Early-onset severe preeclampsia by first trimester pregnancy-associated plasma protein A and total human chorionic

Laura L Jelliffe-Pawlowski1, Rebecca J Baer1, Robert J Currier1

  • 1Genetic Disease Screening Program, California Department of Public Health, Richmond, California.

Insights

First trimester screening for pregnancy-associated plasma protein A (PAPP-A) and human chorionic gonadotropin (hCG) can identify women at high risk for early-onset severe preeclampsia. Abnormal levels of these biomarkers significantly increase the likelihood of developing this serious condition.

Area of Science:

  • Maternal-Fetal Medicine
  • Reproductive Endocrinology
  • Biochemical Markers in Pregnancy

Background:

  • Early-onset severe preeclampsia poses significant risks to both mother and fetus.
  • Accurate prediction of early-onset severe preeclampsia is crucial for timely intervention.
  • First-trimester screening markers are increasingly utilized for risk assessment in pregnancy.

Purpose of the Study:

  • To evaluate the association between first-trimester serum levels of PAPP-A and total hCG and the risk of developing early-onset severe preeclampsia.
  • To determine if abnormal levels of PAPP-A and total hCG in early pregnancy predict increased risk for early-onset severe preeclampsia.

Main Methods:

  • A large cohort study of singleton pregnancies (n=129,488) with integrated prenatal serum screening.
  • Logistic binomial regression analysis was used to estimate the relative risk (RR) of early-onset severe preeclampsia.
  • Serum levels of PAPP-A and total hCG were measured in the first trimester and compared between cases and controls.

Main Results:

  • Low first-trimester PAPP-A or high first-trimester total hCG levels were associated with a significantly increased risk of early-onset severe preeclampsia, regardless of parity.
  • Women with low PAPP-A (≤10th percentile in nulliparous, ≤5th in multiparous) or high total hCG (≥90th percentile in nulliparous, ≥95th in multiparous) had more than a threefold increased risk.
  • Relative risks (RR) were 4.2 (95% CI, 3.0-5.9) for low PAPP-A and 3.3 (95% CI, 2.1-5.2) for high total hCG.

Conclusions:

  • First-trimester measurements of PAPP-A and total hCG are valuable predictors of early-onset severe preeclampsia.
  • Routine biochemical screening in early pregnancy provides unique risk information for this condition.
  • These markers can aid in identifying high-risk pregnancies for closer monitoring and potential intervention.
Abstract

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