Memi Eleni, Pavli Polina, Papagianni Maria, Vrachnis Nikolaos, Mastorakos George
Unit of Endocrinology, Diabetes mellitus, and Metabolism, Aretaieion Hospital, School of Medicine, National and Kapodistrian University of Athens, Vas. Sophias Av. 76, 11528, Athens, Greece.
Department of Nutrition and Dietetics, School of Physical Education, Sport Science and Dietetics, University of Thessaly, 42100, Trikala, Greece.
Rev Endocr Metab Disord. 2024 Aug;25(4):751-772. doi: 10.1007/s11154-024-09882-0. Epub 2024 Apr 23.
Progesterone is a natural steroid hormone, while progestins are synthetic molecules. In the female reproductive system, progesterone contributes to the control of luteinizing hormone and follicle-stimulating hormone secretion and their pulsatility, via its receptors on the kisspeptin, neurokinin B, and dynorphin neurons in the hypothalamus. Progesterone together with estradiol controls the cyclic changes of proliferation and decidualization of the endometrium; exerts anti-mitogenic actions on endometrial epithelial cells; regulates normal menstrual bleeding; contributes to fertilization and pregnancy maintenance; participates in the onset of labor. In addition, it exerts numerous effects on other endocrine systems. Micronized progesterone (MP) is natural progesterone with increased bioavailability, due to its pharmacotechnical micronized structure, which makes it an attractive diagnostic and therapeutic tool. This critical literature review aims to summarize and put forward the potential diagnostic and therapeutic uses of MP in the field of endocrinology. During reproductive life, MP is used for diagnostic purposes in the evaluation of primary or secondary amenorrhea as a challenge test. Moreover, it can be prescribed to women presenting with amenorrhea or oligomenorrhea for induction of withdrawal bleeding, in order to time blood-sampling for diagnostic purposes in early follicular phase. Therapeutically, MP, alone or combined with estrogens, is a useful tool in various endocrine disorders including primary amenorrhea, abnormal uterine bleeding due to disordered ovulation, luteal phase deficiency, premenstrual syndrome, polycystic ovary syndrome, secondary amenorrhea [functional hypothalamic amenorrhea, premature ovarian insufficiency], perimenopause and menopause. When administrated per os, acting as a neurosteroid directly or through its metabolites, it exerts beneficial effects on brain function such as alleviation of symptoms of anxiety and depression, asw well as of sleep problems, while it improves working memory in peri- and menopausal women. Micronized progesterone preserves full potential of progesterone activity, without presenting many of the side-effects of progestins. Although it has been associated with more frequent drowsiness and dizziness, it can be well tolerated with nocturnal administration. Because of its better safety profile, especially with regard to metabolic ailments, breast cancer risk and veno-thromboembolism risk, MP is the preferred option for individuals with an increased risk of cardiovascular and metabolic diseases and of all-cause mortality.
孕酮是一种天然甾体激素,而孕激素是合成分子。在女性生殖系统中,孕酮通过其在下丘脑 kisspeptin、神经激肽 B 和强啡肽神经元上的受体,参与控制促黄体生成素和促卵泡激素的分泌及其脉冲性。孕酮与雌二醇共同控制子宫内膜增殖和蜕膜化的周期性变化;对子宫内膜上皮细胞发挥抗有丝分裂作用;调节正常月经出血;有助于受精和维持妊娠;参与分娩发动。此外,它对其他内分泌系统也有诸多影响。微粉化孕酮(MP)是具有更高生物利用度的天然孕酮,因其药物技术微粉化结构,使其成为一种有吸引力的诊断和治疗工具。这篇重要的文献综述旨在总结并提出 MP 在内分泌学领域的潜在诊断和治疗用途。在生殖期,MP 作为一种激发试验用于评估原发性或继发性闭经的诊断目的。此外,对于出现闭经或月经过少的女性,可开具 MP 以诱导撤退性出血,以便在卵泡早期进行诊断性采血。在治疗方面,MP 单独使用或与雌激素联合使用,是治疗各种内分泌疾病的有用工具,包括原发性闭经、排卵障碍导致的异常子宫出血、黄体期缺陷、经前期综合征、多囊卵巢综合征、继发性闭经[功能性下丘脑性闭经、卵巢早衰]、围绝经期和绝经。口服给药时,MP 直接或通过其代谢产物作为神经甾体发挥作用,对脑功能产生有益影响,如缓解焦虑和抑郁症状以及睡眠问题,同时改善围绝经期和绝经后女性的工作记忆。微粉化孕酮保留了孕酮活性的全部潜能,而没有许多孕激素的副作用。虽然它与更频繁的嗜睡和头晕有关,但夜间给药时耐受性良好。由于其更好的安全性,特别是在代谢疾病、乳腺癌风险和静脉血栓栓塞风险方面,MP 是心血管和代谢疾病风险以及全因死亡率增加的个体的首选。