Liver–lung interactions in acute respiratory distress syndrome

• Published in: Intensive care medicine experimental 2020-12, Vol.8 (Suppl 1), p.48-48, Article 48
• Main Authors: Herrero, Raquel, Sánchez, Gema, Asensio, Iris, López, Eva, Ferruelo, Antonio, Vaquero, Javier, Moreno, Laura, de Lorenzo, Alba, Bañares, Rafael, Lorente, José A.
• Format: Article
• Language: English
• Subjects: Acute respiratory distress syndrome; Acute-phase response; Critical Care Medicine; Immunomodulation; Intensive; Intensive care; Liver; Liver diseases; Liver dysfunction; Liver–lung interaction; Lungs; Mechanisms; Medical prognosis; Medicine; Medicine & Public Health; Pathogenesis; Respiratory distress syndrome
• ISSN: 2197-425X; 2197-425X
• DOI: 10.1186/s40635-020-00337-9

Patients with liver diseases are at high risk for the development of acute respiratory distress syndrome (ARDS). The liver is an important organ that regulates a complex network of mediators and modulates organ interactions during inflammatory disorders. Liver function is increasingly recognized as a critical determinant of the pathogenesis and resolution of ARDS, significantly influencing the prognosis of these patients. The liver plays a central role in the synthesis of proteins, metabolism of toxins and drugs, and in the modulation of immunity and host defense. However, the tools for assessing liver function are limited in the clinical setting, and patients with liver diseases are frequently excluded from clinical studies of ARDS. Therefore, the mechanisms by which the liver participates in the pathogenesis of acute lung injury are not totally understood. Several functions of the liver, including endotoxin and bacterial clearance, release and clearance of pro-inflammatory cytokines and eicosanoids, and synthesis of acute-phase proteins can modulate lung injury in the setting of sepsis and other severe inflammatory diseases. In this review, we summarized clinical and experimental support for the notion that the liver critically regulates systemic and pulmonary responses following inflammatory insults. Although promoting inflammation can be detrimental in the context of acute lung injury, the liver response to an inflammatory insult is also pro-defense and pro-survival. A better understanding of the liver–lung axis will provide valuable insights into new diagnostic targets and therapeutic strategies for clinical intervention in patients with or at risk for ARDS.