Diurnal rhythm and effects of oral contraceptives on serum dehydroepiandrosterone sulfate (DHEAS) are related to alterations in serum albumin rather than to changes in adrenocortical steroid secretion

被引:32
作者
Carlström, K
Karlsson, R
Von Schoultz, B
机构
[1] Huddinge Univ Hosp, Dept Obstet & Gynecol, Karolinska Inst, SE-14186 Huddinge, Sweden
[2] Huddinge Univ Hosp, Clin Res Ctr, Karolinska Inst, SE-14186 Huddinge, Sweden
[3] Univ Hosp, Dept Gen Med, Umea, Sweden
[4] Karolinska Inst, Karolinska Hosp, Dept Obstet & Gynecol, S-10401 Stockholm, Sweden
关键词
albumin; cortisol; dehydroepiandrosterone; dehydroepiandrosterone sulfate; diurnal variation; oral contraceptives;
D O I
10.1080/00365510260296519
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Dehydroepiandrosterone sulfate (DHEAS), which is of almost exclusive adrenal origin, is important for the androgen status in women and prepubertal children, and DHEAS assays are used in the investigation of hyperandrogenism. There are conflicting reports concerning a diurnal variation in serum DHEAS. Although of adrenocortical origin, serum DHEAS levels are decreased by oral contraceptives (OCs). DHEAS is strongly bound to serum albumin and has a very low metabolic clearance rate. The present study was performed in order to investigate whether a diurnal variation in serum DHEAS exists and, if so, whether this diurnal variation and the decreased DHEAS levels following OC use are related to alterations in adrenocortical steroids or to changes in serum albumin. Serum concentrations of DHEAS, dehydroepiandrosterone (DHEA), cortisol and albumin were determined in blood samples taken every half hour over a 24-h period in 10 healthy women before and during use of combined OCs. Significant and frequently synchronous diurnal variations in serum DHEAS and albumin were found before as well as during OC use. These variations were not synchronous with the diurnal variation in DHEA. OCs significantly decreased serum DHEAS and albumin levels. A multiple regression analysis showed changes in albumin to be the most decisive factor for the diurnal variation as and for OC-induced changes in DHEAS. Changes in serum DHEAS during the day and following OC use are related to alterations in its main binding protein, serum albumin, rather than to changes in adrenocortical steroid secretion.
引用
收藏
页码:361 / 368
页数:8
相关论文
共 33 条
[1]   A randomized cross-over study on various hormonal parameters of two triphasic oral contraceptives [J].
Aden, U ;
Jung-Hoffmann, C ;
Kuhl, H .
CONTRACEPTION, 1998, 58 (02) :75-81
[2]   EFFECT OF STEROIDAL CONTRACEPTIVES ON LEVELS OF PLASMA ANDROGEN SULFATES AND CORTISOL [J].
BULBROOK, RD ;
HERIAN, M ;
TONG, D ;
HAYWARD, JL ;
SWAIN, MC ;
WANG, DY .
LANCET, 1973, 1 (7804) :628-631
[3]   ADRENOCORTICAL FUNCTION IN PROSTATIC-CANCER PATIENTS - EFFECTS OF ORCHIDECTOMY OR DIFFERENT MODES OF ESTROGEN-TREATMENT ON BASAL STEROID-LEVELS AND ON THE RESPONSE TO EXOGENOUS ADRENOCORTICOTROPIC HORMONE [J].
CARLSTROM, K ;
STEGE, R .
UROLOGIA INTERNATIONALIS, 1990, 45 (03) :160-163
[4]   DEHYDROEPIANDROSTERONE SULFATE AND DEHYDROEPIANDROSTERONE IN SERUM - DIFFERENCES RELATED TO AGE AND SEX [J].
CARLSTROM, K ;
BRODY, S ;
LUNELL, NO ;
LAGRELIUS, A ;
MOLLERSTROM, G ;
POUSETTE, A ;
RANNEVIK, G ;
STEGE, R ;
VONSCHOULTZ, B .
MATURITAS, 1988, 10 (04) :297-306
[5]   SEX STEROIDS AND STEROID BINDING-PROTEINS IN FEMALE ALCOHOLIC LIVER-DISEASE [J].
CARLSTROM, K ;
ERIKSSON, S ;
RANNEVIK, G .
ACTA ENDOCRINOLOGICA, 1986, 111 (01) :75-79
[6]   ON THE BINDING OF STEROID SULFATES TO ALBUMIN [J].
CEKAN, SZ ;
XING, S ;
RITZEN, M .
EXPERIENTIA, 1984, 40 (09) :949-951
[7]  
Coenen C M, 1995, Int J Fertil Menopausal Stud, V40 Suppl 2, P92
[8]   Changes in androgens during treatment with four low-dose contraceptives [J].
Coenen, CMH ;
Thomas, CMG ;
Borm, GF ;
Hollanders, JMG ;
Rolland, R .
CONTRACEPTION, 1996, 53 (03) :171-176
[9]  
CREPY O, 1970, RES STEROIDS, V4, P61
[10]   SEASONAL-VARIATION OF PLASMA DEHYDROEPIANDROSTERONE SULFATE AND URINARY ANDROGEN EXCRETION IN POST-MENOPAUSAL WOMEN [J].
DESLYPERE, JP ;
DEBISCOP, G ;
VERMEULEN, A .
CLINICAL ENDOCRINOLOGY, 1983, 18 (01) :25-30