Growth hormone therapy of Turner's syndrome: beneficial effect on adult height
Abstract
Objective To carry out a multicenter, prospective, randomized trial of human growth hormone (GH), alone or in combination with oxandrolone (OX), in patients with Turner's syndrome (TS).Methods In an initial phase lasting 12 to 24 months, 70 girls with TS, verified by karyotype, were randomly assigned to one of four groups: (1) observation, (2) OX, (3) GH, or (4) GH plus OX. After completion of the first phase, group 3 subjects continued to receive GH only. All other subjects were treated with GH plus OX. Subjects were followed up until attainment of adult height and/or cessation of treatment. Data from this trial were compared with growth characteristics of 25 American historical subjects with TS (matched for age, height, parental target height, and karyotype) who never received either GH or androgens.Results Of the 70 subjects enrolled, 60 completed the clinical trial. The 17 subjects receiving GH alone all completed the trial and reached a height of 150.4+/-5.5 cm (mean +/- SD), 8.4+/-4.5 cm taller than their mean projected adult height at enrollment (95% confidence interval [CI]: 6.3 to 10.6 cm). The 43 subjects receiving GH plus OX attained a mean height of 152.1+/-5.9 cm, 10.3+/-4.7 cm taller than their mean projected adult height (95% CI: 8.9 to 11.7 cm). The historical control subjects had a mean adult height of 144.2+/-6.0 cm, precisely matching their original projected adult height of 144.2+/-6.1 cm.Conclusions GH, either alone or in combination with OX, is capable of stimulating short-term growth and augmenting adult height in girls with TS. With early diagnosis and initiation of treatment, an adult height of more than 150 cm is a reasonable goal for most girls with TS.
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Only six RCTs have compared GH treatment with concurrent non-treatment or placebo control for at least one year.
“Despite numerous studies of GH treatment in TS, only six randomized, controlled trials (RCTs) have compared GH treatment with a concurrent non-treatment or placebo control for at least one year157-162”
From Clinical practice guidelines for the care of girls and women with Turner syndrome. (2024) · cites this paper as [159]
A 2007 Cochrane review concluded that girls treated with GH grew 3 cm/year more than untreated girls in the first 12-18 months.
“a 2007 Cochrane Center review156 concluded that girls treated with GH grew 3 cm year−1 more than untreated girls in the first 12-18 months of therapy”
From Clinical practice guidelines for the care of girls and women with Turner syndrome. (2024) · cites this paper as [159]
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- Authors
- Rosenfeld, R. G., Attie, K. M., Frane, J., Brasel, A., Burstein, S., Cara, J. F., Chernausek, S., Gotlin, R. W., Kuntze, J., Lippe, B. M., Mahoney, C. P., Moore, W. V., Saenger, P., & Johanson, A. J.
- Affiliations
- Oregon Health & Science University (US)
- Venue
- The Journal of Pediatrics
- Publisher
- Elsevier BV
- Published
- 1998-02
- Volume
- 132
- Issue
- 2
- Pages
- 319-324
- ISSN
- 0022-3476 (ISSN-L)
- OpenAlex
- W2013492072
- Cited by
- 265
- References
- 19
- Citations by year
- 2026: 2 · 2024: 7 · 2023: 2 · 2022: 6 · 2021: 4 · 2020: 4 · 2019: 8 · 2018: 4 · 2017: 3 · 2016: 10 · 2015: 7 · 2014: 8 · 2013: 9 · 2012: 6
- FWCI
- 14.31
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Pediatrics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Growth Hormone and Insulin-like Growth Factors
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
- Keywords
- Turner syndrome, growth hormone therapy, oxandrolone, adult height, short stature, growth promotion, girls
- MeSH terms
- Body Height, Child, Child, Preschool, Drug Therapy, Combination, Female, Humans, Oxandrolone, Prospective Studies, Growth Hormone, Turner Syndrome, Treatment Outcome, Anabolic Agents
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