Interleukin-8 for diagnosis of neonatal sepsis: a meta-analysis

PLoS One. 2015 May 21;10(5):e0127170. doi: 10.1371/journal.pone.0127170. eCollection 2015.

Abstract

Background: Neonatal sepsis (NS) is a life-threatening disorder and an important cause of morbidity and mortality in neonates. Previous studies showed that interleukin 8 (IL-8) may effectively and rapidly diagnose NS.

Objective: We conducted the systematic review and meta-analysis to investigate the diagnostic value of the IL-8 in NS.

Methods: The literature was searched in PUBMED, EMBASE, Cochrane Library, CNKI, VIP and other Chinese Medical Databases during October 1998 to January 2014 using set search criteria. Each included study was evaluated by quality assessment of diagnostic accuracy studies tool. Two investigators independently extracted the data and study characteristics, and disagreements, if any, were resolved by consensus. Meta-disc software was used to calculate the pooled sensitivity, specificity and summary diagnostic odds ratio (SDOR), I² or Cochrane Q to test heterogeneity, and meta-regression to investigate the source of heterogeneity. Funnel plots were used to test the potential presence of publication bias. False-positive report probability (FPRP) was calculated to confirm the significance of the results.

Results: Eight studies (548 neonates) were included in this meta-analysis. The pooled sensitivity and specificity of IL-8 were 0.78 and 0.84, respectively, which had moderate accuracy in the diagnosis of NS. The pooled diagnostic odds ratio (DOR) and area under curve (AUC) was 21.64 and 0.8908 (Q*=0.8215), respectively. The diagnostic threshold analysis showed that there was no threshold effect. The meta-regression analysis showed the cut-off, QUADAS and onset time have no effect on the heterogeneity. The funnel plots showed the existence of publication bias.

Conclusion: Meta-analysis showed IL-8 had a moderate accuracy (AUC=0.8908) for the diagnosis of NS. IL-8 is a helpful biomarker for early diagnosis of NS. However, we should combine the results with clinical symptoms and signs, laboratory and microbial results.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't
  • Systematic Review

MeSH terms

  • Biomarkers
  • Humans
  • Infant, Newborn
  • Interleukin-8 / blood*
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Sepsis / blood*
  • Sepsis / diagnosis*

Substances

  • Biomarkers
  • Interleukin-8

Grants and funding

This work was supported by the Natural Science Foundation of Chongqing Grants (cstc2014jctjA10052), affiliated Children's hospital of Chongqing medical university clinical research projects (lcyj2014-8). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.