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Perspective

Should preimplantation genetic diagnosis be offered universally?

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Pages 729-733 | Published online: 10 Jan 2014

References

  • Gianaroli L, Magli MC, Ferraretti AP. The in vivo and in vitro efficiency and efficacy of PGD for aneuploidy. Mol. Cell. Endocrinol.183, S13–S18 (2001).
  • Verlinsky Y, Cohen J, Munne S et al. Over a decade of preimplantation genetic diagnosis experience – a multicenter report. Fertil. Steril.82, 292–294 (2004).
  • Munne S, Gianaroli L. Chromosomal status of human embryo. In: Human Preimplantation Embryo Selection. Elder K, Cohen J (Eds). Informa Healthcare, London, UK, 209–234 (2007).
  • Verlinsky Y, Kuliev A. Practical Preimplantation Genetic Diagnosis. Springer, NY, USA, 204 (2006).
  • Munné S, Chen S, Colls P et al. Maternal age, morphology, development and chromosome abnormalities in over 6000 cleavage stage embryos. Reprod. Biomed. Online14, 628–634 (2007).
  • Verlinsky Y, Kuliev A. Atlas of Preimplantation Genetic Diagnosis. Taylor & Francis, NY, USA, 288 (2005)
  • Cieslak J, Tur-Kaspa I, Ilkevitch Y, Bernal A, Morris R, Verlinsky Y. Multiple micromanipulations for preimplantation genetic diagnosis do not affect embryo development to the blastocyst stage. Fertil. Steril.85, 1826–1829 (2006).
  • Magli MC, Gianaroli L, Ferraretti A, Toschi M, Esposito F, Fasolino MC. The combination of polar body and embryo biopsy does not affect embryo viability. Hum. Reprod.19, 1163–1169 (2004).
  • Munne S. Preimplantation genetic diagnosis of numerical and structural chromosome abnormalities. Reprod. Biomed. Online4, 183–196 (2002).
  • Kuliev A, Cieslak J, Illkewitch Y, Verlinsky Y. Chromosomal abnormalities in a series of 6733 human oocytes in preimplantation diagnosis of age-related aneuploidies. Reprod. Biomed. Online6, 54–59 (2003).
  • Kahraman S, Benkalifa M, Donmez E. Overall results of aneuploidy screening in 276 couples undergoing assisted reproductive techniques. Prenat. Diagn.24, 307–311 (2004).
  • Kuliev A, Cieslak J, Verlinsky Y. Frequency and distribution of chromosomal abnormalities in human oocytes. Cytogenet. Genome Res.111, 193–198 (2005).
  • Hassold T, Merril M, Adkins K, Freemen S, Sherman S. Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16. Am. J. Hum. Genet.57, 867–874 (1995).
  • Peterson MB, Mikkelsen M. Nondisjunction in trisomy 21: origin and mechanisms. Cytogenet. Cell Genet.91, 199–203 (2000).
  • Sherman SL, Peterson MB, Freeman SB. Nondisjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination. Hum. Mol. Genet.3, 1529–1535 (1994).
  • Hassold T and Hunt P. To err in human: the genesis of human aneuploidy. Nat. Rev. Genet.2, 280–291 (2001).
  • Templado C, Bosch M, Benet J. Frequency and distribution of chromosome abnormalities in human spermatozoa. Cytogenet. Genome Res.111, 199–205 (2005).
  • Kuliev A, Kuznetsova I, Cieslak J et al. Aneuploidy in human oogenesis. Presented at: 7th Preimplantation Genetic Diagnosis International Society Conference, PGDIS. Melbourne, Australia, 13–16 June 2007.
  • Magli C, Ferraretti A, Crippa A, Lappi M, Feliciani E, Gianaroli L. First meiosis errors in immature oocytes generated by stimulated cycles. Fertil. Steril.86, 629–635 (2006).
  • Munne S, Bahce M, Sandalinas M et al. Differences in chromosome susceptibility to aneuploidy and survival to first trimester. Reprod. Biomed. Online8, 81–90 (2004).
  • Munne S. Chromosome abnormalities and their relationship to morphology and development of human embryos. Reprod. Biomed. Online12, 234–253 (2006).
  • Gianaroli L, Magli MC, Ferraretti AP, Munne S. Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with poor prognosis: identification of the categories for which it should be proposed. Fertil. Steril.72, 837–844 (1999).
  • Munné S, Sandalinas M, Escudero T et al. Improved implantation after preimplantation genetic diagnosis of aneuploidy. Reprod. Biomed. Online7, 91–97 (2003).
  • Munne S, Fisher J, Warner A et al. Preimplantation genetic diagnosis significantly reduces pregnancy loss in infertile couples: a multi-center study. Fertil. Steril.85, 326–332 (2006).
  • Staessen C, Platteau P, Van Assche E et al. A comparison of blastocyst transfer with or without preimplantation genetic diagnosis for aneuploidy in couples with advanced maternal age: a prospective randomized controlled trial. Hum. Reprod.19, 2849–2858 (2004).
  • Platteau P, Staessen C, Michiels A, Van Steirteghem A, Liebaers I, Devroey P. Preimplantation genetic diagnosis for aneuploidy in patients with unexplained recurrent miscarriages. Fertil. Steril.83, 393–397 (2005).
  • Cohen J, Wells D, Munne S. Removal of 2 cells from cleavage stage embryos is likely to reduce the efficacy of chromosomal tests that are used to enhance implantation rates. Fertil. Steril.87, 496–503 (2007).
  • Mastenbroek S, Twisk M, Van Echten-Arends J et al. In vitro fertilization with preimplantation genetic screening. N. Engl. J. Med.357, 9–17 (2007).
  • Shahine LK, Cedar MI. Preimplantation genetic diagnosis does not increase pregnancy rates in patients at risk for aneuploidy. Fertil. Steril.85, 51–56 (2006).
  • Denoso P, Staessen C, Fauser BCJM, Devroey P. Current value of preimplantation genetic aneuploidy screening in IVF. Hum. Reprod. Update13, 15–25 (2007).
  • Gianaroli L, Magli MC, Ferraretti A et al. The beneficial effects of PGD for aneuploidy support extensive clinical application. Reprod. Biomed. Online10, 633–640 (2005).
  • Verlinsky Y, Tur-Kaspa I, Cieslak J et al. Preimplantation testing for chromosomal disorders improves reproductive outcome of poor-prognosis IVF patients. Reprod. Biomed. Online11, 219–225 (2005).
  • Magli MC, Jones GM, Gras L, Gianaroli L, Korman I, Trounson AO. Chromosome mosaicism in day 3 aneuploid embryos that develop to morphologically normal blastocysts in vitro. Hum. Reprod.15, 1781–1786 (2000).
  • Sandalinas M, Sadowy S, Alikani M, Calderon G, Cohen J, Munne S. Developmental ability of chromosomally abnormal human embryos to develop to the blastocyst stage. Hum. Reprod.16, 1954–1958 (2001).

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