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Updated: Jul 20, 2025

Author Spotlight: Modeling an Aspect of Preeclampsia in Female Mice Using Hypoxic Human Placenta-Derived Small Extracellular Vesicles
Published on: January 26, 2024
Is There a Predictable Cost-Benefit Ratio in Preeclampsia?
Dogukan Ozkan1, Betul Tokgoz Cakir1, Ceren Polat Kamaci1
1Obstetrics and Gynaecology, Etlik Zübeyde Hanim EAH, Ankara, TUR.
This study found that neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and aspartate aminotransferase-to-platelet ratio index (APRI) cannot predict preeclampsia (PE). These inflammatory markers lack clinical significance for assessing PE risk.
Area of Science:
- Obstetrics and Gynecology
- Perinatal Medicine
- Inflammatory Markers in Pregnancy
Background:
- Preeclampsia (PE) affects 2-8% of pregnancies and is linked to systemic inflammatory response (SIR) markers.
- Identifying predictive markers for PE is crucial for high-risk pregnancies.
Purpose of the Study:
- To investigate the predictive role of neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and aspartate aminotransferase-to-platelet ratio index (APRI) in preeclampsia.
- To determine the clinical significance of these SIR markers in predicting PE development.
Main Methods:
- A cohort of 300 pregnant women (151 with PE, 149 controls) was studied.
- Blood samples were analyzed for NLR, PLR, and APRI at hospitalization.
- Receiver operating characteristic (ROC) curve analysis was used to assess predictive capabilities.
Main Results:
- No significant differences were observed in mean NLR, PLR, and APRI values between the PE and control groups.
- ROC analysis indicated that none of these parameters could reliably predict preeclampsia.
- Hypertensive individuals were hospitalized earlier, with significantly higher blood pressure.
Conclusions:
- Neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and APRI do not possess clinical significance for predicting preeclampsia.
- These inflammatory markers are not useful in assessing the developmental risk of PE.
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