Testosterone concentrations and prescription patterns of 1% testosterone gel in transgender and gender diverse individuals.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2022-03-11 eCollection Date: 2022-01-01 DOI:10.1177/20420188221083512
Brendan J Nolan, Sav Zwickl, Alex F Q Wong, Peter Locke, Satu Simpson, Ling Li, Jeffrey D Zajac, Ada S Cheung
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Abstract

Background: Masculinising hormone therapy with testosterone is used to align an individual's physical characteristics with their gender identity. Standard testosterone doses and formulations recommended for hypogonadal cisgender men are typically administered, although there are currently limited data evaluating the use of 1% testosterone gel in gender-affirming hormone therapy regimens.

Objectives: The objective of the study was to assess the prescription patterns and serum total testosterone concentrations achieved with 1% testosterone gel in trans and gender diverse individuals.

Materials and methods: A retrospective cross-sectional analysis was undertaken of trans individuals at a primary and secondary care clinic in Melbourne, Australia. Sixty-seven individuals treated with 1% testosterone gel were included. Primary outcomes were testosterone dose and serum total testosterone concentration achieved.

Results: Median age was 25 (22-30) years and median duration of testosterone therapy was 12 (7-40) months. Thirty-five (52%) individuals had a nonbinary gender identity. Initial median testosterone dose was 25 mg (12.5-31.3) daily. Fifty-two (78%) individuals commenced doses <50 mg daily, the recommended starting dose for hypogonadal cisgender men. Median total testosterone concentration achieved was 11.9 nmol/l (7.3-18.6). Polycythaemia (haematocrit >0.5) was documented in eight of 138 (6%) laboratory results in six individuals.

Discussion and conclusions: One percent testosterone gel achieves serum total testosterone concentrations in the cisgender male reference range. A high proportion of individuals had a nonbinary gender identity and most individuals commenced a lower dose than that typically administered to hypogonadal cisgender men, potentially related to slow or 'partial' masculinisation goals.

1%睾酮凝胶在跨性别和不同性别人群中的浓度和处方模式
背景:使用睾酮进行男性化激素治疗是为了使个人的身体特征与其性别认同相一致。尽管目前评估在性别确认激素治疗方案中使用1%睾酮凝胶的数据有限,但通常会给性腺功能减退的顺性别男性推荐标准睾酮剂量和配方。目的:本研究的目的是评估跨性别和性别不同个体使用1%睾酮凝胶的处方模式和血清总睾酮浓度。材料和方法:在澳大利亚墨尔本的一家初级和二级护理诊所对跨性别者进行了回顾性横断面分析。包括67名接受1%睾酮凝胶治疗的患者。主要结果是获得睾酮剂量和血清总睾酮浓度。结果:中位年龄为25(22-30)岁,睾酮治疗的中位持续时间为12(7-40)个月。35人(52%)具有非二元性别认同。睾酮的初始中位剂量为每日25 mg(12.5-31.3)。在6名受试者的138份(6%)实验室结果中,有8份记录了52名(78%)受试者开始服用0.5)。讨论和结论:1%的睾酮凝胶达到了顺性别男性参考范围内的血清总睾酮浓度。高比例的个体具有非二元性别认同,大多数个体开始服用的剂量低于性腺功能减退的顺性别男性,这可能与缓慢或“部分”的男性化目标有关。
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
CiteScore
7.20
自引率
4.30%
发文量
567
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