Clinical patterns in asthma based on proximal and distal airway nitric oxide categories
- Equal contributors
1 Department of Biomedical Engineering, 2420 Engineering Tower, University of California, Irvine, Irvine, CA 92697, USA
2 Institute for Clinical Translational Science, 1115 Hewitt Hall, University of California, Irvine, Irvine, CA 92697, USA
3 Children's Hospital of Orange County, 804 W. Collins, Orange, CA 92868, USA
4 Department of Medicine, 2420 Engineering Tower, University of California, Irvine, Irvine, CA 92697, USA
5 Department of Chemical Engineering and Materials Science, 2420 Engineering Tower, University of California, Irvine, Irvine, CA 92697, USA
Respiratory Research 2010, 11:47 doi:10.1186/1465-9921-11-47Published: 28 April 2010
The exhaled nitric oxide (eNO) signal is a marker of inflammation, and can be partitioned into proximal [J'awNO (nl/s), maximum airway flux] and distal contributions [CANO (ppb), distal airway/alveolar NO concentration]. We hypothesized that J'awNO and CANO are selectively elevated in asthmatics, permitting identification of four inflammatory categories with distinct clinical features.
In 200 consecutive children with asthma, and 21 non-asthmatic, non-atopic controls, we measured baseline spirometry, bronchodilator response, asthma control and morbidity, atopic status, use of inhaled corticosteroids, and eNO at multiple flows (50, 100, and 200 ml/s) in a cross-sectional study design. A trumpet-shaped axial diffusion model of NO exchange was used to characterize J'awNO and CANO.
J'awNO was not correlated with CANO, and thus asthmatic subjects were grouped into four eNO categories based on upper limit thresholds of non-asthmatics for J'awNO (≥ 1.5 nl/s) and CANO (≥ 2.3 ppb): Type I (normal J'awNO and CANO), Type II (elevated J'awNO and normal CANO), Type III (elevated J'awNO and CANO) and Type IV (normal J'awNO and elevated CANO). The rate of inhaled corticosteroid use (lowest in Type III) and atopy (highest in Type II) varied significantly amongst the categories influencing J'awNO, but was not related to CANO, asthma control or morbidity. All categories demonstrated normal to near-normal baseline spirometry; however, only eNO categories with increased CANO (III and IV) had significantly worse asthma control and morbidity when compared to categories I and II.
J'awNO and CANO reveal inflammatory categories in children with asthma that have distinct clinical features including sensitivity to inhaled corticosteroids and atopy. Only categories with increase CANO were related to poor asthma control and morbidity independent of baseline spirometry, bronchodilator response, atopic status, or use of inhaled corticosteroids.