Sepsis & infection

Host–Microbe Multiomic Profiling Predicts Mortality in Sepsis

Am J Respir Crit Care MedPublished Prognostic cohort study

Authors' conclusion

Taken together, our findings provide a conceptual advance in the understanding of host and microbial factors associated with mortality in critical illness and demonstrate a new approach to mortality prediction in sepsis.

Study context

Population
Critically ill adults with adjudicated sepsis status; whole blood and plasma within 24 h of admission
Participants
321 adults
Comparison
Host-microbe metagenomic and host transcriptomic classifiers vs APACHE III score for sepsis mortality prediction
Outcome
Prediction of sepsis mortality
Methodological detailsmultiomic (transcriptomic, proteomic, metagenomic), support vector machine-based classifiers
  • Multiomic (transcriptomic, proteomic, metagenomic)
  • Support vector machine-based classifiers

Performance

As reported in the abstract

Test or modelAUC
Host-microbe metagenomic classifier0.79
Host transcriptomic classifier0.75
APACHE III0.69

AUC

Host-microbe metagenomic classifier0.79
Host transcriptomic classifier0.75
APACHE III0.69
  • Host-microbe metagenomic classifier vs APACHE III: P < 0.05 — paired DeLong test; performed better
  • Host transcriptomic classifier vs APACHE III: P < 0.05 — paired DeLong test; performed better

Further findings

Host factors associated with mortality in sepsis

Mortality associated with increased expression of neutrophil degranulation genes, lower expression of T-cell signaling genes, and higher IL-8 levels

Microbial factors associated with mortality in sepsis

Mortality associated with greater microbial mass and greater bacterial relative dominance

Broader group incl. culture-negative or indeterminate sepsis (subgroup)

Similar findings observed

Parts of this Brief are withheld: the automatic checks could not confirm them against the abstract.

Original publication

Host–Microbe Multiomic Profiling Predicts Mortality in Sepsis. Am J Respir Crit Care Med. Published 11 August 2025. doi:10.1164/rccm.202410-1996oc

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