Impact of follicular-fluid meiosis-activating sterol in an albumin-based formulation on the incidence of human pre-embryos with chromosome abnormalities

Fertil Steril. 2005 Oct:84 Suppl 2:1269-76. doi: 10.1016/j.fertnstert.2005.05.017.

Abstract

Objective: To evaluate the effect of adding follicular-fluid meiosis-activating sterol (FF-MAS) in a novel 0.2% recombinant human albumin-based formulation to cumulus-enclosed oocytes on chromosomal status and development of pre-embryos.

Design: Multicenter, prospective, randomized, open (double-blind for vehicle and FF-MAS groups), four parallel groups, controlled trial.

Setting: Four public IVF clinics in Denmark.

Patient(s): Two hundred eighteen women undergoing IVF donated 483 oocytes.

Intervention(s): Follicle-stimulating hormone/hCG-primed cumulus-enclosed oocytes randomized to 4 hours of exposure to medium with 1 or 10 micromol/L of FF-MAS dissolved in 0.2% recombinant human albumin, medium with 0.2% recombinant human albumin (vehicle control), or medium alone (control) before insemination.

Main outcome measure(s): Primary endpoint: incidence of human pre-embryos with chromosomal abnormalities. Secondary endpoint: fertilization rate, cleavage rate, and pre-embryo quality assessed after 68 hours of culture.

Result(s): At pre-embryo level, the overall abnormality rates in the control, vehicle control, and 1- and 10-micromol/L FF-MAS groups were 53%, 39%, 42%, 53%, respectively, and at blastomere level 49%, 44%, 44%, and 48%, respectively. After 20 and 26 hours, the fertilization rates were between 67% and 71% in all groups. No differences in the cleavage rates were observed.

Conclusion(s): The concentrations of FF-MAS in a novel 0.2% recombinant human albumin-based formulation of FF-MAS did not increase the risk of chromosomal abnormalities in pre-embryos or blastomeres. No statistically significant differences in fertilization rate, cleavage rate, or number of good quality pre-embryos were found among the four groups.

Publication types

  • Clinical Trial, Phase I
  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Albumins / adverse effects
  • Albumins / pharmacology*
  • Blastomeres / drug effects
  • Blastomeres / pathology
  • Cells, Cultured
  • Cholestenes / adverse effects
  • Cholestenes / pharmacology*
  • Chromosome Disorders / chemically induced
  • Chromosome Disorders / epidemiology*
  • Chromosome Disorders / pathology
  • Confidence Intervals
  • Double-Blind Method
  • Drug-Related Side Effects and Adverse Reactions
  • Embryo, Mammalian / drug effects*
  • Embryo, Mammalian / pathology
  • Female
  • Follicular Fluid / chemistry
  • Follicular Fluid / physiology*
  • Humans
  • Incidence
  • Meiosis / physiology*
  • Odds Ratio
  • Prospective Studies

Substances

  • Albumins
  • Cholestenes
  • 4,4-dimethylcholesta-8,14,24-trienol