Impact on hepatic estrogen-sensitive proteins by a 1-year contraceptive vaginal ring delivering Nestorone® and ethinyl estradiol

被引:14
作者
Archer, D. F. [1 ]
Thomas, M. A. [2 ]
Conard, J. [3 ]
Merkatz, R. B. [4 ]
Creasy, G. W. [4 ]
Roberts, K. [4 ]
Plagianos, M. [4 ]
Blithe, D. [5 ]
Sitruk-Ware, R. [4 ]
机构
[1] Eastern Virginia Med Sch, Dept Obstet & Gynecol, Clin Res Ctr, Norfolk, VA 23507 USA
[2] Ctr Reprod Hlth, Cincinnati, OH 45219 USA
[3] Hotel Dieu Cochin Hosp, Dept Biol Hematol, F-75014 Paris, France
[4] Populat Council, Ctr Biomed Res, New York, NY 10017 USA
[5] Eunice Kennedy Shrivel Natl Inst Child Hlth & Hum, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
Contraception; Vaginal ring; Coagulation proteins; SHBG; Nestorone; Ethinyl estradiol; HORMONE-BINDING GLOBULIN; COMBINED ORAL-CONTRACEPTIVES; VENOUS THROMBOEMBOLISM; MU-G; RISK; THROMBOSIS; WOMEN; LEVONORGESTREL; DESOGESTREL; DROSPIRENONE;
D O I
10.1016/j.contraception.2015.09.008
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objectives: Estrogen-sensitive hepatic proteins were assessed in women using a contraceptive vaginal ring (CVR) delivering 150 mcg Nestorone (NES) and 15 mcg ethinyl estradiol (EE). Study design: A substudy of the Contraceptive Clinical Trials Network of the National Institute of Child Health and Human Development enrolled 129 participants, with assessments of factor VIII, fibrinogen, protein S (PS) and sex hormone binding globulin (SHBG). Thirty-six participants had used combined hormonal contraceptives (CHCs) in the cycle preceding first CVR use (recent users) and 70 had no history of recent use (nonusers). Results: Mean values at baseline were within the normal range for all four proteins but were higher for factor VIII, fibrinogen and SHBG and significantly lower for PS in recent compared to nonusers. During NES/EE CVR use, factor VIII, fibrinogen and PS were within the normal range; however, SHBG levels were increased by nearly 100% at Cycle 13. The change from baseline to final evaluation was statistically significant for all proteins in nonusers. The change in recent users was significant for factor VIII at Cycle 6 and for SHBG at Cycles 6 and 13, but not for PS or fibrinogen. Conclusion: NES/EE CVR for up to 13 cycles was associated with changes from baseline in plasma levels of factor VIII, fibrinogen and PS that were within the normal range, with SHBG levels above the normal range by Cycle 6. Nonusers of CHC before CVR showed wider changes in values versus recent users whose baseline values were increased by previous BE exposure. Implications: Recent use of CHCs demonstrated significant changes in all four measured hepatic proteins at baseline compared to nonusers. Use of the NES/EE CVR further changed these hepatic protein markers, but values remained within the normal range. Prebaseline exposure to estrogen can obscure interpretation of hepatic proteins changes associated with a second CHC. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:58 / 64
页数:7
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