Serum KL-6 as a novel disease marker in adolescent and adult cystic fibrosis

Cystic fibrosis (CF) is a chronic progressive disease leading to obstructive pulmonary impairment, fibrosis and shortened life expectancy. Serum levels of KL-6, high molecular weight human MUC1 mucin, are increased in the majority of patients with various interstitial lung disorders. Whether they ar...

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Veröffentlicht in:	Sarcoidosis, vasculitis, and diffuse lung diseases vasculitis, and diffuse lung diseases, 2009-07, Vol.26 (1), p.47-53
Hauptverfasser:	Ohshimo, S, Bonella, F, Grammann, N, Starke, K, Cui, A, Bauer, P C, Teschler, H, Kohno, N, Guzman, J, Costabel, U
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Age Factors Biomarkers - blood C-Reactive Protein - metabolism Case-Control Studies Cross-Sectional Studies Cystic Fibrosis - diagnosis Cystic Fibrosis - immunology Cystic Fibrosis - physiopathology Female Forced Expiratory Volume Humans L-Lactate Dehydrogenase - blood Lung - physiopathology Male Middle Aged Mucin-1 - blood Predictive Value of Tests ROC Curve Severity of Illness Index Up-Regulation Vital Capacity Young Adult
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