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雌三醇的重新发现及其对雌激素治疗的意义。

The rediscovery of estetrol and its implications for estrogen treatment.

作者信息

Coelingh Bennink Herjan J T, Gosden Roger, Stanczyk Frank Z, Adashi Eli Y

机构信息

Pandora Endocrine Innovation, Bergen, The Netherlands.

Department of Biology, William & Mary, Williamsburg, VA.

出版信息

Menopause. 2025 Jul 1;32(7):648-651. doi: 10.1097/GME.0000000000002537.

Abstract

OBJECTIVES

To summarize the literature on the rediscovery and clinical exploration of the fourth natural estrogen estetrol (E4), more than 100 years after the discovery of estrone (E1), estradiol (E2), and estriol (E3).

METHODS

Literature review of E4 publications.

RESULTS

Preclinical and clinical research and development of E4 revealed that: (1) contrary to the other 3 natural estrogens, E4 has a high oral bioavailability, and (2) oral E4 has limited effect on hemostasis and other liver functions, and is, therefore, expected to be a safer estrogen. Since 2022, E4 combined with drospirenone has been registered worldwide as an oral contraceptive. E4 for menopausal hormone therapy is expected to become available in 2026. Clinical development of the use of E4 for the treatment of advanced breast cancer and advanced prostate cancer is ongoing, and E4 has been proposed as a component of an oral male contraceptive.

CONCLUSION

The recognition of E4 as a useful and safe natural estrogen for human use is expected to change the scene of estrogen treatment in women and men significantly.

摘要

目的

在雌酮(E1)、雌二醇(E2)和雌三醇(E3)被发现100多年后,总结关于第四种天然雌激素雌四醇(E4)重新发现及临床探索的文献。

方法

对E4相关出版物进行文献综述。

结果

E4的临床前和临床研究与开发表明:(1)与其他3种天然雌激素不同,E4具有较高的口服生物利用度;(2)口服E4对止血和其他肝功能的影响有限,因此有望成为一种更安全的雌激素。自2022年以来,E4与屈螺酮联合已在全球范围内注册为口服避孕药。用于绝经激素治疗的E4预计将于2026年上市。E4用于治疗晚期乳腺癌和晚期前列腺癌的临床开发正在进行中,并且E4已被提议作为口服男性避孕药的一个成分。

结论

E4作为一种对人类有用且安全的天然雌激素,预计将显著改变男女雌激素治疗的局面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e84/12188799/ec63ace350c8/gme-32-648-g001.jpg

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