Slack Daniel J, Di Via Ioschpe Anaïs, Saturno Michael, Kihuwa-Mani Sky, Amakiri Uchechukwu O, Guerra Daniel, Karim Subha, Safer Joshua D
Division of Endocrinology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York; Center for Transgender Medicine and Surgery, Mount Sinai Health System, New York, New York.
Department of Surgery, Icahn School of Medicine at Mount Sinai, New York, New York.
Endocr Pract. 2025 Jan;31(1):19-27. doi: 10.1016/j.eprac.2024.10.002. Epub 2024 Oct 12.
Individuals may seek gender-affirming hormone therapy (GAHT) to align their physical appearance with their gender identity. Feminizing GAHT typically involves the use of estrogen. This study investigates the effect of route of administration (ROA) and dose of estradiol on estradiol (E2) and testosterone (T) levels in transfeminine individuals.
We conducted a chart review of 573 patients with an active prescription for estradiol for feminizing GAHT and serum hormone levels available. Multiple linear regression and analysis of variance were used to analyze the effect of dose and ROA of estradiol on serum E2 and T.
Oral estradiol was the only ROA demonstrating a linear dose-response, with each 1 mg/d increase associated with a reduction in T of 19.03 ng/dL (P = .005). Lower T levels were seen with higher doses of transdermal estradiol but a significant dose-response was not demonstrated. Intramuscular estradiol was associated with lower T and higher E2 compared to oral and transdermal ROAs (P < .001), with many achieving target hormone levels even at low doses. Higher doses of oral estradiol were associated with lower mean serum leutenizing hormone and follicle stimulating hormone levels (P < .05).
Oral estradiol can be titrated to achieve a stepwise decrease in serum T. The intramuscular ROA appears to be the most potent delivery of estradiol with impact on serum hormone levels with doses on the low end of guideline-suggested ranges. Serum leutenizing hormone and follicle stimulating hormone may also help with the management of feminizing GAHT.
个体可能会寻求性别肯定激素疗法(GAHT),以使自己的外貌与性别认同相符。女性化GAHT通常涉及使用雌激素。本研究调查了给药途径(ROA)和雌二醇剂量对跨性别女性个体中雌二醇(E2)和睾酮(T)水平的影响。
我们对573例有雌二醇活性处方用于女性化GAHT且有血清激素水平数据的患者进行了病历回顾。采用多元线性回归和方差分析来分析雌二醇的剂量和ROA对血清E2和T的影响。
口服雌二醇是唯一呈现线性剂量反应的ROA,每增加1mg/d,T水平降低19.03ng/dL(P = 0.005)。经皮雌二醇剂量越高,T水平越低,但未显示出显著的剂量反应。与口服和经皮ROA相比,肌肉注射雌二醇与较低的T水平和较高的E2水平相关(P < 0.001),许多患者即使在低剂量时也能达到目标激素水平。较高剂量的口服雌二醇与较低的平均血清促黄体生成素和促卵泡生成素水平相关(P < 0.05)。
口服雌二醇可以进行滴定,以使血清T逐步降低。肌肉注射ROA似乎是雌二醇最有效的给药方式,在指南建议范围的低端剂量就能对血清激素水平产生影响。血清促黄体生成素和促卵泡生成素也可能有助于女性化GAHT的管理。