Istanbul University, Faculty of Medicine, Department of Obstetrics and Gynecology, Fatih, Istanbul, Turkey.
Istanbul University, Faculty of Medicine, Department of Obstetrics and Gynecology, Fatih, Istanbul, Turkey.
J Pediatr Adolesc Gynecol. 2022 Dec;35(6):634-637. doi: 10.1016/j.jpag.2022.05.004. Epub 2022 May 26.
To evaluate the effects of physiological dose 17 beta-estradiol (E) replacement on low bone mineral density (BMD) and compare the results of oral and transdermal (TD) E administration in adolescents and young women with hypogonadism DESIGN, SETTING, AND PARTICIPANTS: We retrospectively reviewed the medical records of patients aged 15 to 24 years who were diagnosed with hypogonadism, who had begun receiving oral or TD E replacement, and whose initial dual-energy X-ray absorptiometry scan detected a lumbar spine BMD Z-score of -1 or lower between 2014 and 2018. The patients were divided into 2 groups according to the E route of administration as those who received 2 mg orally (Group 1) and 0.1 mg TD (Group 2).
None MAIN OUTCOME MEASURE: BMD scans of the patients at baseline and repeated within 2 years after E replacement RESULTS: In total, 43 patients who met the inclusion criteria were included in the study. Two groups did not differ for BMD scores at baseline. A significant improvement in BMD was observed with physiological dose E replacement in both groups. Mean BMD Z-score increased by +0.7 (95% CI, 0.47-0.93) in response to TD E administration, compared with +0.41 (95% CI, 0.25-0.58) during oral E replacement (P = .037).
We conclude that physiological dose E replacement, even within a short period of 2 years, has a significant beneficial effect on bone mass acquisition on the lumbar spine. Our study also demonstrates the possible superiority of TD E2 replacement over the oral route in increasing lumbar spine BMD.
评估生理剂量 17β-雌二醇(E)替代治疗对低骨密度(BMD)的影响,并比较口服和经皮(TD)E 给药在青春期和年轻女性性腺功能减退症患者中的效果。
设计、地点和参与者:我们回顾性分析了 2014 年至 2018 年间诊断为性腺功能减退症、开始接受口服或 TD E 替代治疗且初始双能 X 线吸收法(DXA)扫描腰椎 BMD Z 评分低于-1 的 15 至 24 岁患者的病历。根据 E 给药途径将患者分为 2 组,即口服 2 mg(组 1)和 0.1 mg TD(组 2)。
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E 替代治疗前和治疗后 2 年内患者的 BMD 扫描结果。
共有 43 名符合纳入标准的患者纳入研究。两组患者的 BMD 评分在基线时无差异。两组患者均接受生理剂量 E 替代治疗后 BMD 均显著改善。TD E 给药后 BMD Z 评分平均增加 0.7(95%置信区间,0.47-0.93),而口服 E 替代治疗时增加 0.41(95%置信区间,0.25-0.58)(P=0.037)。
我们得出结论,即使在短短 2 年内,生理剂量 E 替代治疗对腰椎骨量的获得有显著的有益影响。我们的研究还表明,TD E2 替代治疗在增加腰椎 BMD 方面可能优于口服途径。