Literature DB >> 12124698

Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data. National Institute of Child Health and Development Fetal Cell Isolation Study.

D W Bianchi1, J L Simpson, L G Jackson, S Elias, W Holzgreve, M I Evans, K A Dukes, L M Sullivan, K W Klinger, F Z Bischoff, S Hahn, K L Johnson, D Lewis, R J Wapner, F de la Cruz.   

Abstract

OBJECTIVES: The National Institute of Child Health and Human Development Fetal Cell Isolation Study (NIFTY) is a prospective, multicenter clinical project to develop non-invasive methods of prenatal diagnosis. The initial objective was to assess the utility of fetal cells in the peripheral blood of pregnant women to diagnose or screen for fetal chromosome abnormalities.
METHODS: Results of fluorescence in situ hybridization (FISH) analysis on interphase nuclei of fetal cells recovered from maternal blood were compared to metaphase karyotypes of fetal cells obtained by amniocentesis or chorionic villus sampling (CVS). After the first 5 years of the study we performed a planned analysis of the data. We report here the data from 2744 fully processed pre-procedural blood samples; 1292 samples were from women carrying singleton male fetuses.
RESULTS: Target cell recovery and fetal cell detection were better using magnetic-based separation systems (MACS) than with flow-sorting (FACS). Blinded FISH assessment of samples from women carrying singleton male fetuses found at least one cell with an X and Y signal in 41.4% of cases (95% CI: 37.4%, 45.5%). The false-positive rate of gender detection was 11.1% (95% CI: 6.1,16.1%). This was higher than expected due to the use of indirectly labeled FISH probes in one center. The detection rate of finding at least one aneuploid cell in cases of fetal aneuploidy was 74.4% (95% CI: 76.0%, 99.0%), with a false-positive rate estimated to be between 0.6% and 4.1%.
CONCLUSIONS: The sensitivity of aneuploidy detection using fetal cell analysis from maternal blood is comparable to single marker prenatal serum screening, but technological advances are needed before fetal cell analysis has clinical application as part of a multiple marker method for non-invasive prenatal screening. The limitations of the present study, i.e. multiple processing protocols, are being addressed in the ongoing study. Copyright 2002 John Wiley & Sons, Ltd.

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Mesh:

Year:  2002        PMID: 12124698     DOI: 10.1002/pd.347

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  44 in total

1.  Placental mRNA in maternal plasma: prospects for fetal screening.

Authors:  Malcolm A Ferguson-Smith
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-07       Impact factor: 11.205

2.  Are fetal cells in maternal plasma really there? We think they are.

Authors:  Pınar Bayrak-Toydemir; Eugene Pergament; Morris Fiddler
Journal:  J Hum Genet       Date:  2003-11-08       Impact factor: 3.172

3.  MALDI-TOF MS in Prenatal Genomics.

Authors:  Xiao Yan Zhong; Wolfgang Holzgreve
Journal:  Transfus Med Hemother       Date:  2009-06-25       Impact factor: 3.747

Review 4.  From prenatal genomic diagnosis to fetal personalized medicine: progress and challenges.

Authors:  Diana W Bianchi
Journal:  Nat Med       Date:  2012-07-06       Impact factor: 53.440

Review 5.  Next-generation molecular diagnosis: single-cell sequencing from bench to bedside.

Authors:  Wanjun Zhu; Xiao-Yan Zhang; Sadie L Marjani; Jialing Zhang; Wengeng Zhang; Shixiu Wu; Xinghua Pan
Journal:  Cell Mol Life Sci       Date:  2016-10-13       Impact factor: 9.261

6.  Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma.

Authors:  Rossa W K Chiu; K C Allen Chan; Yuan Gao; Virginia Y M Lau; Wenli Zheng; Tak Y Leung; Chris H F Foo; Bin Xie; Nancy B Y Tsui; Fiona M F Lun; Benny C Y Zee; Tze K Lau; Charles R Cantor; Y M Dennis Lo
Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-10       Impact factor: 11.205

Review 7.  Noninvasive prenatal testing: the future is now.

Authors:  Errol R Norwitz; Brynn Levy
Journal:  Rev Obstet Gynecol       Date:  2013

8.  A microfluidics approach for the isolation of nucleated red blood cells (NRBCs) from the peripheral blood of pregnant women.

Authors:  R Huang; T A Barber; M A Schmidt; R G Tompkins; M Toner; D W Bianchi; R Kapur; W L Flejter
Journal:  Prenat Diagn       Date:  2008-10       Impact factor: 3.050

Review 9.  Recent advances in the prenatal interrogation of the human fetal genome.

Authors:  Lisa Hui; Diana W Bianchi
Journal:  Trends Genet       Date:  2012-11-15       Impact factor: 11.639

10.  Placenta-derived fetal specific mRNA is more readily detectable in maternal plasma than in whole blood.

Authors:  Macy M S Heung; Shengnan Jin; Nancy B Y Tsui; Chunming Ding; Tak Y Leung; Tze K Lau; Rossa W K Chiu; Y M Dennis Lo
Journal:  PLoS One       Date:  2009-06-10       Impact factor: 3.240

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