| Literature DB >> 3102162 |
S K Smith, R J Kirkman, B B Arce, A S McNeilly, N B Loudon, D T Baird.
Abstract
The effect of deliberate omission of a phased formulation pill, Trinordiol (ethinyl estradiol 30 micrograms + levonorgestrel 50 micrograms: 6 tablets; ethinyl estradiol 40 micrograms + levonorgestrel 75 micrograms: 5 tablets; ethinyl estradiol 30 micrograms + levonorgestrel 125 micrograms: 10 tablets) or a low-dose, combined, oral contraceptive pill, Microgynon (ethinyl estradiol 30 micrograms + levonorgestrel 150 micrograms: 21 tablets) on the hypothalamo-pituitary-ovarian axis were studied. Thirty-six women were recruited to the study and divided equally between the two types of pill. Medication was begun on the 8th pill-free day of the cycle and continued for 7 days (Group 1), 14 days (Group 2) or 21 days (Group 3). Levels of FSH, LH, estradiol (E2) and progesterone (P) were measured in plasma on alternate days during the final week of pill therapy, and daily for the 7 days after stopping the pill. For the first 2 weeks of pill therapy, follicular activity, as judged by plasma levels of E2, was greater in women taking Trinordiol than in those taking Microgynon, but was similar in both groups by the third week of pill treatment. Five women taking Trinordiol (2 in Group 1 and 3 in Group 2) had plasma levels of E2 in excess of 500 pmol/l whilst taking the pills, and only 1 patient achieved this degree of follicular activity after stopping the tablets. One woman who had taken 7 days of Trinordiol (Group 1) showed a rise of plasma levels of P to 6.8 nmol/l, but luteinization did not occur in any of the remaining 35 women who took Trinordiol or Microgynon. These findings suggest that follicular activity is less completely suppressed by Trinordiol than Microgynon, at least in the first 2 weeks of pill therapy, but that normal ovulation is still a rare event in the week after cessation of either of these pills, even if only 7 days of medication have been taken.Entities:
Keywords: Biology; Clinical Research; Contraception--pharmacodynamics; Contraceptive Agents, Estrogen--pharmacodynamics; Contraceptive Agents, Female--pharmacodynamics; Contraceptive Agents, Progestin--pharmacodynamics; Contraceptive Agents--pharmacodynamics; Contraceptive Effectiveness; Contraceptive Methods--pharmacodynamics; Contraceptive Mode Of Action; Corpus Luteum Hormones; Developed Countries; Endocrine System; England; Estradiol; Estrogens; Ethinyl Estradiol--pharmacodynamics; Europe; Family Planning; Follicle Stimulating Hormone; Gonadotropins; Gonadotropins, Pituitary; Hormones--pharmacodynamics; Levonorgestrel--pharmacodynamics; Luteinizing Hormone; Northern Europe; Oral Contraceptives, Combined--pharmacodynamics; Oral Contraceptives, Low-dose--pharmacodynamics; Oral Contraceptives, Phasic--pharmacodynamics; Oral Contraceptives--pharmacodynamics; Ovulation; Ovulation Suppression; Physiology; Progesterone; Reproduction; Reproductive Control Agents; Research Methodology; Research Report; United Kingdom; Use-effectiveness
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Year: 1986 PMID: 3102162 DOI: 10.1016/0010-7824(86)90060-0
Source DB: PubMed Journal: Contraception ISSN: 0010-7824 Impact factor: 3.375