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. 2014 Jul 3;2(7):e12069. doi: 10.14814/phy2.12069

Table 2.

Patient characteristics.

Parameters Discovery set (n = 39) Verification set (n = 32) P 1
Age 70.0 ± 7.5 72.2 ± 6.4 0.15
Gender (male/female) 39/0 27/5 0.01
Smoking status at the time of enrollment (current/ex) 7/32 2/30 0.17
GOLD stage (I/II/III/IV) 5/14/15/5 8/8/14/2 0.39
Pulmonary function tests
%VC 86.6 ± 15.6 90.6 ± 22.1 0.39
FEV1 1.48 ± 0.66 1.38 ± 0.68 0.24
FEV1% 49.5 ± 12.4 48.4 ± 18.5 0.46
FEV1% predicted 52.8 ± 20.6 54.0 ± 23.8 0.86
%DLCO/VA 55.8 ± 23.5 57.5 ± 23.9 0.98
Computer tomography
Low attenuation area (%) 36.0 ± 14.7 34.6 ± 15.6 0.91
Therapy (%)
Long‐acting β2 agonist 87 91 1.00
Long‐acting muscarinic antagonist 82 94 0.29
Inhaled corticosteroid2 100 84 0.01
Systemic corticosteroid 0 0

%VC, actual/predicted vital capacity (VC) ratio, in percentage; FEV1, forced expiratory volume in 1 sec; FEV1%, FEV1/FVC ratio, in percentage; FEV1% predicted, actual/predicted FEV1 ratio, in percentage; %DLCO/VA, diffusing capacity for carbon monoxide/alveolar volume, in percentage.

Parameters are shown as mean ± standard deviation, unless indicated otherwise.

1

Comparison between discovery and verification sets. Fisher's exact test (gender, smoking status, and therapy), chi‐square test (GOLD stage), and Student's t‐test (other parameters) were used to compare the two groups.

2

Inhaled (low dose) corticosteroid is prescribed to most patients as a part of therapy during stable period, while systemic (high dose) corticosteroid may be prescribed/administered to patients only during exacerbation. Blood samples were not collected from those patients who were undergoing systemic corticosteroid treatment for the episode of exacerbation.