Related Experiment Video
Updated: Dec 13, 2025

Author Spotlight: Modeling an Aspect of Preeclampsia in Female Mice Using Hypoxic Human Placenta-Derived Small Extracellular Vesicles
Published on: January 26, 2024
The first-trimester serum decorin levels as a potential predictor of preeclampsia
Gültekin Adanaş Aydın1, Habibe Ayvacı2, Gülten Özgen1
1Department of Obstetrics and Gynecology, Bursa Yüksek İhtisas Training and Research Hospital, Bursa, Turkey.
Insights
Serum decorin levels in early pregnancy do not predict preeclampsia. This study found no significant difference in decorin levels between pregnant women who developed preeclampsia and healthy controls.
Area of Science:
- Obstetrics and Gynecology
- Maternal-Fetal Medicine
- Biochemistry
Background:
- Preeclampsia (PE) is a major cause of maternal and neonatal mortality.
- Inadequate trophoblast invasion is a key factor in PE pathogenesis.
- Decidua-derived factors like transforming growth factor beta (TGF-β) and decorin regulate trophoblast function.
Purpose of the Study:
- To investigate the clinical utility of serum decorin levels in early pregnancy (11-14 weeks) for predicting preeclampsia.
- To assess decorin as a potential biomarker for early-onset preeclampsia (EOS-PE).
Main Methods:
- A cohort of 600 pregnant women (18-40 years) was recruited.
- Serum samples were collected between 11-14 gestational weeks.
- Serum decorin levels were analyzed in women who later developed PE and in matched healthy controls.
Main Results:
- Mean serum decorin level was 8.76 ± 6.88 ng/mL in the PE group.
- Mean serum decorin level was 9.75 ± 9.82 ng/mL in the control group.
- No statistically significant difference in serum decorin levels was observed between the PE and control groups (p=0.838).
Conclusions:
- Serum decorin levels measured in the first trimester do not appear to have predictive value for preeclampsia.
- Further research with larger sample sizes, including early-onset preeclampsia cases, is needed to definitively assess decorin's role as a biomarker.
Abstract:
Background Preeclampsia (PE) is a multisystem disease and is still among the leading causes of maternal and neonatal morbidity and mortality. Inadequate trophoblast invasion plays a key role in the PE pathogenesis. The proliferation, migration, and invasion of extravillous trophoblasts (EVTs) is primarily controlled by the decidua-derived transforming growth factor beta (TGF-β) and decorin. In this study, we aimed to investigate the clinical utility of serum decorin levels measured in the 11th to 14th gestational weeks to predict preeclampsia during the following weeks of gestation. Materials and Methods A total of 600 pregnant women, whose age and gestational age ranged from 18 to 40 years and 11 to 14 weeks, were included. Venous blood samples were obtained and stored at -80 °C. Subsequently, the patients who developed preeclampsia and healthy controls with a similar body mass index were identified and their first-trimester blood samples were analyzed for serum decorin levels. Results The mean serum decorin level was 8.76 ± 6.88 ng/mL for the PE group while 9.75 ± 9.82 ng/mL for the control group. No statistically significant difference was found between the two groups (p=0.838). Conclusion We observed that the serum decorin levels during the 11th to 14th weeks of gestation showed no predictive value for preeclampsia in pregnant women. However, more accurate conclusions about the clinical utility of decorin as a biomarker of preeclampsia would require further studies with larger samples including more patients with EOS-PE.
Related Concept Videos
Pathophysiology of Diabetes
Type 1 diabetes is characterized by autoimmune-mediated destruction of pancreatic β cells, with environmental factors potentially triggering this process in genetically susceptible individuals. Despite many not having a family history, certain genes increase susceptibility,...
Teratogenicity

