Pucarelli Ida, Segni Maria, Ortore Massimiliano, Arcadi Elena, Pasquino Anna Maria
Pediatric Endocrinology Unit, Pediatric Department, University La Sapienza, Rome, Italy.
J Pediatr Endocrinol Metab. 2003 Sep;16(7):1005-10. doi: 10.1515/jpem.2003.16.7.1005.
Out of 35 girls with idiopathic central precocious puberty (CPP) treated with gonadotropin-releasing hormone agonist (GnRHa) (depot-triptorelin) at a dose of 100 microg/kg every 21 days i.m. for at least 2-3 years whose growth velocity fell below the 25th percentile for chronological age (CA), 17 received growth hormone (GH) in addition at a dose of 0.3 mg/kg/week, s.c., 6 days per week, for 2-4 years. The other 18, matched for bone age (BA), CA and duration of GnRHa treatment, who showed the same growth pattern but refused GH treatment, remained on GnRHa alone, and were used as a control group to evaluate GH efficacy. No patient was GH deficient. Both groups discontinued treatment at a comparable BA (mean +/- SD): BA 13.4 +/- 0.6 in GnRHa plus GH group vs 13.0 +/- 0.5 years in the GnRHa alone group. The 35 patients have reached adult height (i.e. growth during the preceding year was less than 1 cm, with a BA of over 15 years). Patients of the group treated with GH plus GnRHa showed an adult height (161.2 +/- 4.8 cm) significantly higher (p < 0.001) than pre-treatment predicted adult height (PAH) calculated according to tables either for accelerated girls (153.2 +/- 5.0 cm) or for average girls (148.6 +/- 4.3 cm). The adult height of the GnRH alone treated group (156.6 +/- 5.7) was not significantly higher than pre-treatment PAH if calculated on Bayley and Pinneau tables for accelerated girls (153.9 +/- 3.8 cm), whilst it remained significantly higher if calculated on tables for average girls (149.6 +/- 4.0 cm) (p < 0.001). The gain between pre-treatment PAH and final height was 8.2 +/- 4.8 cm according to tables for accelerated girls and 12.7 +/- 4.8 cm according to tables for average girls in patients treated with GH plus GnRHa; while in patients treated with GnRH alone the gain calculated between pre-treatment PAH for accelerated girls was just 2.3 +/- 2.9 cm and 7.1 +/- 2.7 cm greater than pre-treatment PAH for average girls. The difference between the gain obtained in the two groups (about 6 cm) remained the same, however PAH was calculated. The addition of GH to GnRHa in a larger cohort of patients with CPP with a longer follow-up confirms the safety of the combined treatment and the still significant but more variable gain in the group with the combined treatment, probably due to the larger number of patients analyzed. Caution is advised in using such an invasive and expensive treatment, and there is need for further studies before widespread clinical use outside a research setting.
35名患有特发性中枢性性早熟(CPP)的女孩接受促性腺激素释放激素激动剂(GnRHa)(长效曲普瑞林)治疗,剂量为每21天100μg/kg,肌肉注射,至少持续2 - 3年,其生长速度低于按实际年龄(CA)计算的第25百分位数。其中17名女孩另外接受了生长激素(GH)治疗,剂量为0.3mg/kg/周,皮下注射,每周6天,持续2 - 4年。另外18名女孩,根据骨龄(BA)、CA和GnRHa治疗持续时间进行匹配,她们具有相同的生长模式但拒绝GH治疗,仅继续使用GnRHa,作为对照组来评估GH的疗效。所有患者均无GH缺乏。两组在相近的骨龄时(平均值±标准差)停止治疗:GnRHa加GH组为13.4±0.6岁,单纯GnRHa组为13.0±0.5岁。这35名患者已达到成人身高(即前一年生长不足1cm,骨龄超过15岁)。接受GH加GnRHa治疗组的患者成人身高(161.2±4.8cm)显著高于(p<0.001)根据加速生长女孩表格(153.2±5.0cm)或平均生长女孩表格(148.6±4.3cm)计算的治疗前预测成人身高(PAH)。单纯GnRHa治疗组的成人身高(156.6±5.7),如果根据贝利和皮诺表格计算加速生长女孩的PAH(153.9±3.8cm),则不显著高于治疗前PAH;而如果根据平均生长女孩表格计算(149.6±4.0cm),则仍显著高于治疗前PAH(p<0.001)。根据加速生长女孩表格,接受GH加GnRHa治疗的患者治疗前PAH与最终身高之间的增长为8.2±4.8cm,根据平均生长女孩表格为12.7±4.8cm;而在单纯接受GnRHa治疗的患者中,根据加速生长女孩的PAH计算,增长仅为2.3±2.9cm,比根据平均生长女孩的PAH计算的治疗前PAH高7.1±2.7cm。无论PAH如何计算,两组之间的增长差异(约6cm)保持不变。在更大队列的CPP患者中加入GH并进行更长时间的随访,证实了联合治疗的安全性,以及联合治疗组仍有显著但更具变异性的身高增长,这可能是由于分析的患者数量较多。建议谨慎使用这种侵入性且昂贵的治疗方法,在研究环境之外广泛临床应用之前需要进一步研究。