Literature DB >> 23361110

Exhaled molecular profiles in the assessment of cystic fibrosis and primary ciliary dyskinesia.

T Paff1, M P van der Schee, J M A Daniels, G Pals, P E Postmus, P J Sterk, E G Haarman.   

Abstract

BACKGROUND: Early diagnosis and monitoring of disease activity are essential in cystic fibrosis (CF) and primary ciliary dyskinesia (PCD). We aimed to establish exhaled molecular profiles as the first step in assessing the potential of breath analysis.
METHODS: Exhaled breath was analyzed by electronic nose in 25 children with CF, 25 with PCD and 23 controls. Principle component reduction and canonical discriminant analysis were used to construct internally cross-validated ROC curves.
RESULTS: CF and PCD patients had significantly different breath profiles when compared to healthy controls (CF: sensitivity 84%, specificity 65%; PCD: sensitivity 88%, specificity 52%) and from each other (sensitivity 84%, specificity 60%). Patients with and without exacerbations had significantly different breath profiles (CF: sensitivity 89%, specificity 56%; PCD: sensitivity 100%, specificity 90%).
CONCLUSION: Exhaled molecular profiles significantly differ between patients with CF, PCD and controls. The eNose may have potential in disease monitoring based on the influence of exacerbations on the VOC-profile.
Copyright © 2012 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cystic fibrosis; Electronic nose; Exhaled breath; Primary ciliary dyskinesia; Volatile Organic Compounds

Mesh:

Year:  2013        PMID: 23361110     DOI: 10.1016/j.jcf.2012.12.010

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  12 in total

Review 1.  Mapping targetable inflammation and outcomes with cystic fibrosis biomarkers.

Authors:  Olivia Giddings; Charles R Esther
Journal:  Pediatr Pulmonol       Date:  2017-07-17

Review 2.  Electronic Nose Technology in Respiratory Diseases.

Authors:  Silvano Dragonieri; Giorgio Pennazza; Pierluigi Carratu; Onofrio Resta
Journal:  Lung       Date:  2017-02-25       Impact factor: 2.584

3.  Detection of Airway Colonization by Aspergillus fumigatus by Use of Electronic Nose Technology in Patients with Cystic Fibrosis.

Authors:  K de Heer; M G M Kok; N Fens; E J M Weersink; A H Zwinderman; M P C van der Schee; C E Visser; M H J van Oers; P J Sterk
Journal:  J Clin Microbiol       Date:  2015-12-16       Impact factor: 5.948

4.  Exhaled breath analysis using electronic nose in cystic fibrosis and primary ciliary dyskinesia patients with chronic pulmonary infections.

Authors:  Odin Joensen; Tamara Paff; Eric G Haarman; Ib M Skovgaard; Peter Ø Jensen; Thomas Bjarnsholt; Kim G Nielsen
Journal:  PLoS One       Date:  2014-12-26       Impact factor: 3.240

5.  BreathDx - molecular analysis of exhaled breath as a diagnostic test for ventilator-associated pneumonia: protocol for a European multicentre observational study.

Authors:  Pouline M P van Oort; Tamara Nijsen; Hans Weda; Hugo Knobel; Paul Dark; Timothy Felton; Nicholas J W Rattray; Oluwasola Lawal; Waqar Ahmed; Craig Portsmouth; Peter J Sterk; Marcus J Schultz; Tetyana Zakharkina; Antonio Artigas; Pedro Povoa; Ignacio Martin-Loeches; Stephen J Fowler; Lieuwe D J Bos
Journal:  BMC Pulm Med       Date:  2017-01-03       Impact factor: 3.317

Review 6.  The electronic nose technology in clinical diagnosis: A systematic review.

Authors:  Mariana Valente Farraia; João Cavaleiro Rufo; Inês Paciência; Francisca Mendes; Luís Delgado; André Moreira
Journal:  Porto Biomed J       Date:  2019-07-22

Review 7.  Potential of the Electronic Nose for the Detection of Respiratory Diseases with and without Infection.

Authors:  Johann-Christoph Licht; Hartmut Grasemann
Journal:  Int J Mol Sci       Date:  2020-12-10       Impact factor: 5.923

8.  Exhaled volatile organic compounds analysis in clinical pediatrics: a systematic review.

Authors:  Rosa A Sola Martínez; José M Pastor Hernández; Óscar Yanes Torrado; Manuel Cánovas Díaz; Teresa de Diego Puente; María Vinaixa Crevillent
Journal:  Pediatr Res       Date:  2020-09-12       Impact factor: 3.756

9.  Lessons learned from metabolomics in cystic fibrosis.

Authors:  Marianne S Muhlebach; Wei Sha
Journal:  Mol Cell Pediatr       Date:  2015-10-20

Review 10.  Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review.

Authors:  Adam J Shapiro; Maimoona A Zariwala; Thomas Ferkol; Stephanie D Davis; Scott D Sagel; Sharon D Dell; Margaret Rosenfeld; Kenneth N Olivier; Carlos Milla; Sam J Daniel; Adam J Kimple; Michele Manion; Michael R Knowles; Margaret W Leigh
Journal:  Pediatr Pulmonol       Date:  2015-09-29
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