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Magnesium Sulfate-Mediated Inflammatory Modulation in High-Risk Pregnancies: Dynamic Shifts in CBC-Derived Markers
Şebnem Karagün1, Hamza Yıldız2, Yusuf Dal1
1Department of Obstetrics and Gynecology, Division of Perinatology, Mersin University Faculty of Medicine, Mersin, Turkey.
Magnesium sulfate (MgSO4) therapy alters maternal inflammatory markers like neutrophil-to-lymphocyte ratio (NLR). These hematologic changes may offer limited prediction for adverse neonatal outcomes in high-risk pregnancies.
Area of Science:
- Obstetrics and Gynecology
- Hematology
- Neonatal Medicine
Background:
- High-risk pregnancies often involve interventions like magnesium sulfate (MgSO4) therapy.
- Maternal inflammatory markers can reflect systemic changes during pregnancy.
- Understanding hematologic shifts during MgSO4 treatment is crucial for assessing maternal and fetal well-being.
Purpose of the Study:
- To evaluate the impact of MgSO4 therapy on dynamic changes in maternal inflammation-based hematologic indices.
- To assess the predictive value of these hematologic changes for neonatal outcomes in high-risk pregnancies.
Main Methods:
- Retrospective cohort study of 236 singleton pregnancies receiving MgSO4.
- Comparison of complete blood count (CBC)-derived inflammatory markers (NLR, PLR, SIRI, MPV) pre- and 24-h post-treatment.
- Analysis of percentage changes (Δ) and their correlation with adverse perinatal outcomes using ROC curves.
Main Results:
- MgSO4 administration significantly altered maternal inflammatory markers: increased NLR, WBC, SIRI; decreased PLR, LMR, platelet count (p < 0.05).
- ΔNLR, ΔMPV, and ΔWBC correlated negatively with gestational age and birth weight, and positively with NICU admission.
- ΔNLR ≥ -15.132 predicted NICU admission (AUC = 0.609, p = 0.016).
Conclusions:
- Magnesium sulfate therapy induces measurable dynamic changes in maternal inflammatory hematologic profiles.
- These shifts, particularly in NLR and MPV, show limited predictive value for adverse neonatal outcomes.
- Monitoring Δ-inflammatory indices may aid risk stratification but requires further clinical validation.
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