Literature DB >> 20562125

Cyanide in bronchoalveolar lavage is not diagnostic for Pseudomonas aeruginosa in children with cystic fibrosis.

M D Stutz1, C L Gangell, L J Berry, L W Garratt, B Sheil, P D Sly.   

Abstract

Early detection of the cyanobacterium Pseudomonas aeruginosa in the lungs of young children with cystic fibrosis (CF) is considered the key to delaying chronic pulmonary disease. We investigated whether cyanide in bronchoalveolar lavage (BAL) fluid could be used as an early diagnostic biomarker of infection. Cyanide was measured in 226 BAL samples (36 P. aeruginosa infected) obtained from 96 infants and young children with CF participating in an early surveillance programme involving annual BAL. Cyanide was detected in 97.2% of P. aeruginosa infected and 60.5% of uninfected samples. Cyanide concentrations were significantly higher in BALs infected with P. aeruginosa (median (25th-75th percentile) 27.3 (22.1-33.3) μM) than those which were not (17.2 (7.85-23.0) μM, p<0.001). The best sensitivity, specificity, positive and negative predictive values were obtained with a cut-off concentration of 20.6 μM, and were 83%, 66%, 32% and 96%, respectively. Neutrophil number in BAL was a significant predictor of cyanide concentration (p<0.001). Cyanide concentration can distinguish between P. aeruginosa infected and uninfected BALs as a group, but not individually; therefore, cyanide is a poor diagnostic biomarker of P. aeruginosa infection. Cyanide levels in BAL are related to the level of neutrophilic inflammation.

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Year:  2010        PMID: 20562125     DOI: 10.1183/09031936.00024210

Source DB:  PubMed          Journal:  Eur Respir J        ISSN: 0903-1936            Impact factor:   16.671


  6 in total

1.  The mucoid switch in Pseudomonas aeruginosa represses quorum sensing systems and leads to complex changes to stationary phase virulence factor regulation.

Authors:  Ben Ryall; Marta Carrara; James E A Zlosnik; Volker Behrends; Xiaoyun Lee; Zhen Wong; Kathryn E Lougheed; Huw D Williams
Journal:  PLoS One       Date:  2014-05-22       Impact factor: 3.240

Review 2.  The Pseudomonas aeruginosa AlgZR two-component system coordinates multiple phenotypes.

Authors:  Yuta Okkotsu; Alexander S Little; Michael J Schurr
Journal:  Front Cell Infect Microbiol       Date:  2014-06-20       Impact factor: 5.293

3.  Cutaneotrichosporon (Cryptococcus) cyanovorans, a basidiomycetous yeast, isolated from the airways of cystic fibrosis patients.

Authors:  Tjomme van der Bruggen; Anna Kolecka; Bart Theelen; Johanna M Kwakkel-van Erp; Bert Arets; Teun Boekhout
Journal:  Med Mycol Case Rep       Date:  2018-07-18

4.  Airway, but not serum or urinary, levels of YKL-40 reflect inflammation in early cystic fibrosis lung disease.

Authors:  Emmanuelle Fantino; Catherine L Gangell; Dominik Hartl; Peter D Sly
Journal:  BMC Pulm Med       Date:  2014-02-27       Impact factor: 3.317

5.  Volatile molecules from bronchoalveolar lavage fluid can 'rule-in' Pseudomonas aeruginosa and 'rule-out' Staphylococcus aureus infections in cystic fibrosis patients.

Authors:  Mavra Nasir; Heather D Bean; Agnieszka Smolinska; Christiaan A Rees; Edith T Zemanick; Jane E Hill
Journal:  Sci Rep       Date:  2018-01-16       Impact factor: 4.379

Review 6.  The two faces of cyanide: an environmental toxin and a potential novel mammalian gasotransmitter.

Authors:  Karim Zuhra; Csaba Szabo
Journal:  FEBS J       Date:  2021-08-05       Impact factor: 5.622

  6 in total

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