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Prenatal Diagnosis of Common Aneuploidies in Transcervical Samples Using Quantitative Fluorescent-PCR Analysis

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Abstract

Aim: The aim of this study was to test the feasibility of diagnosing common fetal chromosomal aneuploidies using quantitative fluorescent (QF)-PCR on transcervical cell (TCC) samples collected in the first trimester of pregnancy by means of intrauterine lavage (IUL).

Methods: A total of 181 TCC samples were retrieved from pregnant women between 5 and 12 weeks of gestation, immediately before elective termination of pregnancy, at which time corresponding placental tissue and maternal blood specimens were also obtained. Isolation of trophoblastic cells by micromanipulation was attempted in all TCC samples. Micromanipulated specimens were analyzed by multiplex QF-PCR, including short tandem repeats for the chromosomes X, Y, 21, 18, and 13.

Results: The micromanipulation was successful in 152 of 181 cases (84.8%) where chorionic villous filaments and/or cell clumps of seeming trophoblastic origin could be isolated. All 152 samples were tested by QF-PCR analysis and peaks of paternal origin could be documented in all cases. Two cases of trisomy 21 and two cases of monosomy X0 were detected by means of QF-PCR assay, in accordance with the results obtained in corresponding placental samples.

Conclusion: This study provides evidence that the use of multiplex QF-PCR amplification of selected microsatellites could be applied to micromanipulated TCC samples and in particular to IUL samples, which often contain trophoblastic cells, for the detection of chromosomal aneuploidies. The approach described in this study appears, therefore, a very promising tool toward non-invasive prenatal genetic diagnosis in the early stage of gestation.

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References

  1. Canadian Collaborative CVS-Amniocentesis Clinical Trial Group. Multicentre randomized clinical trial of chorion villus sampling and amniocentesis. Lancet 1989; I: 1–6

    Google Scholar 

  2. Bianchi DW. Prenatal diagnosis by analysis of fetal cells in maternal blood. J Pediatr 1995; 127: 847–56

    Article  PubMed  CAS  Google Scholar 

  3. Lo YM. Fetal DNA in maternal plasma: biology and diagnostic applications. Clin Chem 2000; 46: 1903–6

    PubMed  CAS  Google Scholar 

  4. Adinolfi M, Sherlock J. First trimester prenatal diagnosis using transcervical cells: an evaluation. Hum Reprod Update 1997; 3: 383–92

    Article  PubMed  CAS  Google Scholar 

  5. Cioni R, Bussani C, Scarselli B, et al. Comparison of two techniques for transcervical cell sampling performed in the same study population. Prenat Diagn 2005; 25: 198–202

    Article  PubMed  Google Scholar 

  6. Cioni R, Bussani C, Scarselli B, et al. Detection of fetal cells in intrauterine lavage samples collected in the first trimester of pregnancy. Prenat Diagn 2002; 22: 52–5

    Article  PubMed  Google Scholar 

  7. Ergin T, Baltaci V, Zeyneloglu HB, et al. Non-invasive early prenatal diagnosis using fluorescent in situ hybridization on transcervical cells: comparison of two different methods for retrieval. Eur J Obstet Gynecol Reprod Biol 2001; 95: 37–41

    Article  PubMed  CAS  Google Scholar 

  8. Adinolfi M, El-Hashemite N, Sherlock J, et al. Prenatal detection of Hb mutations using transcervical cells. Prenat Diagn 1997; 17: 539–43

    Article  PubMed  CAS  Google Scholar 

  9. Cioni R, Bussani C, Scarselli B, et al. Fetal cells in cervical mucus in the first trimester of pregnancy. Prenat Diagn 2003; 23: 168–71

    Article  PubMed  Google Scholar 

  10. Bussani C, Cioni R, Scarselli B, et al. Strategies for the isolation and detection of fetal cells in transcervical samples. Prenat Diagn 2002; 22: 1098–101

    Article  PubMed  Google Scholar 

  11. Bussani C, Scarselli B, Cioni R, et al. Use of the quantitative fluorescent-PCR assay in the study of fetal DNA from micromanipulated transcervical samples. Mol Diagn 2004; 8: 259–63

    Article  PubMed  Google Scholar 

  12. Cioni R, Bussani C, Bucciantini S, et al. Fetal cells in a transcervical cell sample collected at 5 weeks of gestation. J Mat Fet Neonat Med 2005; 18: 271–3

