Effect of Vitamin D3 Supplementation on Severe Asthma Exacerbations in Children With Asthma and Low Vitamin D Levels: The VDKA Randomized Clinical Trial

Erick Forno; Leonard B Bacharier; Wanda Phipatanakul; Theresa W Guilbert; Michael D Cabana; Kristie Ross; Ronina Covar; James E Gern; Franziska J Rosser; Joshua Blatter; Sandy Durrani; Yueh-Ying Han; Stephen R Wisniewski; Juan C Celedón

doi:10.1001/jama.2020.12384

. 2020 Aug 25;324(8):1–9. doi: 10.1001/jama.2020.12384

Effect of Vitamin D₃ Supplementation on Severe Asthma Exacerbations in Children With Asthma and Low Vitamin D Levels

The VDKA Randomized Clinical Trial

Erick Forno ¹, Leonard B Bacharier ², Wanda Phipatanakul ³, Theresa W Guilbert ⁴, Michael D Cabana ⁵, Kristie Ross ⁶, Ronina Covar ⁷, James E Gern ⁸, Franziska J Rosser ¹, Joshua Blatter ², Sandy Durrani ⁴, Yueh-Ying Han ¹, Stephen R Wisniewski ⁹, Juan C Celedón ^1,^✉

¹Division of Pulmonary Medicine, Department of Pediatrics, University of Pittsburgh Medical Center Children’s Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, Pennsylvania

²Division of Allergy, Immunology, and Pulmonary Medicine, Department of Pediatrics, St Louis Children’s Hospital, Washington University at St Louis, St Louis, Missouri

³Division of Allergy and Immunology, Boston Children’s Hospital, Harvard Medical School, Boston, Massachusetts

⁴Division of Pulmonary Medicine, Department of Pediatrics, Cincinnati Children’s Hospital, University of Cincinnati, Cincinnati, Ohio

⁵Division of General Pediatrics, Department of Pediatrics, University of California, San Francisco Benioff Children’s Hospital, University of California, San Francisco

⁶Division of Pediatric Pulmonology, University Hospitals Rainbow Babies and Children’s Hospital, Case Western Reserve University, Cleveland, Ohio

⁷Division of Allergy and Immunology, Department of Pediatrics, National Jewish Health, University of Colorado, Denver

⁸Department of Pediatrics, University of Wisconsin-Madison School of Medicine and Public Health, Madison

⁹Department of Epidemiology, University of Pittsburgh, Pittsburgh, Pennsylvania

^✉

Corresponding Author: Juan C. Celedón, MD, DrPH, Division of Pulmonary Medicine, UMPC Children’s Hospital of Pittsburgh, 4401 Penn Ave, Pittsburgh, PA 15224 (juan.celedon@chp.edu).

Accepted for Publication: June 25, 2020.

Author Contributions: Drs Celedón and Wisniewski had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.

Concept and design: Wisniewski, Celedón.

Acquisition, analysis, or interpretation of data: All authors.

Drafting of the manuscript: Forno, Bacharier, Phipatanakul, Durrani, Wisniewski, Celedón.

Critical revision of the manuscript for important intellectual content: All authors.

Statistical analysis: Blatter, Wisniewski.

Obtained funding: Cabana, Celedón.

Administrative, technical, or material support: Forno, Phipatanakul, Guilbert, Covar, Gern, Rosser, Blatter, Durrani, Han, Celedón.

Supervision: Forno, Bacharier, Phipatanakul, Ross, Covar, Rosser, Wisniewski, Celedón.

Conflict of Interest Disclosures: Dr Bacharier reported receiving grants from the National Heart, Lung, and Blood Institute (NHLBI) during the conduct of the study and personal fees from AstraZeneca, GlaxoSmithKline, Sanofi, Regeneron, Novartis, Genentech, Boeringher Ingelheim, Vectura, DBV Technologies, Circassia, Merck, Teva, Medscape, and Rockpointe outside the submitted work, as well as receiving royalties as associate editor from Elsevier (Journal of Allergy and Clinical Immunology). Dr Phipatanakul reported serving as a consultant for GlaxoSmithKline, Genentech, Novartis, Regeneron, Sanofi, and Teva; receiving clinical trial support or medications from Genentech, Novartis, Regeneron, Sanofi, Circassia, Monaghen, Thermo Fisher, Alk Abello, Lincoln Diagnostics, GlaxoSmithKline, Kaleo, and Merck; and funding to the institution by Genentech, Regeneron, Novartis, and the National Institutes of Health (NIH)—all for projects unrelated to the current work. Dr Guilbert reported receiving personal fees from GlaxoSmithKline, TEVA, Novartis, and the American Board of Pediatrics (pediatric pulmonary subboard); grants and personal fees from Sanofi/Regeneron; grants from AstraZeneca and Novartis; and royalties from UpToDate outside the submitted work. Dr Cabana reported serving as a member of the United States Preventive Services Task Force (USPSTF); this manuscript does not necessarily represent the views of the USPSTF. Dr Ross reported receiving grants from the NIH during the conduct of the study and grants and nonfinancial support from TEVA, nonfinancial support from Merck, and grants from Flamel, the NHLBI, AstraZeneca, and Novartis outside the submitted work. Dr Covar reported receiving grants from GlaxoSmithKline during the conduct of the study. Dr Gern reported receiving personal fees from AstraZeneca outside the submitted work. Dr Rosser reported receiving grants from the NIH/National Center for Advancing Translational Sciences during the conduct of the study. Dr Celedón reported receiving nonfinancial support from Pharmavite and GlaxoSmithKline during the conduct of the study and nonfinancial support (Asmanex) for an NIH-funded study from Merck outside the submitted work. No other disclosures were reported.

