Table 1.
Healthy Control Subjects | Nonsevere Asthma | Severe Asthma | |
---|---|---|---|
No. | 10 | 9 | 9 |
Age, yr | 39.0 ± 11.3 | 31.8 ± 16 | 41.4 ± 12 |
Sex, female/male | 5/5 | 4/5 | 5/4 |
Duration of asthma, yr | N/A | 18.2 ± 3.8 | 25.7 ± 9.7* |
Inhaled corticosteroid dose, μg BDP equivalent | N/A | 622 ± 290 | 2160 ± 466* |
Atopy,† n | 3 | 6 | 5 |
Receiving oral prednisolone, n | N/A | N/A | 6 |
FEV1, L | 3.15 ± 1.860 | 2.96 ± 0.46 | 2.0 ± 0.47‡ |
FEV1,% predicted | 91.0 ± 15.6 | 81.5 ± 8.3 | 61.59 ± 4.9§ |
FEV1/FVC, % | 77.2 ± 3.9 | 75.0 ± 3.1 | 69.0 ± 5.9* |
β-Agonist reversibility, %|| | N/A | 24.0 ± 3.5 | 31.0 ± 4.11* |
PC20, mg/ml | >16 | 2.7 ± 0.104 | 0.331 ± 0.13 (4/9) |
Definition of abbreviations: BDP = beclomethasone dipropionate; N/A = not applicable; PC20 = provocative concentration of methacholine causing a 20% fall in FEV1.
P < 0.05 versus patients with nonsevere asthma.
Defined as positive skin prick tests to one or more common aeroallergens.
P < 0.01 versus patients with nonsevere asthma.
P < 0.001 versus patients with nonsevere asthma.
Measured as percent increase in FEV1 after 400 μg salbutamol.