AsthmaNet Vitamin D Add-on Therapy Enhances Corticosteroid Responsiveness in Asthma (VIDA)
Note that you will be prompted to log in or register an account
Open BioLINCC Study See bottom of this webpage for request information
April 2011 – January 2014
February 21, 2020
Clinical Trial URLs
Primary Publication URLs
Commercial Use Data Restrictions No
Data Restrictions Based On Area Of Research No
Specific Consent Restrictions
To evaluate if vitamin D supplementation would improve the clinical efficacy of inhaled corticosteroids in patients with symptomatic asthma and lower vitamin D levels.
At the time of this study, guidelines recommended the use of inhaled corticosteroids as the primary anti-inflammatory controller therapy for patients with persistent asthma. However, previous studies have shown that up to 45% of patients do not have a clinical or physiological response to these agents. In children and adults with asthma, serum 25-hydroxyvitamin D levels of less than 30 ng/mL have been linked to airway hyperresponsiveness, impaired lung function, increased exacerbation frequency, and reduced corticosteroid responsiveness. VIDA was designed to determine if vitamin D supplementation would improve responsiveness to corticosteroids in patients with persistent asthma and low levels of vitamin D at baseline.
Eligible participants were aged 18 years or older with asthma and a serum 25-hydroxyvitamin D level of less than 30 ng/mL. Asthma entry criteria included physician-diagnosed disease and evidence of either bronchodilator reversibility (FEV1≥12% following 180 µg of levalbuterol) or airway hyperresponsiveness (provocative concentration of methacholine at which FEV1 decreased by 20%). A total of 408 patients were randomized, with 201 randomized to the vitamin D3 group and 207 randomized to the placebo group.
The study was a randomized, double-masked, parallel group trial, with each eligible participant randomly assigned to either placebo or high-dose vitamin D3 (100 000 IU once, followed by 4000 IU per day for 28 weeks) added to inhaled corticosteroid (ciclesonide at a dose of 320 µg per day) and levalbuterol. Computer-generated randomization was stratified by clinical center, body mass index (BMI ≤25 vs BMI >25), and race (blacks vs all others), with treatment assignments made in random permuted blocks of size 2. The placebo vitamin D soft gelatin capsules matched in appearance those containing vitamin D3.
After completing a 4-week run-in period of treatment with only ciclesonide and levalbuterol (prior asthma treatments were discontinued), participants were randomized. After randomization, participants entered a 12-week stability phase, in which they continued to receive 320 µg per day of ciclesonide. If the participant’s asthma symptoms were controlled, at 12 weeks patients were tapered to 160 µg per day of ciclesonide for 8 weeks, and then at 20 weeks patients were tapered to 80 µg per day of ciclesonide for 8 weeks. Participants were terminated or withdrawn from the study if they had more than 2 treatment failures or exacerbations.
Asthma symptoms were measured using an electronic diary and the Asthma Symptom Utility Index (ASUI). Participants were instructed to complete the electronic diary every morning and evening and asked to grade the following symptoms: shortness of breath, chest tightness, wheezing, cough, and phlegm or mucus. Symptoms were graded from 0 (absent) to 3 (severe). The scores on the ASUI range from 0 to 1; a higher score indicates better symptom control. Asthma control was measured using the Asthma Control Test (ACT). The scores on the ACT range from 5 to 25; higher scores indicate better asthma control. Asthma-specific quality of life was measured using the Asthma Bother Profile questionnaire. The scores on the Asthma Bother Profile range from 0 to 75; higher scores indicate poorer quality of life. Serum 25-hydroxyvitamin D level was measured at baseline and at the end of each ciclesonide treatment phase. Airway inflammation was measured by performing a differential cell count from induced sputum samples collected at the end of the 4-week run-in and at 12 weeks.
The primary end point was time to first asthma treatment failure during the 28-week study period. Treatment failure was defined as one or more of the following: peak expiratory flow of 65% or less of baseline measurement on two of three consecutive measurements; FEV1 of 80% or less of baseline measurement on two consecutive measurements; increase in levalbuterol dose of 8 puffs per day or more for 48 hours (as compared to baseline); additional use of inhaled corticosteroids or use of oral or parenteral corticosteroids for asthma; emergency department or hospitalization for asthma with systemic corticosteroid use; participant lack of satisfaction with treatment; and physician clinical judgment for safety reasons.
Vitamin D3 did not reduce the rate of first treatment failure or exacerbation in adults with persistent asthma and vitamin D insufficiency.
Castro M, King TS, Kunselman SJ, et al. Effect of vitamin D3 on asthma treatment failures in adults with symptomatic asthma and lower vitamin D levels: the VIDA randomized clinical trial. JAMA. 2014;311(20):2083–2091. doi:10.1001/jama.2014.5052
Please note that researchers must be registered on this site to submit a request, and you will be prompted to log in. If you are not registered on this site, you can do so via the Request button. Registration is quick, easy and free.
Resources AvailableStudy Datasets Only
Persons using assistive technology may not be able to fully access information in the study documents. For assistance, Contact BioLINCC and include the web address and/or publication title in your message. If you need help accessing information in different file formats such as PDF, XLS, DOC, see Instructions for Downloading Viewers and Players.