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Published in: BMC Pulmonary Medicine 1/2008

Open Access 01-12-2008 | Research article

Hospital acquired pneumonia with high-risk bacteria is associated with increased pulmonary matrix metalloproteinase activity

Authors: Bernhard Schaaf, Cornelia Liebau, Volkhard Kurowski, Daniel Droemann, Klaus Dalhoff

Published in: BMC Pulmonary Medicine | Issue 1/2008

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Abstract

Background

Neutrophil products like matrix metalloproteinases (MMP), involved in bacterial defence mechanisms, possibly induce lung damage and are elevated locally during hospital- acquired pneumonia (HAP). In HAP the virulence of bacterial species is known to be different. The aim of this study was to investigate the influence of high-risk bacteria like S. aureus and pseudomonas species on pulmonary MMPconcentration in human pneumonia.

Methods

In 37 patients with HAP and 16 controls, MMP-8, MMP-9 and tissue inhibitors of MMP (TIMP) were analysed by ELISA and MMP-9 activity using zymography in bronchoalveolar lavage (BAL).

Results

MMP-9 activity in mini-BAL was increased in HAP patients versus controls (149 ± 41 vs. 34 ± 11, p < 0.0001). In subgroup analysis, the highest MMP concentrations and activity were seen in patients with high-risk bacteria: patients with high-risk bacteria MMP-9 1168 ± 266 vs. patients with low-risk bacteria 224 ± 119 ng/ml p < 0.0001, MMP-9 gelatinolytic activity 325 ± 106 vs. 67 ± 14, p < 0.0002. In addition, the MMP-8 and MMP-9 concentration was associated with the state of ventilation and systemic inflammatory marker like CRP.

Conclusion

Pulmonary MMP concentrations and MMP activity are elevated in patients with HAP. This effect is most pronounced in patients with high-risk bacteria. Artificial ventilation may play an additional role in protease activation.
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Metadata
Title
Hospital acquired pneumonia with high-risk bacteria is associated with increased pulmonary matrix metalloproteinase activity
Authors
Bernhard Schaaf
Cornelia Liebau
Volkhard Kurowski
Daniel Droemann
Klaus Dalhoff
Publication date
01-12-2008
Publisher
BioMed Central
Published in
BMC Pulmonary Medicine / Issue 1/2008
Electronic ISSN: 1471-2466
DOI
https://doi.org/10.1186/1471-2466-8-12

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