Literature DB >> 18359020

Accuracy of FISH analysis in predicting chromosomal status in patients undergoing preimplantation genetic diagnosis.

Catherine M DeUgarte1, Man Li, Mark Surrey, Hal Danzer, David Hill, Alan H DeCherney.   

Abstract

OBJECTIVE: The purpose of this study was to determine the positive predictive value (PPV) and negative predictive value (NPV) of FISH analysis and to determine which chromosomal abnormalities are most frequently confirmed.
DESIGN: Prospective observational.
SETTING: IVF laboratory. PATIENT(S): Two hundred forty-one embryos were analyzed from 98 patients. INTERVENTION(S): FISH reanalysis. MAIN OUTCOME MEASURE(S): Embryos that would have been discarded in patients undergoing preimplantation genetic diagnosis (PGD) were fixed and FISH reanalysis was performed. Results of reanalysis were compared with the day 3 diagnosis while PPV and NPV were calculated. RESULT(S): Among the 241 embryos, 198 embryos were abnormal and 43 were normal by day 3 FISH analysis. The PPV was 83% and the NPV was 81%. PPV was also determined for specific categories of aneuploidy, and certain abnormalities such as monosomies, trisomies, tetrasomies, and polyploidies were frequently confirmed on reanalysis (PPV >80%), whereas Turner syndrome diagnosis was not (PPV = 17%). CONCLUSION(S): FISH analysis offers a PPV of 83% and NPV of 81% when evaluating a single blastomere in conjunction with PGD. FISH errors and mosaicism are primarily responsible for the errors associated with FISH analysis in PGD.

Entities:  

Mesh:

Year:  2008        PMID: 18359020     DOI: 10.1016/j.fertnstert.2007.07.1337

Source DB:  PubMed          Journal:  Fertil Steril        ISSN: 0015-0282            Impact factor:   7.329


  11 in total

1.  Twenty-four chromosome FISH in human IVF embryos reveals patterns of post-zygotic chromosome segregation and nuclear organisation.

Authors:  D Ioannou; K G L Fonseka; E J Meershoek; A R Thornhill; A Abogrein; M Ellis; D K Griffin
Journal:  Chromosome Res       Date:  2012-06-29       Impact factor: 5.239

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Review 3.  Preimplantation genetic screening: does it help or hinder IVF treatment and what is the role of the embryo?

Authors:  Kim Dao Ly; Ashok Agarwal; Zsolt Peter Nagy
Journal:  J Assist Reprod Genet       Date:  2011-07-09       Impact factor: 3.412

4.  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

Review 5.  Prenatal Diagnosis: Screening and Diagnostic Tools.

Authors:  Laura M Carlson; Neeta L Vora
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6.  Germinal and Somatic Trisomy 21 Mosaicism: How Common is it, What are the Implications for Individual Carriers and How Does it Come About?

Authors:  Maj A Hultén; Jon Jonasson; Ann Nordgren; Erik Iwarsson
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7.  An update of preimplantation genetic diagnosis in gene diseases, chromosomal translocation, and aneuploidy screening.

Authors:  Li-Jung Chang; Shee-Uan Chen; Yi-Yi Tsai; Chia-Cheng Hung; Mei-Ya Fang; Yi-Ning Su; Yu-Shih Yang
Journal:  Clin Exp Reprod Med       Date:  2011-09-30

8.  The parental origin correlates with the karyotype of human embryos developing from tripronuclear zygotes.

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Journal:  Clin Exp Reprod Med       Date:  2015-03-31

9.  Direct Single-Cell Analysis of Human Polar Bodies and Cleavage-Stage Embryos Reveals No Evidence of the Telomere Theory of Reproductive Ageing in Relation to Aneuploidy Generation.

Authors:  Kara Turner; Colleen Lynch; Hannah Rouse; Vimal Vasu; Darren K Griffin
Journal:  Cells       Date:  2019-02-16       Impact factor: 6.600

Review 10.  Preimplantation Genetic Diagnosis: Prenatal Testing for Embryos Finally Achieving Its Potential.

Authors:  Harvey J Stern
Journal:  J Clin Med       Date:  2014-03-17       Impact factor: 4.241

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