Key result
Active cigarette smoking in asthmatics was associated with higher sputum angiopoietin-2 levels compared to non-smoking asthmatics.
Why the study?
Does inhaled beclomethasone dipropionate alter angiopoietin-1 and -2 levels in smoking and non-smoking asthmatics?
Observational (n=84)
Does inhaled beclomethasone dipropionate alter angiopoietin-1 and -2 levels in smoking and non-smoking asthmatics?
Angiopoietin-2 levels are elevated in smoking asthmatics and decrease with inhaled corticosteroids only when accompanied by smoking cessation, which correlates with improved lung function.
Answers are grounded in this paper and cite their sources.
Elevated airway angiopoietin-2 in smoking asthmatics may mark increased vascular permeability; leaves open whether it drives severity or offers a therapeutic target.
BACKGROUND: Active cigarette smoking has detrimental effects on asthma morbidity and severity. Angiopoietin-1 has been shown to protect the microvessels against plasma leakage, whereas angiopoietin-2 enhances vascular permeability and subsequently induces airway mucosal oedema. Therefore, it is recently thought that angiopoietin-2 may contribute to the pathophysiology of asthma. OBJECTIVE: To determine whether angiopoietin-2 levels in the airways are associated with clinical profiles in smoking asthmatics. METHODS: We measured angiopoietin-1 and -2 levels in induced sputum in 35 normal controls (18 non-smokers and 17 smokers) and 49 asthmatics (24 non-smokers and 25 smokers) before and after inhaled beclomethasone dipropionate (BDP: 800 microg/day) therapy for 12 weeks. RESULTS: Angiopoietin-1 and -2 levels in induced sputum were significantly higher in asthmatics than in normal controls. Moreover, angiopoietin-2 levels were significantly higher in smoking asthmatics than in non-smoking asthmatics (P=0.0001). The airway vascular permeability index was also higher in smoking asthmatics than in non-smoking asthmatics. Moreover, the angiopoietin-2 level was positively correlated with the airway vascular permeability index (non-smoking asthmatics: r=0.87, P<0.001, smoking asthmatics: r=0.64, P=0.002). After BDP therapy, angiopoietin-1 levels were significantly decreased in non-smoking asthmatics, smoking-cessation asthmatics, and active-smoking asthmatics. In contrast, angiopoietin-2 levels did not differ from before to after BDP therapy in non-smoking asthmatics and active-smoking asthmatics. However, its levels were significantly decreased from before to after BDP therapy in smoking-cessation asthmatics (P=0.002). Although forced expiratory volume in 1 s (FEV(1))/forced vital capacity (FVC) before BDP therapy was comparable in all subgroups, this parameter after BDP therapy was significantly lower in active-smoking asthmatics than in non-smoking and smoking-cessation asthmatics. Moreover, the reduction in angiopoietin-2 levels after BDP therapy in smoking-cessation asthmatics was significantly correlated with an improvement in FEV(1)/FVC. CONCLUSION: Angiopoietin-2 levels were elevated in the airways of smoking asthmatics, and its levels were associated with impaired airway responses.
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Kanazawa et al. (2009) conducted an observational in Asthma (n=84). Active cigarette smoking vs. Non-smoking was evaluated on Angiopoietin-2 levels in induced sputum (p=0.0001). Active cigarette smoking in asthmatics was associated with higher sputum angiopoietin-2 levels compared to non-smoking asthmatics.
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