Published October 11, 2010 | Version v1
Journal article Open

Soluble fms-Like Tyrosine Kinase 1 (sFlt1), Endoglin and Placental Growth Factor (PlGF) in Preeclampsia among High Risk Pregnancies

  • 1. University of Pittsburgh
  • 2. George Washington University
  • 3. Medical University of South Carolina
  • 4. University of Alabama at Birmingham
  • 5. Eunice Kennedy Shriver National Institute of Child Health and Human Development
  • 6. University of Chicago
  • 7. University of Tennessee
  • 8. The Ohio State University
  • 9. University of Cincinnati

Description

Background: Differences in circulating concentrations of antiangiogenic factors sFlt1 and soluble endoglin (sEng) and the pro-angiogenic growth factor PlGF are reported to precede the onset of preeclampsia weeks to months in low-risk pregnant women. The objective of this study was to investigate whether similar changes can be detected in pregnant women at high-risk to develop the syndrome.

Methods: This study is a secondary analysis of the NICHD MFMU trial of aspirin to prevent preeclampsia in high-risk pregnancies. Serum samples were available from 194 women with pre-existing diabetes, 313 with chronic hypertension, 234 with multifetal gestation, and 252 with a history of preeclampsia in a previous pregnancy. Samples collected across pregnancy were analyzed in a blinded fashion for sFlt1, sEng and PlGF.

Results: The odds of developing preeclampsia were significantly increased among women with multiple fetuses for each 2-fold elevation in sFlt1, sEng and the ratio of angiogenic factors (e.g. OR 2.18, 95% CI 1.46-3.32), and significantly decreased for each 2-fold elevation in circulating PlGF (OR 0.50, 95% CI 0.30-0.82) between 7 and 26 weeks' gestation. Cross-sectional analysis of the angiogenic factors across gestation showed significant differences during the third trimester in women who develop preeclampsia compared with appropriate controls in all high-risk groups. However, when data were examined in relation to the gestational week when preeclampsia was diagnosed only sFlt1 was significantly higher 2 to 5 weeks before the clinical onset of preeclampsia and only in women with previous preeclampsia.

Conclusions: The pattern of elevated concentrations of sFlt1 and sEng, and low PlGF in high-risk pregnant subjects who develop preeclampsia is similar to that reported in low-risk pregnant women. However, differences in these factors among high-risk women who do and do not develop preeclampsia are modest, and do not appear to be clinically useful predictors in these high-risk pregnant women.

Files

journal.pone.0013263.pdf

Files (3.0 MB)

Name Size Download all
Article
md5:fa889db62add07f72eaca356dc8dece3
3.0 MB Preview Download

Additional details

Identifiers

DOI
10.1371/journal.pone.0013263
Other
oai:uchicago.tind.io:8559

Funding

Eunice Kennedy Shriver National Institute of Child Health and Human Development
HD19897
Eunice Kennedy Shriver National Institute of Child Health and Human Development
HD36801
Eunice Kennedy Shriver National Institute of Child Health and Human Development
HD21410
Eunice Kennedy Shriver National Institute of Child Health and Human Development
HD21414
Eunice Kennedy Shriver National Institute of Child Health and Human Development
HD21434
Eunice Kennedy Shriver National Institute of Child Health and Human Development
HD27860
Eunice Kennedy Shriver National Institute of Child Health and Human Development
HD27861
Eunice Kennedy Shriver National Institute of Child Health and Human Development
HD27869
Eunice Kennedy Shriver National Institute of Child Health and Human Development
HD27883
Eunice Kennedy Shriver National Institute of Child Health and Human Development
HD27889
Eunice Kennedy Shriver National Institute of Child Health and Human Development
HD27905
Eunice Kennedy Shriver National Institute of Child Health and Human Development
HD27915
Eunice Kennedy Shriver National Institute of Child Health and Human Development
HD27917
National Institutes of Health
2P01-HD30367

UChicago Information

Division(s)
Pritzker School of Medicine, Biological Sciences Division
Department(s)
Obstetrics and Gynecology