Abstract

Acute respiratory distress syndrome (ARDS) is an acute-onset hypoxic condition with radiographic bilateral lung infiltration. It is characterized by an acute exudative phase combining diffuse alveolar damage and lung edema followed by a later fibroproliferative phase. Despite an improved understanding of ARDS pathobiology, our ability to predict the development of ARDS and risk-stratify patients with the disease remains limited. Biomarkers may help to identify patients at the highest risk of developing ARDS, assess response to therapy, predict outcome, and optimize enrollment in clinical trials. After a short description of ARDS pathobiology, here, we review the scientific evidence that supports the value of various ARDS biomarkers with regard to their major biological roles in ARDS-associated lung injury and/or repair. Ongoing research aims at identifying and characterizing novel biomarkers, in order to highlight relevant mechanistic explorations of lung injury and repair, and to ultimately develop innovative therapeutic approaches for ARDS patients. This review will focus on the pathophysiologic, diagnostic, and therapeutic implications of biomarkers in ARDS and on their utility to ultimately improve patient care.

Highlights

  • The acute respiratory distress syndrome (ARDS) is a heterogeneous syndrome defined by the association of bilateral radiographic pulmonary opacities, arterial hypoxemia (partial pressure of arterial oxygen (PaO2) to fraction of inspired oxygen (FiO2) ratio

  • It is characterized by diffuse alveolar epithelial and lung endothelial injury leading to increased permeability pulmonary edema and alveolar filling [2]

  • Agrawal et al found in a prospective study of 230 patients admitted to the intensive care unit (ICU) without ARDS that higher levels of Ang-2 were significantly associated with increased development of ARDS [130]

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Summary

Introduction

The acute respiratory distress syndrome (ARDS) is a heterogeneous syndrome defined by the association of bilateral radiographic pulmonary opacities, arterial hypoxemia (partial pressure of arterial oxygen (PaO2) to fraction of inspired oxygen (FiO2) ratio

Pathogenesis of ARDS
Biomarkers of ARDS: A Pathophysiologic Approach
Perspectives
Biomarkers in ARDS
Conclusion
Findings
Conflict of Interests
Full Text
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