Short-term testosterone treatment at bone age of 12 to 13 years does not reduce adult height in boys with constitutional delay of growth and adolescence.

Helvetica paediatrica acta Pub Date : 1987-06-01
M Zachmann, S Studer, A Prader
{"title":"Short-term testosterone treatment at bone age of 12 to 13 years does not reduce adult height in boys with constitutional delay of growth and adolescence.","authors":"M Zachmann,&nbsp;S Studer,&nbsp;A Prader","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Growth data and adult height from 22 untreated patients with constitutional delay of growth and adolescence (group 1) were compared retrospectively with those of 19 patients, who had received long-acting testosterone esters (100 to 250 mg per month, mean total dosage 1029 mg/m2) during 2 months to 3.25 years (mean duration 8.5 months, group 2). Age (group 1 15.4 +/- 1.2, group 2 16.2 +/- 1.4 years), bone age (group 1 12.6 +/- 1.3, group 2 13.1 +/- 1.2 years) at first examination (group 1) or start of treatment (group 2), and adult height (172.8 +/- 7.5 cm group 1, 176.8 +/- 8.0 cm group 2) were not significantly different. In group 2, there was no negative correlation between the total testosterone dose and adult height, and the latter corresponded to predicted height in the same way as in the untreated patients. It is concluded that short-term treatment with long-acting testosterone esters (100 to 250 mg per month during 6 months, starting at a bone age of about 12.5 years), which has positive psychosocial effects, does not have negative somatic effects and does not reduce adult height in these patients.</p>","PeriodicalId":75904,"journal":{"name":"Helvetica paediatrica acta","volume":"42 1","pages":"21-8"},"PeriodicalIF":0.0000,"publicationDate":"1987-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Helvetica paediatrica acta","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Growth data and adult height from 22 untreated patients with constitutional delay of growth and adolescence (group 1) were compared retrospectively with those of 19 patients, who had received long-acting testosterone esters (100 to 250 mg per month, mean total dosage 1029 mg/m2) during 2 months to 3.25 years (mean duration 8.5 months, group 2). Age (group 1 15.4 +/- 1.2, group 2 16.2 +/- 1.4 years), bone age (group 1 12.6 +/- 1.3, group 2 13.1 +/- 1.2 years) at first examination (group 1) or start of treatment (group 2), and adult height (172.8 +/- 7.5 cm group 1, 176.8 +/- 8.0 cm group 2) were not significantly different. In group 2, there was no negative correlation between the total testosterone dose and adult height, and the latter corresponded to predicted height in the same way as in the untreated patients. It is concluded that short-term treatment with long-acting testosterone esters (100 to 250 mg per month during 6 months, starting at a bone age of about 12.5 years), which has positive psychosocial effects, does not have negative somatic effects and does not reduce adult height in these patients.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
在12至13岁的骨骼年龄短期睾酮治疗不会降低患有体质性生长迟缓和青春期的男孩的成年身高。
回顾性比较22例未经治疗的体质性生长迟缓和青春期患者的生长数据和成人身高(1组)与19例接受长效睾酮酯(100 - 250 mg/月,平均总剂量1029 mg/m2)治疗2个月至3.25年(平均持续时间8.5个月,2组)的患者的生长数据和身高。年龄(1组15.4 +/- 1.2岁,2组16.2 +/- 1.4岁),骨龄(1组12.6 +/- 1.3岁,1组12.6 +/- 1.3岁)。组2首次检查(组1)或治疗开始(组2)时年龄13.1 +/- 1.2岁,成人身高(组1 172.8 +/- 7.5 cm,组2 176.8 +/- 8.0 cm)差异无统计学意义。在第二组中,睾酮总剂量与成人身高之间没有负相关,后者与未治疗患者的预测身高的对应关系相同。结论是,短期使用长效睾酮酯治疗(从12.5岁左右的骨龄开始,6个月内每月100 - 250毫克)具有积极的心理社会效应,没有负面的躯体效应,也不会降低这些患者的成人身高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Greig cephalopolysyndactyly syndrome Successful treatment of superior vena cava syndrome with urokinase in an infant with a central venous catheter. The testicular lesion and sexual differentiation in congenital lipoid adrenal hyperplasia. [43 years of Helvetica Paediatrica Acta--retrospect and prospects]. Authentic recombinant human growth hormone. Results of a multicenter clinical trial in patients with growth hormone deficiency.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1