Fagundes Vitor Luis, Barreiro Marques Nathália Carolina, Franco de Lima Amanda, de Fátima Cobre Alexandre, Stumpf Tonin Fernanda, Luna Lazo Raul Edison, Pontarolo Roberto
Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Paraná, Curitiba 80210-170, Brazil.
Health and Technology Research Center (H&TRC), Escola Superior de Tecnologia da Saúde (ESTeSL-IPL), 1990-096 Lisbon, Portugal.
Pharmaceutics. 2025 May 11;17(5):638. doi: 10.3390/pharmaceutics17050638.
Gestrinone is a synthetic hormone derived from 19-nortestosterone, exhibiting androgenic, anabolic, anti-progestogenic, and antiestrogenic effects. Gestrinone subcutaneous implants have been used "off label" for aesthetic purposes due to their anabolic action, promoting accelerated metabolism and muscle gain. Our goal is to conduct a systematic review focused exclusively on identifying the safety profile of gestrinone use, without addressing efficacy. This systematic review was performed according to the Joanna Briggs Institute and Cochrane Collaboration recommendations and is reported following the Preferred Reporting Items for Systematic Reviews and Network Meta-Analyses. This article's searches were carried out in the PubMed, Embase, and Web of Science databases. : A total of 32 articles were included in this study. The reported adverse events associated with the use of gestrinone were amenorrhea (41.4% of cases), acne, seborrhea (42.7% of reports), decreased libido (26.5%), and hot flushes (24.2%). Other nonspecific symptoms such as hoarseness and cramps were also fairly reported (3.5% and 18.6%, respectively). Other reported effects were associated with breast size reduction (23.7% of patients) and increased transaminases (15.1%). Most studies (40%, n = 24 studies) found significant weight gain (ranging from 0.9 to 8 kg per patient). Abnormalities in bone mineral density were reported in four studies. The evidence remains insufficient to fully understand the risks of gestrinone uses associated with its widespread, unregulated use. Thus, further standardized studies and regulatory oversight to ensure patient safety are needed to mitigate potential health risks.
孕三烯酮是一种源自19-去甲睾酮的合成激素,具有雄激素、同化激素、抗孕激素和抗雌激素作用。由于其同化作用可促进新陈代谢加快和肌肉增加,孕三烯酮皮下植入物已被“超适应症”用于美容目的。我们的目标是进行一项系统评价,专门聚焦于确定孕三烯酮使用的安全性概况,而不涉及疗效。本系统评价是根据乔安娜·布里格斯研究所和Cochrane协作网的建议进行的,并按照系统评价和网络荟萃分析的首选报告项目进行报告。本文的检索在PubMed、Embase和科学网数据库中进行。本研究共纳入32篇文章。报告的与使用孕三烯酮相关的不良事件有闭经(41.4%的病例)、痤疮、脂溢性皮炎(42.7%的报告)、性欲减退(26.5%)和潮热(24.2%)。其他非特异性症状如声音嘶哑和痉挛也有相当比例的报告(分别为3.5%和18.6%)。其他报告的影响与乳房缩小(23.7%的患者)和转氨酶升高(15.1%)有关。大多数研究(40%,n = 24项研究)发现有显著体重增加(每位患者增加0.9至8千克)。四项研究报告了骨矿物质密度异常。现有证据仍不足以充分了解孕三烯酮广泛、无监管使用所带来的风险。因此,需要进一步的标准化研究和监管监督以确保患者安全,从而降低潜在的健康风险。