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使用促性腺激素释放激素(GnRH)鼻内类似物(布舍瑞林)治疗中枢性性早熟。

Treatment of central precocious puberty with an intranasal analogue of GnRH (Buserelin).

作者信息

Bourguignon J P, Van Vliet G, Vandeweghe M, Malvaux P, Vanderschueren-Lodeweyckx M, Craen M, Du Caju M V, Ernould C

机构信息

Department of Pediatrics, University of Liege, CHU du Sart Tilman, Belgium.

出版信息

Eur J Pediatr. 1987 Nov;146(6):555-60. doi: 10.1007/BF02467352.

Abstract

One boy and 13 girls with central precocious puberty were treated for 1 year using Buserelin, a GnRH analogue, given intranasally (0.3 mg, four times a day). After 1, 3 and 12 months of therapy, the gonadotropin responses to GnRH were abolished in all the patients whereas mean basal serum concentrations of luteinizing hormone (LH) remained similar to those of pubertal controls. During Buserelin treatment, genital development in the boy and breast development in the girls showed no further progress or some regression. In the boy, serum testosterone levels returned to prepubertal values. In the girls, serum oestradiol levels were variable and, in four of them, vaginal smears showed the persistence of a slight oestrogenic effect during therapy. Pelvic ultrasonography did not show any significant variation in ovarian and uterine lengths. Among the 14 patients, 3 had some progression of pubic hair development, irrespective of serum dehydroepiandrosterone sulphate (DHEAS) levels. In eight patients previously treated with cyproterone, elevated prolactin levels were observed before and during the first month of Buserelin administration. During treatment, mean height velocity was markedly reduced from 11.6 to 6.1 cm/year and mean bone age velocity (+/- 1SD) was 0.85 +/- 0.38 year/year. After 1 year of treatment, the differences in predicted adult height ranged between -0.74 and + 1.04 SDS (standard deviation score). These differences were inversely related (r = -0.72) to the prognosis of adult height calculated before treatment. We conclude that, in central precocious puberty, intranasal administration of Buserelin 1.2 mg/day, may arrest sexual development and reduce height velocity and bone maturation. Improvement of adult height prognosis may occur, especially when it was markedly impaired before treatment.

摘要

一名患有中枢性性早熟的男孩和13名患有中枢性性早熟的女孩使用促性腺激素释放激素类似物布舍瑞林进行了为期1年的治疗,通过鼻内给药(0.3毫克,每日4次)。治疗1、3和12个月后,所有患者对促性腺激素释放激素的促性腺激素反应均消失,而黄体生成素(LH)的平均基础血清浓度仍与青春期对照者相似。在布舍瑞林治疗期间,男孩的生殖器发育和女孩的乳房发育没有进一步进展或出现一些退化。在男孩中,血清睾酮水平恢复到青春期前的值。在女孩中,血清雌二醇水平各不相同,其中4名女孩的阴道涂片显示在治疗期间仍存在轻微的雌激素作用。盆腔超声检查未显示卵巢和子宫长度有任何显著变化。在这14名患者中,3名患者的阴毛发育有一定进展,与血清硫酸脱氢表雄酮(DHEAS)水平无关。在8名先前接受过醋酸环丙孕酮治疗的患者中,在布舍瑞林给药前及给药第一个月期间观察到催乳素水平升高。治疗期间,平均身高增长速度从11.6厘米/年显著降至6.1厘米/年,平均骨龄增长速度(±1标准差)为0.85±0.38岁/年。治疗1年后,预测成人身高的差异在-0.74至+1.04 SDS(标准差评分)之间。这些差异与治疗前计算的成人身高预后呈负相关(r=-0.72)。我们得出结论,在中枢性性早熟中,每天鼻内给予1.2毫克布舍瑞林可能会阻止性发育,降低身高增长速度和骨骼成熟度。成人身高预后可能会改善,尤其是在治疗前明显受损的情况下。

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