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Diagnostic and prognostic significance of systemic alkyl quinolones for P. aeruginosa in cystic fibrosis: A longitudinal study.
Barr, Helen L; Halliday, Nigel; Barrett, David A; Williams, Paul; Forrester, Douglas L; Peckham, Daniel; Williams, Kate; Smyth, Alan R; Honeybourne, David; L Whitehouse, Joanna; Nash, Edward F; Dewar, Jane; Clayton, Andrew; Knox, Alan J; Cámara, Miguel; Fogarty, Andrew W.
Afiliación
  • Barr HL; Division of Respiratory Medicine, University of Nottingham, City Hospital Campus, Nottingham, UK. Electronic address: Helen.barr@nottingham.ac.uk.
  • Halliday N; School of Life Sciences, Centre for Biomolecular Sciences, University of Nottingham, Nottingham, UK.
  • Barrett DA; Centre for Analytical Bioscience, School of Pharmacy, University of Nottingham, Nottingham, UK.
  • Williams P; School of Life Sciences, Centre for Biomolecular Sciences, University of Nottingham, Nottingham, UK.
  • Forrester DL; Division of Respiratory Medicine, University of Nottingham, City Hospital Campus, Nottingham, UK.
  • Peckham D; Leeds Adult Cystic Fibrosis Centre, St James's University Hospital, Leeds, UK.
  • Williams K; Leeds Adult Cystic Fibrosis Centre, St James's University Hospital, Leeds, UK.
  • Smyth AR; Division of Child Health, Obstetrics and Gynaecology, University of Nottingham, UK.
  • Honeybourne D; West Midlands Adult CF Centre, Heart of England, NHS Foundation Trust, Birmingham, UK.
  • L Whitehouse J; West Midlands Adult CF Centre, Heart of England, NHS Foundation Trust, Birmingham, UK.
  • Nash EF; West Midlands Adult CF Centre, Heart of England, NHS Foundation Trust, Birmingham, UK.
  • Dewar J; Wolfson Cystic Fibrosis Centre, Department of Respiratory Medicine, Nottingham University Hospitals NHS Trust, Nottingham, UK.
  • Clayton A; Wolfson Cystic Fibrosis Centre, Department of Respiratory Medicine, Nottingham University Hospitals NHS Trust, Nottingham, UK.
  • Knox AJ; Division of Respiratory Medicine, University of Nottingham, City Hospital Campus, Nottingham, UK.
  • Cámara M; School of Life Sciences, Centre for Biomolecular Sciences, University of Nottingham, Nottingham, UK.
  • Fogarty AW; Division of Epidemiology and Public Health, University of Nottingham, Clinical Sciences Building, University of Nottingham, Nottingham, UK.
J Cyst Fibros ; 16(2): 230-238, 2017 Mar.
Article en En | MEDLINE | ID: mdl-27773591
BACKGROUND: Pulmonary P. aeruginosa infection is associated with poor outcomes in cystic fibrosis (CF) and early diagnosis is challenging, particularly in those who are unable to expectorate sputum. Specific P. aeruginosa 2-alkyl-4-quinolones are detectable in the sputum, plasma and urine of adults with CF, suggesting that they have potential as biomarkers for P. aeruginosa infection. AIM: To investigate systemic 2-alkyl-4-quinolones as potential biomarkers for pulmonary P. aeruginosa infection. METHODS: A multicentre observational study of 176 adults and 68 children with CF. Cross-sectionally, comparisons were made between current P. aeruginosa infection using six 2-alkyl-4-quinolones detected in sputum, plasma and urine against hospital microbiological culture results. All participants without P. aeruginosa infection at baseline were followed up for one year to determine if 2-alkyl-4-quinolones were early biomarkers of pulmonary P. aeruginosa infection. RESULTS: Cross-sectional analysis: the most promising biomarker with the greatest diagnostic accuracy was 2-heptyl-4-hydroxyquinoline (HHQ). In adults, areas under the ROC curves (95% confidence intervals) for HHQ analyses were 0.82 (0.75-0.89) in sputum, 0.76 (0.69-0.82) in plasma and 0.82 (0.77-0.88) in urine. In children, the corresponding values for HHQ analyses were 0.88 (0.77-0.99) in plasma and 0.83 (0.68-0.97) in urine. Longitudinal analysis: Ten adults and six children had a new positive respiratory culture for P. aeruginosa in follow-up. A positive plasma HHQ test at baseline was significantly associated with a new positive culture for P. aeruginosa in both adults and children in follow-up (odds ratio (OR)=6.67;-95% CI:-1.48-30.1;-p=0.01 and OR=70; 95% CI: 5-956;-p<0.001 respectively). CONCLUSIONS: AQs measured in sputum, plasma and urine may be used to diagnose current infection with P. aeruginosa in adults and children with CF. These preliminary data show that plasma HHQ may have potential as an early biomarker of pulmonary P. aeruginosa. Further studies are necessary to evaluate if HHQ could be used in clinical practice to aid early diagnosis of P. aeruginosa infection in the future.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pseudomonas aeruginosa / Infecciones por Pseudomonas / Infecciones del Sistema Respiratorio / Quinolonas / Fibrosis Quística Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adult / Child / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: J Cyst Fibros Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pseudomonas aeruginosa / Infecciones por Pseudomonas / Infecciones del Sistema Respiratorio / Quinolonas / Fibrosis Quística Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adult / Child / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: J Cyst Fibros Año: 2017 Tipo del documento: Article
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