Literature DB >> 12470583

Preimplantation genetic diagnosis of numerical and structural chromosome abnormalities.

Santiago Munné1.   

Abstract

The causes of the decline in implantation rates observed with increasing maternal age are still a matter for debate. Data from oocyte donation strongly suggest that in women of advanced reproductive age, the ability to become pregnant is largely unaffected while oocyte quality is compromised. The incidence of chromosomal abnormalities in embryos is considerably higher than that reported in spontaneous abortions, suggesting that a sizable percentage of chromosomally abnormal embryos are eliminated before any prenatal diagnosis. Such loss may partly account for the decline in implantation in older women. Because of the correlation between aneuploidy and reduced implantation, it has been postulated that selection of chromosomally normal embryos could reverse this trend. Preimplantation genetic diagnosis (PGD) for aneuploidy had three objectives relevant to the present paper: (i) to increase rates of implantation, (ii) to reduce risks of spontaneous abortion, and (iii) to avoid chromosomally abnormal births. Implantation rates did not increase when only five chromosomes were analysed in blastomeres. With eight chromosomes, a significant increase in implantation was achieved. PGD can significantly reduce the incidence of spontaneous abortion. In our clinic, a significant decrease in spontaneous abortions was found, from 23 to 11% after PGD. Currently in cases diagnosed at Saint Barnabas, 0.8% chromosomally abnormal conceptions have been observed after PGD versus an expected 3.2% in a control age-matched group. It seems clear that PGD reduces the possibility of trisomic conceptions under all conditions. If a couple's main interest is to improve their chances of conceiving (improve implantation), then one should consider maternal age and number of available embryos. Improvements in conception after PGD again increase after 37 years of age with eight or nine probes. Carriers of translocations are at a high risk of miscarriage or chromosomally unbalanced offspring, and a high proportion have secondary infertility. PGD of translocations has been approached through a variety of methods, here reviewed, and has resulted in a significant reduction in spontaneous abortions. However, implantation rates in translocation carriers are directly correlated with the proportion of normal gametes, and male patients with 70% or more unbalanced spermatozoa have great difficulty in achieving pregnancy with PGD.

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Year:  2002        PMID: 12470583     DOI: 10.1016/s1472-6483(10)61938-4

Source DB:  PubMed          Journal:  Reprod Biomed Online        ISSN: 1472-6483            Impact factor:   3.828


  16 in total

1.  Preimplantation genetic diagnosis for Down syndrome pregnancy.

Authors:  Yu Zhang; Chen-ming Xu; Yi-min Zhu; Min-yue Dong; Yu-li Qian; Fan Jin; He-feng Huang
Journal:  J Zhejiang Univ Sci B       Date:  2007-07       Impact factor: 3.066

2.  Benefits and drawbacks of preimplantation genetic diagnosis (PGD) for reciprocal translocations: lessons from a prospective cohort study.

Authors:  Paul N Scriven; Frances A Flinter; Yakoub Khalaf; Alison Lashwood; Caroline Mackie Ogilvie
Journal:  Eur J Hum Genet       Date:  2013-02-06       Impact factor: 4.246

3.  Interchromosomal effect in carriers of translocations and inversions assessed by preimplantation genetic testing for structural rearrangements (PGT-SR).

Authors:  E Mateu-Brull; L Rodrigo; V Peinado; A Mercader; I Campos-Galindo; F Bronet; S García-Herrero; M Florensa; M Milán; C Rubio
Journal:  J Assist Reprod Genet       Date:  2019-11-06       Impact factor: 3.412

4.  Aneuploidy involving chromosome 1 in failed-fertilized human oocytes is unrelated to maternal age.

Authors:  Jingly Fung Weier; Heinz-Ulrich G Weier; Aida Nureddin; Roger A Pedersen; Catherine Racowsky
Journal:  J Assist Reprod Genet       Date:  2005-08       Impact factor: 3.412

5.  Rapid mapping of chromosomal breakpoints: from blood to BAC in 20 days.

Authors:  Chun-Mei Lu; Johnson Kwan; Jingly F Weier; Adolf Baumgartner; Mei Wang; Tomas Escudero; Santiago Munné; Heinz-Ulrich G Weier
Journal:  Folia Histochem Cytobiol       Date:  2009-01       Impact factor: 1.698

6.  DNA probe pooling for rapid delineation of chromosomal breakpoints.

Authors:  Chun-Mei Lu; Johnson Kwan; Adolf Baumgartner; Jingly F Weier; Mei Wang; Tomas Escudero; Santiago Munné; Horst F Zitzelsberger; Heinz-Ulrich G Weier
Journal:  J Histochem Cytochem       Date:  2009-02-16       Impact factor: 2.479

7.  Chromosome segregation analysis in human embryos obtained from couples involving male carriers of reciprocal or Robertsonian translocation.

Authors:  Ahmet Yilmaz; Xiao Yun Zhang; Jin-Tae Chung; Seang Lin Tan; Hananel Holzer; Asangla Ao
Journal:  PLoS One       Date:  2012-09-27       Impact factor: 3.240

8.  Increasing live birth rate by preimplantation genetic screening of pooled polar bodies using array comparative genomic hybridization.

Authors:  Michael Feichtinger; Tina Stopp; Christian Göbl; Elisabeth Feichtinger; Enrico Vaccari; Ulrike Mädel; Franco Laccone; Monika Stroh-Weigert; Markus Hengstschläger; Wilfried Feichtinger; Jürgen Neesen
Journal:  PLoS One       Date:  2015-05-29       Impact factor: 3.240

9.  Bioinformatic Tools Identify Chromosome-Specific DNA Probes and Facilitate Risk Assessment by Detecting Aneusomies in Extra-embryonic Tissues.

Authors:  Hui Zeng; Jingly F Weier; Mei Wang; Haig J Kassabian; Aris A Polyzos; Adolf Baumgartner; Benjamin O'Brien; Heinz-Ulli G Weier
Journal:  Curr Genomics       Date:  2012-09       Impact factor: 2.236

10.  Origin of germ cells and formation of new primary follicles in adult human ovaries.

Authors:  Antonin Bukovsky; Michael R Caudle; Marta Svetlikova; Nirmala B Upadhyaya
Journal:  Reprod Biol Endocrinol       Date:  2004-04-28       Impact factor: 5.211

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