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[促性腺激素释放激素类似物治疗中枢性性早熟。治疗2年后对生长和骨成熟的影响]

[Treatment of central precocious puberty with an LHRH analog. Effect on growth and bone maturation after 2 years of treatment].

作者信息

Brauner R, Rappaport R

出版信息

Arch Fr Pediatr. 1987 Apr;44(4):271-6.

PMID:3109347
Abstract

Eighteen children (15 girls and 3 boys) with true precocious puberty have been treated with an LHRH analogue (HOE 766, Buserelin suprefact) given subcutaneously during one (n = 11) or two (n = 7) years. Six of 18 children had organic precocious puberty, but their responses to therapy did not show any difference. A satisfactory suppression was achieved in 16 cases with plasma testosterone below 0.5 ng/ml (boys) or estradiol below 25 pg/ml and vaginal maturation index below 35 (girls). The mean annual height gain diminished from 9.5 +/- 0.8 cm during the control year to 7.7 +/- 0.7 cm and 5.1 +/- 0.7 cm during the first and second years of therapy respectively (p less than 0.05). Simultaneously, the mean bone age of 10.4 +/- 0.4 yr at onset of treatment, was 11.4 +/- 0.4 yr after one year and 11.8 +/- 0.3 yr after two years. These changes explain an average increase of predicted height of 5.7 cm after two years of treatment with the LHRH analogue. At least on the basis of these data with two years follow-up, this treatment seems satisfactory. We did not find anti-Buserelin antibodies in any of these patients.

摘要

18名真性性早熟儿童(15名女孩和3名男孩)接受了促黄体生成素释放激素类似物(HOE 766,布舍瑞林,Suprefact)治疗,皮下注射给药,疗程为1年(11例)或2年(7例)。18名儿童中有6名患有器质性性早熟,但他们对治疗的反应没有显示出任何差异。16例患者实现了满意的抑制效果,血浆睾酮低于0.5 ng/ml(男孩)或雌二醇低于25 pg/ml,阴道成熟指数低于35(女孩)。平均每年身高增长从对照年的9.5±0.8 cm分别降至治疗第一年的7.7±0.7 cm和第二年的5.1±0.7 cm(p<0.05)。同时,治疗开始时平均骨龄为10.4±0.4岁,1年后为11.4±0.4岁,2年后为11.8±0.3岁。这些变化说明使用促黄体生成素释放激素类似物治疗两年后预测身高平均增加了5.7 cm。至少基于这些两年随访的数据,这种治疗似乎是令人满意的。我们在这些患者中均未发现抗布舍瑞林抗体。

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