Literature DB >> 10599727

Normalization of height in girls with Turner syndrome after long-term growth hormone treatment: results of a randomized dose-response trial.

T C Sas1, S M de Muinck Keizer-Schrama, T Stijnen, M Jansen, B J Otten, J J Hoorweg-Nijman, T Vulsma, G G Massa, C W Rouwe, H M Reeser, W J Gerver, J J Gosen, C Rongen-Westerlaken, S L Drop.   

Abstract

Short stature and ovarian failure are the main features in Turner syndrome (TS). To optimize GH and estrogen treatment, we studied 68 previously untreated girls with TS, age 2-11 yr, who were randomly assigned to one of three GH dosage groups: group A, 4 IU/m2 day (approximately 0.045 mg/kg x day); group B, first yr 4, thereafter 6 IU/m2 x day (approximately 0.0675 mg/kg/day); group C, first yr 4, second yr 6, thereafter 8 IU/m2 x day (approximately 0.090 mg/kg x day). In the first 4 yr of GH treatment, no estrogens for pubertal induction were given to the girls. Thereafter, girls started with 17beta-estradiol (5 microg/kg bw x day, orally) when they had reached the age of 12 yr. Subjects were followed up until attainment of adult height or until cessation of treatment because of satisfaction with the height achieved. Seven-year data of all girls were evaluated to compare the growth-promoting effects of three GH dosages during childhood. After 7 yr, 85% of the girls had reached a height within the normal range for healthy Dutch girls. The 7-yr increment in height SD-score was significantly higher in groups B and C than in group A. In addition, we evaluated the data of 32 of the 68 girls who had completed the trial after a mean duration of treatment of 7.3 yr (range, 5.0 - 8.75). Mean (SD) height was 158.8 cm (7.1), 161.0 cm (6.8), and 162.3 cm (6.1) in groups A, B, and C, respectively. The mean (SD) difference between predicted adult height before treatment and achieved height was 12.5 cm (2.1), 14.5 cm (4.0), and 16.0 cm (4.1) for groups A, B, and C, respectively, being significantly different between group A and group C. GH treatment was well tolerated in all three GH dosage groups. In conclusion, GH treatment starting in relatively young girls with TS results in normalization of height during childhood, as well as of adult height, in most of the individuals. With this GH and estrogen treatment regimen, most girls with TS can grow and develop much more in conformity with their healthy peers.

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Year:  1999        PMID: 10599727     DOI: 10.1210/jcem.84.12.6241

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  27 in total

Review 1.  Growth hormone: new ideas, recurring themes.

Authors:  E O Reiter
Journal:  Endocrine       Date:  2001-06       Impact factor: 3.633

Review 2.  Long-term results of growth hormone therapy in Turner syndrome.

Authors:  J H Bramswig
Journal:  Endocrine       Date:  2001-06       Impact factor: 3.633

3.  Which children should receive growth hormone treatment. Cost-benefit analysis is the key.

Authors:  C J Kelnar
Journal:  Arch Dis Child       Date:  2000-08       Impact factor: 3.791

4.  Towards evidence based referral criteria for growth monitoring.

Authors:  S van Buuren; P van Dommelen; G R J Zandwijken; F K Grote; J M Wit; P H Verkerk
Journal:  Arch Dis Child       Date:  2004-04       Impact factor: 3.791

Review 5.  Sex hormone replacement in Turner syndrome.

Authors:  Christian Trolle; Britta Hjerrild; Line Cleemann; Kristian H Mortensen; Claus H Gravholt
Journal:  Endocrine       Date:  2011-12-07       Impact factor: 3.633

Review 6.  Growth hormone therapy.

Authors:  Anurag Bajpai; P Sn Menon
Journal:  Indian J Pediatr       Date:  2005-02       Impact factor: 1.967

Review 7.  Turner syndrome and GH treatment: the state of the art.

Authors:  A M Pasquino
Journal:  J Endocrinol Invest       Date:  2004-12       Impact factor: 4.256

8.  Adult height in sixty girls with Turner syndrome treated with growth hormone matched with an untreated group.

Authors:  A M Pasquino; I Pucarelli; M Segni; L Tarani; V Calcaterra; D Larizza
Journal:  J Endocrinol Invest       Date:  2005-04       Impact factor: 4.256

9.  Cardiovascular anomalies in children and young adults with Ullrich-Turner syndrome the Erlangen experience.

Authors:  Thomas M K Völkl; Karin Degenhardt; Andreas Koch; Diemud Simm; Helmuth G Dörr; Helmut Singer
Journal:  Clin Cardiol       Date:  2005-02       Impact factor: 2.882

10.  Recombinant human growth hormone in the treatment of Turner syndrome.

Authors:  Bessie E Spiliotis
Journal:  Ther Clin Risk Manag       Date:  2008-12       Impact factor: 2.423

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