Assessment of day-3 morphology and euploidy for individual chromosomes in embryos that develop to the blastocyst stage
Objective
To examine the relationship between day-3 morphology and euploidy for individual chromosomes in embryos that develop to the blastocyst stage by day 5.
Design
Retrospective cohort study.
Setting
Boston IVF, a large university-affiliated reproductive medicine practice.
Patient(s)
Ninety-nine patients undergoing their first preimplantation genetic screening (PGS) cycle between January 1 and December 31, 2006.
Intervention(s)
In vitro fertilization (IVF) and preimplantation genetic screening (PGS).
Main Outcome Measure(s)
Prevalence of euploidy for chromosomes X, Y, 8, 13, 14, 15, 16, 17, 18, 20, 21, and 22 in day-3 high implantation potential (HIP) versus non-HIP embryos that grew to day-5 blastocysts.
Result(s)
Seven hundred three embryos from 99 cycles in 99 patients underwent PGS. Three hundred sixty-four (52%) embryos from 88 cycles in 88 patients developed to the blastocyst stage by day 5. High implantation potential embryos were more likely to be euploid for chromosomes X/Y, 8, 15, 16, 18, and 22 compared with non-HIP embryos, with similar trends for chromosomes 14 and 17. There were no statistically significant differences between HIP and non-HIP embryos in euploidy prevalence for chromosomes 13, 20, and 21.
Conclusion(s)
Our data suggest that PGS may detect potentially viable but detrimental chromosomal abnormalities that are not detected by embryo morphology alone.
Key Words: Preimplantation genetic screening, embryo morphology, euploidy, aneuploidy, in vitro fertilization, assisted reproductive technology, ART outcomes
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J.L.E. has nothing to disclose. M.R.H. is a consultant and member of the data safety monitoring board of Bayer Pharmaceuticals. D.H. has spouse with Incept Biosystems. K.L.T. is a consultant for and receives research support from Organon, is a speaker for and receives research support from EMD Serono, and receives research support from Ferring Pharmaceuticals. A.S.P. receives grant support from EMD Serono, Organon, and Ferring Pharmaceuticals, and is on the speakers bureau of Ferring Pharmaceuticals.
Presented at the American Society for Reproductive Medicine 63rd Annual Meeting, Washington, DC, October 13–17, 2007.
PII: S0015-0282(08)00581-5
doi:10.1016/j.fertnstert.2008.03.008
© 2009 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

