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Thorax. 2007 August; 62(8): 653–654.
PMCID: PMC2117263

Linking ventilation heterogeneity and airway hyperresponsiveness in asthma

Short abstract

Heterogeneity indices derived from the multiple breath nitrogen washout technique are strongly associated with AHR in asthma

Airway hyperresponsiveness (AHR), inflammation and heterogeneity in airway constriction and ventilation within the airway tree are fundamental features of asthma.1 Heterogeneity in ventilation is relevant not only because it affects gas exchange efficiency (ventilation/perfusion in asthma), but also because it can theoretically magnify the degree of mechanical obstruction2 which could affect the degree of AHR. By thickening of airway walls, increasing airway secretions and releasing mediators, inflammation could also be linked to ventilation heterogeneity and AHR in asthma.3,4 Indeed, the exhaled nitric oxide concentration (FeNO) is substantially increased by inflammation in asthma and has been proposed as a non‐invasive biological marker to guide treatment.5

In this issue of Thorax, Downie and coworkers6 present convincing evidence that ventilation heterogeneity is strongly associated with AHR in patients with asthma, regardless of the level of inflammation (see page 684). In a group of subjects with a wide range of asthma severity, the authors measured, among other parameters, the heterogeneity of the conducting airways by multiple breath nitrogen washout (Scond) and FeNO with AHR to methacholine. A subgroup of patients with poorly controlled symptoms was also studied after 3 months of treatment with inhaled corticosteroids. Analysis of the whole group of patients at baseline showed a positive correlation of AHR with FeNO and Scond, although Scond accounted for almost twice the variance in AHR compared with FeNO. Remarkably, in the treated subgroup, AHR was uniquely associated with Scond, and not with FeNO both before and after corticosteroid treatment. Moreover, the relationship between AHR and Scond was virtually unchanged by treatment (fig 1A and B in their paper). Based on these results, the authors suggest that normalisation of ventilation heterogeneity could be a potential goal of asthma treatment.

These experimental data lead to two important questions: what are the mechanisms responsible for the relationship between Scond and AHR and why is that relationship unchanged by the anti‐inflammatory treatment?

The heterogeneity of ventilation in asthma is well recognised and was noted in very early studies measuring radioactive gas distribution at low spatial resolution using external scintillation counters.7,8,9 More recent studies using single photon emission computed tomography (SPECT)10,11 reported regions of reduced deposition of very small particles (<0.1 μm, Technegas) in asymptomatic subjects with asthma, suggesting the presence of regions of severe hypoventilation or airway closure. Similar regions of low Technegas deposition were seen in subjects with asthma after bronchoprovocation with methacholine, together with foci of increased particle deposition attributed to turbulence within flow‐limiting airways,12 thus linking heterogeneous ventilation with the potential for heterogeneous agonist deposition. Detailed imaging of individual airways by CT scanning has also shown substantial heterogeneity in response to constrictive challenges in animals13 and in patients with asthma.14 Consistent with these findings, magnetic resonance imaging of hyperpolarised 3He has demonstrated large ventilation defective areas in the lungs of asymptomatic individuals15 and in patients with asthma challenged with methacholine and exercise.16 This patchy pattern of ventilation distribution has been quantitatively characterised by positron emission tomography.17,18,19 Because the transport and deposition of an inhaled aerosol strongly depend on the movement of air along the bronchial tree, it can be expected that the regional delivery of methacholine to airways feeding ventilation defective areas in a bronchoconstricted lung could be substantially lower than the delivery to airways feeding well ventilated regions of the lung. This non‐uniform delivery of the agonist would have two additive effects: first, it would expose airways leading to ventilating regions to higher doses of agonist, thus increasing their constrictive response; and, second, this would lead to a greater fraction of the tidal volume being distributed to ventilation defective areas and hence to airways already obstructed. Even if this distributional effect of agonist was relatively small, a recent computational model of the airway tree18 showed that interdependence of forces between parenchyma and airways, the bronchodilating effect of dynamic airway stretching during breathing20 and the dynamic interactions between airways of the bronchial tree could lead to an inherently unstable system during bronchoconstriction that could magnify any small existing heterogeneity.21

The basic mechanism can be visualised by considering two identical daughter branches at an airway bifurcation. Both airways receive equal flows, pressures and tidal volumes, and their behaviour is symmetrical until airway smooth muscle constriction narrows the airway lumen to a critical level. Beyond this point, any small perturbation breaks the equilibrium and a small decrease in tidal volume to one branch reduces stretch to its walls, increasing smooth muscle forces and causing progressive airway narrowing. At the same time, the redistribution of flow to the other branch would cause it to dilate. It has been shown that airway interactions of this kind along the airway tree can lead to a highly heterogeneous response,18 and it is therefore conceivable that a small degree of heterogeneity in baseline ventilation can be greatly magnified during bronchoprovocation, increasing airway hyperreactivity. This could explain why, in spite of a significant reduction in ventilation hetero‐geneity in the subjects treated with inhaled corticosteroid, the association of AHR with the post‐treatment ventilation heterogeneity was virtually unchanged.

Even though AHR was correlated with FeNO in the baseline group of subjects, the puzzling question remains why such an association was not present in the treatment group before or after steroid treatment. Extensive experimental and modelling work has shown that exhaled nitric oxide originates both from airways and parenchyma,22,23 but the effect of ventilation heterogeneity on the FeNO signal remains unexplored. The lack of correlation between FeNO and AHR in the subgroup reportedly selected for having poorly controlled symptoms could in part have been the result of the increased heterogeneity in ventilation affecting the measurement of FeNO.

