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Plasma sRAGE is independently associated with increased mortality in ARDS: a meta-analysis of individual patient data
PURPOSE: The soluble receptor for advanced glycation end-products (sRAGE) is a marker of lung epithelial injury and alveolar fluid clearance (AFC), with promising values for assessing prognosis and lung injury severity in acute respiratory distress syndrome (ARDS). Because AFC is impaired in most pa...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132684/ https://www.ncbi.nlm.nih.gov/pubmed/30051136 http://dx.doi.org/10.1007/s00134-018-5327-1 |
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author | Jabaudon, Matthieu Blondonnet, Raiko Pereira, Bruno Cartin-Ceba, Rodrigo Lichtenstern, Christoph Mauri, Tommaso Determann, Rogier M. Drabek, Tomas Hubmayr, Rolf D. Gajic, Ognjen Uhle, Florian Coppadoro, Andrea Pesenti, Antonio Schultz, Marcus J. Ranieri, Marco V. Brodska, Helena Mrozek, Ségolène Sapin, Vincent Matthay, Michael A. Constantin, Jean-Michel Calfee, Carolyn S. |
author_facet | Jabaudon, Matthieu Blondonnet, Raiko Pereira, Bruno Cartin-Ceba, Rodrigo Lichtenstern, Christoph Mauri, Tommaso Determann, Rogier M. Drabek, Tomas Hubmayr, Rolf D. Gajic, Ognjen Uhle, Florian Coppadoro, Andrea Pesenti, Antonio Schultz, Marcus J. Ranieri, Marco V. Brodska, Helena Mrozek, Ségolène Sapin, Vincent Matthay, Michael A. Constantin, Jean-Michel Calfee, Carolyn S. |
author_sort | Jabaudon, Matthieu |
collection | PubMed |
description | PURPOSE: The soluble receptor for advanced glycation end-products (sRAGE) is a marker of lung epithelial injury and alveolar fluid clearance (AFC), with promising values for assessing prognosis and lung injury severity in acute respiratory distress syndrome (ARDS). Because AFC is impaired in most patients with ARDS and is associated with higher mortality, we hypothesized that baseline plasma sRAGE would predict mortality, independently of two key mediators of ventilator-induced lung injury. METHODS: We conducted a meta-analysis of individual data from 746 patients enrolled in eight prospective randomized and observational studies in which plasma sRAGE was measured in ARDS articles published through March 2016. The primary outcome was 90-day mortality. Using multivariate and mediation analyses, we tested the association between baseline plasma sRAGE and mortality, independently of driving pressure and tidal volume. RESULTS: Higher baseline plasma sRAGE [odds ratio (OR) for each one-log increment, 1.18; 95% confidence interval (CI) 1.01–1.38; P = 0.04], driving pressure (OR for each one-point increment, 1.04; 95% CI 1.02–1.07; P = 0.002), and tidal volume (OR for each one-log increment, 1.98; 95% CI 1.07–3.64; P = 0.03) were independently associated with higher 90-day mortality in multivariate analysis. Baseline plasma sRAGE mediated a small fraction of the effect of higher ΔP on mortality but not that of higher V(T). CONCLUSIONS: Higher baseline plasma sRAGE was associated with higher 90-day mortality in patients with ARDS, independently of driving pressure and tidal volume, thus reinforcing the likely contribution of alveolar epithelial injury as an important prognostic factor in ARDS. Registration: PROSPERO (ID: CRD42018100241). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00134-018-5327-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6132684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-61326842018-09-13 Plasma sRAGE is independently associated with increased mortality in ARDS: a meta-analysis of individual patient data Jabaudon, Matthieu Blondonnet, Raiko Pereira, Bruno Cartin-Ceba, Rodrigo Lichtenstern, Christoph Mauri, Tommaso Determann, Rogier M. Drabek, Tomas Hubmayr, Rolf D. Gajic, Ognjen Uhle, Florian Coppadoro, Andrea Pesenti, Antonio Schultz, Marcus J. Ranieri, Marco V. Brodska, Helena Mrozek, Ségolène Sapin, Vincent Matthay, Michael A. Constantin, Jean-Michel Calfee, Carolyn S. Intensive Care Med Original PURPOSE: The soluble receptor for advanced glycation end-products (sRAGE) is a marker of lung epithelial injury and alveolar fluid clearance (AFC), with promising values for assessing prognosis and lung injury severity in acute respiratory distress syndrome (ARDS). Because AFC is impaired in most patients with ARDS and is associated with higher mortality, we hypothesized that baseline plasma sRAGE would predict mortality, independently of two key mediators of ventilator-induced lung injury. METHODS: We conducted a meta-analysis of individual data from 746 patients enrolled in eight prospective randomized and observational studies in which plasma sRAGE was measured in ARDS articles published through March 2016. The primary outcome was 90-day mortality. Using multivariate and mediation analyses, we tested the association between baseline plasma sRAGE and mortality, independently of driving pressure and tidal volume. RESULTS: Higher baseline plasma sRAGE [odds ratio (OR) for each one-log increment, 1.18; 95% confidence interval (CI) 1.01–1.38; P = 0.04], driving pressure (OR for each one-point increment, 1.04; 95% CI 1.02–1.07; P = 0.002), and tidal volume (OR for each one-log increment, 1.98; 95% CI 1.07–3.64; P = 0.03) were independently associated with higher 90-day mortality in multivariate analysis. Baseline plasma sRAGE mediated a small fraction of the effect of higher ΔP on mortality but not that of higher V(T). CONCLUSIONS: Higher baseline plasma sRAGE was associated with higher 90-day mortality in patients with ARDS, independently of driving pressure and tidal volume, thus reinforcing the likely contribution of alveolar epithelial injury as an important prognostic factor in ARDS. Registration: PROSPERO (ID: CRD42018100241). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00134-018-5327-1) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-07-26 2018 /pmc/articles/PMC6132684/ /pubmed/30051136 http://dx.doi.org/10.1007/s00134-018-5327-1 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Jabaudon, Matthieu Blondonnet, Raiko Pereira, Bruno Cartin-Ceba, Rodrigo Lichtenstern, Christoph Mauri, Tommaso Determann, Rogier M. Drabek, Tomas Hubmayr, Rolf D. Gajic, Ognjen Uhle, Florian Coppadoro, Andrea Pesenti, Antonio Schultz, Marcus J. Ranieri, Marco V. Brodska, Helena Mrozek, Ségolène Sapin, Vincent Matthay, Michael A. Constantin, Jean-Michel Calfee, Carolyn S. Plasma sRAGE is independently associated with increased mortality in ARDS: a meta-analysis of individual patient data |
title | Plasma sRAGE is independently associated with increased mortality in ARDS: a meta-analysis of individual patient data |
title_full | Plasma sRAGE is independently associated with increased mortality in ARDS: a meta-analysis of individual patient data |
title_fullStr | Plasma sRAGE is independently associated with increased mortality in ARDS: a meta-analysis of individual patient data |
title_full_unstemmed | Plasma sRAGE is independently associated with increased mortality in ARDS: a meta-analysis of individual patient data |
title_short | Plasma sRAGE is independently associated with increased mortality in ARDS: a meta-analysis of individual patient data |
title_sort | plasma srage is independently associated with increased mortality in ards: a meta-analysis of individual patient data |
topic | Original |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132684/ https://www.ncbi.nlm.nih.gov/pubmed/30051136 http://dx.doi.org/10.1007/s00134-018-5327-1 |
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