Literature DB >> 20351658

Metabolomics of volatile organic compounds in cystic fibrosis patients and controls.

Charlotte M H H T Robroeks1, Joep J B N van Berkel, Jan W Dallinga, Quirijn Jöbsis, Luc J I Zimmermann, Han J E Hendriks, Miel F M Wouters, Chris P M van der Grinten, Kim D G van de Kant, Frederik-Jan van Schooten, Edward Dompeling.   

Abstract

In cystic fibrosis (CF), airway inflammation causes an increased production of reactive oxygen species, responsible for degradation of cell membranes. During this process, volatile organic compounds (VOCs) are formed. Measurement of VOCs in exhaled breath of CF patients may be useful for the assessment of airway inflammation. This study investigates whether "metabolomics' of VOCs could discriminate between CF and controls, and between CF patients with and without Pseudomonas colonization. One hundred five children (48 with CF, 57 controls) were included in this study. After exhaled breath collection, samples were transferred onto tubes containing active carbon to adsorb and stabilize VOCs. Samples were analyzed by gas chromatography-time of flight-mass spectrometry to assess VOC profiles. Analysis showed that 1099 VOCs had a prevalence of at least 7%. By using 22 VOCs, a 100% correct identification of CF patients and controls was possible. With 10 VOCs, 92% of the subjects were correctly classified. The reproducibility of VOC measurements with a 1-h interval was very good (match factor 0.90 +/- 0.038). We conclude that metabolomics of VOCs in exhaled breath was possible in a reproducible way. This new technique was able to discriminate not only between CF patients and controls but also between CF patients with or without Pseudomonas colonization.

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Year:  2010        PMID: 20351658     DOI: 10.1203/PDR.0b013e3181df4ea0

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  51 in total

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5.  Proof of concept for identifying cystic fibrosis from perspiration samples.

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Review 7.  Bacterial volatiles and diagnosis of respiratory infections.

Authors:  James E Graham
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Review 8.  Clinical implications of shared genetics and pathogenesis in autoimmune diseases.

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9.  Urinary metabolomics reveals unique metabolic signatures in infants with cystic fibrosis.

Authors:  B T Kopp; E Joseloff; D Goetz; B Ingram; S L Heltshe; D H Leung; B W Ramsey; K McCoy; D Borowitz
Journal:  J Cyst Fibros       Date:  2018-11-23       Impact factor: 5.482

10.  Robust detection of P. aeruginosa and S. aureus acute lung infections by secondary electrospray ionization-mass spectrometry (SESI-MS) breathprinting: from initial infection to clearance.

Authors:  Jiangjiang Zhu; Jaime Jiménez-Díaz; Heather D Bean; Nirav A Daphtary; Minara I Aliyeva; Lennart K A Lundblad; Jane E Hill
Journal:  J Breath Res       Date:  2013-07-18       Impact factor: 3.262

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