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首页> 外文期刊>Clinical Pediatric Endocrinology >Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols
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Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols

机译:男性小儿促性腺激素性性腺功能减退症的治疗情况以及睾丸激素和促性腺激素替代治疗方案的建议

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摘要

Male hypogonadotropic hypogonadism (MHH), a disorder associated with infertility, is treated with testosterone replacement therapy (TRT) and/or gonadotropins replacement therapy (GRT) (TRT and GRT, together with HRT hormone replacement therapy). In Japan, guidelines have been set for treatment during adolescence. Due to the risk of rapid maturation of bone age, low doses of testosterone or gonadotropins have been used. However, the optimal timing and methods of therapeutic intervention have not yet been established. The objective of this study was to investigate the current situation of treatment for children with MHH in Japan and to review a primary survey involving councilors of the Japanese Society for Pediatric Endocrinology and a secondary survey obtained from 26 facilities conducting HRT. The subjects were 55 patients with MHH who reached their adult height after HRT. The breakdown of the patients is as follows: 7 patients with Kallmann syndrome, 6 patients with isolated gonadotropin deficiency, 18 patients with acquired hypopituitarism due to intracranial and pituitary tumor, 22 patients with classical idiopathic hypopituitarism due to breech delivery, and 2 patients with CHARGE syndrome. The mean age at the start of HRT was 15.7 yrs and mean height was 157.2 cm. The mean age at reaching adult height was 19.4 yrs, and the mean adult height was 171.0 cm. The starting age of HRT was later than the normal pubertal age and showed a significant negative correlation with pubertal height gain, but it showed no correlation with adult height. As for spermatogenesis, 76% of the above patients treated with hCG-rFSH combined therapy showed positive results, though ranging in levels; impaired spermatogenesis was observed in some with congenital MHH, and favorable spermatogenesis was observed in all with acquired MHH. From the above, we propose the establishment of a treatment protocol for the start low-dose testosterone or low-dose gonadotropins by dividing subjects into two groups to determine different treatment protocols, acquired and congenital MHH, and to conduct them at a timing closer to the onset of puberty, namely, at a timing near entrance to junior high school. We also propose a new HRT protocol using preemptive FSH therapy prior to GRT aimed at achieving future fertility in patients with congenital MHH.
机译:与睾丸激素替代疗法(TRT)和/或促性腺激素替代疗法(GRT)(TRT和GRT以及HRT激素替代疗法)一起治疗与生殖不育相关的男性性腺功能低下性腺机能减退(MHH)。在日本,已经为青春期治疗制定了指南。由于骨龄快速成熟的风险,已使用低剂量的睾丸激素或促性腺激素。但是,尚未确定治疗干预的最佳时机和方法。这项研究的目的是调查日本MHH儿童的治疗现状,并审查涉及日本小儿内分泌学会理事的初次调查和从26个进行HRT的机构获得的二次调查。受试者为55名MHH患者,他们在HRT后达到了成人身高。患者的分类如下:7例Kallmann综合征,6例单纯性促性腺激素缺乏症,18例因颅内和垂体瘤而获得性垂体功能低下,22例因臀位分娩引起的典型特发性垂体功能低下,2例CHARGE患者综合症。 HRT开始时的平均年龄为15.7岁,平均身高为157.2 cm。达到成年人身高的平均年龄为19.4岁,成年人平均身高为171.0厘米。 HRT的起始年龄晚于正常的青春期年龄,并且与青春期身高增加呈显着负相关,但与成人身高没有相关性。至于精子发生,上述接受hCG-rFSH联合治疗的患者中有76%表现出阳性结果,尽管水平有所不同。先天性MHH患儿的精子发生受损,获得性MHH患儿的精子发生良好。综上所述,我们建议通过将受试者分为两组来确定不同的治疗方案(先天性和先天性MHH),并在更接近的时间进行,从而为开始低剂量的睾丸激素或低剂量的促性腺激素建立治疗方案。青春期开始,即在初中入学附近的某个时间。我们还提出了一种新的HRT方案,该方案在GRT之前使用先行FSH治疗,旨在实现先天性MHH患者的未来生育能力。

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