Taylor Jo, Mitchell Alex, Hall Ruth, Heathcote Claire, Langton Trilby, Fraser Lorna, Hewitt Catherine Elizabeth
Department of Health Sciences, University of York, York, UK
Department of Health Sciences, University of York, York, UK.
Arch Dis Child. 2024 Oct 30;109(Suppl 2):s33-s47. doi: 10.1136/archdischild-2023-326669.
Treatment to suppress or lessen effects of puberty are outlined in clinical guidelines for adolescents experiencing gender dysphoria/incongruence. Robust evidence concerning risks and benefits is lacking and there is a need to aggregate evidence as new studies are published.
To identify and synthesise studies assessing the outcomes of puberty suppression in adolescents experiencing gender dysphoria/incongruence.
A systematic review and narrative synthesis. Database searches (Medline, Embase, CINAHL, PsycINFO, Web of Science) were performed in April 2022, with results assessed independently by two reviewers. An adapted version of the Newcastle-Ottawa Scale for cohort studies was used to appraise study quality. Only moderate-quality and high-quality studies were synthesised. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses reporting guidelines were used.
11 cohort, 8 cross-sectional and 31 pre-post studies were included (n=50). One cross-sectional study was high quality, 25 studies were moderate quality (including 5 cohort studies) and 24 were low quality. Synthesis of moderate-quality and high-quality studies showed consistent evidence demonstrating efficacy for suppressing puberty. Height increased in multiple studies, although not in line with expected growth. Multiple studies reported reductions in bone density during treatment. Limited and/or inconsistent evidence was found in relation to gender dysphoria, psychological and psychosocial health, body satisfaction, cardiometabolic risk, cognitive development and fertility.
There is a lack of high-quality research assessing puberty suppression in adolescents experiencing gender dysphoria/incongruence. No conclusions can be drawn about the impact on gender dysphoria, mental and psychosocial health or cognitive development. Bone health and height may be compromised during treatment. More recent studies published since April 2022 until January 2024 also support the conclusions of this review.
CRD42021289659.
针对有性别焦虑/性别不一致问题的青少年,临床指南中概述了抑制或减轻青春期影响的治疗方法。目前缺乏关于风险和益处的有力证据,且随着新研究的发表,有必要汇总证据。
识别并综合评估有性别焦虑/性别不一致问题的青少年青春期抑制结果的研究。
进行系统综述和叙述性综合分析。2022年4月进行数据库检索(Medline、Embase、CINAHL、PsycINFO、Web of Science),结果由两名评审员独立评估。采用纽卡斯尔-渥太华队列研究量表的改编版评估研究质量。仅综合了中等质量和高质量的研究。使用系统评价和Meta分析的首选报告项目报告指南。
纳入了11项队列研究、8项横断面研究和31项前后对照研究(n = 50)。1项横断面研究为高质量,25项研究为中等质量(包括5项队列研究),24项为低质量。中等质量和高质量研究的综合分析显示,有一致证据表明青春期抑制有效。多项研究中身高有所增加,尽管不符合预期生长情况。多项研究报告治疗期间骨密度降低。在性别焦虑、心理和社会心理健康、身体满意度、心血管代谢风险、认知发展和生育能力方面,证据有限且/或不一致。
缺乏评估有性别焦虑/性别不一致问题的青少年青春期抑制的高质量研究。无法得出关于对性别焦虑、心理和社会心理健康或认知发展影响的结论。治疗期间骨骼健康和身高可能会受到影响。2022年4月至2024年1月发表的最新研究也支持本综述的结论。
PROSPERO注册号:CRD42021289659。