性腺功能减退的青春期男孩的睾酮治疗及其监测:来自I-DSD登记处的一项国际调查结果。

IF 2.4 4区 医学 Q2 DEVELOPMENTAL BIOLOGY
Marianna R Stancampiano, Angela K Lucas-Herald, Jillian Bryce, Gianni Russo, Graziano Barera, Antonio Balsamo, Federico Baronio, Silvano Bertelloni, Margherita Valiani, Martine Cools, Lloyd J W Tack, Feyza Darendeliler, Sukran Poyrazoglu, Evgenia Globa, Romina Grinspon, Sabine E Hannema, Ieuan A Hughes, Rieko Tadokoro-Cuccaro, Ajay Thankamony, Violeta Iotova, Vilhelm Mladenov, Daniel Konrad, Inas Mazen, Marek Niedziela, Zofia Kolesinska, Anna Nordenström, S Faisal Ahmed
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引用次数: 4

摘要

受一系列可能与性腺功能减退相关的内分泌疾病影响的青春期男孩,睾酮替代疗法(TRT)是否特别普遍,目前尚不清楚。本研究的目的是评估纳入I-DSD登记处的男孩进行TRT的当代实践。I-DSD登记处的所有参与中心都被邀请在2019年提供进一步的信息,这些中心的男孩年龄在10至18岁之间,并且患有可能与性腺功能减退有关的疾病。从15个中心收集了162名男孩的信息,每个中心的中位数(范围)为6名男孩(1.35名)。其中,来自9个中心的30名(19%)接受了TRT,开始时的年龄中位数(范围)为12.6岁(10.8-16.2岁),6名男孩(20%)开始接受TRT
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Testosterone Therapy and Its Monitoring in Adolescent Boys with Hypogonadism: Results of an International Survey from the I-DSD Registry.

It is unclear whether testosterone replacement therapy (TRT) in adolescent boys, affected by a range of endocrine diseases that may be associated with hypogonadism, is particularly common. The aim of this study was to assess the contemporary practice of TRT in boys included in the I-DSD Registry. All participating centres in the I-DSD Registry that had boys between 10 and 18 years of age and with a condition that could be associated with hypogonadism were invited to provide further information in 2019. Information on 162 boys was collected from 15 centres that had a median (range) number of 6 boys per centre (1.35). Of these, 30 (19%) from 9 centres were receiving TRT and the median (range) age at the start was 12.6 years (10.8-16.2), with 6 boys (20%) starting at <12 years. Median (range) age of boys not on TRT was 11.7 years (10.7-17.7), and 69 out of 132 (52%) were <12 years. TRT had been initiated in 20 of 71 (28%) boys with a disorder of gonadal development, 3 of 14 (21%) with a disorder of androgen synthesis, and all 7 (100%) boys with hypogonadotropic hypogonadism. The remainder who did not have TRT included 15 boys with partial androgen insensitivity, 52 with non-specific XY DSD, and 3 with persistent Müllerian duct syndrome. Before starting TRT, liver function and blood count were checked in 19 (68%) and 18 boys (64%), respectively, a bone age assessment was performed in 23 (82%) and bone mineral density assessment in 12 boys (43%). This snapshot of contemporary practice reveals that TRT in boys included in the I-DSD Registry is not very common, whilst the variation in starting and monitoring therapy is quite marked. Standardisation of practice may lead to more effective assessment of treatment outcomes.

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来源期刊
Sexual Development
Sexual Development 生物-发育生物学
CiteScore
4.00
自引率
4.30%
发文量
25
审稿时长
>12 weeks
期刊介绍: Recent discoveries in experimental and clinical research have led to impressive advances in our knowledge of the genetic and environmental mechanisms governing sex determination and differentiation, their evolution as well as the mutations or endocrine and metabolic abnormalities that interfere with normal gonadal development. ‘Sexual Development’ provides a unique forum for this rapidly expanding field. Its broad scope covers all aspects of genetics, molecular biology, embryology, endocrinology, evolution and pathology of sex determination and differentiation in humans and animals. It publishes high-quality original research manuscripts, review articles, short reports, case reports and commentaries. An internationally renowned and multidisciplinary editorial team of three chief editors, ten prominent scientists serving as section editors, and a distinguished panel of editorial board members ensures fast and author-friendly editorial processing and peer reviewing.
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