Funding/Support: This study was funded by grant HL119952 from the US NIH. The project was also supported by the Pediatric Clinical and Translational Research Center (PCTRC) at University of Pittsburgh Medical Center Children’s Hospital of Pittsburgh through NIH grant UL1TR001857. Pharmavite LLC provided the vitamin D and placebo capsules for the study, and GlaxoSmithKline provided the Flovent given to study participants.

Role of the Funder/Sponsor: The funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

Group Information: The VDKA group members include the following: University of Pittsburgh Medical Center Children’s Hospital of Pittsburgh and University of Pittsburgh: design of the study: John M. Brehm, MD, MPH. Collection of the data: Jonathan D. Finder, MD, Mark E. Dovey, MD, Jonathan E. Spahr, MD, David M. Orenstein, MD, Geoffrey Kurland, MD, Daniel J. Weiner, MD, Gregory Burg, MD, Sandeep Puranik, MD, Allyson Larkin, MD, Hiren Muzumdar, MD, Deborah Albright, MD, Hey Chong, MD, PhD, David Nash, MD, Todd Green, MD, Natalie Baldauff, DO, Robert W. Hickey, MD, John Broyles, MS, CRNP, Lori Holt, MSN, CRNP, Rose Lanzo, Jamie Adams, Elizabeth Hartigan, RN, MPH, Cynthia Granny, and Pamela Vincent. Data management and data analysis: Zachary Doyle, Heather Eng, and Jim Luther.

Boston Children’s Hospital: Data collection: Jonathan Gaffin, MD, MMSc, Perdita Permaul, MD, Margee Louisias, MD, MPH, Marissa Hauptman, MD, MPH, Nicole Akar-Ghibril, MD, Elizabeth Burke Roberts, RN, PNP, Sachin Baxi, MD, Lisa Bartnikas, MD, William Sheehan, MD, Britanny Esty MD, David Kantor MD, PhD, Peggy Lai, MD, MPH, Michelle Maciag, MD, Elena Crestani, MD, Mehtap Haktanir-Abul, MD, Amparito Cunningham MD, MPH, Anna Cristina Vasquez-Muniz, BA, Nicole Adler, BS, Reid Mathews, BS, Brian Volonte, BS, John Pacheco, BA, Anna Ramsey, BS, Vanessa Konzelmann, BS, Aiza Zia, BS, Julianne Saia, BS, Alma Castillo-Hernandez, BS, Benjamin Peterson, BS, Jennifer Rooney, MS, and Robert Rega, BS.

Cincinnati Children’s Hospital Medical Center: Data collection: Cassie Shipp, MD, Carolyn Kercsmar, MD, Karen McDowell, MD, Stephanie (Logsdon) Ward, MD, Nancy Lin, MD, Alisha George, MD, Will Corwin, Grant Geigle, Alisha Hartmann, and John Broderick.

Rainbow Babies and Children’s Hospital: Data collection: Laurie Logan, RN, Laura Veri, Daniel Craven MD, Ben Gaston MD, Amy DiMarino MD, Erica Roesch MD, and Ross Myers, MD.

Washington University at St Louis: Data collection: Wanda Caldwell, Tina Norris, and Roseanne Donato.

Data Sharing Statement: See Supplement 3.

Additional Contributions: We thank all study participants and their families; the research coordinators and research teams at each of the study sites and the data coordinating center; the data and safety monitoring board; and the clinical trials specialist (Julie Bamdad, MSE) and program officer (Patricia Noel, PhD) for the project at the federal agency that funded the study (the National Heart, Lung, and Blood Institute) for monitoring the study progress.

^✉

Corresponding author.

