Can the neutrophil-to-lymphocyte ratio (NLR) predicts fetal loss in preeclampsia with severe features?

Pregnancy Hypertens. 2020 Oct:22:14-16. doi: 10.1016/j.preghy.2020.07.005. Epub 2020 Jul 15.

Abstract

Introduction: Preeclampsia (PE) is one of the most common causes of major maternal and fetal adverse events including mortality and preterm birth Grill et al. (2009). The neutrophil-to-lymphocyte ratio (NLR) and other hematologic indexes of systemic inflammation have been investigated in patients with PE for the prediction of the severity or presence of the disease. Despite these studies, we found no trials investigating the relationship between NLR and fetal outcomes in PE patients. In this study, we aimed to investigate the relationship between NLR and fetal outcomes.

Methods: We retrospectively analyzed the demographic data and laboratory tests to determine the NLR of 175 pregnant women with severe PE admitted to our clinic between January 2015 and December 2018.

Results: NLR in the first (2.4 ± 1.1 vs 2.9 ± 1.4, P = 0.18) and second trimesters (3.6 ± 0.7 vs 3.8 ± 1.3, P = 0.25) were not different between the groups, but third trimester NLR was significantly higher in patients with fetal loss (6.5 ± 5.4 vs 4.2 ± 2.7, P = 0.009). The area under the receiver operating characteristic curve for NLR in the third trimester was 0.66 and NLR > 3.9 predicted fetal loss with a sensitivity of 75% and a specificity of 61% (0.684, 95% confidence interval 0.48-0.83, P = 0.05).

Conclusion: We demonstrated that third trimester NLR is associated with fetal loss in patients with severe PE.

Keywords: Fetal outcome; Neutrophil-to-lymphocyte ratio; Preeclampsia.

MeSH terms

  • Adult
  • Biomarkers / blood
  • Case-Control Studies
  • Female
  • Fetal Death*
  • Humans
  • Inflammation Mediators / blood
  • Lymphocyte Count
  • Neutrophils / immunology
  • Pre-Eclampsia / blood*
  • Pre-Eclampsia / immunology
  • Pregnancy
  • Pregnancy Trimester, Third
  • Premature Birth / diagnosis*
  • ROC Curve
  • Retrospective Studies

Substances

  • Biomarkers
  • Inflammation Mediators