Elevated glucose concentrations in respiratory droplets of cystic fibrosis patients

R. M. Effros, J. Biller, F. Sun, B. Foss (Milwaukee, United States Of America)

Source: Annual Congress 2002 - Respiratory problems and new ways of evaluating the patient with cystic fibrosis
Session: Respiratory problems and new ways of evaluating the patient with cystic fibrosis
Session type: Thematic Poster Session
Number: 3281
Disease area: Respiratory infections

Congress or journal article abstract

Rating: 0
You must login to grade this presentation.

Share or cite this content

Citations should be made in the following way:
R. M. Effros, J. Biller, F. Sun, B. Foss (Milwaukee, United States Of America). Elevated glucose concentrations in respiratory droplets of cystic fibrosis patients. Eur Respir J 2002; 20: Suppl. 38, 3281

You must login to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.

Member's Comments

No comment yet.
You must Login to comment this presentation.


Related content which might interest you:
Serum lipid concentrations and malnutrition in adult cystic fibrosis patients
Source: Eur Respir J 2006; 28: Suppl. 50, 58s
Year: 2006

KL-6 serum levels in adult cystic fibrosis patients
Source: Annual Congress 2011 - Cystic fibrosis: clinical and laboratory studies
Year: 2011

Serum lipid levels in patients with bronchiectasis
Source: Annual Congress 2008 - Aetiology of respiratory infections: mycobacteria and fungi
Year: 2008

Lung function parameters influence serum concentration after antibiotic inhalation in patients with cystic fibrosis
Source: Eur Respir J 2001; 18: Suppl. 33, 537s
Year: 2001

Glucose tolerance during pulmonary exacerbations in children with cystic fibrosis
Source: Annual Congress 2011 - Cystic fibrosis: new basic, clinical and bacteriological knowledge
Year: 2011


Sputum glucose as a marker of disease severity in adult patients with cystic fibrosis
Source: International Congress 2018 – Cystic fibrosis in adults: current research
Year: 2018


Plasma leakage is elevated in COPD airways
Source: Eur Respir J 2005; 26: Suppl. 49, 441s
Year: 2005

Plasma surfactant protein A levels are increased in smokers but do not correlate with respiratory symptoms and airway obstruction
Source: Annual Congress 2010 - COPD: phenotyping and monitoring
Year: 2010

Detection of elevated 2-propanol in breath samples from children with cystic fibrosis
Source: Eur Respir J 2006; 28: Suppl. 50, 309s
Year: 2006

Reduced uptake of inhaled carbon in airway macrophages from children with cystic fibrosis
Source: International Congress 2018 – Latest developments in cystic fibrosis
Year: 2018



Relation of serum IGF-1 and IGFBP3 levels with acute exacerbation in cystic fibrosis
Source: International Congress 2018 – Clinical problems in paediatric pulmonology
Year: 2018

Airway bacterial colonization is associated with low vitamin D serum levels in children with cystic fibrosis
Source: Annual Congress 2013 –Cystic fibrosis: clinical problems, genetics and microbiology in children
Year: 2013


Serum lipid profile and iron content in serum and pulmonary tissue in experimental pulmonary emphysema
Source: Annual Congress 2011 - Recent developments in COPD
Year: 2011

Serum bactericidal activity in non cystic fibrosis bronchiectasis in patients with pseudomonas aeruginosa colonisation
Source: Annual Congress 2011 - Pseudomonas aeruginosa infection and non-cystic fibrosis bronchiectasis
Year: 2011

Serial change in serum KL-6 levels correlate with the pulmonary function variables in cystic fibrosis
Source: Annual Congress 2010 - Cystic fibrosis: lung disease and much more
Year: 2010

Serum progranulin levels in idiopathic pulmonary fibrosis and other interstitial lung diseases
Source: International Congress 2018 – Idiopathic interstital pneumonias other than idiopathic pulmonary fibrosis (IPF)
Year: 2018

Changes in lung gas mixing after physiotherapy in adults with cystic fibrosis
Source: Annual Congress 2007 - Critical care and airways clearance
Year: 2007


Sputum and plasma adiponectin levels in clinically stable adult cystic fibrosis patients with CFTR I1234V mutation
Source: International Congress 2018 – Cystic fibrosis in adults: current research
Year: 2018


Pathological mucus and impaired mucus clearance in cystic fibrosis patients result from increased concentration, not altered pH
Source: Eur Respir J, 52 (6) 1801297; 10.1183/13993003.01297-2018
Year: 2018



Cyanide levels found in infected cystic fibrosis sputum inhibit airway ciliary function
Source: Eur Respir J 2014; 44: 1253-1261
Year: 2014