Document Detail


Triple colour fluorescent in-situ hybridization for chromosomes X,Y and 1 on spare human embryos.
MedLine Citation:
PMID:  9159447     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The potential for implantation of human embryos obtained by in-vitro fertilization is presumably determined to a large extent by their chromosomal constitution but cytogenetic analysis of preimplantation embryos has been hampered by a number of practical and technical problems. With the advent of fluorescent in-situ hybridization (FISH) a practical method for numerical chromosomal analysis has become available. A limited amount of data has been obtained with FISH on human embryos using probes binding to chromosomes X, Y, 16, 18 and 13/21 combined or for chromosomes X and Y or 1 and 17. It was our purpose to extend these data by the combined analysis of chromosomes X, Y and 1 in spare human embryos. A short fluorescent in-situ hybridization procedure involving the simultaneous use of three deoxyribonucleic acid probes detected with red, green, and a mixture of red and green was used to determine chromosomal abnormalities in 116 spare embryos with a poor morphological score and/or displaying one or more multinucleated blastomeres. The majority of the embryos was obtained by intracytoplasmic sperm injection. Less than half of the embryos (n = 54) were diploid and only 39 of them were uniformly XY11 or XX11; two embryos showed a non-disjunction and 13 embryos were aneuploid. Of the remainder, 22 were mosaic, nine were either haploid, triploid or tetraploid and 12 embryos were classified as chaotic. The latter pattern was particularly frequent in multinucleated blastomeres. Our data are comparable with those obtained with FISH using other chromosomal probes and confirm that the majority of preimplantation embryos carry a numerical chromosomal defect. Aneuploidy for chromosome 1 does not appear to be more common in preimplantation embryos than is reported for other chromosomes. Although the high incidence of chromosomal anomalies is presumably biased by the fact that only embryos with a poor morphological score were analysed, it nevertheless indicates that natural selection is the foremost reason for the low implantation rates of human preimplantation embryos in in-vitro fertilization (IVF) programmes.
Authors:
H Laverge; P De Sutter; M R Verschraegen-Spae; A De Paepe; M Dhont
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Publication Detail:
Type:  Clinical Trial; Journal Article    
Journal Detail:
Title:  Human reproduction (Oxford, England)     Volume:  12     ISSN:  0268-1161     ISO Abbreviation:  Hum. Reprod.     Publication Date:  1997 Apr 
Date Detail:
Created Date:  1997-07-22     Completed Date:  1997-07-22     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  8701199     Medline TA:  Hum Reprod     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  809-14     Citation Subset:  IM    
Affiliation:
Infertility Centre, Department of Obstetrics and Gynaecology, University Hospital, Gent, Belgium.
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MeSH Terms
Descriptor/Qualifier:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Color
Embryo, Mammalian / pathology,  physiology*
Embryonic Development
Female
Fertilization in Vitro
Humans
In Situ Hybridization, Fluorescence / methods*
Male
Ploidies
Pregnancy
X Chromosome*
Y Chromosome*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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