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Conversion of a Capture ELISA to a Luminex xMAP Assay using a Multiplex Antibody Screening Method
Published on: July 6, 2012
Early pregnancy protein multiplex screening reflects circulating and urinary divergences associated with the
Margarita L Martinez-Fierro1,2, Claudia Castruita-De La Rosa1, Idalia Garza-Veloz1,2
1a Molecular Medicine Laboratory, Unidad Academica de Medicina Humana y Ciencias de la Salud, Universidad Autonoma de Zacatecas , Zacatecas , Mexico.
Insights
Early detection of preeclampsia is possible using specific angiogenic proteins. Measuring levels of proteins like soluble epidermal growth factor receptor (sEGFR) and vascular endothelial growth factor A (VEGF-A) in pregnant women can predict preeclampsia risk.
Area of Science:
- Reproductive biology and obstetrics.
- Biomarker discovery and validation.
- Maternal-fetal medicine.
Background:
- Preeclampsia is a major cause of maternal and fetal mortality globally.
- Accurate biomarkers are needed for early preeclampsia detection and improved patient outcomes.
- Current diagnostic methods require enhancement for predictive capabilities.
Purpose of the Study:
- To assess the predictive value of 34 angiogenic-related proteins for preeclampsia development.
- To identify specific protein biomarkers for early identification of preeclampsia risk.
- To evaluate protein profiles at multiple gestational weeks for predictive accuracy.
Main Methods:
- A nested case-control study involving pregnant women.
- Analysis of 34 angiogenic proteins in urine and plasma samples at 12, 16, and 20 gestational weeks.
- Utilized Bio-Plex Pro™ Human Cancer Biomarker Panels for protein profiling.
Main Results:
- Significant differences in urine concentrations of sEGFR, HGF, ANG-2, ENG, sFASL, IL-6, PLGF, and VEGF-A at 12 GW.
- Distinct levels of PRL, ANG-2, TGF-α, and VEGF-A identified at 16 GW.
- Elevated sIL-6Rα, ANG-2, and sFASL concentrations at 20 GW were associated with preeclampsia.
Conclusions:
- Multiple angiogenic proteins, including sEGFR, HGF, ANG-2, sFASL, IL-6, PLGF, VEGF-A, PRL, TGF-α, FGF-b, sHER2/Neu, sIL-6Rα, ENG, uPA, and IGFBP-1, are predictive of preeclampsia.
- These proteins show potential as early diagnostic markers for preeclampsia.
- Further consideration of these biomarkers for clinical use is warranted.
Background:
Preeclampsia, a pregnancy disorder characterized by hypertension and proteinuria, represents the leading cause of fetal and maternal morbidity and mortality in developing countries. The identification of novel and accurate biomarkers that are predictive of preeclampsia is necessary to improve the prognosis of patients with preeclampsia.
Objective:
To evaluate the preeclampsia predictive value of 34 angiogenic-related proteins.
Methods:
We performed a nested cohort case-control study of pregnant women. The profile of the 34 proteins was evaluated at 12, 16, and 20 gestational weeks (GWs), using urine/plasma from 16 women who developed preeclampsia and 20 normotensive pregnant controls by Bio-Plex ProTM Human Cancer Biomarker Panels 1 and 2.
Results:
The urine concentration of soluble epidermal growth factor receptor (sEGFR), hepatocyte growth factor (HGF), angiopoietin-2 (ANG-2), endoglin (ENG), soluble fas ligand (sFASL), interleukin 6 (IL-6), placental growth factor (PLGF), and vascular endothelial growth factor A (VEGF-A) at 12 GW, prolactin (PRL), ANG-2, transforming growth factor alpha (TGF-α), and VEGF-A at 16 GW, and soluble IL-6 receptor alpha (sIL-6Rα), ANG-2 and sFASL at 20 GW, were different between groups (p < 0.05). The concentration cut-off values calculated in this study for the mentioned proteins, predicted an increased risk to developing preeclampsia in a range of 3.8-29.8 times in the study population.
Conclusion:
The proteins sEGFR, HGF, ANG-2, sFASL, IL-6, PLGF, VEGF-A, PRL, TGF-α FGF-b, sHER2/Neu sIL-6Rα, ENG, uPA, and insulin-like growth factor binding protein 1 (IGFBP-1), were predictive of the development of preeclampsia and their use as markers for this disease should be considered.
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