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Role of First Trimester Screening Biochemical Markers to Predict Hypertensive Pregnancy Disorders and SGA Neonates-A
Wojciech Górczewski1, Joanna Górecka2, Magdalena Massalska-Wolska3
1Independent Public Health Care Facility "Bl. Marta Wiecka County Hospital", 32-700 Bochnia, Poland.
Insights
Early pregnancy biochemical markers like PAPP-A and PlGF can predict hypertensive disorders and small-for-gestational-age neonates, improving antenatal surveillance and outcomes.
Area of Science:
- Obstetrics and Gynecology
- Biochemistry
- Perinatal Medicine
Background:
- Early identification of high-risk pregnancies is crucial for improved maternal and neonatal outcomes.
- Biochemical markers in the first trimester offer potential for predicting adverse pregnancy complications.
Purpose of the Study:
- To evaluate the predictive value of first-trimester biochemical markers for hypertensive pregnancy disorders (HPD) and small-for-gestational-age (SGA) neonates.
- To synthesize current literature on biochemical markers associated with adverse pregnancy outcomes.
Main Methods:
- A systematic literature search was conducted across PubMed, Scopus, and Web of Science.
- Articles focusing on biochemical markers for HPD and SGA prediction were reviewed.
Main Results:
- Low levels of pregnancy-associated plasma protein A (PAPP-A) and placental growth factor (PlGF) are associated with increased risk.
- Elevated soluble fms-like Tyrosine Kinase-1 (sFlt-1), alfa fetoprotein (AFP), and inflammatory markers (β-HGC, INF-γ, TNF-α) are linked to HPD and fetal growth restriction (FGR).
- PAPP-A and PlGF demonstrated the most significant predictive value for HPD and SGA.
Conclusions:
- First-trimester biochemical markers are valuable indicators for predicting HPD and SGA.
- PAPP-A and PlGF are key biomarkers for early risk assessment in pregnancy.
- Utilizing these markers can enhance antenatal surveillance and potentially improve pregnancy outcomes.
Abstract:
Early recognition of high-risk pregnancies through biochemical markers may promote antenatal surveillance, resulting in improved pregnancy outcomes. The goal of this study is to evaluate the possibilities of using biochemical markers during the first trimester of pregnancy in the prediction of hypertensive pregnancy disorders (HPD) and the delivery of small-for-gestational-age (SGA) neonates. A comprehensive search was conducted on key databases, including PubMed, Scopus, and Web of Science, for articles relating to the use of biochemical markers in the prediction of HPD and SGA. The findings show that changes in the levels of biomarkers in the early pregnancy phases could be an important indicator of adverse pregnancy outcomes. The literature shows that low PAPP-A (pregnancy-associated plasma protein A) and PlGF (placental growth factor) levels, low alkaline phosphatase (AP), higher sFlt-1 (soluble fms-like Tyrosine Kinase-1) levels, higher AFP (alfa fetoprotein) levels, and elevated levels of inflammatory markers such as β-HGC (free beta human chorionic gonadotropin), interferon-gamma (INF-γ), and tumor necrosis factor-α (TNF-α) may be associated with risks including the onset of HPD, fetal growth restriction (FGR), and delivery of SGA neonates. Comparatively, PAPP-A and PlGF appear to be the most important biochemical markers for the prediction of SGA and HPD.
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