ERJ
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Published online before print February 2, 2006
Eur Respir J 2006, doi:10.1183/09031936.06.00085105
This Article
Right arrow Full Text (Rapid PDF)
Right arrow All Versions of this Article:
27/5/929    most recent
09031936.06.00085105v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Permissions
Right arrowRequest Permissions
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Barker, M.
Right arrow Articles by Koppmann, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Barker, M.
Right arrow Articles by Koppmann, R.


ORIGINAL ARTICLE

Volatile organic compounds in the exhaled breath of young patients with cystic fibrosis

M. Barker 1*, M. Hengst 1, J. Schmid 1, H-J. Buers 2, B. Mittermaier 3, D. Klemp 2, R. Koppmann 2

1 Dept. of Paediatrics, University of Technology (RWTH) Medical Center, Aachen, Germany
2 Institute of Chemistry and Dynamics of the Geosphere, Division II: Troposphere
3 Institute of Chemistry and Dynamics of the Geosphere, Division II: Troposphere; and Central Library, Research Center Jülich, Germany

* To whom correspondence should be addressed. E-mail: Barker{at}rwth-aachen.de.


   Abstract

Inflammatory mediators in the exhaled breath are receiving growing medical interest as non-invasive disease markers. Volatile organic compounds have been investigated in this context, but clinical information and methodological standards are limited.

We measured the levels of ethane, propane, n-pentane, methanol, ethanol, 2-propanol, acetone, isoprene, benzene, toluene, dimethylsulfide and limonene in repeated breath samples from 20 cystic fibrosis patients and 20 healthy controls (age 8-29 years). Three end-exhaled and one ambient air sample were collected per person and analysed on a customised gas chromatography system.

Intra-subject coefficients of variation ranged between 9-34%, and hydrocarbon breath levels were influenced by their inspired concentrations. The alveolar gradient for pentane was higher in cystic fibrosis patients than in healthy controls (0.36 vs. 0.21 ppb, p=0.04) and inversely proportional to FEV1 (r=-0.62, p=0.004), highest values were observed in patients with pulmonary exacerbations (0.73 vs. 0.24 ppb, p=0.006). Cystic fibrosis patients also exhibited a lower output of dimethylsulfide (3.9 vs. 7.6 ppb, p=0.003). Group differences were not significant for ethane and the remaining substances.

We conclude that chemical breath analysis for volatile organic compounds is feasible and may hold potential for the non-invasive diagnosis and follow-up of inflammatory processes in cystic fibrosis lung disease.

Keywords:  Biological markers, breath tests, cystic fibrosis, gas chromatography







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2006 by the European Respiratory Society.