Ovarian hyporesponsiveness in combined gonadotropin-releasing hormone agonist and menotropin therapy is associated with low serum follicle-stimulating hormone levels

Fertil Steril. 1991 Feb;55(2):272-5. doi: 10.1016/s0015-0282(16)54114-4.

Abstract

The study was designed to evaluate if ovarian hyporesponsiveness, which is associated with combined gonadotropin-releasing hormone agonist (GnRH-a) and human menopausal gonadotropin (hMG) therapy is because of suboptimal serum follicle-stimulating hormone (FSH) levels. Two groups of 12 patients each were suppressed with GnRH-a and stimulation with a fixed dose of hMG. The control group (n = 10) received equal doses of hMG only. The follicular phase and the number of hMG ampules was significantly higher in the study group. Basal FSH levels and FSH levels during hMG treatment were significantly lower in patients treated with GnRH-a. Peak estradiol levels and the outcome of in vitro fertilization treatment were similar in the three groups. We suggest that the delay in ovarian response in patients treated with a combination of GnRH-a and hMG is because of lack of endogenous contribution of FSH, resulting in low circulating levels of FSH. An increase of serum FSH levels by administration of higher doses of hMG can reverse this effect.

MeSH terms

  • Adult
  • Delayed-Action Preparations
  • Drug Therapy, Combination
  • Embryo Transfer
  • Estradiol / blood
  • Female
  • Fertilization in Vitro*
  • Follicle Stimulating Hormone / blood*
  • Gonadotropin-Releasing Hormone / analogs & derivatives*
  • Gonadotropin-Releasing Hormone / therapeutic use
  • Humans
  • Luteolytic Agents / therapeutic use*
  • Menotropins / therapeutic use*
  • Ovary / drug effects*
  • Triptorelin Pamoate

Substances

  • Delayed-Action Preparations
  • Luteolytic Agents
  • Triptorelin Pamoate
  • Gonadotropin-Releasing Hormone
  • Estradiol
  • Tryptal
  • Menotropins
  • Follicle Stimulating Hormone