PMCID: PMC7448830 PMID: 32840597

Key Points

Question

In high-risk children with persistent asthma and low vitamin D levels, does vitamin D₃ supplementation prolong the time to a severe asthma exacerbation?

Findings

In this randomized clinical trial that included 192 children, vitamin D₃ supplementation, compared with placebo, did not significantly improve the time to a severe asthma exacerbation (adjusted hazard ratio, 1.13).

Meaning

The findings from this trial do not support the use of vitamin D₃ supplementation to improve the time to a severe asthma exacerbation in children with asthma and low serum vitamin D levels.

Abstract

Importance

Severe asthma exacerbations cause significant morbidity and costs. Whether vitamin D₃ supplementation reduces severe childhood asthma exacerbations is unclear.

Objective

To determine whether vitamin D₃ supplementation improves the time to a severe exacerbation in children with asthma and low vitamin D levels.

Design, Setting, and Participants

The Vitamin D to Prevent Severe Asthma Exacerbations (VDKA) Study was a randomized, double-blind, placebo-controlled clinical trial of vitamin D₃ supplementation to improve the time to severe exacerbations in high-risk children with asthma aged 6 to 16 years taking low-dose inhaled corticosteroids and with serum 25-hydroxyvitamin D levels less than 30 ng/mL. Participants were recruited from 7 US centers. Enrollment started in February 2016, with a goal of 400 participants; the trial was terminated early (March 2019) due to futility, and follow-up ended in September 2019.

Interventions

Participants were randomized to vitamin D₃, 4000 IU/d (n = 96), or placebo (n = 96) for 48 weeks and maintained with fluticasone propionate, 176 μg/d (6-11 years old), or 220 μg/d (12-16 years old).

Main Outcomes and Measures

The primary outcome was the time to a severe asthma exacerbation. Secondary outcomes included the time to a viral-induced severe exacerbation, the proportion of participants in whom the dose of inhaled corticosteroid was reduced halfway through the trial, and the cumulative fluticasone dose during the trial.

Results

Among 192 randomized participants (mean age, 9.8 years; 77 girls [40%]), 180 (93.8%) completed the trial. A total of 36 participants (37.5%) in the vitamin D₃ group and 33 (34.4%) in the placebo group had 1 or more severe exacerbations. Compared with placebo, vitamin D₃ supplementation did not significantly improve the time to a severe exacerbation: the mean time to exacerbation was 240 days in the vitamin D₃ group vs 253 days in the placebo group (mean group difference, −13.1 days [95% CI, −42.6 to 16.4]; adjusted hazard ratio, 1.13 [95% CI, 0.69 to 1.85]; P = .63). Vitamin D₃ supplementation, compared with placebo, likewise did not significantly improve the time to a viral-induced severe exacerbation, the proportion of participants whose dose of inhaled corticosteroid was reduced, or the cumulative fluticasone dose during the trial. Serious adverse events were similar in both groups (vitamin D₃ group, n = 11; placebo group, n = 9).

Conclusions and Relevance

Among children with persistent asthma and low vitamin D levels, vitamin D₃ supplementation, compared with placebo, did not significantly improve the time to a severe asthma exacerbation. The findings do not support the use of vitamin D₃ supplementation to prevent severe asthma exacerbations in this group of patients.

Trial Registration

ClinicalTrials.gov Identifier: NCT02687815

This randomized trial compares the effects of vitamin D₃vs placebo on time to severe exacerbation in children with asthma and low vitamin D levels.

Introduction

As of 2018, an estimated 5.5 million children in the US had asthma, a major cause of health care utilization and costs.¹ In 2018, asthma exacerbations led to more than 546 000 emergency department (ED) visits and 80 000 hospitalizations.¹

Several observational studies have linked low serum 25-hydroxyvitamin D (henceforth, “vitamin D”) levels to severe asthma exacerbations, lower lung function, and reduced response to corticosteroids.^2,3,4,5 Such findings may be explained by immune-modulatory and anti-inflammatory effects of vitamin D, including regulatory T-cell induction, attenuation of Th2 and Th17 responses, enhancement of IL-10 production, and inhibition of airway smooth muscle hypertrophy and collagen deposition.^6,7,8,9 Vitamin D may attenuate viral-induced asthma attacks by reducing rhinovirus replication in bronchial epithelium, promoting interferon-mediated antiviral pathways and inducing production of antimicrobial peptides.^10,11

A meta-analysis of clinical trials using participant-level data showed that vitamin D₃ supplementation was associated with lower risk of asthma exacerbations, but the pooled estimate was not significant among children younger than 16 years old.¹² More recently, a comprehensive review of vitamin D₃ for the prevention of wheeze attacks found insufficient evidence to recommend vitamin D₃ supplementation in children.¹³ Previous pediatric randomized clinical trials, however, have not focused on children with low vitamin D levels or who are at high risk for severe asthma exacerbations. Moreover, existing trials did not monitor vitamin D levels or did not show consistently improved levels after supplementation.

