Accuracy of circulating microRNAs in diagnosis of sepsis: a systematic review and meta-analysis

Xiaomin Shen1, Jiajie Zhang2, Yicheng Huang2

  • 1State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Zhejiang Provincial Key Laboratory for Drug Clinical Research and Evaluation, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Journal of Intensive Care
|December 9, 2020
PubMed
Abstract

Insights

This meta-analysis shows circulating microRNAs (miRNAs) are accurate biomarkers for sepsis diagnosis. Specifically, miR-223 demonstrates strong potential as a sepsis indicator.

Area of Science:

  • Biomarkers
  • Molecular Diagnostics
  • Sepsis Research

Background:

  • Sepsis diagnosis relies on clinical criteria and biomarkers like procalcitonin (PCT) and C-reactive protein (CRP).
  • Circulating microRNAs (miRNAs) are emerging as potential diagnostic biomarkers due to their stability and role in disease regulation.
  • A systematic assessment of miRNA accuracy for sepsis diagnosis is needed.

Purpose of the Study:

  • To systematically evaluate the diagnostic accuracy of circulating miRNAs for sepsis using a meta-analysis.
  • To compare the accuracy of miRNAs with established sepsis biomarkers (PCT and CRP).

Main Methods:

  • A comprehensive literature search was conducted across major databases (PubMed, Cochrane, Embase, Web of Science, Scopus, Ovid) up to April 2020.
  • The Quality in Prognostic Studies (QUADAS-2) tool assessed study quality.
  • Meta-analysis techniques were employed to calculate pooled sensitivity, specificity, diagnostic odds ratio (DOR), and area under the curve (AUC).

Main Results:

  • The meta-analysis included 22 studies with 2210 sepsis cases, 426 systemic inflammatory response syndrome (SIRS) cases, and 1076 healthy controls (HC).
  • Circulating miRNAs demonstrated a pooled sensitivity of 0.80, specificity of 0.85, and DOR of 22, outperforming CRP (DOR 7) and comparable to PCT (DOR 17).
  • Subgroup analysis revealed superior diagnostic accuracy for miRNAs in adults, serum samples, downregulated expression, Sepsis-3 criteria, non-U6 internal references, and dysregulated miR-223 expression.

Conclusions:

  • Circulating miRNAs, particularly miR-223, are accurate and promising biomarkers for sepsis diagnosis.
  • The findings support the clinical utility of miRNAs as diagnostic indicators for sepsis.

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