Aneuploidy rates and blastocyst formation after biopsy of morulae and early blastocysts on day 5

Jonathan D. Kort, Ruth B. Lathi, Kathleen Brookfield, Valerie L. Baker, Qianying Zhao, Barry R. Behr

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Purpose Studies have demonstrated high implantation rates after trophectoderm biopsy of day 5 expanded blastocysts. However, biopsy of cleavage stage embryos may adversely affect embryo development and implantation. No studies have assessed the utility of day 5 morulae and early blastocyst biopsy. This study sought to better understand these slower embryos’ aneuploidy rates and implantation potential. Methods This was a retrospective review of all autologous IVF cycles utilizing PGS at a single academic infertility center. Results The biopsy of day 5 morulae and early blastocysts provided 22 % additional euploid blastocysts available for fresh day 6 transfer compared to day 5 biopsy of only expanded blastocysts. Aneuploidy did correlate with embryo stage on day 5, even after controlling for maternal age, with 16 % of morulae and 35 % of blastocysts being euploid. The majority (83 %) of euploid morulae progressed to the blastocyst stage by day 6. Experience transferring slower developing embryos is limited, but preliminary pregnancy and implantation rates appear similar to euploid embryos biopsied as expanded blastocysts. Conclusions The biopsy of all non-arrested embryos on day 5 provides genetic information for all blastocysts on day 6, increasing the pool of euploid blastocysts available for fresh transfer and avoiding the need to cryopreserve developmentally competent embryos without genetic information.

Original languageEnglish (US)
Article numberA007
Pages (from-to)925-930
Number of pages6
JournalJournal of Assisted Reproduction and Genetics
Volume32
Issue number6
DOIs
StatePublished - Jun 1 2015
Externally publishedYes

Keywords

  • Aneuploidy
  • Blastocyst
  • Fresh Transfer
  • Implantation
  • PGD

ASJC Scopus subject areas

  • Reproductive Medicine
  • Genetics
  • Obstetrics and Gynecology
  • Developmental Biology
  • Genetics(clinical)

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