Chromosome anomalies in human oocytes in vitro

Fertil Steril. 1991 May;55(5):964-9.

Abstract

Objective: To determine possible effects on chromosomal status of human oocytes in vitro.

Design: A prospective cytogenetic study of human oocytes fixed at 4, 20 (noninseminated oocytes), or approximately 52 hours after pick-up (inseminated-unfertilized oocytes).

Setting: Primary treatment of infertility in an institutional practice.

Patients, participants: Eighty-eight consecutive in vitro fertilization (IVF) patients (262 inseminated-unfertilized oocytes) and 47 IVF patients with greater than 8 oocytes retrieved (95 noninseminated oocytes).

Interventions: Ultrasound-guided transvaginal follicular aspiration.

Main outcome measure(s): Planned before data collection began.

Results: The incidence of chromosome anomalies did not differ between groups. However, a negative correlation between oocytes apparently without chromosomes and oocytes with fragmented chromosomes was found.

Conclusions: Incubation of oocyte in vitro does not affect the chromosome complement. The mechanisms leading to oocytes apparently without chromosomes and with fragmented chromosomes are self-excluding.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Aberrations*
  • Female
  • Fertilization in Vitro
  • Haploidy
  • Humans
  • Infertility / therapy
  • Oocytes / ultrastructure*