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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.
Objective:
This study aims to evaluate the relationship between early-onset severe preeclampsia and first trimester serum levels of pregnancy-associated plasma protein A (PAPP-A) and total human chorionic gonadotropin (hCG).
Study Design:
The association between early-onset severe preeclampsia and abnormal levels of first trimester PAPP-A and total hCG in maternal serum were measured in a sample of singleton pregnancies without chromosomal defects that had integrated prenatal serum screening in 2009 and 2010 (n = 129,488). Logistic binomial regression was used to estimate the relative risk (RR) of early-onset severe preeclampsia in pregnancies with abnormal levels of first trimester PAPP-A or total hCG as compared with controls.
Results:
Regardless of parity, women with low first trimester PAPP-A or high total hCG were at increased risk for early-onset severe preeclampsia. Women with low PAPP-A (multiple of the median [MoM] ≤ the 10th percentile in nulliparous or ≤ the 5th percentile in multiparous) or high total hCG (MoM ≥ the 90th percentile in nulliparous or ≥ the 95th percentile in multiparous) were at more than a threefold increased risk for early-onset severe preeclampsia (RR, 4.2; 95% confidence interval [CI], 3.0-5.9 and RR, 3.3; 95% CI, 2.1-5.2, respectively).
Conclusion:
Routinely collected first trimester measurements of PAPP-A and total hCG provide unique risk information for early-onset severe preeclampsia.
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