Relationship of circulating cell-free DNA levels to cell-free fetal DNA levels, clinical characteristics and laboratory parameters in preeclampsia

BMC Med Genet. 2009 Nov 21:10:120. doi: 10.1186/1471-2350-10-120.

Abstract

Background: The aim of our study was to examine whether increased circulating total cell-free DNA levels are related to the clinical characteristics and standard laboratory parameters of preeclamptic patients, to markers of inflammation, endothelial activation or injury, oxidative stress and to cell-free fetal DNA levels.

Methods: Circulating total cell-free DNA was measured by real-time quantitative PCR in plasma samples obtained from 67 preeclamptic and 70 normotensive pregnant women. Standard laboratory parameters, C-reactive protein, plasma von Willebrand factor antigen, plasma fibronectin, plasma malondialdehyde and cell-free fetal DNA levels were also determined.

Results and conclusion: Circulating total cell-free and fetal deoxyribonucleic acid levels were significantly elevated in pregnancies complicated by preeclampsia (median: 11.395 vs. 32.460 and 0.001 vs. 0.086 pg/microl; P < .001). The quantity of plasma total cell-free DNA did not correlate with most of the laboratory parameters, except for serum aspartate aminotransferase and alanine aminotransferase activities (correlation coefficient: 0.31; P = 0.012 and 0.46; P < .001). There was no correlation with clinical characteristics, including body mass index. The releases of both free fetal and total cell-free deoxyribonucleic acid were found to be affected in preeclampsia. Hepatocellular necrosis seems to be responsible--at least partly--for increased circulating total DNA levels in preeclampsia, as suggested by the significant correlation with liver enzyme activities.

MeSH terms

  • Adolescent
  • Adult
  • Cell-Free System
  • DNA / metabolism*
  • Female
  • Fetal Blood / metabolism*
  • Humans
  • Male
  • Polymerase Chain Reaction
  • Pre-Eclampsia / blood*
  • Pre-Eclampsia / genetics
  • Pregnancy
  • Retrospective Studies
  • Young Adult

Substances

  • DNA