Table 1– Subject characteristics
Nonobese asthmaObese asthmaNonobese controlsObese controlsp-value
Subjects n68476316
Age yrs56.7 (39.0–64.5)59.0 (52.1–64.6)58.7 (27.9–66.4)57.3 (34.7–65.0)0.671
Females %64.761.763.556.30.933
FEV1 % pred82.0 (67.5–92.5)+,§84.0 (67.0–95.0)+101.0 (94.0–115.0)99.0 (82.0–111.0)<0.001
FVC % pred96.4±17.8+92.8±15.8+,§109.1±12.6104.4±17.3<0.001
FEV1/FVC68.5 (61.5–74.5)+,§72.0 (64.0–80.0)+78.0 (75.0–82.0)76.0 (74.0–78.5)<0.001
Atopy %73.5+,§66.0+,§41.325.0<0.001
BMI kg·m−226.1 (23.8–28.3)§34.7 (33.2–39.9)+,ƒ25.8 (23.4–28.0)§33.0 (31.0–35.0)<0.001
ICS dose# μg·day−1500 (0–1000)1000 (0–2000)ƒNANA0.003
ICS use %58.870.2NANA0.212
ACQ Score0.7 (0.4–1.3)0.9 (0.4–1.6)NANA0.811
GINA classification %0.708
 Intermittent32.440.4NANA
 Mild persistent13.28.5NANA
 Moderate persistent39.734.0NANA
 Severe persistent14.717.0NANA
LogPD15 mL1.81 (-0.35–2.16)1.91 (1.53–2.51)NANA0.104
  • Data are presented as median (interquartile range) or mean±sd, unless otherwise stated. FEV1: forced expiratory volume in 1 s; % pred: % predicted; FVC: forced vital capacity; BMI: body mass index; ICS: inhaled corticosteroid; ACQ: Asthma Control Questionnaire; GINA: Global Initiative for Asthma; PD15: provocation dose of 4.5% hypertonic saline required to induce a drop in FEV1 of 15% from baseline; NA: not available. #: beclomethasone equivalents; : presented as geometric median (interquartile range); +: p<0.01 versus nonobese controls; §: p<0.02 versus obese controls; ƒ: p<0.01 versus nonobese asthma.