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口服与经皮甾体避孕药对雄激素标志物的影响。

Effect of oral versus transdermal steroidal contraceptives on androgenic markers.

作者信息

White Terry, Jain John K, Stanczyk Frank Z

机构信息

Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, University of South California Keck School of Medicine, Los Angeles, USA.

出版信息

Am J Obstet Gynecol. 2005 Jun;192(6):2055-9. doi: 10.1016/j.ajog.2005.02.067.

Abstract

OBJECTIVE

The purpose of this study was to compare biochemical androgen profiles in women treated with the contraceptive patch versus an oral contraceptive (OC).

STUDY DESIGN

Twenty-four healthy women were randomly assigned to receive 3 cycles of either the contraceptive patch (ethinyl estradiol [EE] 20 microg/d and norelgestromin 150 microg/d) or OC (EE 35 mug and norgestimate 250 microg). Blood samples were taken at baseline and end of treatment. Serum levels of sex hormone-binding globulin (SHBG), total testosterone (T), androstenedione (A), dehydroepiandrosterone sulfate (DHEAS), dihydrotestosterone (DHT), and 3alpha-androstanediol glucuronide (3alpha-diol G) were quantified by immunoassay methods; free T was calculated. The paired t and Student t tests were used for statistical analysis.

RESULTS

Nineteen women completed the study (patch, n = 10; OC, n = 9). Despite a 1.6-fold relative increase in SHBG levels with the patch versus OC (449% vs 274%, P = .03), free T decreased equally in both groups (patch 60%, P < .0001; OC 59%, P < .0001). DHEAS decreased by 26% in the patch group (P < .01) and 32% in the OC group (P < .001). 3alpha-diol G was reduced by 52% in the patch group (P < .0001) and 51% in the OC group (P < .0001). In addition, the OC was associated with significant decreases in A and DHT.

CONCLUSION

The contraceptive patch had an effect comparable to the OC on several key androgenic markers. Given these biochemical findings, the contraceptive patch has significant potential as a therapeutic agent for disorders of androgen excess.

摘要

目的

本研究旨在比较使用避孕贴片与口服避孕药(OC)的女性的生化雄激素谱。

研究设计

24名健康女性被随机分配接受3个周期的避孕贴片(炔雌醇[EE]20微克/天和诺孕酯150微克/天)或OC(EE 35微克和诺孕酯250微克)治疗。在基线和治疗结束时采集血样。通过免疫测定方法对血清性激素结合球蛋白(SHBG)、总睾酮(T)、雄烯二酮(A)、硫酸脱氢表雄酮(DHEAS)、双氢睾酮(DHT)和3α-雄烷二醇葡萄糖醛酸苷(3α-二醇G)水平进行定量;计算游离T。采用配对t检验和学生t检验进行统计分析。

结果

19名女性完成了研究(贴片组,n = 10;OC组,n = 9)。尽管贴片组的SHBG水平相对于OC组有1.6倍的相对升高(449%对274%,P = 0.03),但两组的游离T均同等程度下降(贴片组60%,P < 0.0001;OC组59%,P < 0.0001)。贴片组的DHEAS下降了26%(P < 0.01),OC组下降了32%(P < 0.001)。贴片组的3α-二醇G降低了52%(P < 0.0001),OC组降低了51%(P < 0.0001)。此外,OC与A和DHT的显著降低相关。

结论

避孕贴片在几种关键雄激素指标上的效果与OC相当。基于这些生化研究结果,避孕贴片作为治疗雄激素过多症的药物具有巨大潜力。

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