Changes in androgens during treatment with four low-dose contraceptives

被引:123
作者
Coenen, CMH
Thomas, CMG
Borm, GF
Hollanders, JMG
Rolland, R
机构
[1] UNIV NIJMEGEN ST RADBOUD HOSP,ENDOCRINOL & REPROD LAB,6500 HB NIJMEGEN,NETHERLANDS
[2] UNIV NIJMEGEN ST RADBOUD HOSP,DEPT BIOSTAT,6500 HB NIJMEGEN,NETHERLANDS
[3] KING FAHAD NATL GUARD HOSP,RIYADH 11426,SAUDI ARABIA
关键词
androgens; oral contraceptives;
D O I
10.1016/0010-7824(96)00006-6
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The aim of the present study was to compare changes in the endogenous androgen environment in healthy women while on low-dose oral contraceptives (OCs). One-hundred healthy women were randomized to receive one of four OCs during six months: 21 tablets of Cilest((R)), Femodeen(R), Marvelon(R), or Mercilon(R). During the luteal phase of the pretreatment cycle, body weight and blood pressure were recorded and the following parameters were measured: sex hormone-binding globulin (SHBG), corticosteroid-binding globulin (CBG), testosterone (T), free testosterone (FT), 5 alpha-dihydrotestosterone (DHT), androstenedione (A), dehydroepiandrosterone-sulphate (DHEA-S) and 17 alpha-hydroxyprogesterone (17OHP) while also the free androgen index (FAI) was calculated. Measurements were repeated during the 3rd week of pill intake in the 4th and the 6th pill month. There were no differences on body mass and blood pressure with the use of the four OCs. The mean serum DHEA-S decreased significantly in all groups though less in the Mercilon(R) group when compared to Cilest(R) and Marvelon(R) (approximately 20% vs 45%). Mean serum SHBG and CBG increased significantly in all four groups approximately 250% and 100%, respectively. In each group CBG also increased significantly but less in women taking Mercilon(R) (-75%) as compared to the others (-100%). Current low-dose OCs were found to have similar impact on the endogenous androgen metabolism with significant decreases of serum testosterone, DHT, A, and DHEA-S. They may be equally beneficial in woman with androgen related syndromes such as acne and hirsutism.
引用
收藏
页码:171 / 176
页数:6
相关论文
共 22 条
[11]   THE METABOLIC IMPACT OF ORAL-CONTRACEPTIVES [J].
KRAUSS, RM ;
BURKMAN, RT .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1992, 167 (04) :1177-1184
[12]   ORAL CONTRACEPTION AND RISK OF A CEREBRAL THROMBOEMBOLIC ATTACK - RESULTS OF A CASE-CONTROL STUDY [J].
LIDEGAARD, O .
BRITISH MEDICAL JOURNAL, 1993, 306 (6883) :956-963
[13]   PROGESTOGENS AND CARDIOVASCULAR REACTIONS ASSOCIATED WITH ORAL-CONTRACEPTIVES AND A COMPARISON OF THE SAFETY OF 50-MU-G AND 30-MU-G ESTROGEN PREPARATIONS [J].
MEADE, TW ;
GREENBERG, G ;
THOMPSON, SG .
BRITISH MEDICAL JOURNAL, 1980, 280 (6224) :1157-1161
[14]  
MURPHY AA, 1990, FERTIL STERIL, V53, P35
[15]   PRECLINICAL EVALUATION OF NORGESTIMATE, A PROGESTIN WITH MINIMAL ANDROGENIC ACTIVITY [J].
PHILLIPS, A ;
HAHN, DW ;
MCGUIRE, JL .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1992, 167 (04) :1191-1196
[16]  
REIJNDERS FJL, 1988, THESIS CATHOLIC U NI
[17]   NEW PROGESTOGENS IN ORAL-CONTRACEPTIVES [J].
RUNNEBAUM, B ;
RABE, T .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1987, 157 (04) :1059-1063
[18]  
THOMAS CMG, 1986, CLIN CHEM, V32, P702
[19]   AN EPIDEMIOLOGIC SURVEY OF CARDIOVASCULAR-DISEASE IN WOMEN TAKING ORAL-CONTRACEPTIVES [J].
THOROGOOD, M ;
VESSEY, MP .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1990, 163 (01) :274-281
[20]  
Valkenburg H A, 1980, Ned Tijdschr Geneeskd, V124, P183