Exhaled breath profiles to detect lung infection with Staphylococcus aureus in children with cystic fibrosis

被引:6
|
作者
Licht, Johann-Christoph [1 ,2 ,3 ]
Seidl, Elias [1 ,2 ]
Slingers, Gitte [4 ]
Waters, Valerie [1 ,3 ,5 ]
de Vries, Rianne [4 ]
Post, Martin [3 ]
Ratjen, Felix [1 ,2 ,3 ]
Grasemann, Hartmut [1 ,2 ,3 ]
机构
[1] Hosp Sick Children, Dept Pediat, Div Resp Med, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Toronto, ON, Canada
[3] Hosp Sick Children, Translat Med, Res Inst, Toronto, ON M5G 1X8, Canada
[4] Beathomix BV, Bargelaan 200, NL-2333 CW Leiden, Netherlands
[5] Hosp Sick Children, Dept Pediat, Div Infect Dis, Toronto, ON M5G 1X8, Canada
关键词
Electronic nose; Cystic fibrosis; Respiratory disease; Respiratory infections; Volatile organic compounds; Staphylococcus aureus; Pseudomonas aeruginosa; ELECTRONIC NOSE TECHNOLOGY; BRONCHOALVEOLAR LAVAGE; CFTR POTENTIATOR; INFLAMMATION; DIAGNOSIS; BIOMARKER; IVACAFTOR;
D O I
10.1016/j.jcf.2023.02.010
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: An electronic nose (eNose) can be used to detect volatile organic compounds (VOCs). Ex-haled breath contains numerous VOCs and individuals' VOCs mixtures create distinct breath profiles. Previous reports have shown that eNose can detect lung infections. Whether eNose can detect Staphy-lococcus aureus airway infections in breath of children with cystic fibrosis (CF) is currently unclear.Methods: In this cross-sectional observational study, a cloud-connected eNose was used for breath profile analysis of clinically stable paediatric CF patients with airway microbiology cultures positive or negative for CF pathogens. Data-analysis involved advanced signal processing, ambient correction and statistics based on linear discriminant and receiver operating characteristics (ROC) analyses.Results: Breath profiles from 100 children with CF (median predicted FEV1 91%) were obtained and analysed. CF patients with positive airway cultures for any CF pathogen were distinguishable from no CF pathogens (no growth or usual respiratory flora) with accuracy of 79.0% (AUC-ROC 0.791; 95% CI: 0.669- 0.913) and between patients positive for Staphylococcus aureus (SA) only and no CF pathogen with accuracy of 74.0% (AUC-ROC 0.797; 95% CI: 0.698-0.896). Similar differences were seen for Pseudomonas aeruginosa (PA) infection vs no CF pathogens (78.0% accuracy, AUC-ROC 0.876, 95% CI: 0.794-0.958). SA-and PA-specific signatures were driven by different sensors in the SpiroNose suggesting pathogen-specific breath signatures.Conclusions: Breath profiles of CF patients with SA in airway cultures are distinct from those with no infection or PA infection, suggesting the utility of eNose technology in the detection of this early CF pathogen in children with CF.(c) 2023 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:888 / 893
页数:6
相关论文
共 50 条
  • [21] Exhaled breath analysis by ion mobility spectrometry in children with asthma and cystic fibrosis
    Bannier, Michiel
    Van De Kant, Kim
    Baumbach, Jorg
    Jobsis, Quirijn
    Dompeling, Edward
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2018, 52
  • [22] Biomarkers in exhaled breath condensate indicate presence and severity of cystic fibrosis in children
    Robroeks, Charlotte M. H. H. T.
    Rosias, Philippe P. R.
    Van Vliet, Dillys
    Jobsis, Quirijn
    Yntema, Jan-Bart L.
    Brackel, Hein J. L.
    Damoiseaux, Jan G. M. C.
    den Hartog, Gertjan M.
    Wodzig, Will K. W. H.
    Dompeling, Edward
    [J]. PEDIATRIC ALLERGY AND IMMUNOLOGY, 2008, 19 (07) : 652 - 659
  • [23] Linezolid-Resistant Staphylococcus aureus in Children With Cystic Fibrosis
    Yu, Diana
    Stach, Leslie M.
    Newland, Jason G.
    [J]. JOURNAL OF THE PEDIATRIC INFECTIOUS DISEASES SOCIETY, 2015, 4 (04) : E163 - E165
  • [24] Host response to Staphylococcus aureus cytotoxins in children with cystic fibrosis
    Chadha, Ashley D.
    Thomsen, Isaac P.
    Jimenez-Truque, Natalia
    Soper, Nicole R.
    Jones, Lauren S.
    Sokolow, Andrew G.
    Torres, Victor J.
    Creech, C. Buddy
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2016, 15 (05) : 597 - 604
  • [25] VITAMIN D DEFICIENCY IS NOT ASSOCIATED WITH PSEUDOMONAS AERUGINOSA OR STAPHYLOCOCCUS AUREUS INFECTION IN CHILDREN WITH CYSTIC FIBROSIS
    Thursfield, R. M.
    Bush, A.
    Alton, E. W.
    Davies, J. C.
    [J]. PEDIATRIC PULMONOLOGY, 2014, 49 : 346 - 347
  • [26] THE LUNG CLEARANCE INDEX IS SENSITIVE TO DETECT INFLAMMATION AND INFECTION IN PRESCHOOL CHILDREN WITH CYSTIC FIBROSIS
    Ramsey, K.
    Ranganathan, S.
    Grdosic, J.
    Skoric, B.
    Stick, S. M.
    Hall, G.
    [J]. PEDIATRIC PULMONOLOGY, 2015, 50 : 358 - 358
  • [27] Ability of the lung clearance index to detect inflammation and infection in preschool children with cystic fibrosis
    Ramsey, Kathryn
    Ranganathan, Sarath
    Grdosic, Jasmine
    Skoric, Billy
    Stick, Stephen
    Hall, Graham
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2015, 46
  • [28] Slower rise of exhaled breath temperature in cystic fibrosis
    Geetanjali Bade
    Sumita Gupta
    Sushil Kumar Kabra
    Anjana Talwar
    [J]. Indian Pediatrics, 2015, 52 : 125 - 127
  • [29] Exhaled breath condensate pH in patients with cystic fibrosis
    Antus, Balazs
    Barta, Imre
    Csiszer, Eszter
    Kelemen, Krisztina
    [J]. INFLAMMATION RESEARCH, 2012, 61 (10) : 1141 - 1147
  • [30] Increased nitrotyrosine in exhaled breath condensate in cystic fibrosis
    Balint, B
    Kharitonov, SA
    Hanazawa, T
    Donnelly, LE
    Shah, PL
    Hodson, ME
    Barnes, PJ
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2001, 17 (06) : 1201 - 1207