Maternal β-hCG and Neutrophil Lymphocyte Ratio during Pregnancy to Predict High-Risk Neonates: an Observational Study

Megha Panwar1, Akansha Mohanty1, Nidhi Ahuja1

  • 1Dept. of Obstetrics and Gynaecology, Vardhaman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.

Maedica
|August 29, 2022
PubMed

Insights

High maternal levels of neutrophil-to-lymphocyte ratio (NLR) and beta-human chorionic gonadotropin (β-hCG) are linked to adverse neonatal outcomes, including low birth weight and poor APGAR scores. Further research is recommended to explore these biomarker impacts for improved fetal outcomes.

Area of Science:

  • Obstetrics and Gynecology
  • Maternal-Fetal Medicine
  • Neonatal Outcomes

Background:

  • Maternal serum biomarkers are crucial for identifying potential maternal and fetal complications during pregnancy.
  • This study investigated the predictive value of beta-human chorionic gonadotropin (β-hCG) and neutrophil-to-lymphocyte ratio (NLR) for high-risk infant delivery, specifically focusing on low birth weight and poor APGAR scores.

Discussion:

  • Maternal NLR and β-hCG levels demonstrated a negative correlation with neonatal outcomes such as low birth weight and low APGAR scores.
  • Significantly higher mean NLR values were observed in neonates experiencing poor outcomes (low birth weight, low APGAR).

Key Insights:

  • β-hCG showed good sensitivity (83%) and specificity (66-90%) in predicting poor APGAR scores at different gestational weeks (16-18 and 32-34 weeks).
  • NLR also demonstrated predictive capabilities for poor APGAR scores, with sensitivities ranging from 78% to 89% and specificities from 53% to 61% across gestational periods.
  • Elevated maternal NLR and β-hCG levels are associated with increased risk of low birth weight and poor neonatal APGAR scores.

Outlook:

  • The findings suggest that elevated maternal NLR and β-hCG levels are significant indicators of adverse neonatal outcomes.
  • Further large-scale investigations are warranted to fully elucidate the negative impact of these biomarkers on fetal development.
  • Understanding and monitoring these biomarkers could lead to strategies for reducing poor fetal outcomes.