Cocchetti Carlotta, Romani Alessia, Collet Sarah, Greenman Yona, Schreiner Thomas, Wiepjes Chantal, den Heijer Martin, T'Sjoen Guy, Fisher Alessandra Daphne
Andrology, Women's Endocrinology and Gender Incongruence Unit, Florence University Hospital, Viale Pieraccini 6, 50100 Florence, Italy.
Department of Endocrinology, Center for Sexology and Gender, Ghent University Hospital, 9000 Ghent, Belgium.
J Clin Med. 2022 Mar 24;11(7):1784. doi: 10.3390/jcm11071784.
Literature on the efficacy and safety of gender-affirming hormonal treatment (GAHT) in transgender people is limited. For this reason, in 2010 the European Network for the Investigation of Gender Incongruence (ENIGI) study was born. The aim of this review is to summarize evidence emerging from this prospective multicentric study and to identify future perspectives. GAHT was effective in inducing desired body changes in both trans AMAB and AFAB people (assigned male and female at birth, respectively). Evidence from the ENIGI study confirmed the overall safety of GAHT in the short/mid-term. In trans AMAB people, an increase in prolactin levels was demonstrated, whereas the most common side effects in trans AFAB people were acne development, erythrocytosis, and unfavorable changes in lipid profile. The main future perspectives should include the evaluation of the efficacy and safety of non-standardized hormonal treatment in non-binary trans people. Furthermore, long-term safety data on mortality rates, oncological risk, and cardiovascular, cerebrovascular and thromboembolic events are lacking. With this aim, we decided to extend the observation of the ENIGI study to 10 years in order to study all these aspects in depth and to answer these questions.
关于性别肯定激素治疗(GAHT)在跨性别者中的疗效和安全性的文献有限。因此,2010年欧洲性别认同不一致调查网络(ENIGI)研究应运而生。本综述的目的是总结这项前瞻性多中心研究中出现的证据,并确定未来的研究方向。GAHT在诱导出生时被指定为男性(AMAB)和出生时被指定为女性(AFAB)的跨性别者产生期望的身体变化方面是有效的。ENIGI研究的证据证实了GAHT在短期/中期的总体安全性。在出生时被指定为男性的跨性别者中,催乳素水平有所升高,而在出生时被指定为女性的跨性别者中,最常见的副作用是痤疮、红细胞增多症以及血脂谱的不利变化。未来主要的研究方向应包括评估非二元跨性别者中非标准化激素治疗的疗效和安全性。此外,缺乏关于死亡率、肿瘤风险以及心血管、脑血管和血栓栓塞事件的长期安全性数据。出于这个目的,我们决定将ENIGI研究的观察期延长至10年,以便深入研究所有这些方面并回答这些问题。