| Literature DB >> 24581980 |
Alexis Adler1, Hsaio-Ling Lee2, David H McCulloh2, Esmeralda Ampeloquio2, Melicia Clarke-Williams2, Brooke Hodes Wertz2, James Grifo2.
Abstract
Preimplantation genetic diagnosis and screening improves the chances of achieving a viable pregnancy, not only free of undesired single-gene defects but also aneuploidy. In addition, improvements in vitrification provide an efficient means of preserving embryos (blastocysts). By combining trophectoderm biopsy with recent improvements in vitrification methods, only those embryos that have proved themselves viable and potentially more competent are tested. Using array comparative genomic hybridization (aCGH) to assess all 24 chromosomes, aneuploidy rates were compared between day-3 blastomere biopsy and day-5 trophectoderm biopsy. Of those 1603 embryos, 31% were euploid, 62% were aneuploid and 7% not analysable. A significantly larger proportion of embryos were euploid on day-5 biopsy (42%) compared with day-3 biopsy (24%, P<0.0001). The number of euploid embryos per patient was not significantly different. Combining extended culture, trophectoderm biopsy and aneuploidy assessment by aCGH and subsequent vitrification can provide a more efficient means of achieving euploid pregnancies in IVF.Entities:
Keywords: aneuploidy; array comparative genomic hybridization; blastomere biopsy; preimplantation genetic screening; trophectoderm biopsy; whole-genome amplification
Mesh:
Year: 2013 PMID: 24581980 DOI: 10.1016/j.rbmo.2013.11.018
Source DB: PubMed Journal: Reprod Biomed Online ISSN: 1472-6483 Impact factor: 3.828