Sputum biomarkers of inflammation and lung function decline in children with cystic fibrosis

scientific article

Sputum biomarkers of inflammation and lung function decline in children with cystic fibrosis is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1164/RCCM.201203-0507OC
P932PMC publication ID3530222
P698PubMed publication ID22904182

P50authorBrandie D WagnerQ46190894
Edith T ZemanickQ59210801
P2093author name stringScott D Sagel
Margaret M Anthony
Peggy Emmett
P2860cites workBiochemical and pathologic evidence for proteolytic destruction of lung connective tissue in cystic fibrosisQ69907533
Elastin and collagen degradation products in urine of patients with cystic fibrosisQ71842481
Sputum peroxidase activity correlates with the severity of lung disease in cystic fibrosisQ72060753
Bronchoalveolar lavage findings in cystic fibrosis patients with stable, clinically mild lung disease suggest ongoing infection and inflammationQ72105394
alpha 1-Proteinase inhibitor, elastase activity, and lung disease severity in cystic fibrosisQ72647013
Predictors of deterioration of lung function in cystic fibrosisQ74054944
Induced sputum inflammatory measures correlate with lung function in children with cystic fibrosisQ78599646
alpha1-Antitrypsin inhalation reduces airway inflammation in cystic fibrosis patientsQ79271331
Prolastin aerosol therapy and sputum taurine in cystic fibrosisQ80300248
Genetic modifiers of lung disease in cystic fibrosisQ81316734
Pulmonary function is negatively correlated with sputum inflammatory markers and cough clearability in subjects with cystic fibrosis but not those with chronic bronchitisQ83310445
Sputum induction in routine clinical care of children with cystic fibrosisQ84568150
17beta-Estradiol inhibits Ca2+-dependent homeostasis of airway surface liquid volume in human cystic fibrosis airway epitheliaQ22306299
High-dose oral N-acetylcysteine, a glutathione prodrug, modulates inflammation in cystic fibrosisQ24545304
Random-effects models for longitudinal dataQ28279619
Standardization of Spirometry, 1994 Update. American Thoracic SocietyQ29547574
Analysis of left-censored longitudinal data with application to viral load in HIV infectionQ30819879
Gender differences in cystic fibrosis: Pseudomonas aeruginosa infectionQ34058988
Mixed models for longitudinal left-censored repeated measuresQ35769431
Sputum biomarkers of inflammation in cystic fibrosis lung diseaseQ36891552
Potential role of high-mobility group box 1 in cystic fibrosis airway disease.Q36935244
Association between pulmonary function and sputum biomarkers in cystic fibrosisQ37287157
Addressing the complexity of chronic obstructive pulmonary disease: from phenotypes and biomarkers to scale-free networks, systems biology, and P4 medicineQ37822219
Airway inflammation in children with cystic fibrosis and healthy children assessed by sputum inductionQ43796663
Levels of free granulocyte elastase in bronchial secretions from patients with cystic fibrosis: effect of antimicrobial treatment against Pseudomonas aeruginosaQ44412123
Longitudinal analysis of pulmonary function decline in patients with cystic fibrosisQ44923126
Microbiology of sputum from patients at cystic fibrosis centers in the United StatesQ44982403
Pulmonary function between 6 and 18 years of age.Q46340194
Safety and efficacy of recombinant alpha(1)-antitrypsin therapy in cystic fibrosisQ46863950
Induced sputum matrix metalloproteinase-9 correlates with lung function and airway inflammation in children with cystic fibrosisQ47870081
Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: analysis of the Cystic Fibrosis Foundation National CF Patient Registry.Q50664409
Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis.Q51745373
Effect of Treatment with Dornase Alpha on Airway Inflammation in Patients with Cystic FibrosisQ61791581
Sputum and serum calprotectin are useful biomarkers during CF exacerbationQ64450091
Aerosol α1 -antitrypsin treatment for cystic fibrosisQ68291975
P433issue9
P407language of work or nameEnglishQ1860
P921main subjectinflammationQ101991
cystic fibrosisQ178194
sputumQ259346
biomarkerQ864574
P304page(s)857-865
P577publication date2012-08-16
P1433published inAmerican Journal of Respiratory and Critical Care MedicineQ4744267
P1476titleSputum biomarkers of inflammation and lung function decline in children with cystic fibrosis
P478volume186

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