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

T.C. Sas, 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.M. Gerver, J.J. Gosen, C. Rongen-Westerlaken, S.L. Drop

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Sas TC, de Muinck Keizer-Schrama SM, Stijnen T, Jansen M, Otten BJ, Hoorweg-Nijman JJ, Vulsma T, Massa GG, Rouwe CW, Reeser HM, Gerver WJ, Gosen JJ, Rongen-Westerlaken C, Drop SL.

Department of Pediatrics, Sophia Children's Hospital, Rotterdam, The Netherlands. sas@alkg.azr.nl

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.

Publication Types:
Clinical Trial
Randomized Controlled Trial
Original languageEnglish
Pages (from-to)4607-4612
Number of pages6
JournalJournal of Clinical Endocrinology & Metabolism
Volume84
Issue number12
DOIs
Publication statusPublished - 1 Jan 1999

Cite this

Sas, T. C., de Muinck Keizer-Schrama, S. M., Stijnen, T., Jansen, M., Otten, B. J., Hoorweg-Nijman, J. J., Vulsma, T., Massa, G. G., Rouwe, C. W., Reeser, H. M., Gerver, W. J. M., Gosen, J. J., Rongen-Westerlaken, C., & Drop, S. L. (1999). Normalization of height in girls with Turner syndrome after long-term growth hormone treatment: results of a randomized dose-response trial. Journal of Clinical Endocrinology & Metabolism, 84(12), 4607-4612. https://doi.org/10.1210/jc.84.12.4607