Key result
Higher early plasma Ang-2 in sepsis is linked to ~52% greater mortality per log increase.
Why the study?
Elevated circulating Angiopoietin-2 levels may identify critically ill sepsis patients at risk for ARDS and poor clinical outcomes, but this association needed evaluation.
Is early plasma Angiopoietin-2 associated with the development of ARDS and 30-day mortality in critically ill patients with sepsis?
Cohort (n=757)
No
Is early plasma Angiopoietin-2 associated with the development of ARDS and 30-day mortality in critically ill patients with sepsis?
Early plasma Ang-2 levels in sepsis patients are prognostic for the development of ARDS and 30-day mortality, highlighting its potential as a biomarker for risk prediction and targeted therapy.
Answers are grounded in this paper and cite their sources.
Ang-2 may refine mortality risk prediction in sepsis; leaves open its utility for guiding therapy or ARDS prevention.
Angiopoietin-2 (Ang-2) is associated with vascular endothelial injury and permeability in the acute respiratory distress syndrome (ARDS) and sepsis. Elevated circulating Ang-2 levels may identify critically ill patients with distinct pathobiology amenable to targeted therapy. We hypothesized that plasma Ang-2 measured shortly after hospitalization among patients with sepsis would be associated with the development of ARDS and poor clinical outcomes. To test this hypothesis, we measured plasma Ang-2 in a cohort of 757 patients with sepsis, including 267 with ARDS, enrolled in the emergency department or early in their ICU course before the COVID-19 pandemic. Multivariable models were used to test the association of Ang-2 with the development of ARDS and 30-day morality. We found that early plasma Ang-2 in sepsis was associated with higher baseline severity of illness, the development of ARDS, and mortality risk. The association between Ang-2 and mortality was strongest among patients with ARDS and sepsis as compared to those with sepsis alone (OR 1.81 vs. 1.52 per log Ang-2 increase). These findings might inform models testing patient risk prediction and strengthen the evidence for Ang-2 as an appealing biomarker for patient selection for novel therapeutic agents to target vascular injury in sepsis and ARDS.
No takes yet. Share an insight, caveat, or question.
Rosenberger et al. (2023) conducted a cohort in Sepsis (n=757). Early plasma angiopoietin-2 (Ang-2) vs. Lower Ang-2 levels was evaluated on 30-day mortality (OR 1.52, 95% CI 1.28-1.80, p=<0.001). Higher early plasma angiopoietin-2 levels in critically ill patients with sepsis were associated with increased 30-day mortality.
Synapse has enriched 10 related papers. Consider them for comparative context: