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Eur Respir J 2004; 24:122-128
Copyright ©ERS Journals Ltd 2004

Parameters associated with persistent airflow obstruction in chronic severe asthma

D. Bumbacea1, D. Campbell2, L. Nguyen2, D. Carr2, P.J. Barnes2, D. Robinson2 and K.F. Chung2

1 Clinica de Pneumologie, Institutul National de Pneumologie "Marius Nasta", Universitatea de Medicina si Farmacie, Carol Davila, Bucharest, Romania. 2 Asthma and Allergy Research Group, Royal Brompton and Harefield NHS Trust, and National Heart and Lung Institute, Imperial College, London, UK

CORRESPONDENCE: K.F. Chung, National Heart and Lung Institute, Imperial College School ofMedicine, Dovehouse Street, London SW36LY, UK. Fax: 44 2073518126. E-mail: f.chung@imperial.ac.uk

Keywords: Airway remodelling, airway thickening, eosinophils, severe asthma

Received: July 7, 2003
Accepted March 15, 2004

This work was supported by the Royal Brompton and Harefield NHS Trust, and European Respiratory Society Research Fellowships to D. Bumbacea and L. Nguyen.


   Abstract
TOP
 Abstract
Methods
 Results
 Discussion
 References
 
The significance of severe airflow obstruction in severe asthma is unclear. The current study determined whether severe airflow obstruction is related to inflammatory or structural changes in the airways.

Patients with severe asthma from a tertiary referral clinic were divided into two groups according to their postbronchodilator forced expiratory volume in one second (FEV1): severe persistent airflow limitation (FEV1 <50% predicted; group S; n=37) and no obstruction (FEV1 >80% pred; group N; n=29). Smoking history, atopic status, lung function tests, exhaled NO, blood eosinophil count, quality of life scores using St George's Respiratory Questionnaire and high resolution computed tomography (HRCT) of the lungs were assessed.

Patients from group S were older and had longer disease duration. There was no difference in smoking history, atopic status, hospital admissions, quality of life scores and amount of treatment with inhaled or oral corticosteroids. Exhaled NO and peripheral blood eosinophils were higher in group S (21.0±2.4 versus 12.8±2.3 ppb; 0.41±0.06 versus 0.15±0.03x109cells·L–1, respectively). HRCT scores for bronchial wall thickening and dilatation were higher in group S with no differences in air trapping. Peripheral blood eosinophilia and bronchial wall thickening on HRCT scan were the only parameters significantly and independently associated with persistent airflow obstruction.

Patients with severe asthma and irreversible airflow obstruction had longer disease duration, a greater inflammatory process and more high resolution computed tomography airway abnormalities suggestive of airway remodelling, despite being on similar treatments and experiencing equivalent impairment in quality of life.

Asthma is a chronic inflammatory disorder of the airways characterised by recurrent symptoms associated with airflow limitation and by bronchial hyperresponsiveness. Inhaled corticosteroids, which suppress airway inflammation, are efficient in reducing symptoms and exacerbations, and often normalise lung function. However, a proportion of patients with asthma are not controlled and have persistent symptoms, recurrent exacerbations and/or persistent airflow limitation despite using high doses of inhaled corticosteroids (and often oral corticosteroids) and long-acting bronchodilators. This small proportion of asthmatics, labelled with difficult/therapy-resistant 1 or refractory 2 asthma, experience greater morbidity with severe derangement of quality of life and the use of a disproportionate amount of healthcare resources 3.

The clinical spectrum of severe asthma is variable, ranging from life-threatening attacks superimposed on disease-free periods (brittle asthma 4) to severe chronic persistent symptoms. Patients may have normal lung function between exacerbations (reversible disease) or persistent, sometimes severe, airflow limitation that may only be partially reversible to asthma medication, such as ß2-adrenergic bronchodilators or corticosteroids. Persistent airway inflammation with eosinophilic or neutrophilic predominance 5, 6, features of airway remodelling 7, airway inflammation with remodelling in the small airways 8 or a combination of the above have been described. The causes of persistent airflow obstruction in chronic severe asthma are unknown but may be related to the presence of airway wall remodelling, with increased airway smooth muscle mass and airway wall fibrosis, or to persistent airway inflammation that could lead to persistent release of bronchoconstrictor mediators. In a recent study, a strong association between sputum eosinophilia and persistent airflow obstruction in asthmatic patients has been reported 9. However, a forced expiratory volume in one second (FEV1) of <75% predicted was used as a cut-off level for severe airflow obstruction.

In order to further unravel the associations between severe asthma with airflow obstruction, the current study compared various characteristics of severe asthma patients with severe persistent airflow obstruction to those with normal lung function, including noninvasive measures of inflammation using exhaled NO measurements and blood eosinophil counts, and a measure of airway wall thickness as assessed by high resolution computed tomography (HRCT). A more severe value of 50% FEV1 predicted was used as the cut-off point.


   Methods
TOP
 Abstract
 Methods
Results
 Discussion
 References
 
Severe asthma protocol
Patients referred to the Royal Brompton Hospital, London, with a presumed diagnosis of severe asthma underwent a structured assessment protocol as to diagnosis and treatment. Asthma was diagnosed on the basis of chronic symptoms and/or of recurrent exacerbations together with previously documented reversible airflow obstruction of >15% either spontaneously or with treatment. Asthma was considered severe because of persistent symptoms and/or recurrent exacerbations despite the use of high dose inhaled steroid therapy, and often in addition to needing regular oral steroid therapy. For this study, the data from the first 175 patients referred to the severe asthma protocol were examined from the database. The systematic assessment of the first 100 patients of difficult-to-treat asthma has recently been reported 10 and the current authors have also described the distribution of exhaled nitric oxide measurements in the first 52 patients 11.

Patient characteristics
For the purposes of the present study, two groups of patients were obtained from the current authors' database: one with severe persistent airflow obstruction (group S) as defined by a postbronchodilator FEV1 <50% pred (n=51), and the other without airflow obstruction (group N) with a postbronchodilator FEV1 >80% pred (n=41). These were postbronchodilator FEV1, and had not varied by >10% when repeated within 3–6 months. All patients were assessed during a 3-day hospital admission when the history, clinical and laboratory findings regarding the diagnosis of asthma were reviewed. Patients were reviewed again 3–6 months later when the diagnosis of asthma was either confirmed or refuted. In this way, 14 were excluded from group S and 12 from group N. In those in group S that were excluded for the presence ofsignificant concomitant diseases, these included: chronic obstructive pulmonary disease (COPD) (n=5), allergic bronchopulmonary aspergillosis (n=2), Churg Strauss syndrome (n=1), hypereosinophilic syndrome (n=1), bronchiolitis (n=1), bronchiectasis (n=1), pulmonary artery stenosis (n=1), significant exposure to coal dust in an exminer (n=1) and refusal to take oral corticosteroids (n=1). Patients were diagnosed with COPD on the basis of a lack of previous history of reversible airflow obstruction. Patients that were excluded from group N did not fit the criteria for severe asthma and had mild-to-moderate asthma. Therefore, using the criteria for this study, the analysis was performed in 37 S and 29 N patients.

Measurements and investigations
FEV1 and forced vital capacity (FVC) were measured using a spirometer (Erich Jaeger UK Ltd, Market Harborough, UK) using published predicted values 12. Diffusing capacity to carbon monoxide and lung volumes (residual volume (RV), and total lung capacity (TLC)) were measured with a body plethysmograph (Master Lab; Erich Jaeger UK Ltd). The maximal bronchodilator response was determined 30 min after inhaling salbutamol (400 µg) after discontinuation of short-acting ß2-agonist for 4 h, and of long-acting ß-agonist for at least 12 h. Peak flow measurements were recorded in the morning and in the evening, and peak flow variability over 2 weeks was expressed as amplitude mean per cent 13. Patients continued with their maintenance bronchodilator therapy, such as long-acting ß-agonists or subcutaneous terbutaline, while performing these peak flow measurements.

Exhaled NO was measured with a chemiluminescence analyser (model LR2000; Logan Research Ltd., Rochester, UK), as previously described 11. The mean of two consecutive measurements was recorded. Quality of life was assessed using the St George's Respiratory Questionnaire 14. The presence of atopy was defined by the presence of a positive skin-prick test to at least two aeroallergens (house dust mite, mixed grass pollen, cat dander and dog dander).

HRCT scans were performed on full inspiration and at end-expiration using an Imatron Ultrafast CT scanner (Imatron, San Francisco, CA, USA). The abnormalities of intrapulmonary bronchi (wall thickening and dilatation) and the degree of air trapping were evaluated according to a previously published score system 15. Each pulmonary lobe was evaluated for bronchial wall thickening and dilatation (score 0–3) and for air trapping (score 0–2). The total extent of changes for each abnormality for each patient was obtained on a 19-point scale (0–18) for bronchial wall thickening and dilatation and a 13-point scale (0–12) for air trapping.

Statistical analysis
Data were expressed either as mean±sem and compared using the unpaired t-test for normally-distributed continuous variables, or alternatively as median (interquartile range) for ordinal variables and for non-normally distributed continuous variables and compared using the Mann-Whitney U-test. Proportions were compared using the Chi-squared test. Logistic regression analysis was used to compute estimated OR for the presence of severe airflow limitation for each factor found significantly different between the two groups. Multiple logistic regression analysis was used to compute the adjusted OR (for possible confounding factors) and to assess the independence of the relation between each factor and the presence of severe persistent airflow obstruction. The following contrasts were used: ex- or current smoker versus never smoker, atopic versus nonatopic, age of asthma onset (≥18 versus <18 yrs), peak expiratory flow (PEF) variability (>10% versus <10%), FEV1 reversibility (≥9% versus <9%), exhaled NO (≥10 ppb versus <10 ppb), peripheral blood eosinophils (>450 versus ≤450x106·L–1), total immunoglobulin E (IgE) (>100 versus ≤100 IU·mL–1), presence versus absence of bronchial wall thickening, bronchial dilatation and air-trapping on HRCT. Statistical significance was defined by a p-value of <0.05.

Because of the well-known association between smoking and persistent airflow obstruction, and because of the high percentage of current or exsmokers in the population, the same analysis as for the whole group in nonsmokers (22 in group S and 23 in group N) and for the <10 pack-yr history (30 in group S and 27 in group N) was performed.


   Results
TOP
 Abstract
 Methods
 Results
Discussion
 References
 
Patient demographics
Patients with severe persistent airflow limitation were older (p<0.001) and more frequently male (p<0.05), although females dominated both groups (table 1Go). The age at diagnosis was not different between groups, but the duration of disease was longer in group S (p<0.001). The proportion of smokers (current and past) was higher in group S, but this did not achieve statistical significance. Comparisons of level of tobacco consumption (expressed as pack-yrs) between the two groups was not significant, with seven patients in group S andtwo patients in group N with ≥10 pack-yrs tobacco consumption. Although there was no difference in hospital admissions, patients in group S were more likely to have been mechanically ventilated.


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  		Table 1 Demographics, history of asthma and asthma treatment

 
The dose of inhaled corticosteroids was not different between groups. Although the dose of prednisolone was similar, patients in group N had more short courses of prednisolone in the last year. The use of inhaled and nebulised short-acting ß2-agonist as rescue medication was similar, but patients in group N used subcutaneous terbutaline more frequently (41.4% versus 10.8%, p<0.01).

Lung function
FVC was lower in patients with severe airflow limitation (p<0.001) (table 2Go). TLC was similar but RV was significantly higher in the severe airflow limitation group (p<0.001). Diffusing capacity was within normal limits. The maximal bronchodilator response was similar but the diurnal PEF variability was greater in group N (p<0.05).


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  		Table 2 Lung function tests

 
Inflammatory markers
Exhaled NO was increased in group S (21.0±2.4 versus 12.8±2.3 ppb, p<0.05) (fig. 1Go). Peripheral blood eosinophils were higher in group S (0.41±0.06 versus 0.15±0.03x109cells·L–1, p <0.0001). Total serum IgE levels were similar in the two groups (median 133 IU·mL–1 in group S and 127 IU·mL–1 in group N).



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  		Fig. 1.— Individual scores of a) exhaled NO levels and b) blood eosinophil counts in patients with severe asthma with (forced expiratory volume in one second (FEV1) <50% ({blacksquare})) or without (FEV1 >80% ({blacktriangleup})) airflow obstruction. Horizontal bar indicates median. *: p<0.05; ***: p<0.001.

 
Quality of life
The mean scores in each group show a significant impairment of the overall quality of life, as well as in all three domains, with no differences between the groups (table 3Go).


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  		Table 3 St. George's Respiratory Questionnaire scores

 
HRCT evaluation of the airways
HRCT scans were performed in 34 (of 37) patients in the low FEV1 group and in 27 (of 29) in the normal FEV1 group. Bronchial wall thickening was found in 15 patients (44.1%) with severe airflow limitation and in only two (7.4%) with normal lung function (fig. 2Go; p<0.01). Bronchial dilatation was found in 12 patients (35.3%) from group S and three (11.1%) from group N (p<0.05). Air trapping was found in 21 patients (61.8%) in group S and 13 patients (50.0%) in group N (nonsignificant difference). Separate analysis of these alterations for each pair of pulmonary lobes showed a nonsignificant higher involvement of lower lobes as compared with upper or middle lobes. Examples of the HRCT abnormalities are shown in figure 3Go.



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  		Fig. 2.— Scores for a) bronchial wall thickening, b) bronchial dilatation and c) air trapping measured from high resolution computed tomograms for patients with severe asthma with (FEV1 <50% ({blacksquare})) or without (FEV1 >80% ({blacktriangleup})) airflow obstruction. Horizontal bar indicates median. *: p<0.05; **: p<0.01.

 


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  		Fig. 3.— High resolution computed tomography of the lungs from two patients with severe asthma with predicted forced expiratory volume in one second <50%. a) Airway wall thickening and mild dilatation of the intrapulmonary airways in both lower lobes, and b) air-trapping with mosaic pattern, together with bronchial dilatation and thickening of the intrapulmonary airways.

 
Factors associated with severe airflow limitation
Peripheral blood eosinophilia, and bronchial wall thickening and bronchial dilatation on HRCT examination were significantly associated with severe persistent airflow limitation (table 4Go). OR adjusted for age, sex and asthma duration were calculated for several factors (table 5Go) and blood eosinophilia and bronchial wall thickening were the only factors independently associated with the outcome. When analysis was done including the two significant factors in the same model, they proved to be associated with the presence of persistent airflow limitation (blood eosinophilia: OR=24.1; 95% CI: 3.0–192.9 and bronchial wall thickening on HRCT: OR=18.4; 95% CI: 2.3–146.2), independently of each other.


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  		Table 4 Crude OR for the presence of severe persistent airflow obstruction

 

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  		Table 5 Adjusted OR (for age, sex and asthma duration) for the presence of severe persistent airflow obstruction.

 
In order to test the robustness of the analysis, the same comparisons and logistic regression analyses were performed with the nonsmokers, and again with nonsmokers and smokers with <10 pack-yrs tobacco consumption. Bronchial wall thickening and bronchial dilatation were the only factors significantly associated with the presence of severe airflow obstruction inall populations, including the whole population, the nonsmoking population and the <10 pack-yrs population (table 6Go). When adjusted for age, sex and asthma duration, bronchial wall thickening was the only significantly associated factor with the presence of severe persistent airflow obstruction. Thus, the association of bronchial wall thickening with the presence of severe airflow obstruction is independent of age, sex and asthma duration, and is present whether the whole population, the nonsmoking population or the <10 pack-yrs population was examined.


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  		Table 6 Logistic regression analysis in various populations

 

   Discussion
TOP
 Abstract
 Methods
 Results
 Discussion
References
 
In this study of patients with severe asthma, important differences between those with normal lung function and those with severe persistent airflow limitation have been found. Patients have been carefully assessed and characterised in terms of diagnosis, severity of asthma, aggravating factors and associated diseases. It was important to make sure that there were no other significant lung diseases apart from asthma in these patients, and many exclusions in the obstructed group was due to the presence of pulmonary comorbidity factors. Severe persistent airflow obstruction was found to be associated with older age, more prolonged disease course, increased peripheral blood eosinophilia and especially bronchial wall thickening on HRCT. The last factor was associated with airflow obstruction independently of various confounding factors and this association was also found when the analysis was performed in nonsmokers as well as in nonsmokers combined with smokers with <10 pack-yrs of tobacco consumption.

There were no differences between the groups in terms of atopic status, quality of life scores and the amount of asthma treatment they were taking; though one notable exception was the use of subcutaneous terbutaline, which was more frequent in the nonobstructed group. This reflects the authors' practice of prescribing subcutaneous terbutaline mainly for brittle asthma and not for patients with chronic airflow obstruction. There were no differences in the dose of inhaled corticosteroids used between the two groups, but the doses used were very high with a mean of 3,400 µg of beclomethasone equivalent per day. These patients were likely to be overtreated with inhaled corticosteroid therapy given the relatively shallow concentration-response curve. There were significant differences, such as the older age with longer duration of disease of the patients with persistent airflow obstruction, and more importantly these patients, despite having similar rates of hospital admissions, had experienced more episodes of mechanical ventilation for asthma. Diffusing capacity was within normal limits in all patients and HRCT examination showed no evidence of emphysema. Although there was no significant difference in smoking history between the two groups, it is noteworthy that 40.5% of the obstructed asthmatics were either current or past smokers compared with 20.7% in the nonobstructed group. However, there were few current smokers in each group and the level of tobacco consumption was low, with only seven patients in the obstructed group and two patients in the group without airflow obstruction having smoked ≥10 pack-yrs. Cigarette smoking could be a predisposing factor for chronic airflow obstruction in patients with asthma and is in accordance with the accelerated decline in lung function over time observed in asthmatic smokers 16.

Two indirect markers of inflammation, exhaled NO and blood eosinophil count, were increased in patients with persistent airflow obstruction compared with those with normal lung function. Exhaled NO reflects an aspect of airway inflammation in asthma 17, and there is a correlation with the number of eosinophils in induced sputum or bronchial biopsies in mild asthmatics not on inhaled corticosteroid therapy 18, 19. Peripheral blood eosinophilia was significantly associated with severe persistent airflow obstruction in the whole population, but this association was not significant in the nonsmoking population and in the <10 pack-yr population. The number of peripheral blood eosinophils has been related to the level of airway inflammation, asthma severity and lung function as measured by FEV1 20, 21. A strong association between sputum eosinophilia and persistent airflow limitation has been found in severe asthmatic patients. However, airflow obstruction was defined as an FEV1 of <75% pred 9, which is a cut-off point that would include also mild-to-moderate airflow obstruction. The current authors chose a more "severe" limit of <50% FEV1 predicted. Persistence of the inflammatory process in the airways of patients with severe asthma has been reported previously 5, 22, and in the authors' studies of severe asthma, a persistence of eosinophils and neutrophils with high levels of eosinophilic cationic protein in induced sputum was found 6.

The most important differences found between the groups relate to airway abnormalities in terms of bronchial wall thickening and dilatation in patients with severe persistent airflow obstruction rather than in those with normal lung function. Bronchial wall thickening was significantly and independently associated with severe persistent airflow limitation. This association was present when the analysis was performed in nonsmoking population and in the <10 pack-yr population. Bronchial wall thickening and dilatation have been found to be more frequent in patients with asthma than in healthy subjects 23–25 with reported frequencies varying 16–92% for bronchial wall thickening and 31–77% for bronchial dilatation. This variability may be related to the subjective nature of the computed tomography interpretation and to differences in patient populations. The increase in the extent of airways abnormalities (including wall thickening and dilatation) was related to increasing severity and duration of asthma 23, 26, 27. In cross-sectional studies, either a negative correlation 27 or no correlation 28 has been reported between bronchial wall thickness and FEV1.

The extent to which airway wall remodelling features, such as thickening of subepithelial layer, smooth muscle hypertrophy and hyperplasia, angiogenesis, mucous glands hyperplasia contribute to the bronchial alterations seen on HRCT and to persistent airflow limitation is largely unknown. Airway remodelling has been implicated in the accelerated decline of FEV1 in asthmatics 16 and could contribute to the persistence of airflow limitation despite maximal treatment. Subepithelial fibrosis has been inversely related to FEV1 29, but there is no evidence as yet for a relationship between FEV1 decline and the degree of subepithelial fibrosis. Eosinophils produce metalloproteinases, collagenase, and growth factors (transforming growth factor-ß and platelet-derived growth factor), which regulate the proliferation of fibroblasts and airway smooth muscle and matrix production from fibroblasts and other stromal tissues 30, suggesting a role for eosinophils in inducing and maintaining airway remodelling in asthma. However, the data indicate that increased peripheral blood eosinophilia and bronchial wall thickening on HRCT were associated with airflow obstruction, independently of each other. This suggests that eosinophilic inflammation is not related to the structural changes in the airways. Other noneosinophilic aspects of the asthmatic inflammation may be related to airway wall remodelling features.

The quality of life scores were similar in the two groups. Previous studies have either reported a negative relationship between quality of life scores and lung function expressed as FEV1 14, 31, 32 or lack of correlation between the two variables 33. Moy et al. 34 using the Juniper et al. 35 Asthma Quality of Life Questionnaire, showed a weak correlation between the two parameters in mild asthmatics and no correlation in moderate-to-severe asthmatics. These authors found a wide range of quality of life scores for a given level of FEV1 in the moderate-to-severe group, which is similar to the findings in the current study in more severe patients. This may reflect the variability in the patient's adaptation to their disability and the way patients cope with their disease. Other factors, such as the intensity and the persistence of symptoms, may have much greater impact onquality of life than the level of lung function. This is particularly true for severe asthma patients, who experience severe and/or persistent symptoms regardless of persistent airflow limitation.

Patients with severe asthma and severe persistent airflow limitation have certain different characteristics than those with normal lung function, namely longer disease duration, indirect evidence of a persistent inflammatory process, and increased incidence of thickened airways as seen on high resolution computed tomography examination, despite similar impairments in quality of life and similar amounts of treatments for asthma. Persistent airflow obstruction in severe asthma may be associated with a greater degree of inflammation and with structural abnormalities in the airways.


   Footnotes
 
For editorial comments see page 8. Back


   References
TOP
 Abstract
 Methods
 Results
 Discussion
 References
 

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