Microarray-based analysis of ventilator-induced lung injury - PubMed (original) (raw)
Review
Microarray-based analysis of ventilator-induced lung injury
Mark M Wurfel. Proc Am Thorac Soc. 2007 Jan.
Abstract
Acute respiratory distress syndrome (ARDS) and acute lung injury (ALI) are a frequent cause of intensive care unit admission, affecting over 200,000 patients in the United States each year. Mechanical ventilation is a life-saving intervention in the setting of ARDS and ALI, but clinical trials have demonstrated that mechanical ventilation with excessive tidal volumes plays a role in promoting and perpetuating lung injury and leads to excess mortality. This process has been labeled ventilator-induced lung injury (VILI), but the molecular mechanisms driving this process and its interactions with predisposing risk factors such as sepsis and chemical injury remain incompletely understood. Genome-wide measurements of gene expression using microarray technology represent a powerful tool to examine the pathophysiology of VILI. Several recent studies have used this approach to study VILI in isolation and associated with endotoxin instillation or saline lavage. These studies and others examining gene expression profiles in epithelial cells subjected to cyclic stretch have provided novel insights on the molecular mechanisms underlying VILI. This review will summarize these findings and discuss implications for future studies.
Figures
**Figure 1.
Summary of differentially regulated genes. Genes grouped based on differential regulation in the same direction: upper panel, up-regulated; lower panel, down-regulated. 1Genes differentially regulated across murine, rat, canine, and human models of VILI (p < 0.05; black boxes) (25). 2Genes differentially regulated (95% confidence interval for fold-change not containing 1.0) in murine model of mechanical ventilation alone (black boxes) or mechanical ventilation plus intratracheal lipopolysaccharide (grey boxes) (26). 3Genes differentially regulated in rat model of mechanical ventilation (fold change ⩾ 2 and D ⩾ 0.8) (24). 4Genes differentially regulated in murine isolated perfused lung model of mechanical ventilation (false discovery rate ⩽ 0.1; black boxes), or fold change over control ⩾ 2.0 (grey boxes) (27).
References
- Webb HH, Tierney DF. Experimental pulmonary edema due to intermittent positive pressure ventilation with high inflation pressures: protection by positive end-expiratory pressure. Am Rev Respir Dis 1974;110:556–565. - PubMed
- The Acute Respiratory Distress Syndrome Network. Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. N Engl J Med 2000;342:1301–1308. - PubMed
- Tremblay LN, Slutsky AS. Ventilator-induced lung injury: from the bench to the bedside. Intensive Care Med 2006;32:24–33. - PubMed
- DeRisi J, Penland L, Brown PO, Bittner ML, Meltzer PS, Ray M, Chen Y, Su YA, Trent JM. Use of a cDNA microarray to analyse gene expression patterns in human cancer. Nat Genet 1996;14:457–460. - PubMed
- Schena M, Shalon D, Davis RW, Brown PO. Quantitative monitoring of gene expression patterns with a complementary DNA microarray. Science 1995;270:467–470. - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources