Table II.
P-values from adjusted longitudinal analysisll |
|||
---|---|---|---|
FEV1 (%pred)* | FEV1/FVC* | BDR | |
Time† | <0.0001 | <0.0001 | <0.0001 |
Budesonide‡ | <0.0001 | <0.0001 | <0.0001 |
BMI (percentile) | <0.0001 | 0.001 | 0.04 |
BMI* budesonide | 0.15 | 0.0007 | 0.049 |
Gender | <0.0001 | <0.0001 | 0.36 |
Age (years) | 0.02 | 0.29 | 0.29 |
Height (cm) | 0.002 | 0.003 | 0.4 |
Duration of asthma | 0.07 | 0.004 | 0.005 |
Tobacco exposure | 0.02 | 0.91 | 0.6 |
Race§: African-American | 0.56 | 0.19 | 0.01 |
Hispanic/Other | 0.009 | 0.96 | 0.43 |
Vitamin D (log10) | 0.03 | 0.92 | 0.17 |
Shown are the P-values for each variable from the adjusted longitudinal analysis. The interaction between BMI (as a continuous variable) and treatment with budesonide is highlighted in grey. Both budesonide and BMI had significant effects on all three lung function measures (P<0.05), as do some of the covariates. There was a significant interaction between budesonide treatment and BMI (budesonide*BMI) for FEV1/FVC and for BDR.
Pre-bronchodilator FEV1 and FEV1/FVC.
As months of follow-up during CAMP.
Effect of budesonide compared to placebo/nedocromil.
Compared to non-Hispanic whites.
All models were adjusted for all of the variables listed in the first column.