Estimation of chromosomal imbalances in preimplantation embryos from preimplantation genetic diagnosis cycles of reciprocal translocations with or without acrocentric chromosomes

Fertil Steril. 2008 Dec;90(6):2144-51. doi: 10.1016/j.fertnstert.2007.10.035. Epub 2008 Apr 28.

Abstract

Objective: To estimate chromosomal imbalances in preimplantation embryos from reciprocal translocation carriers with or without acrocentric chromosomes (Acro-Ch) 13, 14, 15, 21, and 22 in preimplantation genetic diagnosis (PGD) cycles.

Design: Fluorescence in situ hybridization was applied to PGD cycles for reciprocal translocation carriers.

Setting: University-based centers for reproductive medicine.

Patient(s): Ten and 24 patients of reciprocal translocation with and without Acro-Ch, respectively.

Intervention(s): Fluorescence in situ hybridization in biopsied blastomeres.

Main outcome measure(s): Estimation of meiotic segregation mode in embryos from translocation carriers.

Result(s): The proportion of alternative segregation for normal or balanced chromosome contents in preimplantation embryos from PGD cycles in reciprocal translocations without Acro-Ch was significantly higher than that with Acro-Ch (26.0% vs. 14.6%). The proportion of interchange trisomy in 3:1 segregation was significantly lower in reciprocal translocations without Acro-Ch than that with Acro-Ch (4.3% vs. 9.5%).

Conclusion(s): This is the first report that the incidence of alternative segregation producing normal or balanced embryos was relatively low in reciprocal translocations associated with Acro-Ch. Our data may be useful to predict the possibility of normal or balanced embryos and to counsel with reciprocal translocation carriers for PGD-fluorescence in situ hybridization cycles.

Publication types

  • Multicenter Study

MeSH terms

  • Abortion, Spontaneous / etiology
  • Adult
  • Chromosome Segregation*
  • Chromosomes, Human*
  • Embryo Transfer
  • Female
  • Genetic Testing*
  • Humans
  • In Situ Hybridization, Fluorescence*
  • Infertility / therapy*
  • Karyotyping
  • Korea
  • Live Birth
  • Pregnancy
  • Pregnancy Rate
  • Preimplantation Diagnosis / methods*
  • Reproductive Techniques, Assisted* / adverse effects
  • Retrospective Studies
  • Translocation, Genetic*
  • Treatment Outcome