Rationale: Glutathione is the major antioxidant in the extracellular lining fluid of the lungs and depleted in patients with cystic fibrosis (CF). Objectives: We aimed to assess glutathione delivered by inhalation as a potential treatment for CF lung disease. Methods: This randomized, double-blind, placebo-controlled trial evaluated inhaled glutathione in subjects with CF 8 years of age and older and FEV1 of 40-90% of predicted. Subjects were randomized to receive 646 mg glutathione in 4 ml (n = 73) or placebo (n = 80) via an investigational eFlow nebulizer every 12 hours for 6 months. Measurements and Main Results: FEV1 (absolute values), both as pre-post differences (P = 0.180) and as area under the curves (P = 0.205), were the primary ef...
Rationale: Pulmonary infection and malnutrition in cystic fibrosis are associated with decreased sur...
Background: Impaired mucociliary clearance characterises lung disease in cystic fibrosis (CF).Hypert...
The airway surface liquid (ASL) of Cystic Fibrosis (CF) patients contains a lower concentration of r...
Background: In cystic fibrosis (CF) the defective CF transmembrane conductance regulator protein may...
Background: In cystic fibrosis (CF) the defective CF transmembrane conductance regulator protein may...
In CF patients, Glutathione (GSH), the first-line defence of lungs against oxidative stress, is seve...
Glutathione (GSH) is decreased in cystic fibrosis (CF) airways, thus its resupply by inhalation has ...
The sustained imbalance between oxidant and antioxidant species contributes to lung damage in patien...
This is the publisher's version, also available electronically from http://www.atsjournals.org/doi/a...
AbstractBackground: Reduced glutathione (GSH) is a major antioxidant in the lung. In cystic fibrosis...
AbstractCFTR mutation, which causes cystic fibrosis (CF), has also recently been identified as causi...
Glutathione is an important antioxidant in the lungs but its concentration is low in the airways of ...
AbstractBackground: The lung disease of cystic fibrosis is associated with a chronic inflammatory re...
-Nitrosoglutathione (GSNO), a naturally occurring constituent of airway lining fluid, enhances cilia...
BACKGROUND Cystic fibrosis is an inherited condition resulting in thickened, sticky respiratory s...
Rationale: Pulmonary infection and malnutrition in cystic fibrosis are associated with decreased sur...
Background: Impaired mucociliary clearance characterises lung disease in cystic fibrosis (CF).Hypert...
The airway surface liquid (ASL) of Cystic Fibrosis (CF) patients contains a lower concentration of r...
Background: In cystic fibrosis (CF) the defective CF transmembrane conductance regulator protein may...
Background: In cystic fibrosis (CF) the defective CF transmembrane conductance regulator protein may...
In CF patients, Glutathione (GSH), the first-line defence of lungs against oxidative stress, is seve...
Glutathione (GSH) is decreased in cystic fibrosis (CF) airways, thus its resupply by inhalation has ...
The sustained imbalance between oxidant and antioxidant species contributes to lung damage in patien...
This is the publisher's version, also available electronically from http://www.atsjournals.org/doi/a...
AbstractBackground: Reduced glutathione (GSH) is a major antioxidant in the lung. In cystic fibrosis...
AbstractCFTR mutation, which causes cystic fibrosis (CF), has also recently been identified as causi...
Glutathione is an important antioxidant in the lungs but its concentration is low in the airways of ...
AbstractBackground: The lung disease of cystic fibrosis is associated with a chronic inflammatory re...
-Nitrosoglutathione (GSNO), a naturally occurring constituent of airway lining fluid, enhances cilia...
BACKGROUND Cystic fibrosis is an inherited condition resulting in thickened, sticky respiratory s...
Rationale: Pulmonary infection and malnutrition in cystic fibrosis are associated with decreased sur...
Background: Impaired mucociliary clearance characterises lung disease in cystic fibrosis (CF).Hypert...
The airway surface liquid (ASL) of Cystic Fibrosis (CF) patients contains a lower concentration of r...