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Eckrich, J.* ; Zissler, U.M. ; Serve, F.* ; Leutz, P.* ; Smaczny, C.* ; Schmitt-Grohé, S.* ; Fussbroich, D.* ; Schubert, R.* ; Zielen, S.* ; Eickmeier, O.*

Airway inflammation in mild cystic fibrosis.

J. Cyst. Fibros. 16, 107-115 (2017)
Article in press DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
BACKGROUND: Airway infection and inflammation play major roles in the progression of cystic fibrosis (CF) lung disease. In patients with mild disease, airway inflammation is a clinically relevant and often underdiagnosed feature. Lung function, sputum cell counts, and cytokine profiles in CF with mild disease might be different in patients with and without involvement of small airway disease (SAD). METHODS: Patients with mild CF (n=32) and 22 healthy controls were enrolled in this study. Patients with CF were assigned to two groups: (1) patients without SAD (n=19, median age 12.3years, MEF25>50% predicted), and (2) patients with SAD (n=13 median age, 13.2years, MEF25<50% predicted). Lung function parameters were measured, cells in induced sputum were counted, and cytokines/chemokines (IL-1β, IL-6, IL-8, TNF-α) were analyzed by real-time quantitative PCR (qRT-PCR) and cytometric bead array (CBA). RESULTS: Patients with CF had significant elevated levels of pro-inflammatory genes in qRT-PCR and secreted gene products in CBA compared to controls. Patients with CF and SAD had significantly increased trapped air (RV/TLC) and pronounced airway inflammation compared to controls as indicated by elevated levels of sputum biomarkers like total cells, neutrophils, and IL6. CONCLUSIONS: Our study demonstrated that patients with CF with mild disease defined by lung function might be further endotyped according to their involvement of SAD. In patients with CF and SAD, airway neutrophilic inflammation is more pronounced and is in part distinct from that seen in patients without SAD.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Airway Inflammation ; Cystic Fibrosis ; Gene Expression ; Induced Sputum ; Pro-inflammatory Biomarkers ; Small Airway Disease; Lung Clearance Index; Pseudomonas-aeruginosa; Double-blind; Disease; Children; Association; Antagonist; Profiles; Cftr
ISSN (print) / ISBN 1569-1993
e-ISSN 1873-5010
Zeitschrift Journal of Cystic Fibrosis
Quellenangaben Band: 16, Heft: 1, Seiten: 107-115 Artikelnummer: , Supplement: ,
Verlag Elsevier
Verlagsort Amsterdam
Begutachtungsstatus Peer reviewed
Institut(e) Institute for Allergy Research (IAF)