Growth hormone therapy in Turner's syndrome

An update on final height

Ronald (Ron) Rosenfeld, K. M. Attie, J. Frane, A. J. Johanson, J. Kuntze, J. A. Brasel, S. Burstein, J. F. Cara, S. Chernausek, R. W. Gotlin, B. M. Lippe, P. C. Mahoney, W. V. Moore, P. Saenger

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

The Genentech National Cooperative Study of growth hormone (GH) therapy in Turner's syndrome was initiated in 1983; 70 girls with Turner's syndrome were randomly assigned to observation or to treatment with GH alone, oxandrolone alone, or a combination of GH plus oxandrolone for a period of 12-24 months. After completion of this phase, patients receiving GH alone were continued on GH, while all other patients received the combination of GH plus oxandrolone. Data are currently available on the 62 girls who were treated for a minimum of 3-6 years. When compared with the height velocities anticipated for girls of comparable ages with untreated Turner's syndrome, both GH alone and a combination of GH plus oxandrolone resulted in an increase in height velocity, which was most prominent during the first 2 years of treatment and was sustained for at least 6 years. Although GH therapy is continuing at present in half of the patients, 14 of 17 girls (82%) receiving GH alone and 42 of 45 girls (93%) receiving combination therapy have exceeded their projected adult heights. For the 30 girls who have stopped therapy, the current mean height is 151.9 cm, compared with their original mean projected adult height of 143.8 cm. These results demonstrate that GH therapy can result in short-term (3-6 years) acceleration of growth, as well as in improved adult height.

Original languageEnglish (US)
Pages (from-to)3-6
Number of pages4
JournalActa Paediatrica, International Journal of Paediatrics, Supplement
Volume81
Issue number383
StatePublished - 1992
Externally publishedYes

Fingerprint

Turner Syndrome
Growth Hormone
Oxandrolone
Therapeutics
Observation

Keywords

  • final height
  • growth hormone
  • height velocity
  • oxandrolone
  • Turner's syndrome

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Rosenfeld, R. R., Attie, K. M., Frane, J., Johanson, A. J., Kuntze, J., Brasel, J. A., ... Saenger, P. (1992). Growth hormone therapy in Turner's syndrome: An update on final height. Acta Paediatrica, International Journal of Paediatrics, Supplement, 81(383), 3-6.

Growth hormone therapy in Turner's syndrome : An update on final height. / Rosenfeld, Ronald (Ron); Attie, K. M.; Frane, J.; Johanson, A. J.; Kuntze, J.; Brasel, J. A.; Burstein, S.; Cara, J. F.; Chernausek, S.; Gotlin, R. W.; Lippe, B. M.; Mahoney, P. C.; Moore, W. V.; Saenger, P.

In: Acta Paediatrica, International Journal of Paediatrics, Supplement, Vol. 81, No. 383, 1992, p. 3-6.

Research output: Contribution to journalArticle

Rosenfeld, RR, Attie, KM, Frane, J, Johanson, AJ, Kuntze, J, Brasel, JA, Burstein, S, Cara, JF, Chernausek, S, Gotlin, RW, Lippe, BM, Mahoney, PC, Moore, WV & Saenger, P 1992, 'Growth hormone therapy in Turner's syndrome: An update on final height', Acta Paediatrica, International Journal of Paediatrics, Supplement, vol. 81, no. 383, pp. 3-6.
Rosenfeld RR, Attie KM, Frane J, Johanson AJ, Kuntze J, Brasel JA et al. Growth hormone therapy in Turner's syndrome: An update on final height. Acta Paediatrica, International Journal of Paediatrics, Supplement. 1992;81(383):3-6.
Rosenfeld, Ronald (Ron) ; Attie, K. M. ; Frane, J. ; Johanson, A. J. ; Kuntze, J. ; Brasel, J. A. ; Burstein, S. ; Cara, J. F. ; Chernausek, S. ; Gotlin, R. W. ; Lippe, B. M. ; Mahoney, P. C. ; Moore, W. V. ; Saenger, P. / Growth hormone therapy in Turner's syndrome : An update on final height. In: Acta Paediatrica, International Journal of Paediatrics, Supplement. 1992 ; Vol. 81, No. 383. pp. 3-6.
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