Children with a recent severe asthma exacerbation are at highest risk for subsequent exacerbations, independent of disease severity, treatment, or control.¹⁴ The primary hypothesis for this trial was that supplementation with vitamin D₃ would improve the time to a severe exacerbation in high-risk children, aged 6 to 16 years, with vitamin D insufficiency and taking low-dose inhaled corticosteroids for persistent asthma. The secondary hypotheses were that this protective effect would result from reduced incidence of viral-induced exacerbations or enhanced response to corticosteroids.

Methods

The study protocol was approved by the institutional review board (IRB) at each participating institution, and an independent data and safety monitoring board (DSMB) appointed by the National Heart, Lung, and Blood Institute monitored the study. Written parental consent was obtained for participating children, from whom written assent was also obtained.

Participants

Participants for the Vitamin D to Prevent Severe Asthma Exacerbations (Vit-D-Kids Asthma [VDKA]) Study were recruited from 7 sites across the US: Boston Children’s Hospital, Boston, Massachusetts; Washington University and St Louis Children’s Hospital, St Louis, Missouri; Cincinnati Children’s Hospital, Cincinnati, Ohio; Rainbow Babies and Children’s Hospital, Cleveland, Ohio; the University of California at San Francisco Benioff Children’s Hospital; National Jewish Health, Denver, Colorado; and University of Pittsburgh Medical Center Children’s Hospital of Pittsburgh, Pittsburgh, Pennsylvania. The data coordinating center was based at the University of Pittsburgh Graduate School of Public Health. Based on prior observational studies on vitamin D and asthma outcomes,^2,5 eligible participants were high-risk children with asthma, aged 6 to 16 years, with serum vitamin D levels less than 30 ng/mL but greater than or equal to 10 ng/mL (until July 21, 2017) or greater than or equal to 14 ng/mL (after that date, following a protocol amendment). Entry criteria included (1) physician-diagnosed asthma for at least 1 year; (2) at least 1 severe asthma exacerbation (systemic corticosteroids for at least 3 days, or a hospitalization or ED visit requiring systemic corticosteroids) in the previous year; (3) use of asthma medications (daily controller medications, or inhaled β₂-agonists at least thrice per week) for at least 6 months in the previous year; (4) forced expiratory volume in the first second of expiration (FEV₁) greater than or equal to 70% of predicted; and (5) either bronchodilator responsiveness (an increment in baseline FEV₁ of 8% or more 15 minutes after inhalation of 180-μg albuterol) or, in those without bronchodilator response, increased airway responsiveness (a provocative concentration of methacholine at which FEV₁ decreased by 20% [PC₂₀] <8 mg/mL if not receiving inhaled corticosteroids, or <16 mg/mL if receiving inhaled corticosteroids). Exclusion criteria, listed in the full study protocol (Supplement 1), included chronic respiratory disorders other than asthma, chronic oral corticosteroid therapy, severe asthma, and inability to perform adequate spirometry. Recruitment was conducted at several locations at each study site, including EDs, pulmonary and allergy/immunology clinics, and general pediatric clinics. A study description was also posted in the study website and at IRB-approved websites (eg, Pitt+Me) to reach a broader population.

Study Design and Treatment

The study was a randomized, double-blind, parallel, placebo-controlled clinical trial, with each participant randomly assigned to either daily placebo capsules or daily vitamin D₃, 4000 IU (Pharmavite LLC), plus inhaled fluticasone propionate (88 μg twice per day in children aged 6-11 years and 110 μg twice per day in children ≥12 years). Eligible participants were screened between February of 2016 and March of 2019 and enrolled if they met inclusion criteria. After a 4-week run-in period in which participants received placebo capsules plus inhaled fluticasone and as-needed inhaled albuterol (prior medications were discontinued), those who met inclusion criteria at entry and during run-in were randomized (Figure 1).

Figure 1. — FEV₁ indicates forced expiratory volume in the first second of expiration.

^aSum is greater than 376 because potential participants could fail screening more than once and could fail for more than 1 reason.

^bSum is greater than 27 because participants could enter run-in more than once and could fail for more than 1 reason.

