학술논문

Plasma Angiopoietin-2 Predicts the Onset of Acute Lung Injury in Critically Ill Patients
Document Type
article
Source
American Journal of Respiratory and Critical Care Medicine. 187(7)
Subject
Biomedical and Clinical Sciences
Clinical Sciences
Acute Respiratory Distress Syndrome
Lung
Clinical Research
Rare Diseases
Detection
screening and diagnosis
4.1 Discovery and preclinical testing of markers and technologies
4.2 Evaluation of markers and technologies
Respiratory
Acute Lung Injury
Aged
Aged
80 and over
Angiopoietin-2
Biomarkers
Critical Illness
Decision Support Techniques
Female
Humans
Interleukin-8
Male
Middle Aged
Prospective Studies
ROC Curve
Receptor for Advanced Glycation End Products
Receptors
Immunologic
Regression Analysis
Risk Factors
Sensitivity and Specificity
von Willebrand Factor
acute respiratory distress syndrome
acute lung injury
receptor for advanced glycation end products
angiopoietin-2
Lung Injury Prediction Score
Medical and Health Sciences
Respiratory System
Cardiovascular medicine and haematology
Clinical sciences
Language
Abstract
RationaleCurrent clinical prediction scores for acute lung injury (ALI) have limited positive predictive value. No studies have evaluated predictive plasma biomarkers in a broad population of critically ill patients or as an adjunct to clinical prediction scores.ObjectivesTo determine whether plasma angiopoietin-2 (Ang-2), von Willebrand factor (vWF), interleukin-8 (IL-8), and/or receptor for advanced glycation end products (sRAGE) predict ALI in critically ill patients.MethodsPlasma samples were drawn from critically ill patients (n = 230) identified in the emergency department. Patients who had ALI at baseline or in the subsequent 6 hours were excluded, and the remaining patients were followed for development of ALI.Measurements and main resultsNineteen patients developed ALI at least 6 hours after the sample draw. Higher levels of Ang-2 and IL-8 were significantly associated with increased development of ALI (P = 0.0008, 0.004, respectively). The association between Ang-2 and subsequent development of ALI was robust to adjustment for sepsis and vasopressor use. Ang-2 and the Lung Injury Prediction Score each independently discriminated well between those who developed ALI and those who did not (area under the receiver operating characteristic curve, 0.74 for each), and using the two together improved the area under the curve to 0.84 (vs. 0.74, P = 0.05). In contrast, plasma levels of sRAGE and vWF were not predictive of ALI.ConclusionsPlasma biomarkers such as Ang-2 can improve clinical prediction scores and identify patients at high risk for ALI. In addition, the early rise of Ang-2 emphasizes the importance of endothelial injury in the early pathogenesis of ALI.