Department of Medical and Surgical Sciences for Mother, Child and Adult, University of Modena and Reggio Emilia, Azienda Ospedaliero-Universitaria Di Modena, Modena, Italy.
Expert Rev Clin Pharmacol. 2021 Feb;14(2):211-224. doi: 10.1080/17512433.2021.1878876. Epub 2021 Jan 26.
Norgestimate (NGM) is a testosterone derivative with peculiar receptor activities.
This is a narrative review of the available data on the pharmacotherapy of NGM in combined hormonal contraceptives (CHCs) in terms of contraceptive efficacy, venous thromboembolism (VTE) risk, safety, tolerability and bleeding patterns. A comprehensive literature review was conducted in August 2020 using PubMed with the keyword 'norgestimate'.
NGM shows a mild estrogenic activity associated with anti-mineralocorticoid and anti-androgenic properties, largely responsible for the cardiovascular safety profile. The anti-androgenic property depends on the androgen receptor (AR) nuclear translocation (AR trafficking and its subnuclear distribution), the inhibition of 5α-reductase activity (it possesses higher activity compared to other available progestins), and the increase on sexual hormone binding globulin (SHBG) levels if combined with an estrogenic counterpart. NGM is one of the molecules that best modulates the power of ethinyl-estradiol on the thromboembolic risk, being associated with the lowest VTE risk between different CHCs. NGM has the advantage of retaining peripheral anti-androgenic activity, demonstrated by the impact on lipid and glucose metabolism, and it should be preferred if compared with other similar progestins of the same class of risk which are much more androgenic, such as levonorgestrel.
诺孕酯(NGM)是一种具有特殊受体活性的睾酮衍生物。
本文是对 NGM 在复方激素避孕药(CHC)中的药理学治疗方面的现有数据进行的叙述性综述,涉及避孕效果、静脉血栓栓塞(VTE)风险、安全性、耐受性和出血模式。2020 年 8 月,使用 PubMed 关键词“norgestimate”进行了全面的文献综述。
NGM 表现出轻微的雌激素活性,同时具有抗盐皮质激素和抗雄激素特性,这在很大程度上解释了其心血管安全性。抗雄激素特性取决于雄激素受体(AR)核易位(AR 转运及其亚核分布)、5α-还原酶活性的抑制(与其他可用孕激素相比,其活性更高),以及与雌激素成分联合使用时可增加性激素结合球蛋白(SHBG)水平。NGM 是最佳调节炔雌醇血栓栓塞风险的分子之一,与不同 CHC 之间的最低 VTE 风险相关。NGM 具有保留外周抗雄激素活性的优势,对脂代谢和糖代谢都有影响,如果与其他具有相同风险类别的更具雄激素性的类似孕激素(如左炔诺孕酮)相比,它应该是首选。