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. 2015 Jan 1;191(1):54–62. doi: 10.1164/rccm.201402-0314OC

Table 1.

Subject Characteristics

  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.