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Details

Autor(en) / Beteiligte
Titel
Cystic fibrosis lung disease starts in the small airways: Can we treat it more effectively?
Ist Teil von
  • Pediatric pulmonology, 2010-02, Vol.45 (2), p.107-117
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
2010
Link zum Volltext
Quelle
MEDLINE
Beschreibungen/Notizen
  • The aims of this article are to summarize existing knowledge regarding the pathophysiology of small airways disease in cystic fibrosis (CF), to speculate about additional mechanisms that might play a role, and to consider the available or potential options to treat it. In the first section, we review the evidence provided by pathologic, physiologic, and imaging studies suggesting that obstruction of small airways begins early in life and is progressive. In the second section we discuss how the relationships between CF transmembrane conductance regulator (CFTR), ion transport, the volume of the periciliary liquid layer and airway mucus might lead to defective mucociliary clearance in small airways. In addition, we discuss how chronic endobronchial bacterial infection and a chronic neutrophilic inflammatory response increase the viscosity of CF secretions and exacerbate the clearance problem. Next, we discuss how the mechanical properties of small airways could be altered early in the disease process and how remodeling can contribute to small airways disease. In the final section, we discuss how established therapies impact small airways disease and new directions that may lead to improvement in the treatment of small airways disease. We conclude that there are many reasons to believe that small airways play an important role in the pathophysiology of (early) CF lung disease. Therapy should be aimed to target the small airways more efficiently, especially with drugs that can correct the basic defect at an early stage of disease. Pediatr Pulmonol. 2010; 45:107–117. © 2010 Wiley‐Liss, Inc.
Sprache
Englisch
Identifikatoren
ISSN: 8755-6863
eISSN: 1099-0496
DOI: 10.1002/ppul.21154
Titel-ID: cdi_proquest_miscellaneous_733842097
Format
Schlagworte
Administration, Inhalation, airway obstruction, Airway Obstruction - diagnostic imaging, Airway Obstruction - drug therapy, Airway Obstruction - physiopathology, Airway Remodeling - drug effects, Airway Remodeling - physiology, Anti-Inflammatory Agents - administration & dosage, Anti-Inflammatory Agents - therapeutic use, Biological and medical sciences, Child, Child, Preschool, Chronic obstructive pulmonary disease, asthma, cystic fibrosis, Cystic Fibrosis - diagnostic imaging, Cystic Fibrosis - drug therapy, Cystic Fibrosis - physiopathology, cystic fibrosis transmembrane conductance regulator, Cystic Fibrosis Transmembrane Conductance Regulator - metabolism, Cystic Fibrosis Transmembrane Conductance Regulator - physiology, Deoxycytosine Nucleotides - administration & dosage, Deoxycytosine Nucleotides - therapeutic use, Errors of metabolism, General aspects, Humans, Infant, Ion Transport - physiology, lung diseases, Mannitol - administration & dosage, Mannitol - therapeutic use, Medical sciences, Metabolic diseases, Miscellaneous hereditary metabolic disorders, mucociliary clearance, Mucociliary Clearance - drug effects, Mucus - diagnostic imaging, Mucus - physiology, Neutrophils - drug effects, Neutrophils - pathology, obstructive, Pneumology, Pneumonia, Bacterial - pathology, pulmonary, Pulmonary Alveoli - diagnostic imaging, Pulmonary Alveoli - physiology, Pulmonary Alveoli - physiopathology, Radiography, Respiratory Mucosa - drug effects, Respiratory Mucosa - physiopathology, Sodium Channel Blockers - administration & dosage, Sodium Channel Blockers - therapeutic use, Uridine - administration & dosage, Uridine - analogs & derivatives, Uridine - therapeutic use, Young Adult

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