Sepsis & infection

Identification of a robust metabolic signature associated with hospital-acquired pneumonia and response to interferon-gamma treatment in critically ill patients

Crit CarePublished Prospective observational cohort study with replication in a randomised trial dataset

Authors' conclusion

Longitudinal clustering classified metabolic response patterns into low-, moderate-, and high-risk groups for HAP and can help identify responders and non-responders to interferon gamma-1b after a single treatment injection.

Study context

Population
Critically ill brain-injured patients in two French centres; replication in PREV-HAP trial patients (interferon gamma-1b for hospital-acquired pneumonia (HAP) prevention)330 samples analysed
Participants
128 patients
Comparison
Low- vs moderate- vs high-risk metabolic response patterns
Primary endpoint
Association of metabolic response patterns with HAP
Methodological detailstwo-centre, unsupervised longitudinal consensus clustering, Fast-and-Frugal Tree replication
  • Two-centre
  • Unsupervised longitudinal consensus clustering
  • Fast-and-Frugal Tree replication

Primary result

As reported in the abstract

HAP, discovery cohort
HAP overall
57 (45%)

Further findings

ARDS, discovery cohort

HAP, replication dataset (315 samples, 105 patients)

Acute respiratory distress syndrome (ARDS), discovery cohort — ARDS overall
21 (16%)

Discharge alive from ICU with interferon gamma-1b (replication)

Probability decreased in low-risk and increased in high-risk metabolic response patterns

Original publication

Identification of a robust metabolic signature associated with hospital-acquired pneumonia and response to interferon-gamma treatment in critically ill patients. Crit Care. Published 12 March 2026. doi:10.1186/s13054-026-05946-6

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