Critical Care (Jun 2023)

Early plasma angiopoietin-2 is prognostic for ARDS and mortality among critically ill patients with sepsis

  • Carrie M. Rosenberger,
  • Katherine D. Wick,
  • Hanjing Zhuo,
  • Nelson Wu,
  • Yue Chen,
  • Sharookh B. Kapadia,
  • Alessander Guimaraes,
  • Diana Chang,
  • David F. Choy,
  • Hubert Chen,
  • Melicent Peck,
  • Kathryn M. Sullivan,
  • Serena Ke,
  • Alejandra Jauregui,
  • Aleksandra Leligdowicz,
  • Pratik Sinha,
  • Antonio D. Gomez,
  • Kirsten N. Kangelaris,
  • Kevin Delucchi,
  • Kathleen D. Liu,
  • Carolyn S. Calfee,
  • Michael A. Matthay,
  • Carolyn M. Hendrickson

DOI
https://doi.org/10.1186/s13054-023-04525-3
Journal volume & issue
Vol. 27, no. 1
pp. 1 – 4

Abstract

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Abstract 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.