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对于体质性生长和青春期延迟的男孩,睾酮治疗是否会影响最终身高并抑制下丘脑-垂体-性腺轴?

Is testosterone therapy for boys with constitutional delay of growth and puberty associated with impaired final height and suppression of the hypothalamo-pituitary-gonadal axis?

作者信息

Uruena M, Pantsiotou S, Preece M A, Stanhope R

机构信息

Medical Unit, Institute of Child Health, London, United Kingdom.

出版信息

Eur J Pediatr. 1992 Jan;151(1):15-8. doi: 10.1007/BF02073882.

Abstract

We report the treatment of 44 boys with constitutional delay of growth and puberty (CDGP) at a mean chronological age of 14.3 years (range, 12.4-17.1) and bone age of 12.1 years (range, 9.1-15.0). All were below the 3rd height percentile for chronological age. They received monthly intramuscular injections of depot testosterone esters (50 mg) for a mean period of 0.35 years (range, 0.25-0.5). Means (SD) height velocity was 4.5 (1.5) cm/year during a pretreatment period of 0.5 years. During a period of 0.9 years which included the period of treatment with depot testosterone, mean growth velocity increased to 8.8 (1.9) cm/year (P less than 0.001). In the initial 1.8 years following the cessation of treatment growth velocity was sustained at 7.0 (1.7) cm/year. Pretreatment height standard deviation score (SDS) for bone age was -0.89 and this gradually reduced over the next 1.5 years to a minimum of -1.48. Thereafter, height SDS for bone age gradually increased to attain a value of -1.2, 3 years after the commencement of therapy (P less than 0.02). The same pattern of an initial decrease, followed by an increase, in height prediction was also observed when TW2 height prediction was analysed. Sexual maturation progressed during treatment, with mean testicular volume increasing both during and after treatment, confirming the diagnosis of CDGP. The time interval for progress through puberty was shorter in boys with testosterone therapy than in the normal population. The mean duration of puberty was 2.2 years compared to 3.3 years in normal boys. We conclude that low-dose depot testosterone treatment is safe and effective for boys with CDGP.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们报告了对44名体质性生长和青春期发育延迟(CDGP)男孩的治疗情况,他们的平均实际年龄为14.3岁(范围12.4 - 17.1岁),骨龄为12.1岁(范围9.1 - 15.0岁)。所有人的身高均低于其实际年龄对应的第3百分位。他们每月接受一次长效睾酮酯(50毫克)肌肉注射,平均疗程为0.35年(范围0.25 - 0.5年)。在为期0.5年的治疗前期,平均(标准差)身高增长速度为4.5(1.5)厘米/年。在包括长效睾酮治疗期在内的0.9年期间,平均生长速度增至8.8(1.9)厘米/年(P小于0.001)。治疗停止后的最初1.8年里,生长速度维持在7.0(1.7)厘米/年。治疗前骨龄的身高标准差评分(SDS)为 - 0.89,在接下来的1.5年里逐渐降至最低 - 1.48。此后,治疗开始3年后,骨龄的身高SDS逐渐升至 - 1.2(P小于0.02)。分析TW2身高预测时,也观察到了身高预测先下降后上升的相同模式。治疗期间性成熟进程加快,治疗期间及之后平均睾丸体积均增加,证实了CDGP的诊断。接受睾酮治疗的男孩青春期进展的时间间隔比正常人群短。青春期平均持续时间为2.2年,而正常男孩为3.3年。我们得出结论,低剂量长效睾酮治疗对患有CDGP的男孩安全有效。(摘要截选至250词)

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