Literature DB >> 2147887

Intra- and interindividual variations in contraceptive steroid levels during 12 treatment cycles: no relation to irregular bleedings.

C Jung-Hoffmann1, H Kuhl.   

Abstract

During one year of treatment with oral contraceptives containing 30 micrograms ethinylestradiol and 150 micrograms desogestrel (EE/DG) or 30 micrograms EE and 75 micrograms gestodene (EE/GSD), the serum concentrations of EE, 3-keto-desogestrel (KDG) and GSD were determined on day 1, 10 and 21 of the 1st, 3rd, 6th and 12th cycle. The areas under the time-versus-concentration curves were calculated from the levels before and 0.5, 1, 1.5, 2, 3, 4 and 24 hours after intake of a tablet. There were large intra- and interindividual variations both revealing coefficients of variation (C.V.) between 25% and 80% (EE),, 30% and 50% (KDG) and 30% and 65% (GSD). During each cycle, the EE levels increased significantly between day 1 and 10 by 70% on average reaching a steady-state, while the progestogen concentrations rose by 100% (KDG) and 150% (GSD) up to a steady-state between day 10 and 21. After reaching the steady-state, the C.V. were generally lower. The ratios between the levels of EE and the progestogens showed still higher variations indicating different influences on the estrogen and progestogen component. There was no correlation between the steroid levels and weight, height or age. In spite of the large intraindividual variations, most of the women showed a distinct pattern of the levels of EE and the progestogens throughout the year of treatment indicating a genetic or acquired predisposition. The difference in the average AUC of EE, KDG and GSD between the women was 300% at most. During the first cycle of treatment with EE/DG and EE/GSD, about half of the women recorded intermenstrual bleedings which decreased thereafter. There was no relation between the occurrence of irregular bleedings and the average serum levels of EE and the progestogens of the individual women, neither during the first cycle nor during the whole treatment period of 12 cycles. It is concluded that spottings or breakthrough bleedings during treatment with oral contraceptives are not dependent on a distinct pattern of the serum levels of EE and the progestogen.

Entities:  

Keywords:  Biology; Contraception; Contraceptive Agents, Estrogen--administraction and dosage; Contraceptive Agents, Female--administraction and dosage; Contraceptive Agents, Female--pharmacodynamics; Contraceptive Agents, Progestin--administraction and dosage; Contraceptive Agents, Progestin--pharmacodynamics; Contraceptive Agents--administraction and dosage; Contraceptive Agents--pharmacodynamics; Contraceptive Methods--administraction and dosage; Diseases; Ethinyl Estradiol--administraction and dosage; Family Planning; Female Contraception; Incidence; Measurement; Menstrual Cycle; Menstruation; Menstruation Disorders; Metabolic Effects; Oral Contraceptives, Combined--administraction and dosage; Oral Contraceptives--administraction and dosage; Physiology; Reproduction; Research Methodology; Steroid Metabolic Effects

Mesh:

Substances:

Year:  1990        PMID: 2147887     DOI: 10.1016/0010-7824(90)90050-6

Source DB:  PubMed          Journal:  Contraception        ISSN: 0010-7824            Impact factor:   3.375


  7 in total

1.  Effect of a low-dose contraceptive patch on efficacy, bleeding pattern, and safety: a 1-year, multicenter, open-label, uncontrolled study.

Authors:  Inka Wiegratz; Susana Bassol; Edith Weisberg; Uwe Mellinger; Martin Merz
Journal:  Reprod Sci       Date:  2014-04-30       Impact factor: 3.060

Review 2.  Comparative pharmacology of newer progestogens.

Authors:  H Kuhl
Journal:  Drugs       Date:  1996-02       Impact factor: 9.546

Review 3.  Long-cycle treatment with oral contraceptives.

Authors:  Inka Wiegratz; Herbert Kuhl
Journal:  Drugs       Date:  2004       Impact factor: 9.546

4.  Pharmacokinetic drug-drug interaction between ethinyl estradiol and gestodene, administered as a transdermal fertility control patch, and two CYP3A4 inhibitors and a CYP3A4 substrate.

Authors:  Julia Winkler; Mark Goldammer; Matthias Ludwig; Beate Rohde; Christian Zurth
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2014-07-06       Impact factor: 2.441

5.  Pharmacokinetic overview of ethinyl estradiol dose and bioavailability using two transdermal contraceptive systems and a standard combined oral contraceptive.

Authors:  Birte Hofmann; Isabel Reinecke; Barbara Schuett; Martin Merz; Christian Zurth
Journal:  Int J Clin Pharmacol Ther       Date:  2014-12       Impact factor: 1.366

6.  An open-label, two-period comparative study on pharmacokinetics and safety of a combined ethinylestradiol/gestodene transdermal contraceptive patch.

Authors:  Chao Zhang; Haiyan Li; Xin Xiong; Suodi Zhai; Yudong Wei; Shuang Zhang; Yuanyuan Zhang; Lin Xu; Li Liu
Journal:  Drug Des Devel Ther       Date:  2017-03-10       Impact factor: 4.162

7.  Investigation of the hemostatic effect of a transdermal patch containing 0.55 mg ethinyl estradiol and 2.1 mg gestodene compared with a monophasic oral contraceptive containing 0.03 mg ethinyl estradiol and 0.15 mg levonorgestrel: an open-label, randomized, crossover study.

Authors:  Wolfgang Junge; Doris Heger-Mahn; Dietmar Trummer; Martin Merz
Journal:  Drugs R D       Date:  2013-09
  7 in total

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