Sepsis & infection

The Plasma Lipidomic Landscape in Patients with Sepsis due to Community-acquired Pneumonia

Am J Respir Crit Care MedPublished Observational cohort study

Authors' conclusion

Patients with sepsis due to CAP exhibit a time-dependent and partially disease-specific shift in their plasma lipidome that correlates with disease severity and systemic inflammation and is associated with higher mortality.

Study context

Population
ICU patients with sepsis due to community-acquired pneumonia (CAP)82 reanalyzed at day 4
Participants
169 / 51 / 48
Exposure
Sepsis due to CAP vs noninfected ICU patients and outpatient controls
  • CAP sepsisn = 169
  • Noninfected ICUn = 51
  • Outpatient controlsn = 48reference
Outcome
Plasma lipids vs outpatient controls
Methodological detailspaired analysis, external validation cohorts
  • Paired analysis
  • External validation cohorts

Main finding

As reported in the abstract

Plasma lipids significantly lower in CAP sepsis vs outpatient controls

58%

Plasma lipids higher

6%

Plasma lipids not different

36%

Observational data: associations, not effects.

Further findings

OutcomeORP value
30-day mortality per 10% increase in cholesterol ester levels · absolute mortality, 18 of 820.84P = 0.006

Associations with disease severity and inflammatory biomarkers

Strong lipid class-specific associations with disease severity (validated in two external cohorts) and inflammatory biomarkers; strongest for triacylglycerols, cholesterol esters and lysophospholipids

Change in lipids over time · 4 days after admission

Lipids increased over time
36%
Diverging lipid recovery by survival, confirmed in an external cohort

Comparison with noninfected ICU patients

Common illness response
57.5%
Distinct lipidomic signal for CAP sepsis
37%

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

Original publication

The Plasma Lipidomic Landscape in Patients with Sepsis due to Community-acquired Pneumonia. Am J Respir Crit Care Med. Published 15 April 2024. doi:10.1164/rccm.202308-1321oc

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