Diagnostic efficacy of aneuploidy markers correlated with early onset preeclampsia
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Updated: Aug 16, 2025

Semiconductor Sequencing for Preimplantation Genetic Testing for Aneuploidy
Published on: August 25, 2019
Seung Yeon Pyeon1, Byung Su Kwon2, Young Sun Kim2
1Department of Obstetrics and Gynecology, Kyung Hee University Hospital at Gangdong, Gangdong-gu, Seoul, Republic of Korea.
Insights
Early prediction of preeclampsia (PE) using pregnancy-associated plasma protein A (PAPP-A) and aneuploidy markers can guide timely low-dose aspirin treatment. Combined markers show improved predictive accuracy for early-onset PE.
Area of Science:
- Obstetrics and Gynecology
- Maternal-Fetal Medicine
- Biochemistry
Background:
- Preeclampsia (PE) is a major cause of maternal and fetal morbidity.
- Early intervention with low-dose aspirin before 16 weeks of gestation is effective in preventing PE.
- Accurate prediction of PE onset is crucial for timely treatment initiation.
Purpose of the Study:
- To evaluate the predictive performance of pregnancy-associated plasma protein A (PAPP-A) and aneuploidy markers for preeclampsia onset.
- To compare the utility of individual markers and their combinations in predicting early-onset preeclampsia (EOPE).
- To establish cutoff values for these markers to guide aspirin administration timing.
Main Methods:
- Serum levels of PAPP-A, alpha-fetoprotein (AFP), and human chorionic gonadotropin (hCG) were analyzed in 1053 pregnant women.
- Participants were categorized into normotensive, late-onset PE, and early-onset PE groups.
- The predictive values of marker ratios (AFP/PAPP-A, hCG/PAPP-A) and their combinations for EOPE were assessed.
Main Results:
- Specific ratios, AFP/PAPP-A > 6.89 and hCG/PAPP-A > 7.94, were significantly associated with EOPE (LR 6.52 and 5.77, respectively).
- The combination of these markers demonstrated higher accuracy in predicting EOPE compared to individual markers.
- Established cutoff values provide a basis for early PE risk assessment.
Conclusions:
- PAPP-A and aneuploidy markers, particularly in combination, are valuable predictors of early-onset preeclampsia.
- These markers and their defined thresholds can aid in identifying women who would benefit from early aspirin therapy.
- Optimizing aspirin treatment timing based on these predictive markers can improve maternal and fetal outcomes.
Abstract:
Low-dose aspirin administration before 16 weeks of gestation can prevent preeclampsia (PE) more effectively. In order to determine if aspirin should be administered, this study aimed to investigate the predictive value of pregnancy-associated plasma protein A (PAPP-A) and aneuploidy markers for the onset period of PE. 1053 singleton pregnant women were included in the study, and serum PAPPA-A and aneuploidy markers were analyzed between 3 group (normotensive, late-onset PE, and early-onset PE). The utility of these markers for predicting early-onset preeclampsia (EOPE) was compared using each marker and their combination. Alpha-fetoprotein (AFP)/PAPP-A > 6.89 and human chorionic gonadotropin (hCG)/PAPP-A > 7.94 were associated with EOPE with a positive likelihood ratio (LR) (6.52, 95% confidence interval [CI] 4.9-7.1), and (5.77, 95% CI 3.9-6.4). The combination of markers could predict EOPE more accurately compared to the single markers. AFP/PAPP-A > 6.89 and hCG/PAPP-A > 7.94had a predictive ability for EOPE, and these cutoff values can help determine the use of aspirin at an earlier gestational age (GA).
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