Exeltis Germany GmbH, Ismaning, Germany.
Womens Health (Lond). 2023 Jan-Dec;19:17455057221147388. doi: 10.1177/17455057221147388.
The spironolactone derivative drospirenone is combined with ethinylestradiol or estetrol in combined oral contraceptives. Formulations with 17-β-estradiol are used to treat climacteric symptoms. A drospirenone-only formulation has been introduced for contraception. Here, the pharmacological properties of drospirenone, the impact of the different formulations on metabolic and laboratory parameters, and the resulting clinical implications are reviewed. Ethinylestradiol, an inhibitor of CYP metabolic enzymes, changes the pharmacokinetics of drospirenone, leading to a higher drospirenone exposure with ethinylestradiol/drospirenone compared to the drospirenone-only preparation. In addition, several metabolic alterations have been described. The impact of estetrol is less pronounced, and for 17-β-estradiol/drospirenone and drospirenone-only, decreased triglyceride and cholesterol levels were observed. Ethinylestradiol induces various pro-coagulatory factors, leading to hypercoagulability. The effect is significantly reduced with estetrol, and no influence was observed with the drospirenone-only preparation. The anti-mineralocorticoid activity of drospirenone seems to positively counteract the renin-angiotensin-aldosterone-system-activating action of ethinylestradiol. There is no influence on blood pressure with ethinylestradiol/drospirenone and estetrol/drospirenone formulations, while in clinical trials, a reduction has been observed with 17-β-estradiol/drospirenone and drospirenone-only. Anti-aldosterone activity via non-renal mineralocorticoid receptors is associated with cardiovascular health, while interactions with parathyroid hormone signaling impact bone structure and vascular calcification. Though the clinical relevance is unclear for drospirenone, data in this context are reviewed. To sum up, the advantages of drospirenone in hormonal contraception and treatment of menopausal symptoms have been demonstrated for all the formulations described here. Combination with estrogen confers benefits and risks, which must be considered.
螺内酯衍生物屈螺酮与炔雌醇或雌三醇联合用于复方口服避孕药。含有 17-β-雌二醇的制剂用于治疗更年期症状。一种仅含屈螺酮的制剂已被引入用于避孕。本文综述了屈螺酮的药理学特性、不同制剂对代谢和实验室参数的影响以及由此产生的临床意义。炔雌醇是细胞色素 P450 代谢酶的抑制剂,改变了屈螺酮的药代动力学,使屈螺酮/炔雌醇的屈螺酮暴露量高于仅含屈螺酮的制剂。此外,还描述了几种代谢改变。雌三醇的影响较小,并且观察到 17-β-雌二醇/屈螺酮和屈螺酮仅制剂降低了甘油三酯和胆固醇水平。炔雌醇诱导多种促凝因子,导致血液高凝状态。这种作用在雌三醇的作用下显著降低,而在仅含屈螺酮的制剂中则没有观察到。屈螺酮的抗盐皮质激素活性似乎对炔雌醇的肾素-血管紧张素-醛固酮系统激活作用有积极的拮抗作用。炔雌醇/屈螺酮和雌三醇/屈螺酮制剂对血压没有影响,而在临床试验中,17-β-雌二醇/屈螺酮和屈螺酮仅制剂观察到血压降低。通过非肾性盐皮质激素受体的抗醛固酮作用与心血管健康相关,而与甲状旁腺激素信号的相互作用影响骨结构和血管钙化。尽管屈螺酮在这方面的临床意义尚不清楚,但本文对相关数据进行了综述。总之,本文描述的所有制剂均证实了屈螺酮在激素避孕和治疗更年期症状方面的优势。与雌激素联合使用具有获益和风险,必须加以考虑。