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Human Reproduction, Vol. 16, No. 7, 1527-1535, July 2001
© 2001 European Society of Human Reproduction and Embryology

Ovarian and endometrial function during hormonal contraception

The ESHRE Capri Workshop Group*

This report addresses the balance of benefits and risks from changes in ovarian and endometrial function from hormonal contraception. The main mode of action of hormonal contraception is inhibition of ovulation, due chiefly to the dose of oestrogen in combined oral contraceptives. With 20 µg dosages of ethinyl oestradiol follicular activity is more common so that contraception depends on suppression of the LH surge or disruption of the endometrial cycle. In polycystic ovary syndrome (PCOS) treated with oral contraceptives, cysts become smaller and in time the ovarian volume is reduced, ovarian testosterone secretion is reduced and there are potentially favourable effects on carbohydrate and lipid metabolism. Typical oral contraceptive users in the 1980s had a lower incidence of ovarian cysts, but modern oral contraceptives do not appear to affect the incidence of functional cysts or benign epithelial cysts. Moreover, randomized controlled trials indicate that oral contraception prescriptions are unlikely to prevent the development of functional cysts or to hasten their disappearance. Oral contraceptives, however, greatly reduce pelvic pain in women with symptomatic endometriosis and improve the health-related quality of life. Bleeding is a common response with all types of hormonal contraception, but current methodology is inadequate to make accurate comparisons of different products or of different phasic formulations. With continuing use, however, combined oral contraception is associated with endometrial atrophy, the biological plausibility for a reduced risk of endometrial carcinoma. With progestin-only contraception, a number of endometrial changes are considered as possible mechanisms of the associated bleeding but it remains largely unexplained. Oral contraceptives are frequently used for treatment of dysfunctional uterine bleeding, although only one trial has been reported. Oral contraceptive use confers protection from endometrial [relative risk (RR) 0.5] and ovarian (RR 0.4) cancers and in both cases, the protection lasts for up to 2 decades after stopping use.

Key words: cancer/endometrial function/oral contraceptives/ovarian function

* A meeting was organized by ESHRE (Capri, August 23–25, 2000) with financial support from Schering S.p.A. to discuss the above subjects. The speakers included D.T.Baird (Edinburgh), J.Collins (Hamilton), I.Cooke (Sheffield), A.Glasier (Edinburgh), H.S.Jacobs (London), C.La Vecchia (Milano), G.Stock (Berlin), P.Vercellini (Milano). The discussants included J.Cohen (Paris), P.G.Crosignani (Milano), E.Diczfalusy (Ronninge), J.L.H.Evers (Maastricht), S.Skouby (Copenhagen) and B.Tarlatzis (Thessaloniki). The report was prepared by P.G.Crosignani1 (Milano) and B.L.Rubin (Newtown Square, PA). J.Collins wrote the abstract. Professor G.Stock was a specially invited guest to provide information about the newest approaches to drug development in the field of fertility regulation.

1 To whom correspondence should be addressed at: Department of Obstetrics and Gynaecology, University of Milan, Via Della commenda 12, 20122 Milan, Italy. E-mail: piergorgio.crosignani{at}unimi.it


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