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在正常进入青春期的健康矮小儿童中,联合生长激素和促性腺激素释放激素类似物治疗后的最终身高。

Final height after combined growth hormone and gonadotrophin-releasing hormone analogue therapy in short healthy children entering into normally timed puberty.

作者信息

Lanes R, Gunczler P

机构信息

Unidad de Endocrinologia Pediatrica, Hospital de Clinicas Caracas, Venezuela.

出版信息

Clin Endocrinol (Oxf). 1998 Aug;49(2):197-202. doi: 10.1046/j.1365-2265.1998.00499.x.

Abstract

OBJECTIVE

Combined gonadotrophin-releasing hormone analogue and recombinant human growth hormone therapy has been used in an attempt to improve the final height of short non-GH deficient adolescents with normally timed puberty; its use, however, is still controversial as only short-term studies in a very limited number of patients have been undertaken, with either improvement in height prognosis or no beneficial effect on predicted growth. We have treated a group of extremely short healthy children with very low predicted adult heights entering into normally timed puberty with combined therapy, in order to determine whether we could improve their final height above their pretreatment predicted adult height.

PATIENTS

We treated 10 healthy adolescent short children (7 girls and 3 boys) simultaneously for 30.0 +/- 5.2 months with the GnRH analogue leuprolide acetate (0.3 mg/kg im every 28 days) and with rhGH (0.1 U/kg/day, sc, 6 days a week). The mean chronological age of our patients was 11.8 +/- 1.3 years, with a mean bone age of 11.2 +/- 0.9 years, height of 128.9 +/- 7.5 cm (-2.4 +/- 0.4 SD below the mean) and a predicted adult height of 150.7 +/- 9.8 cm; they were all in Tanner stage II-III of puberty. Ten healthy short children (7 girls and 3 boys) in the early stages of puberty with a mean chronological age of 11.4 +/- 1.0 years, a mean bone age of 11.0 +/- 0.8 years, height of 128.9 +/- 7.8 cm (-2.3 +/- 0.4 SD below the mean) and a mean adult predicted height of 151.8 +/- 10.1 cm served as controls and were simultaneously followed without therapy for the same study period.

MEASUREMENTS

Height and pubertal status were followed every 3 months during combined therapy and until final height of our patients was reached; bone ages were obtained every 6 months. Growth hormone deficiency was ruled out in all our subjects prior to beginning of the study by a normal response to oral clonidine and normal IGF-1 levels. Basal serum testosterone and/or oestradiol levels, as well as LH and FSH following administration of LH-releasing hormone were obtained before treatment and after 6 weeks and 4 months of combined therapy and every 6 months thereafter. Routine biochemistry as well as thyroid function tests were obtained at each visit.

RESULTS

Combined treatment resulted in an interruption of pubertal development with a suppression of gonadal steroids and of the LH response to LH-releasing hormone. Growth velocity decreased from 6.5 +/- 1.6 cm/year before treatment to 5.5 +/- 1.5 cm/year and 3.9 +/- 1.3 cm/year during the first and second year of treatment (P < 0.02 and P < 0.05, respectively) resulting in a height Z score reduction, declining from -2.4 +/- 04 to -2.6 +/- 0.7 SD. Bone age maturation declined averaging 0.75 bone age year/year of treatment but height SDS for bone age declined from -1.7 +/- 0.7 to -2.2 +/- 0.5 at the end of the second year of therapy with no improvement in predicted adult height (150.7 +/- 9.8 cm before and 150.0 +/- 8.0 after 2 years of therapy). After discontinuing treatment growth velocity did not improve and bone maturation advanced more rapidly (averaging 2.0 +/- 0.4 year/year of follow up) and the mean final height of our patients was 151 +/- 2.4 cm (-2.6 +/- 0.6 SD below the mean) which was not greater than the mean pretreatment predicted adult height and well below their target height; these results were also similar to those of the control population in whom the predicted adult height at the beginning of the study and after 2 years of follow up, was not different from their final height and well below their target height.

CONCLUSIONS

We conclude that combined rhGH and GnRH analogue therapy in short adolescents with normally timed puberty does not contribute to increase their final height above their pretreatment predicted adult height; we can therefore not recommend this form of therapy for this group of patients given the poor results obtained, as well as the cost of these medications and the

摘要

目的

促性腺激素释放激素类似物与重组人生长激素联合治疗已被用于试图改善青春期正常时间的非生长激素缺乏型矮身材青少年的最终身高;然而,其应用仍存在争议,因为仅对极少数患者进行了短期研究,结果要么是身高预后有所改善,要么是对预测生长无有益影响。我们对一组进入青春期正常时间、预测成年身高极低的极矮健康儿童进行了联合治疗,以确定我们是否能够使他们的最终身高高于治疗前预测的成年身高。

患者

我们对10名健康的青春期矮身材儿童(7名女孩和3名男孩)同时进行了30.0±5.2个月的治疗,使用促性腺激素释放激素类似物醋酸亮丙瑞林(每28天肌肉注射0.3mg/kg)和重组人生长激素(0.1U/kg/天,皮下注射,每周6天)。我们的患者平均实际年龄为11.8±1.3岁,平均骨龄为11.2±0.9岁,身高为128.9±7.5cm(低于平均水平2.4±0.4标准差),预测成年身高为150.7±9.8cm;他们均处于青春期坦纳II - III期。10名青春期早期的健康矮身材儿童(7名女孩和3名男孩)作为对照,平均实际年龄为11.4±1.0岁,平均骨龄为11.0±0.8岁,身高为128.9±7.8cm(低于平均水平2.3±0.4标准差),平均预测成年身高为151.8±10.1cm,在同一研究期间未接受治疗并同时进行随访。

测量

在联合治疗期间每3个月以及直至我们的患者达到最终身高时,对身高和青春期状态进行随访;每6个月测定骨龄。在研究开始前,通过口服可乐定的正常反应和正常的胰岛素样生长因子 - 1水平排除了所有受试者的生长激素缺乏。在治疗前、联合治疗6周和4个月后以及此后每6个月,获取基础血清睾酮和/或雌二醇水平,以及注射促黄体生成素释放激素后的促黄体生成素和促卵泡生成素水平。每次就诊时进行常规生化检查以及甲状腺功能测试。

结果

联合治疗导致青春期发育中断,性腺类固醇和促黄体生成素对促黄体生成素释放激素的反应受到抑制。生长速度从治疗前的6.5±1.6cm/年降至治疗第一年的5.5±1.5cm/年和第二年的3.

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