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Early plasma angiopoietin-2 is prognostic for ARDS and mortality among critically ill patients with sepsis.
Rosenberger, Carrie M; Wick, Katherine D; Zhuo, Hanjing; Wu, Nelson; Chen, Yue; Kapadia, Sharookh B; Guimaraes, Alessander; Chang, Diana; Choy, David F; Chen, Hubert; Peck, Melicent; Sullivan, Kathryn M; Ke, Serena; Jauregui, Alejandra; Leligdowicz, Aleksandra; Sinha, Pratik; Gomez, Antonio D; Kangelaris, Kirsten N; Delucchi, Kevin; Liu, Kathleen D; Calfee, Carolyn S; Matthay, Michael A; Hendrickson, Carolyn M.
  • Rosenberger CM; Human Pathophysiology and OMNI Reverse Translation, Genentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA. rosenbc4@gene.com.
  • Wick KD; Division of Pulmonary and Critical Care Medicine, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA, USA.
  • Zhuo H; Department of Internal Medicine, University of California, Davis, Davis, CA, USA.
  • Wu N; Division of Pulmonary and Critical Care Medicine, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA, USA.
  • Chen Y; Division of Pulmonary and Critical Care Medicine, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA, USA.
  • Kapadia SB; Division of Pulmonary and Critical Care Medicine, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA, USA.
  • Guimaraes A; Infectious Diseases, Genentech, Inc., 1 DNA Way, South San Francisco, CA, USA.
  • Chang D; Human Pathophysiology and OMNI Reverse Translation, Genentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.
  • Choy DF; Human Genetics, Genentech, Inc., 1 DNA Way, South San Francisco, CA, USA.
  • Chen H; Human Pathophysiology and OMNI Reverse Translation, Genentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.
  • Peck M; Early Clinical Development, Genentech, Inc., 1 DNA Way, South San Francisco, CA, USA.
  • Sullivan KM; Krystal Biotech, Pittsburgh, PA, USA.
  • Ke S; Early Clinical Development, Genentech, Inc., 1 DNA Way, South San Francisco, CA, USA.
  • Jauregui A; Division of Pulmonary and Critical Care Medicine, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA, USA.
  • Leligdowicz A; Division of Pulmonary and Critical Care Medicine, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA, USA.
  • Sinha P; Division of Pulmonary and Critical Care Medicine, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA, USA.
  • Gomez AD; Division of Pulmonary and Critical Care Medicine, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA, USA.
  • Kangelaris KN; Department of Medicine, Division of Critical Care, Western University, London, ON, Canada.
  • Delucchi K; Division of Pulmonary and Critical Care Medicine, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA, USA.
  • Liu KD; Division of Pulmonary and Critical Care Medicine, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA, USA.
  • Calfee CS; Division of Pulmonary and Critical Care Medicine, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA, USA.
  • Matthay MA; Division of Pulmonary and Critical Care Medicine, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA, USA.
  • Hendrickson CM; Division of Pulmonary and Critical Care Medicine, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA, USA.
Crit Care ; 27(1): 234, 2023 06 13.
Artículo en Inglés | MEDLINE | ID: covidwho-20242141
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.
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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Asunto principal: Síndrome de Dificultad Respiratoria / Sepsis / COVID-19 Tipo de estudio: Estudio de cohorte / Estudio observacional / Estudio pronóstico Límite: Humanos Idioma: Inglés Revista: Crit Care Año: 2023 Tipo del documento: Artículo País de afiliación: S13054-023-04525-3

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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Asunto principal: Síndrome de Dificultad Respiratoria / Sepsis / COVID-19 Tipo de estudio: Estudio de cohorte / Estudio observacional / Estudio pronóstico Límite: Humanos Idioma: Inglés Revista: Crit Care Año: 2023 Tipo del documento: Artículo País de afiliación: S13054-023-04525-3