rage: it’s relevance in ards
TRANSCRIPT
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RAGE: It’s relevance in ARDS
Professor Timothy EvansImperial College & Royal Brompton &
Harefield NHS Foundation Trust
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Potential conflicts of interest
– None to declare
– Ben Creagh Brown, Anne Burke Gaffney, Doverdale Trust
Acknowledgements
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RAGE: What is it? • The receptor for advanced glycation end products;
trans membrane receptor of immunoglobulin superfamily; constitutively expressed in all cells
• Diverse ligands upregulate [HMGB1, S100]
• Two hit hypothesis of inflammation:• Chronic inflammation (eg diabetes) up
regulates RAGE & RAGE ligands• Superimposed acute inflammation
further elevates leading to excessive and prolonged inflammation
RAGE: What does it do?
Intensive Care Medicine 2010; 36: 1644-1656
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RAGE axis in critical illness: The two hit hypothesis [Biochim Biophys Acta 2000; 1498: 99-111] Intensive Care Medicine 2010; 36: 1644-1656
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RAGE subtypes: Genesis, structure, signal transduction capacity: Intensive Care Medicine 2010; 36: 1644-1656
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RAGE: Where is it?
• Probably ubiquitous in all cells• Certainly in vascular tissue (eg
endothelium), neural tissue, neutrophils • Most abundantly isolated in lung so far;
primarily located on basal surface of alveolar type 1 cells
• Levels in BAL higher in permeabilty than hydrostatic pulmonary oedema
• In specific populations associated with longer mechanical ventilation and ICU LOS
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• Animal studies: RAGE & RAGE ligands• Clinical studies:
• The ARDSNet study• RAGE ligands in uncomplicated
pneumonia & when complicated by sepsis• sRAGE in ALI; & in ALI with sepsis• sRAGE and RAGE ligands in a population
at risk of developing ALI• Conclusions
RAGE: What do we know in experimental & clinical settings?
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Murine studies, RAGE inhibition. Intensive Care Medicine 2010; 36: 1644-1656
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Critical Care Medicine 2010: 38: 1414-1422
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RAGE & sepsis syndromes: Human studies. Intensive Care Med 2010; 36: 1644
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Thorax 2008; 63: 1083-1089
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Thorax 2008; 63: 1083-1089RAGE and survival
RAGE: baseline and day 3
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Thorax 2008; 63: 1083-1089
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• Baseline levels of plasma RAGE associated independently with clinical outcome in patients randomised to 12 ml/kg TV
• In this group, higher baseline RAGE associated with increased mortality, fewer VF and organ failure free days
• 6 ml/kg increased the fall in RAGE seen between day 0 and 3
Thorax 2008; 63: 1083-1089
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Critical Care Medicine 2007; 37: 1061-1067
A marker of the (activated) host response to infection; not a ’late’ mediator
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Critical Care Medicine 2011; 39: 480-8
• 64 patients with ALI/ARDS; ALI/ARDS plus sepsis/septic shock; sepsis/SS alone; ventilated controls
• sRAGE at baseline and day 3,6,28/ICU discharge
• Correlations sought between sRAGE and clinical and radiographic markers of severity
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Critical Care Medicine 2011; 39: 480-8
sRAGE and (A) PaO2:FiO2 and (B) LIS
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Critical Care Medicine 2011; 39: 480-8
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Critical Care Medicine 2011; 39: 480-8
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Critical Care Medicine 2011; 39: 480-8
• sRAGE correlated with clinical and radiographic severity of ALI
• Focal loss of aeration on CT associated with significantly lower sRAGE levels
• BAL levels in pARDS and non pARDS not different • Plasma levels decreased over time (?repair)• sRAGE elevated in ALI/ARDS regardless of presence
of sepsis/septic shock
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• Surgery necessitating CPB leads to inflammation & is a risk factor for ALI
• Levels and expression of sRAGE and ligands (S100B, S100A8/9, S100A12, HMGB1) measured; associations sought with relevant markers (IL-8, CRP) & clinical outcomes
• Patients undergoing CPB (n=177)
Preoperative RAGE: An independent predictor of outcome in patients at risk of ALI?
Creagh Brown B et al [submitted]
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Creagh-Brown B et al; Submitted to Intensive Care Medicine 2011
Patient demographics and operative variables
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Creagh-Brown B et al; Submitted 2011
Post operative variables; † p<0.001; ‡ p<0.005
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Plasma RAGE ligand levels pre and 2hr post CPB; * p<0.05; *** p<0.001
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Plasma sRAGE levels:
(A)Pre and 2hr post CPB [n=162]
(B)Pre intra and post CPB [n=13]
(C)esRAGE and shed RAGE levels pre and 2 hr post [n=19]
[*** p<0.001; * p<0.01]
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• Neutrophil membrane RAGE expression significantly reduced post op
• Intra cellular RAGE unaltered
[* p<0.01]
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Creagh-Brown B et al; Submitted to Intensive Care Medicine 2011
Assn of clinical and assay variables, > median ICU LOS (34.5 hrs)
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Creagh-Brown |B et al, Submitted 2011
Preoperative RAGE: An independent predictor of outcome in patients at risk of ALI?
Conclusions
• Surgery necessitating CPB leads to substantial increases in 4 RAGE ligands
• Strong relationship between duration of CPB and S100 release
• Elevated sRAGE maximal in surgery; pre op levels predictive of ICU LOS
• Leukocytes probable contributors• sRAGE: biomarker/mediator of SIRS?
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Critical Care Medicine 2011; 39: 589-590
• Is biologically plausible as a mediator or a marker • Relates to clinical outcomes in:
– Acute lung injury (regardless of presence of sepsis)– In SIRS
• Has some relationship to structural changes in patients with acute lung injury:– Radiographic (CT) but not BAL
• BUT as yet sparse evidence it is: – Predictive of ALI in at risk populations – Modified by therapeutic intervention – Easily and reliably measured
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Creagh-Brown B et al; Submitted 2011
Assn of clinical and assay variables, > 75% percentile ICU LOS [MBLR]
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