    Article  Google Scholar 

  13. Cirigliano V, Voglino G, Marongiu A, et al. Rapid prenatal diagnosis by QF-PCR: evaluation of 30,000 consecutive clinical samples and future applications. Ann N Y Acad Sci 2006; 1075: 288–98

    Article  PubMed  CAS  Google Scholar 

  14. Cirigliano V, Maijo E, Canadas MP, et al. Clinical application of multiplex quantitative fluorescent polymerase chain reaction (QF-PCR) for the rapid prenatal detection of common chromosome aneuploidies. Mol Hum Reprod 2001; 7: 1001–6

    Article  PubMed  CAS  Google Scholar 

  15. Cirigliano V, Maijo E, Fuster C, et al. X chromosome dosage by quantitative fluorescent PCR and rapid prenatal diagnosis of sex chromosome aneuploidies. Mol Hum Reprod 2002; 8: 1042–5

    Article  PubMed  CAS  Google Scholar 

  16. Adinolfi M, Pertl B, Sherlock J. Rapid detection of aneuploidies by microsatellite and the quantitative fluorescent polymerase chain reaction. Prenat Diagn 1997; 17: 1299–311

    Article  PubMed  CAS  Google Scholar 

  17. Shettles LB. Use of the Y chromosome in prenatal sex determination. Nature 1971; 230: 52

    Article  PubMed  CAS  Google Scholar 

  18. Bischoff FZ, Simpson JL. Endocervical fetal trophoblast for prenatal genetic diagnosis. Curr Opin Obstet Gynecol 2006; 18: 216–20

    Article  PubMed  Google Scholar 

  19. Chang SD, Lin SL, Chu KK, et al. Minimally-invasive early prenatal diagnosis using fluorescence in situ hybridization on samples from uterine lavage. Prenat Diagn 1997; 17: 1019–25

    Article  PubMed  CAS  Google Scholar 

  20. Tutschek B, Sherlock J, Halder A, et al. Isolation of fetal cells from transcervical samples by micromanipulation: molecular confirmation of their fetal origin and diagnosis of fetal aneuploidy. Prenat Diagn 1995; 15: 951–60

    Article  PubMed  CAS  Google Scholar 

  21. Sherlock JK, Halder A, Tutschek B, et al. Prenatal detection of fetal aneuploidies using transcervical cell samples. J Med Genet 1997; 34: 302–5

    Article  PubMed  CAS  Google Scholar 

  22. Adinolfi M, Davies A, Sharif S, et al. Detection of trisomy 18 and Y-derived sequences in fetal nucleated cells obtained by transcervical flushing. Lancet 1993; 342: 403–4

    Article  PubMed  CAS  Google Scholar 

  23. Maggi F, Berdusco F, Liuti R, et al. First-trimester chromosome diagnosis by lavage of the uterine cavity. Prenat Diagn 1996; 16: 823–7

    Article  PubMed  CAS  Google Scholar 

  24. Massari A, Novelli G, Colosimo A, et al. Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. Hum Genet 1996; 97: 150–5

    Article  PubMed  CAS  Google Scholar 

  25. Ishai D, Amiel A, Diukman R, et al. Uterine lavage: adding FISH to conventional cytogenetics for embryonic sexing and diagnosing common chromosomal abnormalities. Prenat Diagn 1995; 15: 961–5

    Article  PubMed  CAS  Google Scholar 

  26. Kagan KO, Avgidou K, Molina FS, et al. Relation between increased fetal nuchal translucency thickness and chromosomal defects. Obstet Gynecol 2006; 107: 6–10

    Article  PubMed  Google Scholar 

  27. Kharrat R, Yamamoto M, Roume J, et al. Karyotype and outcome of fetuses diagnosed with cystic hygroma in the first trimester in relation to nuchal translucency thickness. Prenat Diagn 2006; 26: 369–72

    Article  PubMed  Google Scholar 

  28. Hulten MA, Dhanjal S, Pertl B. Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR. Reproduction 2003; 126: 279–97

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

The authors would like to thank the “Ente Cassa di Risparmio di Firenze” for financial support.

The authors have no conflicts of interest that are directly relevant to the content of this study.

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Correspondence to Cecilia Bussani.

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Bussani, C., Cioni, R., Mattei, A. et al. Prenatal Diagnosis of Common Aneuploidies in Transcervical Samples Using Quantitative Fluorescent-PCR Analysis. Mol Diag Ther 11, 117–121 (2007). https://doi.org/10.1007/BF03256231

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