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Published on: August 7, 2017
Markers of systemic and lung inflammation in childhood asthma
M Navratil1, D Plavec, S Dodig
1Srebrnjak Children's Hospital, Reference Center for Clinical Pediatric Allergology of the Ministry of Health and Social Welfare, Zagreb, Croatia.
Insights
In children with asthma, higher serum high-sensitivity C-reactive protein (hs-CRP) indicates uncontrolled disease. Hs-CRP and lymphocyte counts effectively differentiate asthma control, with hs-CRP inversely correlating with exhaled nitric oxide (F(E)NO).
Area of Science:
- Pediatric Allergy and Immunology
- Respiratory Medicine
- Biomarker Research
Background:
- Asthma control in children is crucial for long-term health.
- Identifying reliable biomarkers for asthma control is an ongoing challenge.
- Inflammation plays a key role in asthma pathophysiology.
Purpose of the Study:
- To compare inflammatory biomarkers in children with controlled versus uncontrolled asthma.
- To investigate the relationship between biomarkers and clinical asthma control indices.
- To assess the diagnostic accuracy of biomarkers for asthma control.
Main Methods:
- Studied 62 children with asthma (19 controlled, 43 uncontrolled).
- Measured spirometry, exhaled nitric oxide (F(E)NO), high-sensitivity C-reactive protein (hs-CRP), and white blood cell counts.
- Utilized discriminant analysis to identify significant factors for asthma control.
Main Results:
- Serum hs-CRP levels were significantly higher in children with uncontrolled asthma.
- Hs-CRP and lymphocyte counts were significant discriminators of asthma control with 82.3% accuracy.
- Hs-CRP showed a significant inverse association with F(E)NO, with lower F(E)NO at higher hs-CRP levels.
Conclusions:
- Elevated serum hs-CRP is associated with uncontrolled asthma in children.
- Hs-CRP and F(E)NO may reflect different underlying etiologies for asthma control loss.
- Further research is needed on the role of peripheral blood biomarkers in pediatric 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:
A total of 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 (F(E)NO), high-sensitivity C-reactive protein (hs-CRP), peripheral blood white blood cells (WBC) counts, and differentials.
Results:
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 association with F(E)NO (F = 7.359, p = 0.003, ANOVA) with no significant difference for asthma control (F = 1.032, p = 0.386). Post-hoc analysis revealed that F(E)NO values were significantly lower in the third and the fourth quartile of hs-CRP in comparison to the first and the second one (p < 0.05 for all).
Conclusion:
In asthmatic children with uncontrolled asthma serum hs-CRP was increased compared to children with controlled asthma. Although F(E)NO 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 required.
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