[Puberty induction in boys with congenital isolated hypogonadotropic hypogonadism].

Q4 Medicine
K D Kokoreva, I S Chugunov, M A Kareva, O B Bezlepkina
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引用次数: 0

Abstract

Background: Gonadotropin therapy in boys with congenital isolated hypogonadotropic hypogonadism helps to increase testes volume and induce spermatogenesis in comparison with testosterone therapy. However, difficulties with dose titration, partial therapy success, absence of generally accepted regimen protocols don't allow to use this therapy in order to induce puberty in adolescents with Kallmann syndrome or normosmic hypogonadotropic hypogonadism.

Aim: To assess the effectiveness of combination hormonal replacement therapy via human chorionic gonadotropin and recombinant follicle stimulation hormone in adolescents with congenital isolated normosmic hypogonadotropic hypogonadism and with Kallmann syndromeMATERIALS AND METHODS: This is an open single-center prospective non-controlled study. Boys with hypogonadotropic hypogonadism were receiving hormonal replacement therapy for 12 months. Initial dose of human chorionic gonadotropin was 500 IU per week. Initial dose of recombinant follicle stimulation hormone was 37.5 IU per week. Doses were doubled in 6 months. Antropometric data, Tanner stage, testes volumes, inhibin B and anti-Mullerian hormone (AMH) levels were evaluated in all the patients before the treatment, after 6 and 12 months of the therapy.

Results: 8 boys with hypogonadotropic hypogonadism were included into the study. Median age before therapy initiation was 15.7 years [15.33; 16.41]. In 12 months after the therapy initiation puberty development, testosterone increase from 0.44 [0.34;0.62] to 4.39 [0.88;10.51] nmol/l (p=0.012), AMH decrease from 35.70 [18.00;59.00] to 14.41 [11.60;16.65] ng/ml were noted in all the patients (p=0.017). Testes volumes increase and inhibin B level increase were not statistically significant.

Conclusion: Gonadotropin therapy is effective in order to puberty initiation in adolescents with congenital hypogonadotropic hypogonadism. In helps to achieve not only androgenization, but also to Sertoli cells maturation.

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[先天性孤立性促性腺功能减退症男孩的青春期诱导]。
背景:与睾酮治疗相比,促性腺激素治疗先天性孤立性促性腺功能低下的男孩有助于增加睾丸体积和诱导精子发生。然而,剂量滴定的困难,部分治疗成功,缺乏普遍接受的方案,不允许使用这种疗法来诱导青春期的青少年与Kallmann综合征或正常的促性腺功能低下。目的:评价人绒毛膜促性腺激素和重组卵泡刺激激素联合激素替代治疗先天性孤立性正常促性腺功能低下和Kallmann综合征的青少年的有效性。材料和方法:这是一项开放的单中心前瞻性非对照研究。患有促性腺功能减退症的男孩接受激素替代治疗12个月。人绒毛膜促性腺激素的初始剂量为每周500国际单位。重组卵泡刺激激素的初始剂量为37.5 IU /周。剂量在6个月内增加了一倍。在治疗前、治疗6个月和治疗12个月后,评估所有患者的静压指标、Tanner分期、睾丸体积、抑制素B和抗苗勒管激素(AMH)水平。结果:本组共纳入8例促性腺功能减退症男童。治疗开始前的中位年龄为15.7岁[15.33;16.41]。治疗开始后12个月,所有患者青春期发育睾酮水平由0.44[0.34;0.62]上升至4.39 [0.88;10.51]nmol/l (p=0.012), AMH水平由35.70[18.00;59.00]下降至14.41 [11.60;16.65]ng/ml (p=0.017)。睾丸体积增大,抑制素B水平升高无统计学意义。结论:促性腺激素治疗对先天性促性腺功能低下的青少年青春期启动是有效的。In不仅有助于实现雄激素化,而且有助于支持细胞成熟。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Problemy endokrinologii
Problemy endokrinologii Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
1.40
自引率
0.00%
发文量
59
期刊介绍: Since 1955 the “Problems of Endocrinology” (or “Problemy Endocrinologii”) Journal publishes timely articles, balancing both clinical and experimental research, case reports, reviews and lectures on pressing problems of endocrinology. The Journal is aimed to the most topical issues of endocrinology: to chemical structure, biosynthesis and metabolism of hormones, the mechanism of their action at cellular and molecular level; pathogenesis and to clinic of the endocrine diseases, new methods of their diagnostics and treatment. The Journal: features original national and foreign research articles, reflecting world endocrinology development; issues thematic editions on specific areas; publishes chronicle of major international congress sessions and workshops on endocrinology, as well as state-of-the-art guidelines; is intended for scientists, endocrinologists diabetologists and specialists of allied trade, general practitioners, family physicians and pediatrics.
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