绝经期补充雄激素的风险。

S M Slayden
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引用次数: 25

摘要

有越来越多的兴趣使用绝经期雄激素替代疗法(MART)在有症状的妇女接受自然或手术绝经。然而,与传统的雌激素/黄体酮激素替代疗法相比,MART在缓解这些症状方面的疗效仍然存在争议。因此,必须注意各种MART制剂的副作用。这些化合物的剂量、烷基化和给药途径影响副作用的发生。虽然所有雄激素都是潜在的壮阳剂,但烷基化化合物无论其给药途径如何,都有诱发严重肝脏后果的额外风险。幸运的是,与男性相比,女性服用的剂量较低,没有导致明显的肝脏事件。产生不利的脂蛋白谱是可能的,但不解决在这篇文章。因此,阳刚之气和皮肤副作用仍然是主要关注的问题。虽然一些观察性研究表明,痤疮和/或多毛症在口服甲基睾酮治疗的患者中分别高达38%和36%,但其他前瞻性研究表明,发病率要低得多,约为5%。其他被报道的男性化效果包括声音变深和阴蒂变大。当MART与雌激素联合使用时,其他的担忧与发生子宫内膜增生的风险有关。幸运的是,同时服用黄体酮具有保护作用。最后,有一个理论上的担忧,MART可能会增加患乳腺癌的风险,但这还没有在临床实践中得到证实。总的来说,当剂量避免超生理睾酮水平时,MART的安全性似乎是可以接受的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risks of menopausal androgen supplementation.

There is increasing interest in the use of menopausal androgen replacement therapy (MART) in symptomatic women undergoing natural or surgical menopause. However, the efficacy of MART in alleviating these symptoms compared to traditional estrogen/progestin hormone replacement therapy remains a subject of debate. Accordingly, attention must be focused on the side-effects of the various MART preparations. The dose, alkylation, and route of administration of these compounds influences the development of side effects. While all androgens are potential virilizing agents, alkylated compounds have an additional risk of inducing severe hepatic consequences, regardless of their route of administration. Fortunately, the lower doses administered to women compared to men has not resulted in significant hepatic events. Generation of an adverse lipoprotein profile is possible but is not addressed in this article. Thus, virilizing and cutaneous side effects remain the primary concern. While some observational studies indicate acne and/or hirsutism are evident in up to 38% and 36% of oral methyltestosterone-treated patients, respectively, other studies performed in a prospective fashion suggest a much lower incidence of approximately 5%. Other reported virilizing effects include deepening of the voice and clitoromegaly. Additional concerns are related to risks of developing endometrial hyperplasia when MART is used in conjunction with estrogens. Fortunately, concomitant progestin administration is protective. Finally, there is a theoretical concern that MART may increase the risk of developing breast cancer but this has not been demonstrated in clinical practice. Overall, the safety profile of MART appears to be acceptable when dosing avoids supraphysiologic testosterone levels.

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