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Association between first-trimester maternal serum pregnancy-associated plasma protein-A and obstetric complications
Francesco D'Antonio1, Claudia Rijo, Basky Thilaganathan
1Fetal Medicine Unit, Division of Developmental Sciences, St. George's University of London, London, UK.
Insights
First-trimester maternal serum pregnancy-associated plasma protein-A (PAPP-A) is lower in pregnancies complicated by preeclampsia, small-for-gestational age, or preterm delivery. However, PAPP-A alone is a poor screening tool for these conditions.
Area of Science:
- Obstetrics and Gynecology
- Maternal-Fetal Medicine
- Reproductive Endocrinology
Background:
- First-trimester screening is crucial for identifying pregnancies at risk.
- Pregnancy-associated plasma protein-A (PAPP-A) is a biomarker used in early pregnancy assessment.
- Preeclampsia (PE), small-for-gestational age (SGA) fetus, and preterm delivery (PD) are significant adverse pregnancy outcomes.
Purpose of the Study:
- To evaluate the association between first-trimester maternal serum PAPP-A levels and the development of PE, early PE, SGA fetus, and PD.
- To determine the predictive value of PAPP-A for these adverse pregnancy outcomes.
Main Methods:
- Retrospective analysis of 12,355 deliveries between 2008 and 2011.
- Maternal serum PAPP-A multiples of the median (MoM) were categorized into percentiles.
- Statistical analysis using Mann-Whitney U-test and chi-squared test to compare outcomes.
Main Results:
- Significantly lower PAPP-A MoM levels were observed in women who developed PE, early PE, SGA fetus, and PD compared to the general study population.
- A lower PAPP-A MoM percentile was associated with increased odds ratios for developing PE, early PE, SGA fetus, and PD.
- The odds ratio for PE ranged from 1.76 to 2.41 for the lowest PAPP-A percentiles.
Conclusions:
- First-trimester maternal serum PAPP-A is significantly lower in pregnancies affected by PE, SGA fetus, and PD.
- Maternal serum PAPP-A, when used alone, demonstrates poor performance as a screening test for PE, SGA fetus, and PD.
- Further research may explore PAPP-A in combination with other biomarkers for improved screening.
Objective:
This study aimed to investigate the relationship between maternal serum pregnancy-associated plasma protein-A (PAPP-A) in the first trimester of pregnancy and the development of preeclampsia (PE), early PE, small-for-gestational age (SGA) fetus and preterm delivery (PD).
Method:
This is a retrospective study of 12,355 pregnant women that delivered between 2008 and 2011. We define the first, third and fifth percentiles of maternal serum PAPP-A multiples of the median (MoM). The primary outcome measures were the occurrence of PE, early PE (PE requiring delivery before 34 weeks), SGA fetus (birth weight < 5th centile) and PD. The Mann-Whitney U-test and chi-squared test were used to analyze continuous and dichotomous variables, respectively.
Results:
Maternal serum PAPP-A was significantly lower in women with PE, early PE, SGA fetus and PD (0.91, 0.74, 0.80 and 0.84 MoM, respectively) than in the study population (0.99 MoM) (p < 0.05). The lower the MoM percentile of PAPP-A, the higher are the odds ratio (OR) to develop PE, early PE, SGA fetus and PD.
Conclusions:
Maternal serum PAPP-A levels are lower in women who develop preeclampsia, those with SGA fetus and those who deliver preterm. However, on its own, maternal serum PAPP-A performs poorly (OR for PE between 1.76 and 2.41 with the lower percentile of PAPP-A) as a screening test for these conditions.
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