Table 2.
Baseline Characteristics of VIDA Randomized Participants with Colds: Continuous Variables
| Vitamin D (N = 110) |
Placebo (N = 93) |
P Value* | |||||
|---|---|---|---|---|---|---|---|
| Characteristic | N | Mean | SD | N | Mean | SD | |
| Age, yr | 110 | 39.6 | 12.1 | 93 | 39.2 | 12.8 | 0.85† |
| Duration of asthma since doctor first diagnosed, yr | 110 | 24.9 | 13.2 | 93 | 25.0 | 13.4 | 0.94† |
| BMI, kg/m2 | 110 | 32.42 | 8.39 | 93 | 31.47 | 9.85 | 0.46† |
| Number of positive skin tests‡ | 106 | 4.00 | (2.00–6.00) | 88 | 3.50 | (2.00–6.00) | 0.41§ |
| Peak flow, 2-wk average, L/min | |||||||
| a.m. | 110 | 401.5 | 97.3 | 93 | 393.1 | 106.6 | 0.56† |
| p.m. | 110 | 406.5 | 102.6 | 93 | 395.4 | 106.7 | 0.45† |
| Symptoms, 2-wk average over 5 types║ | |||||||
| a.m. | 110 | 0.36 | 0.27 | 93 | 0.40 | 0.36 | 0.34† |
| p.m. | 110 | 0.38 | 0.29 | 93 | 0.46 | 0.41 | 0.13† |
| Prebronchodilator FEV1, L | 110 | 2.62 | 0.76 | 93 | 2.61 | 0.83 | 0.98† |
| Prebronchodilator FEV1% predicted | 110 | 80.9 | 14.0 | 93 | 81.1 | 14.2 | 0.92† |
| Prebronchodilator FEV1/FVC ratio | 110 | 0.73 | 0.09 | 93 | 0.71 | 0.09 | 0.24† |
| Improvement in prebronchodilator FEV1 over OCS response period, % | 92 | −0.93 | 7.42 | 78 | −0.17 | 8.04 | 0.52† |
| Imputed PC20¶, mg/ml | 106 | 2.14 | 1.58 | 88 | 2.09 | 1.61 | 0.92** |
| Sputum eosinophils‡, % | 90 | 0.25 | (0.00–1.30) | 80 | 0.25 | (0.00–1.30) | 0.81§ |
| Maximum post-albuterol FEV1% predicted | 110 | 91.61 | 14.30 | 92 | 93.16 | 13.98 | 0.44† |
| Maximum reversibility, % change | 110 | 16.03 | 11.91 | 92 | 18.41 | 11.80 | 0.16† |
| Vitamin D, ng/ml | 110 | 18.05 | (13.70–23.70) | 93 | 19.70 | (14.80–24.80) | 0.29§ |
| Melanin level | |||||||
| Upper inner arm | 108 | 63.6 | (51.4–68.1) | 91 | 65.3 | (61.5–67.5) | 0.16§ |
| Outer forearm | 107 | 56.7 | (45.4–60.9) | 92 | 58.3 | (52.7–62.4) | 0.04§ |
| Exposed forehead | 108 | 56.0 | (44.8–60.9) | 92 | 58.2 | (52.7–62.3) | 0.02§ |
| Abdomen | 108 | 62.0 | (45.8–68.0) | 92 | 64.5 | (57.6–68.8) | 0.08§ |
| ASUI score | 110 | 0.84 | 0.10 | 92 | 0.82 | 0.12 | 0.18† |
| ACT score†† | 110 | 20.0 | (17.0–22.0) | 93 | 20.0 | (17.0–22.0) | 0.80§ |
| Asthma control days | |||||||
| Proportion of controlled days, 2-wk average | 110 | 0.20 | 0.27 | 93 | 0.17 | 0.24 | 0.39† |
| Number of controlled days, 2-wk sum | 110 | 2.81 | 3.75 | 93 | 2.38 | 3.39 | 0.39† |
| ABP score | 110 | 19.0 | (13.0–26.0) | 93 | 18.0 | (13.0–28.0) | 0.66§ |
Definition of abbreviations: ABP = Asthma Bother Profile; ACT = Asthma Control Test; ASUI = Asthma Symptom Utility Index; BMI = body mass index; OCS = oral corticosteroid response to prednisone 40 mg by mouth once daily for 5–7 days; PC20 = provocative concentration of methacholine that decreased FEV1 by 20%, with maximum reversibility after up to eight puffs (360 μg) of inhaled levalbuterol; VIDA = Vitamin D Add-on Therapy Enhances Corticosteroid Responsiveness trial.
Placebo versus vitamin D.
t test for differences between specified groups.
Median (interquartile range) is reported.
Wilcoxon rank-sum test for differences between specified groups.
Symptoms scale: 0 = absent, 1 = mild, 2 = moderate, 3 = severe. Symptom types: shortness of breath, chest tightness, wheezing, cough, and phlegm/mucus.
Geometric mean (coefficient of variation) reported.
t test for differences between specified groups on logarithmic scale.
Individual ACT questions are scaled 1–5, with higher values representing better asthma control. ACT score is sum of answers to questions 1–5.