Computer-generated randomization was stratified according to study site and race/ethnicity, with treatment assignments made in random permuted block sizes of 2 and 4. The soft gelatin placebo capsules were matched in appearance to those containing vitamin D₃. At the randomization visit, participants and their parents received dietary counseling, including a list of foods rich in vitamin D. After randomization, participants were followed up for 48 weeks, including a total of 6 in-person visits every 8 weeks and telephone calls in-between visits. Following randomization, participants continued taking the same dose of fluticasone until the 24-week visit, when their fluticasone dose was reduced by 50% if their asthma was well controlled and if they had FEV₁ and FEV₁ to forced vital capacity (FEV₁/FVC) greater than or equal to 80% of predicted, were using a rescue inhaler 4 or fewer times per week, and had asthma symptoms preventing full participation in daily activities no more than once per month. Asthma control was assessed using the Asthma Control Test (ACT [score range, 5-25], for participants aged ≥12 years)¹⁵ or the Childhood ACT (C-ACT [score range, 0-27], for participants aged <12 years)¹⁶; for both tests, higher scores mean better symptom control, and more than 19 points is considered well-controlled asthma. Per protocol, study medications were discontinued in participants who had 3 or more severe asthma exacerbations (n = 6); those participants were followed up and analyzed in the group to which they were randomized.

During the trial, vitamin D levels were measured during in-person study visits at 0 (randomization), 16, 32, and 48 weeks. Study medications were discontinued in participants with a vitamin D level less than 10 ng/mL (n = 2), who were referred to a pediatric endocrinologist for evaluation and followed up in the group to which they were randomized. Participants whose vitamin D level was between 10 and 13 ng/mL (n = 10) received additional dietary counseling along with a randomly selected participant (to prevent unblinding); if their vitamin D level was less than 14 ng/mL at a subsequent visit (n = 2), study medications were discontinued and the participant was referred to a pediatric endocrinologist and followed up in the group to which they were randomized. Adherence to placebo or vitamin D capsules was assessed both through returned pill counts and electronically, using the MEMS monitor (Aardex).

Viral Polymerase Chain Reaction

Nasal blows for polymerase chain reaction (PCR) assessment of a viral infection were collected within 7 days of a severe exacerbation. Nasal mucus specimens were tested for common respiratory viruses (influenza, respiratory syncytial virus A and B, parainfluenza 1-4, bocavirus, metapneumovirus, rhinoviruses and enteroviruses, and coronavirus [HKU1, NL63, OC43, and 229E]) using the NxTAG Respiratory Pathogen Panel (Luminex). Sensitivity and specificity vary by virus but on average were approximately 95% and 99%, respectively. Rhinoviruses were typed by partial sequencing as previously described.¹⁷

Outcome Measures

The primary end point was time to a severe asthma exacerbation during the 48-week trial period. A severe asthma exacerbation was defined as the occurrence of either (1) use of systemic corticosteroids (tablets, suspension, or injection) for at least 3 days or (2) a hospitalization or ED visit because of asthma, requiring systemic corticosteroids.¹⁸

There were 3 prespecified secondary outcomes: (1) the time to a viral-induced severe asthma exacerbation, defined by having both a severe exacerbation and a positive PCR result to a panel of common respiratory viruses, (2) the ability to reduce the dose of inhaled steroids by 50% at the 24-week study visit, and (3) the cumulative dose of inhaled steroids during the study period. We also evaluated 2 exploratory outcomes: (1) the mean number of severe asthma exacerbations and (2) the mean number of viral-induced severe exacerbations.

Prespecified Power Calculations

Based on prior studies,⁵ the trial was designed to have a sample size of 400 participants for 88% power to detect an absolute reduction in the rate of severe asthma exacerbations of 16% (from 40% in the placebo group¹⁹ to 24% in the intervention group), assuming an overall α of .05, a 2-sided test, and a withdrawal rate of 15%. Such calculations were conservative because they did not reflect the primary time-to-event analysis.

Statistical Analysis

During the trial, all children were followed up in the group to which they were randomized. In the primary analysis, treatment groups were compared in a Cox proportional hazards regression model that estimated a hazard ratio (HR) for the time to a severe asthma exacerbation across the 48-week study period. The model included dropouts as censored observations and, per protocol, was stratified by site and race/ethnicity, as well as by potential confounders that were not balanced by randomization. A similar approach was used for the analysis of time to a viral-induced severe asthma exacerbation. Both asthma severity and vitamin D level may vary by race/ethnicity; information was ascertained by parental report using fixed categories for race and a separate question for Hispanic/Latino ethnicity, and analyzed using a combined variable (non-Hispanic White, non-Hispanic Black, and other). The proportionality assumption was tested visually and by fitting models with covariates and their interactions with time; none of the interactions were significant.

