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Age-dependent differences in pulmonary host responses in ARDS: a prospective observational cohort study

Authors :
Laura R. Schouten
Anton H. van Kaam
Franziska Kohse
Floor Veltkamp
Lieuwe D. Bos
Friso M. de Beer
Roosmarijn T. van Hooijdonk
Janneke Horn
Marleen Straat
Esther Witteveen
Gerie J. Glas
Luuk Wieske
Lonneke A. van Vught
Maryse A. Wiewel
Sarah A. Ingelse
Bart Cortjens
Job B. van Woensel
Albert P. Bos
Thomas Walther
Marcus J. Schultz
Roelie M. Wösten-van Asperen
for the MARS consortium
Source :
Annals of Intensive Care, Vol 9, Iss 1, Pp 1-9 (2019)
Publication Year :
2019
Publisher :
SpringerOpen, 2019.

Abstract

Abstract Background Results from preclinical studies suggest that age-dependent differences in host defense and the pulmonary renin–angiotensin system (RAS) are responsible for observed differences in epidemiology of acute respiratory distress syndrome (ARDS) between children and adults. The present study compares biomarkers of host defense and RAS in bronchoalveolar lavage (BAL) fluid from neonates, children, adults, and older adults with ARDS. Methods In this prospective observational study, we enrolled mechanical ventilated ARDS patients categorized into four age groups: 20 neonates ( 65 years of age). All patients underwent a nondirected BAL within 72 h after intubation. Activities of the two main enzymes of RAS, angiotensin converting enzyme (ACE) and ACE2, and levels of biomarkers of inflammation, endothelial activation, and epithelial damage were determined in BAL fluid. Results Levels of myeloperoxidase, interleukin (IL)-6, IL-10, and p-selectin were higher with increasing age, whereas intercellular adhesion molecule-1 was higher in neonates. No differences in activity of ACE and ACE2 were seen between the four age groups. Conclusions Age-dependent differences in the levels of biomarkers in lungs of ARDS patients are present. Especially, higher levels of markers involved in the neutrophil response were found with increasing age. In contrast to preclinical studies, age is not associated with changes in the pulmonary RAS.

Details

Language :
English
ISSN :
21105820
Volume :
9
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Annals of Intensive Care
Publication Type :
Academic Journal
Accession number :
edsdoj.0eb053f78b0a436991dd632c9fd09910
Document Type :
article
Full Text :
https://doi.org/10.1186/s13613-019-0529-4