Context: GnRH analogs (GnRHa) are considered the treatment of choice for central precocious puberty (CPP). During GnRHa administration, the suppression of the pituitary-gonadal axis results in decreased rates of linear growth and skeletal maturation and in improved adult height. However, in some patients, the growth deceleration is so marked that the expected improvement in predicted adult height is not achieved. Objective: The objective of this study was to assess whether the addition of oxandrolone (Ox) may affect the height outcome of patients with CPP and growth deceleration during GnRHa treatment. Design: This was an open-label, clinical study. Setting: The study was performed at a pediatric endocrinology referral clinic. Patients: Twenty patients with CPP and marked growth deceleration during GnRHa treatment were studied. Interventions: Treatment consisted of GnRHa (Leuprorelina, 3.75 mg im every 28 d) alone (10 patients) or in combination with Ox (0.06 mg/kgd by mouth) (10 patients). Main Outcome Measure: The main outcome measure was the patients’ adult height. Results: The adult height of the patients treated with GnRHa plus Ox was significantly higher than pretreatment predicted adult height (162.6 2.3 vs. 154.8 1.7 cm, mean SEM; P 0.05) and target height (162.6 2.3 vs. 158.0 1.9; P 0.05). Patients treated with GnRHa alone reached an adult height similar to the pretreatment predicted adult height (151.9 1.2 vs. 155.4 2.1 cm) but significantly lower than target height (151.9 1.2 vs. 156.6 1.4 cm; P 0.005). No side effects were recorded in either group of patients. Conclusions: Combined GnRHa and Ox therapy is a viable treatment option for children with CPP and marked growth deceleration during treatment with GnRHa alone. (J Clin Endocrinol Metab 91: 1284–1287, 2006
Final height in girls with central idiopathic precociou puberty treated with gonadotropin-releasing hormon analog and oxandrolone / Vottero, A.; Pedori, S; Verna, M; Pagano, B; Cappa, M; Loche, S; Bernasconi, Sergio; Ghizzoni, L.. - In: THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM. - ISSN 0021-972X. - 91 (4):(2006), pp. 1284-1287. [10.1210/jc.2005-1693]
Final height in girls with central idiopathic precociou puberty treated with gonadotropin-releasing hormon analog and oxandrolone.
BERNASCONI, Sergio;
2006-01-01
Abstract
Context: GnRH analogs (GnRHa) are considered the treatment of choice for central precocious puberty (CPP). During GnRHa administration, the suppression of the pituitary-gonadal axis results in decreased rates of linear growth and skeletal maturation and in improved adult height. However, in some patients, the growth deceleration is so marked that the expected improvement in predicted adult height is not achieved. Objective: The objective of this study was to assess whether the addition of oxandrolone (Ox) may affect the height outcome of patients with CPP and growth deceleration during GnRHa treatment. Design: This was an open-label, clinical study. Setting: The study was performed at a pediatric endocrinology referral clinic. Patients: Twenty patients with CPP and marked growth deceleration during GnRHa treatment were studied. Interventions: Treatment consisted of GnRHa (Leuprorelina, 3.75 mg im every 28 d) alone (10 patients) or in combination with Ox (0.06 mg/kgd by mouth) (10 patients). Main Outcome Measure: The main outcome measure was the patients’ adult height. Results: The adult height of the patients treated with GnRHa plus Ox was significantly higher than pretreatment predicted adult height (162.6 2.3 vs. 154.8 1.7 cm, mean SEM; P 0.05) and target height (162.6 2.3 vs. 158.0 1.9; P 0.05). Patients treated with GnRHa alone reached an adult height similar to the pretreatment predicted adult height (151.9 1.2 vs. 155.4 2.1 cm) but significantly lower than target height (151.9 1.2 vs. 156.6 1.4 cm; P 0.005). No side effects were recorded in either group of patients. Conclusions: Combined GnRHa and Ox therapy is a viable treatment option for children with CPP and marked growth deceleration during treatment with GnRHa alone. (J Clin Endocrinol Metab 91: 1284–1287, 2006File | Dimensione | Formato | |
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