Linear regression was used for the analysis of the difference in mean cumulative dose of inhaled steroids between the vitamin D₃ and placebo groups at the end of the trial with treatment group as the primary explanatory variable, adjusting for study site, sex, time in study (ie, follow-up time), and race/ethnicity. Logistic regression was used for the analysis of the proportion of participants achieving a reduction in inhaled corticosteroid dose at or after the 24-week visit, adjusting for site, sex, time in study, and race/ethnicity. Missing data for the primary and secondary outcomes were minimal (Figure 1) and, thus, listwise deletion was used in the analyses. Two-sided P values less than .05 were considered significant. Because of the potential for type I error due to multiple comparisons, findings for analyses of secondary end points should be interpreted as exploratory. All analyses were performed using SAS version 9.4 (SAS Institute).

Results

Early Termination

After review of the second interim analysis, on March 11, 2019, the DSMB recommended that no new participants be randomized due to futility (lack of efficacy of vitamin D₃ supplementation), based on the protocol threshold of less than 30% conditional power to detect the prespecified effect (a 16% reduction in severe exacerbations). At that time, there had been 26 events in 90 participants (28.9%) in the placebo group and 25 events in 91 participants (27.5%) in the vitamin D₃ group. Conditional power was evaluated under 3 conditions: under the null (based on no treatment effect); under the alternative hypothesis (based on the original assumption of effect); and under the observed rates. Under all 3, conditional power was less than 30%. A close-out plan to complete follow-up of randomized participants was reviewed and approved by the National Heart, Lung, and Blood Institute; the DSMB; and the IRBs at all participating institutions in August of 2019. Follow-up of the last participant was completed in September of 2019.

Enrollment and Study Completion

After screening, a total of 219 participants entered run-in, and 192 were randomized (96 each to the vitamin D₃ and placebo groups), of whom 180 (93.8%) completed the trial (92 [51%] in the vitamin D₃ group and 88 [49%] in the placebo group) (Figure 1). The median duration of follow-up was 332 days. The most common reasons for study discontinuation were loss to follow-up (n = 6), family decision (n = 5), and administrative decision (n = 1) (Figure 1).

Baseline Characteristics

The trial enrolled children with a mean (SD) age of 9.8 (2.5) years, a mean (SD) ACT or C-ACT score of 21.7 (3.4), and a median of 1 (interquartile range [IQR], 1-2) severe asthma exacerbation in the prior year (Table 1). A total of 77 girls (40%) and 115 boys (60%) were enrolled, with 44 girls (46%) in the vitamin D₃ group and 33 girls (34%) in the placebo group. Both groups were similar in terms of age, race/ethnicity, parental education, household smoke exposure, season of enrollment, body mass index z score, FEV₁, and FEV₁/FVC. The mean (SD) baseline serum vitamin D level was 22.5 (4.6) ng/mL in the vitamin D₃ group and 22.8 (4.6) ng/mL in the placebo group.

Table 1. Baseline Characteristics of Randomized Participants.

Characteristic	Participants, No. (%)
Characteristic	Vitamin D₃ (n = 96)	Placebo (n = 96)
Sex
Female	44 (46)	33 (34)
Male	52 (54)	63 (66)
Race^a
White	27 (28)	32 (33)
Black	51 (53)	49 (51)
Other race	18 (19)	15 (16)
Hispanic/Latino ethnicity^a	7 (7)	6 (6)
Parental education, No./total No. (%)
High school or less	21/94 (22)	20/95 (21)
Some college	22/94 (23)	22/95 (23)
Completed college	37/94 (39)	32/95 (34)
Postgraduate education	14/94 (16)	21/95 (22)
Household smoke exposure, No./total No. (%)
Before age 2 y	31/94 (33)	32/94 (34)
During study	25/93 (27)	22/93 (24)
Season of enrollment
January-March	30 (31)	25 (26)
April-June	26 (27)	26 (27)
July-September	22 (23)	22 (23)
October-December	18 (19)	23 (24)
Asthma Control Test score >19^b	76 (79)	73 (76)
Age at randomization, mean (SD), y	9.9 (2.5)	9.7 (2.5)
BMI z score, mean (SD)^c	0.9 (1.1) [n = 95]	0.9 (1.3)
No. of severe exacerbations in the previous year, median (IQR)	1 (1-2) [n = 88]	1 (1-2) [n = 86]
Vitamin D, mean (SD), ng/mL	22.5 (4.6)	22.8 (4.6)
FEV₁, mean (SD), % predicted^d	93.9 (15.8)	90.6 (17.3)
FEV₁/FVC, mean (SD), % predicted^d	91.5 (9.3)	89.6 (10.1)
Asthma Control Test score, mean (SD)^b	22.0 (3.2)	21.3 (3.6)

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Abbreviations: BMI, body mass index (calculated as weight in kilograms divided by height in meters squared); FEV₁, forced expiratory volume in the first second of expiration; FVC, forced vital capacity; IQR, interquartile range.

