Serum concentrations of enclomiphene and zuclomiphene across consecutive cycles of clomiphene citrate therapy in anovulatory infertile women

Citation
Sl. Young et al., Serum concentrations of enclomiphene and zuclomiphene across consecutive cycles of clomiphene citrate therapy in anovulatory infertile women, FERT STERIL, 71(4), 1999, pp. 639-644
Citations number
21
Categorie Soggetti
Reproductive Medicine","da verificare
Journal title
FERTILITY AND STERILITY
ISSN journal
00150282 → ACNP
Volume
71
Issue
4
Year of publication
1999
Pages
639 - 644
Database
ISI
SICI code
0015-0282(199904)71:4<639:SCOEAZ>2.0.ZU;2-K
Abstract
Objective: To determine the serum concentrations of enclomiphene and zuclom iphene across consecutive cycles of clomiphene citrate treatment in anovula tory infertile women. Design: Prospective cohort. Setting: Tertiary institutional infertility clinic. Patient(s): Fourteen consenting anovulatory infertile women receiving stand ardized, cyclic, incremental treatment with clomiphene citrate for ovulatio n induction. Intervention(s): Clomiphene citrate treatment (50-150 mg/d, cycle days 5-9) , titrated to the minimum effective ovulation-inducing dose, was administer ed for three to six total cycles. Blood samples were obtained on cycle days 3 and 10 in each treatment cycle. Main Outcome Measure(s): Serum concentrations of enclomiphene and zuclomiph ene. Result(s): Cycle day 3 zuclomiphene levels were below assay limits in all i nitial cycles, increased progressively across three consecutive cycles, and thereafter plateaued. Cycle day 3 enclomiphene concentrations were uniform ly undetectable. Cycle day 10 enclomiphene levels increased with dose admin istered, but these observations were not statistically significant. Conclusion(s): Clomiphene citrate induction of ovulation results in an isom er-specific systemic accumulation of zuclomiphene across consecutive cycles of treatment. The combined maximum concentration of enclomiphene and zuclo miphene attained in practice approximates 100 nmol/L and is generally well below levels previously demonstrated to have adverse effects in vitro. (Fer til Steril(R) 1999;71:639-44. (C)1999 by American Society for Reproductive Medicine.).