Dynamics of the development of multiple follicles during ovarian stimulation for in vitro fertilization using recombinant follicle-stimulating hormone (Puregon) and various doses of the gonadotropin-releasing hormone antagonist ganirelix (Orgalutran/Antagon)

Citation
D. De Jong et al., Dynamics of the development of multiple follicles during ovarian stimulation for in vitro fertilization using recombinant follicle-stimulating hormone (Puregon) and various doses of the gonadotropin-releasing hormone antagonist ganirelix (Orgalutran/Antagon), FERT STERIL, 75(4), 2001, pp. 688-693
Citations number
28
Categorie Soggetti
Reproductive Medicine","da verificare
Journal title
FERTILITY AND STERILITY
ISSN journal
00150282 → ACNP
Volume
75
Issue
4
Year of publication
2001
Pages
688 - 693
Database
ISI
SICI code
0015-0282(200104)75:4<688:DOTDOM>2.0.ZU;2-Q
Abstract
Objective: To investigate relations between dose of GnRH antagonist and fol licular phase characteristics. Design: Randomized controlled multicenter trial. Setting: Tertiary referral fertility centers. Patient(s): Three hundred and twenty-nine IVF patients. Intervention(s): Ovarian stimulation for IVF with recombinant FSH starting on cycle day 2. From cycle day 7 onwards, cotreatment was provided with 0.0 625, 0.125. 0.25, 0.5, 1.0, or 2.0 mg/d GnRH antagonist. Main Outcome Measure(s): Number of follicles, total follicular surface area , gonadotropin, and serum steroid concentrations. Result(s): In 311 patients, similar follicular growth was observed in all t reatment groups. FSH levels increased during the follicular phase. Late fol licular phase LH, androstenedione (AD), and E, levels showed a GnRH antagon ist dose-related decrease (P<0.05). Late follicular phase E, levels correla ted with total follicular surface area, AD, LH, and FSH (all P<0.001), incr easing GnRH antagonist doses exhibited additional suppressive action on E, levels. Conclusion(s): Follicular growth was unaffected by the dose of GnRH antagon ist. A rise in follicular phase FSH serum concentrations during the follicu lar phase, largely related to exogenous FSH, enabled ongoing follicular gro wth in all treatment groups. The effect of GnRH;l antagonist on late follic ular phase E, levels could not be exclusively attributed to suppression of LH, (C) 2001 1 by American Society far Reproductive Medicine.