical Research Council
ID : MR/R010692/1
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Emma Jane Gault (EJ)

University of Glasgow College of Medical, Veterinary and Life Sciences, Glasgow, UK.

Tim J Cole (TJ)

Policy and Practice Programme, UCL Great Ormond Street, Institute of Child Health, London, UK.

Sarah Casey (S)

Pharmacy (Clinical Trials) Department, NHS Greater Glasgow and Clyde, Glasgow, UK.

Peter C Hindmarsh (PC)

Clinical and Molecular Genetics Unit, UCL Great Ormond Street Institute of Child Health, London, UK.

Peter Betts (P)

Paediatrics, Southampton University Hospitals NHS Trust, Southampton, UK.

David B Dunger (DB)

Paediatrics, University of Cambridge, Cambridge, UK.

Malcolm D C Donaldson (MDC)

Section of Child Health, Royal Hospital for Sick Children, University of Glasgow School of Medicine, Glasgow, UK malcolm.donaldson@glasgow.ac.uk.

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Classifications MeSH