Markers of Systemic and Lung Inflammation in Childhood Asthma (CROSBI ID 155155)
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Navratil, Marta ; Plavec, Davor ; Dodig, Slavica ; Jelčić, Žaneta ; Nogalo, Boro ; Erceg, Damir ; Turkalj, Mirjana
engleski
Markers of Systemic and Lung Inflammation in Childhood Asthma
Aim: To compare different biomarkers of inflammation in children with controlled and uncontrolled asthma and to investigate their relationship with other clinical indices of asthma control (symptoms, lung function, serum IgE, and prn beta agonist use). Materials and Methods: 62 consecutive asthmatic children (age 11± ; ; 3.3 years, 32 girls) with controlled ([C], n=19) and uncontrolled asthma ([NC], n=43)were studied. Measured lung function and inflammatory biomarkers included: spirometry, exhaled NO (FENO), high-sensitivity C-reactive protein (hs-CRP), peripheral blood white blood cells (WBC) counts and differentials. Result: Hs-CRP was significantly higher in uncontrolled than in controlled asthma (hs-CRP, median[IQR], mg/L ; 0.56 [0.60]vs 0.25 [0.34], P=0.008).Discriminant analysis (backward stepwise)depicted hs-CRP and lymphocytes (as Z-score for absolute count)as significant discriminative factors for asthma control (F=8.319, P=0.0007) with 82.3% diagnostic accuracy. Divided into quartiles hs-CRP showed the significant inverse assocition with FENO (F=7.359, P=0.003, ANOVA)with no significant difference for asthma control (F=1.032, P=0.386). Post-hoc analysis reveled that FENO values were significantly lower in the third and the fourth quartile of hs-CRP in comparsion to the first and second one (P<0.05 for all). Conclusion: In asthmatic children with uncontrolled asthma serum hs-CRP was increased compared to children with cintrolled asthma. Although FENO values were also increased (insignificantly) and inversely correlated with hs-CRP they were probably reflecting different etiology underlying the loss of control. The role of peripheral blood biomarkers in asthmatics is still poorly investigated so new studies are requred.
asthma; biomarkers; C-reactive protein; exhaled nitric oxide; inflammation
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