Sepsis & infection

Prognostic implication of downregulated exosomal microRNA (miRNAs) in patients with sepsis: a cross-sectional study with bioinformatics analysis

J Intensive CarePublished Cross-sectional study

Authors' conclusion

Among the differentially-expressed miRNAs detected in microarrays, the top four downregulated exosomal miRNAs (hsa-let-7f-5p, miR-331-3p miR-301a-3p, and miR-335-5p) were identified as independent prognostic factors for in-hospital and 90-day mortalities among sepsis patients.

Study context

Population
Critically ill adults with sepsis admitted to the ICU, from an ongoing prospective registryvalidation: 35 sepsis, 10 controls
Participants
135 vs 11
Exposure
Sepsis patients vs healthy controls
  • Sepsisn = 135
  • Healthy controlsn = 11reference
Outcome
Differential expression of plasma exosomal miRNAs
Methodological detailsbioinformatics analysis, external validation cohort, prospective registry
  • Bioinformatics analysis
  • External validation cohort
  • Prospective registry

Main finding

As reported in the abstract

Differentially expressed exosomal miRNAs

miRNAs significantly changed in sepsis vs healthy controls

25

Upregulated miRNAs

8

Downregulated miRNAs

17

Observational data: associations, not effects.

Further findings

Prediction of in-hospital mortality (AUC)

hsa-let-7f-5p AUC
0.913
miR-331-3p AUC
0.931
miR-301a-3p AUC
0.929
miR-335-5p AUC
0.957
  • p < 0.001
  • Confirmed in external validation cohort

90-day mortality, high vs low miRNA levels (Kaplan-Meier)

Significant difference in 90-day mortality between high and low miR-335-5p, miR-301a-3p, hsa-let-7f-5p and miR-331-3p levels
  • p < 0.001, log-rank test

KEGG pathway analysis

Most common pathways for the four miRNAs: PI3K-Akt and mitogen-activated protein kinase (MAPK) signaling

Original publication

Prognostic implication of downregulated exosomal miRNAs in patients with sepsis: a cross-sectional study with bioinformatics analysis. J Intensive Care. Published 3 August 2023. doi:10.1186/s40560-023-00683-2

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