In summary, this elegant study shows that the indices of heterogeneity derived from the multiple breath nitrogen washout technique are strongly associated with AHR in asthma, and opens up a wide range of clinical and basic research avenues to elucidate the topographical and mechanistic basis of relationships between ventilation heterogeneity, exhaled nitric oxide analysis and AHR.

Footnotes

Funded by HL068011.

Competing interests: None.

References

1. Brown R H. Marching to the beat of different drummers: individual airway response diversity. Eur Respir J 2004. 24193–194.194 [PubMed]
2. Lutchen K R, Jensen A, Atileh H. et al Airway constriction pattern is a central component of asthma severity: the role of deep inspirations. Am J Respir Crit Care Med 2001. 164207–215.215 [PubMed]
3. Obase Y, Shimoda T, Mitsuta K. et al Correlation between airway hyperresponsiveness and airway inflammation in a young adult population: eosinophil, ECP, and cytokine levels in induced sputum. Ann Allergy Asthma Immunol 2001. 86304–310.310 [PubMed]
4. Reid D W, Johns D P, Feltis B. et al Exhaled nitric oxide continues to reflect airway hyperresponsiveness and disease activity in inhaled corticosteroid‐treated adult asthmatic patients. Respirology 2003. 8479–486.486 [PubMed]
5. Taylor D R. Nitric oxide as a clinical guide for asthma management. J Allergy Clin Immunol 2006. 117259–262.262 [PubMed]
6. Downie S R, Salome C M, Verbanck S. et al Ventilation heterogeneity is a major determinant of airway hyperresponsiveness in asthma, independent of airway inflammation. Thorax 2007. 62684–689.689 [PMC free article] [PubMed]
7. Engel L A, Landau L, Taussig L. et al Influence of bronchomotor tone on regional ventilation distribution at residual volume. J Appl Physiol 1976. 40411–416.416 [PubMed]
8. Siegler D, Fukuchi Y, Engel L. Influence of bronchomotor tone on ventilation distribution and airway closure in asymptomatic asthma. Am Rev Respir Dis 1976. 114123–130.130 [PubMed]
9. Filuk R B, Berezanski D J, Anthonisen N R. Airway closure with methacholine‐induced bronchoconstriction. J Appl Physiol 1987. 632223–2230.2230 [PubMed]
10. King G G, Eberl S, Salome C M. et al Airway closure measured by a Technegas bolus and SPECT. Am J Respir Crit Care Med 1997. 155682–688.688 [PubMed]
11. King G G, Eberl S, Salome C M. et al Differences in airway closure between normal and asthmatic subjects measured with single‐photon emission computed tomography and technegas. Am J Respir Crit Care Med 1998. 1581900–1906.1906 [PubMed]
12. Pellegrino R, Biggi A, Papaleo A. et al Regional expiratory flow limitation studied with Technegas in asthma. J Appl Physiol 2001. 912190–2198.2198 [PubMed]
13. Brown R H, Herold C J, Hirshman C A. et al Individual airway constrictor response heterogeneity to histamine assessed by high‐resolution computed tomography. J Appl Physiol 1993. 742615–2620.2620 [PubMed]
14. Kotaru C, Coreno A, Skowronski M. et al Morphometric changes after thermal and methacholine bronchoprovocations. J Appl Physiol 2005. 981028–1036.1036 [PubMed]
15. Altes T A, Powers P L, Knight‐Scott J. et al Hyperpolarized 3He MR lung ventilation imaging in asthmatics: preliminary findings. J Magn Reson Imaging 2001. 13378–384.384 [PubMed]
16. Samee S, Altes T, Powers P. et al Imaging the lungs in asthmatic patients by using hyperpolarized helium‐3 magnetic resonance: assessment of response to methacholine and exercise challenge. J Allergy Clin Immunol 2003. 1111205–1211.1211 [PubMed]
17. Harris R S, Winkler T, Tgavalekos N. et al Regional pulmonary perfusion, inflation, and ventilation defects in bronchoconstricted patients with asthma. Am J Respir Crit Care Med 2006. 174245–253.253 [PMC free article] [PubMed]
18. Venegas J G, Winkler T, Musch G. et al Self‐organized patchiness in asthma as a prelude to catastrophic shifts. Nature 2005. 434777–782.782 [PubMed]
19. Tgavalekos N T, Musch G, Harris R S. et al Relationship between airway narrowing, patchy ventilation and lung mechanics in asthmatics. Eur Respir J. 2007 (epub ahead of print).
20. Fredberg J J, Inouye D, Miller B. et al Airway smooth muscle, tidal stretches, and dynamically determined contractile states. Am J Respir Crit Care Med 1997. 1561752–1759.1759 [PubMed]
21. Anafi R C, Wilson T A. Airway stability and heterogeneity in the constricted lung. J Appl Physiol 2001. 911185–1192.1192 [PubMed]
22. Shin H W, Condorelli P, George S C. A new and more accurate technique to characterize airway nitric oxide using different breath‐hold times. J Appl Physiol 2005. 981869–1877.1877 [PubMed]
23. Shin H W, Schwindt C D, Aledia A S. et al Exercise‐induced bronchoconstriction alters airway nitric oxide exchange in a pattern distinct from spirometry. Am J Physiol Regul Integr Comp Physiol 2006. 291R1741–R1748.R1748 [PubMed]

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