American Journal of Obstetrics & Gynecology
Volume 201, Issue 5 , Pages 472.e1-472.e7, November 2009

First-trimester maternal plasma cell-free fetal DNA and preeclampsia

  • Stavros Sifakis, MD

      Affiliations

    • Harris Birthright Research Center for Fetal Medicine, King's College Hospital, London, UK
    • Laboratory of Clinical Virology, Medical School, University of Crete, Heraklion, Greece
  • ,
  • Apostolos Zaravinos, PhD

      Affiliations

    • Laboratory of Clinical Virology, Medical School, University of Crete, Heraklion, Greece
  • ,
  • Nerea Maiz, MD

      Affiliations

    • Harris Birthright Research Center for Fetal Medicine, King's College Hospital, London, UK
  • ,
  • Demetrios A. Spandidos, PhD

      Affiliations

    • Laboratory of Clinical Virology, Medical School, University of Crete, Heraklion, Greece
  • ,
  • Kypros H. Nicolaides, MD

      Affiliations

    • Harris Birthright Research Center for Fetal Medicine, King's College Hospital, London, UK
    • Corresponding Author InformationReprints: Kypros H. Nicolaides, MD, Harris Birthright Research Center for Fetal Medicine, King's College Hospital, Denmark Hill, London SE5 9RS, UK

Received 21 January 2009; received in revised form 16 March 2009; accepted 14 May 2009. published online 27 July 2009.

Objective

The purpose of this study was to determine whether, in pregnancies that experience preeclampsia, plasma cell-free fetal DNA (cffDNA) at 11-13 weeks of gestation is increased and whether this increase is related to the uterine artery pulsatility index (PI).

Study Design

Plasma cffDNA and uterine artery PI were measured in 44 cases with preeclampsia, which included 11 cases that required delivery at <34 weeks of gestation and 176 normal control subjects. All fetuses were male, and cffDNA was assessed by amplification of the DYS14 gene. The association between cffDNA and uterine artery PI was assessed by regression analysis.

Results

Median cffDNA was higher in early preeclampsia (median, 95.5 genome equivalents/mL; interquartile range, 72.7-140.9 genome equivalents/mL), but not late preeclampsia (median, 50.8 genome equivalents/mL; interquartile range, 25.0-103.8 genome equivalents/mL), than control subjects (median, 51.5 genome equivalents/mL; interquartile range, 31.1-84.9 genome equivalents/mL). There was a significant association between cffDNA and uterine artery PI (P = .038) but not in the control subjects (P = .174).

Conclusion

The increase in plasma cffDNA in pregnancies that experience preeclampsia is associated with the degree of impairment in placental perfusion.

Key words: cell-free fetal DNA, Doppler, preeclampsia, screening, uterine artery

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 Cite this article as: Sifakis S, Zaravinos A, Maiz N, et al. First-trimester maternal plasma cell-free fetal DNA and preeclampsia. Am J Obstet Gynecol 2009;201:472.e1-7.

 This study was supported by a Grant from the Fetal Medicine Foundation (UK Charity no. 1037116).

PII: S0002-9378(09)00533-X

doi:10.1016/j.ajog.2009.05.025

American Journal of Obstetrics & Gynecology
Volume 201, Issue 5 , Pages 472.e1-472.e7, November 2009