^{^a}

Race and ethnicity were ascertained per parental report. “Other race” includes American Indian, Alaskan Native, Asian, mixed, and those reported as “other.”

^{^b}

Asthma Control Test (ACT)¹⁵ was for participants aged 12 years or older, and Childhood Asthma Control Test (C-ACT)¹⁶ was for participants aged 6 to younger than 12 years. The ACT is calculated based on 5 self-administered questions and has a score range of 5 to 25. The C-ACT is calculated based on 7 questions (3 answered by the parent and 4 answered with the child’s input) and has a score range of 0 to 27. For both, higher scores indicate better symptom control, and a score greater than 19 indicates well-controlled asthma symptoms.

^{^c}

BMI z scores calculated using US Centers for Disease Control and Prevention equations,²⁰ which create z scores and percentiles for the child’s sex and age. A BMI z score of 0 is equivalent to the 50th percentile.

^{^d}

All participants performed spirometry following American Thoracic Society/European Respiratory Society guidelines.²¹ Calculated using reference values from the third National Health and Nutrition Examination Survey.²² Values 80% of predicted or greater are considered normal.

Serum Vitamin D Levels

Compared with participants in the placebo group, those in the vitamin D₃ group were significantly more likely to achieve a vitamin D level of 30 ng/mL or higher (94.4% in the vitamin D₃ group vs 40.7% in the placebo group at 16 weeks; and 87.2% vs 30.1%, respectively, at 48 weeks; both P < .001) and to have a higher vitamin D level at all visits during the trial. In the vitamin D₃ group, the mean vitamin D levels were 57.2 ng/mL (95% CI, 52.9-61.5) at 16 weeks, 53.8 ng/mL (95% CI, 48.9-58.6) at 32 weeks, and 49.4 ng/mL (95% CI, 44.9-53.9) at 48 weeks. In the placebo group, vitamin D serum levels were 27.5 ng/mL (95% CI, 25.2-29.9) at 16 weeks, 25.4 ng/mL (95% CI, 23.6-27.3) at 32 weeks, and 24.6 ng/mL (95% CI, 22.9-26.3) at 48 weeks (Figure 2), with similar levels after excluding participants who received open-label vitamin D₃ supplementation due to very low levels during the trial (eTable in Supplement 2). A total of 23% and 12% of participants had vitamin D levels less than 20 ng/mL at the baseline visit and study exit visit, respectively. In the vitamin D₃ group, no participants reported taking (nonstudy) vitamin D₃ supplements at randomization, and 2 reported such supplementation at study exit; those numbers were 1 and 6 participants, respectively, in the placebo group. The median adherence with study medication was 85% (IQR, 72%-93%) in the vitamin D₃ group and 87% (IQR, 76%-94%) in the placebo group.

Figure 2. — Boxes represent median and interquartile ranges with error bars indicating the highest and lowest values within 1.5 times the interquartile range; dots represent outlying data.

Primary Outcome: Time to Severe Asthma Exacerbation

A total of 36 participants (37.5%) in the vitamin D₃ group and 33 participants (34.4%) in the placebo group had at least 1 severe asthma exacerbation during the trial. Vitamin D₃ supplementation did not significantly prolong the time to a severe asthma exacerbation: the mean number of days until a severe exacerbation was 240 in the vitamin D₃ group and 253 in the placebo group, with a mean group difference of −13.1 days (95% CI, −42.6 to 16.4) and adjusted HR of 1.13 (95% CI, 0.69-1.85; P = .63) (Table 2 and Figure 3).

Table 2. VDKA Trial Outcomes and Serious Adverse Events for Vitamin D₃ Supplementation vs Placebo.

Measure	Vitamin D₃		Placebo		Group difference (95% CI)	Adjusted analysis
Measure	No.	Mean	No.	Mean	Group difference (95% CI)	Parameter estimate (95% CI)	P value
Primary outcome
Days to a severe exacerbation^a	96	240	96	253	−13.1 (−42.6 to 16.4)	1.13 (0.69 to 1.85)^b	.63
Secondary outcomes
Days to viral-induced severe exacerbation^c	82	272	83	281	−9.1 (−35.5 to 17.2)	1.32 (0.63 to 2.75)^b	.46
Proportion of participants in whom fluticasone dose was halved, No. (%)	91	28 (30.8)	91	29 (31.9)	−1.1 (−14.6 to 12.4)	0.99 (0.66 to 1.52)^d	.99
Cumulative fluticasone dose, mg	96	59.6	96	55.2	4.41 (−0.99 to 9.80)	4.40 (0.001 to 8.80)^e	.049
Exploratory outcomes
No. of severe exacerbations	96	0.58^f	96	0.51^f	0.07 (−0.14 to 0.28)	0.13 (−0.25 to 0.52)^e	.50
No. of viral-induced severe exacerbations	86	0.26^f	85	0.22^f	0.03 (−0.11 to 0.18)	0.18 (−0.44 to 0.81)^g	.56
Serious adverse events^h
Participants with ≥1 serious adverse events, No. (%)	96	9 (9.4)	96	7 (7.3)
Total No. of serious adverse eventsⁱ	96	11	96	9
Hospitalizations for asthma exacerbation, No.	96	8	96	6

Open in a new tab

Abbreviation: VDKA, Vitamin D to Prevent Severe Asthma Exacerbations.

