Screening models using multiple markers for early detection of late-onset preeclampsia in low-risk pregnancy

BMC Pregnancy Childbirth. 2014 Jan 20:14:35. doi: 10.1186/1471-2393-14-35.

Abstract

Background: Our primary objective was to establish a cutoff value for the soluble fms-like tyrosine kinase 1(sFlt-1)/placental growth factor (PlGF) ratio measured using the Elecsys assay to predict late-onset preeclampsia in low-risk pregnancies. Our secondary objective was to evaluate the ability of combination models using Elecsys data, second trimester uterine artery (UtA) Doppler ultrasonography measurements, and the serum fetoplacental protein levels used for Down's syndrome screening, to predict preeclampsia.

Methods: This prospective cohort study included 262 pregnant women with a low risk of preeclampsia. Plasma levels of pregnancy-associated plasma protein-A (PAPP-A) and serum levels of alpha-fetoprotein, unconjugated estriol, human chorionic gonadotropin, and inhibin-A were measured, and sFlt-1/PlGF ratios were calculated. All women underwent UtA Doppler ultrasonography at 20 to 24 weeks of gestation.

Results: Eight of the 262 women (3.0%) developed late-onset preeclampsia. Receiver operating characteristic curve analysis showed that the third trimester sFlt-1/PlGF ratio yielded the best detection rate (DR) for preeclampsia at a fixed false-positive rate (FPR) of 10%, followed by the second trimester sFlt-1/PlGF ratio, sFlt-1 level, and PlGF level. Binary logistic regression analysis was used to determine the five best combination models for early detection of late-onset preeclampsia. The combination of the PAPP-A level and the second trimester sFlt-1/PlGF ratio yielded a DR of 87.5% at a fixed FPR of 5%, the combination of second and third trimester sFlt-1/PlGF ratios yielded a DR of 87.5% at a fixed FPR of 10%, the combination of body mass index and the second trimester sFlt-1 level yielded a DR of 87.5% at a fixed FPR of 10%, the combination of the PAPP-A and inhibin-A levels yielded a DR of 50% at a fixed FPR of 10%, and the combination of the PAPP-A level and the third trimester sFlt-1/PlGF ratio yielded a DR of 62.5% at a fixed FPR of 10%.

Conclusions: The combination of the PAPP-A level and the second trimester sFlt-1/PlGF ratio, and the combination of the second trimester sFlt-1 level with body mass index, were better predictors of late-onset preeclampsia than any individual marker.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / blood
  • Chorionic Gonadotropin
  • Down Syndrome / diagnosis
  • Early Diagnosis*
  • Female
  • Follow-Up Studies
  • Gestational Age
  • Glycosylphosphatidylinositols
  • Humans
  • Inhibins / blood
  • Maternal Serum Screening Tests / methods*
  • Membrane Proteins / blood*
  • Placenta
  • Placenta Growth Factor
  • Pre-Eclampsia / blood
  • Pre-Eclampsia / diagnosis*
  • Pregnancy
  • Pregnancy Proteins / blood
  • Pregnancy Trimester, Third
  • Pregnancy-Associated Plasma Protein-A / metabolism*
  • Prospective Studies
  • ROC Curve
  • Risk Factors
  • Time Factors
  • Ultrasonography, Doppler
  • Ultrasonography, Prenatal / methods*
  • Vascular Endothelial Growth Factor Receptor-1 / blood*
  • Young Adult

Substances

  • Biomarkers
  • Chorionic Gonadotropin
  • Glycosylphosphatidylinositols
  • Membrane Proteins
  • PGF protein, human
  • PIGF protein, human
  • Pregnancy Proteins
  • inhibin A
  • Placenta Growth Factor
  • Inhibins
  • FLT1 protein, human
  • Vascular Endothelial Growth Factor Receptor-1
  • Pregnancy-Associated Plasma Protein-A