TABLE III.
Clinical phenotype | OR | 95% CI | P value |
---|---|---|---|
Serum eosinophil count <500 cells/μL | 1.79 | 1.02–3.21 | .045 |
Inhaled budesonide treatment‡ | 2.05 | 1.11–3.83 | .02 |
Inhaled nedocromil treatment‡ | 1.30 | 0.70–2.42 | .41 |
FEV1/FVC ratio ≥90%§ | 73.81 | 13.07–1404.13 | <.001 |
FEV1/FVC ratio 80% to 89%§ | 25.10 | 5.16–453.35 | .002 |
FEV1/FVC ratio 70% to 79%§ | 6.59 | 1.28–120.93 | .07 |
Covariates included in the cross-validated model: age, race, CAMP treatment group, clinic site, household income level, history of wheezing with colds, history of exacerbations after exercise, history of exposure to home tobacco smoke, baseline asthma severity, and serum IgE level.
Quantitative variables were modeled categorically.
Reference group is placebo treatment.
Reference level is an FEV1/FVC ratio of less than 70%.