Skip to main content
Log in

Advantages of Day 4 Embryo Transfer in Patients Undergoing Preimplantation Genetic Diagnosis of Aneuploidy

  • Published:
Journal of Assisted Reproduction and Genetics Aims and scope Submit manuscript

Abstract

Purpose: Following preimplantation genetic diagnosis of aneuploidy, embryo transfer was executed on day 4, with the aim of providing more time for expanding from six to nine the number of diagnosed chromosomes per single cell (Group 2; 45 cycles). The results obtained were compared to those derived from conventional day 3 transfer (Group 1; 71 cycles).

Methods: For multicolor fluorescence in situ hybridization analysis, two panels of probes were used: the first, specific for chromosomes XY, 13, 16, 18, and 21, was tested in all patients (Groups 1 and 2); the second was implemented only in Group 2 patients for the detection of chromosomes 14, 15, and 22.

Results: A total of 406 embryos underwent fluorescence in situ hybridization analysis in Group 1, and 236 in Group 2. Comparable percentages of both chromosomal abnormalities (61% and 62%) and pregnancy and implantation rates (36% and 24.5% in Group 1, 41% and 23.6% in Group 2) resulted, regardless of the higher mean age in Group 2.

Conclusions: The diagnosis of the nine chromosomes which are most frequently associated with aneuploidy in humans could have an immediate impact on the rate of spontaneous abortions. Additional advantages are represented by the more accurate morphological evaluation of euploid embryos; the advanced compaction, which means that embryos are less exposed to damage during the transfer procedure; and the possibility of performing a reanalysis in cases where a fluorescence in situ hybridization diagnosis is not obtained.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

REFERENCES

  1. Plachot M, Mandelbaum J: Oocyte maturation, fertilization and embryonic growth in vitro. Br Med Bull 1990;46:675-694

    Google Scholar 

  2. Delhanty JDA, Griffin DK, Handyside AH, Harper J, Atkinson GH, Pieters MH, Winston RM: Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridization (FISH). Hum Mol Genet 1993;2:1183-1185

    Google Scholar 

  3. Munné S, Alikani M, Tomkin G, Grifo J, Cohen J: Embryo morphology, developmental rates and maternal age are correlated with chromosomal abnormalities. Fertil Steril 1995;64:382-391

    Google Scholar 

  4. Verlinsky Y, Cieslak J, Freidine M, Ivakhnenko V, Wolf G, Kovalinskaya L, White M, Lifchez A, Kaplan B, Moise J, Valle J, Ginsberg N, Strom C, Kuliev A: Polar body diagnosis of common aneuploidies by FISH. J Assist Reprod Genet 1996;13:157-162

    Google Scholar 

  5. Gianaroli L, Magli MC, Munné S, Fiorentino A, Montanaro N, Ferraretti AP: Will preimplantation genetic diagnosis assist patients with a poor prognosis to achieve pregnancy? Hum Reprod 1997;12:1762-1767

    Google Scholar 

  6. Gianaroli L, Magli MC, Ferraretti AP, Fiorentino A, Garrisi J, Munné S: Preimplantation genetic diagnosis increases the implantation rate in human in vitro fertilization by avoiding the transfer of chromosomally abnormal embryos. Fertil Steril 1997;68:1128-1131

    Google Scholar 

  7. Magli MC, Gianaroli L, Munné S, Ferraretti AP: Incidence of chromosomal abnormalities from a morphologically normal cohort of embryos in poor-prognosis patients. J Assist Reprod Genet 1998;15:297-301

    Google Scholar 

  8. Ferraretti AP, Magli MC, Feliciani E, Montanaro N, Gianaroli L: Relationship of timing agonist administration in the cycle phase to the ovarian response to gonadotropins in the long down-regulation protocols for assisted reproductive technologies. Fertil Steril 1996;65:114-121

    Google Scholar 

  9. Munné S, Lee A, Rosewaks Z, Grifo J, Cohen J: Diagnosis of major chromosome aneuploidies in human preimplantation embryos. Hum Reprod 1993;8:2185-2191

    Google Scholar 

  10. Munné S, Marquez C, Magli C, Morton P, Morrison L: Scoring criteria for preimplantation genetic diagnosis of numerical abnormalities for chromosomes X, Y, 13, 16, 18 and 21. Mol Hum Reprod 1998;4:863-870

    Google Scholar 

  11. Munné S, Weier U: Simultaneous enumeration of chromosomes 13, 18, 21, X and Y in interphase cells for preimplantation genetic diagnosis. Cytogenet Cell Genet 1996;75:263-270

    Google Scholar 

  12. Grifo JA, Giatras K, Tang YX, Krey LC: Successful outcome with day 4 embryo transfer after preimplantation diagnosis for genetically transmitted diseases. Hum Reprod 1998;13:1656-1659

    Google Scholar 

  13. Menezo Y, Hazout A, Dumont M, Herbaut N, Nicollet B: Co-culture of embryos on Vero cells and transfer of blastocysts in humans. Hum Reprod 1992;Suppl 1:101-106

    Google Scholar 

  14. Dawson KJ, Conaghan J, Ostera GR, Winston RM, Hardy K: Delaying transfer to the third day post-insemination, to select non arrested embryos, increases development to the fetal heart stage. Hum Reprod 1995;10:177-182

    Google Scholar 

  15. Jones GM, Trounson, AO, Gardner DK, Kausche A, Lolatgis N, Wood C: Evolution of a culture protocol for successful blastocyst development and pregnancy. Hum Reprod 1998;13:169-177

    Google Scholar 

  16. Magli MC, Fortini D, Gianaroli L, et al.: Performance of thawed biopsied embryos. In Abstracts from the 14th ESHRE Meeting. Hum Reprod 1998;13:131 (abstr R-119)

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gianaroli, L., Magli, M.C., Munné, S. et al. Advantages of Day 4 Embryo Transfer in Patients Undergoing Preimplantation Genetic Diagnosis of Aneuploidy. J Assist Reprod Genet 16, 170–175 (1999). https://doi.org/10.1023/A:1020356605408

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1020356605408

Navigation