^{^a}

Defined as a hospitalization or emergency department visit for asthma requiring systemic corticosteroids, or an asthma exacerbation leading to use of systemic corticosteroids (tablets, suspension, or injection) for at least 3 days.

^{^b}

Hazard ratio stratified by site, sex, and race/ethnicity.

^{^c}

Defined as a nasal blow, collected within 7 days of the exacerbation, in which at least 1 virus was detected by polymerase chain reaction in a panel of common respiratory viruses (average, approximately 95% sensitivity and 99% specificity).

^{^d}

Relative risk ratio adjusted for sex, race/ethnicity, and days of follow-up in the study (model failed to converge when site included as covariate).

^{^e}

Parameter estimate (beta coefficient, or adjusted difference in means) from Poisson regression adjusted for study site, sex, race/ethnicity, and days of follow-up in the study.

^{^f}

Mean number of exacerbations per participant.

^{^g}

Parameter estimate (beta coefficient, or adjusted difference in means) from Poisson regression adjusted for sex, race/ethnicity, and days of follow-up in the study (model failed to converge when site included as covariate).

^{^h}

Serious adverse events reported as comparative frequencies alone; sample size not sufficient to allow meaningful statistical comparisons.

^ⁱ

Serious adverse events included hospitalizations (9 in each group), eosinophilia (1), and severe neutropenia (1). There were no instances of hypercalcemia in either group.

Figure 3. — Vertical bars represent single censored events. The adjusted hazard ratio for time from randomization to a first severe exacerbation was 1.13 (95% CI, 0.69-1.85) for the vitamin D₃ vs placebo treatment groups (P = .63). Models were stratified by study site, sex, and race/ethnicity. The median observation time was 274.5 days (interquartile range [IQR], 163-333) in the vitamin D₃ group and 321 days (IQR, 196.5-334) in the control group.

Secondary Outcomes

Vitamin D₃ supplementation did not significantly prolong the time to a first viral-induced severe exacerbation compared with placebo: the mean number of days was 272 in the vitamin D₃ group and 281 in the placebo group, with a mean group difference of −9.1 days (95% CI, −35.5 to 17.2) and an adjusted HR of 1.32 (95% CI, 0.63-2.75; P = .46; Table 2; eFigure in Supplement 2). The proportion of participants whose inhaled corticosteroid dose could be reduced (halved) at the midpoint of the trial was not significantly different between the vitamin D₃ (28 participants [31%]) and the placebo (29 participants [32%]) groups (group difference, −1.1% [95% CI, −14.6% to 12.4%]; adjusted relative risk ratio, 0.99 [95% CI, 0.66-1.52]; P = .99) (Table 2). Vitamin D₃ supplementation, compared with placebo, did not lead to a significant reduction in the cumulative dose of fluticasone during the trial (59.6 mg vs 55.2 mg, respectively; mean group difference, 4.41 mg [95% CI, −0.99 to 9.80]; adjusted mean difference, 4.40 mg [95% CI, 0.001 to 8.80]; P = .049) (Table 2).

Exploratory Outcomes

Compared with placebo, vitamin D₃ supplementation did not significantly reduce the number of severe asthma exacerbations (mean number of exacerbations, 0.58 in the vitamin D₃ group vs 0.51 in the placebo group; mean group difference, 0.07 [95% CI, −0.14 to 0.28]; P = .50) or viral-induced severe exacerbations (mean number of viral-induced exacerbations, 0.26 in the vitamin D₃ group vs 0.22 in the placebo group; mean group difference, 0.03 [95% CI, −0.11 to 0.18]; P = .56) (Table 2).

Adverse Events

Nine participants in the vitamin D₃ group and 7 in the placebo group had a serious adverse event (Table 2). The most common serious adverse events were hospitalizations for asthma (8 in the vitamin D₃ group and 6 in the placebo group). After randomization, no participant in the vitamin D₃ group and 2 participants in the placebo group had medication stopped due to vitamin D levels less than 10 ng/mL. Two participants had a level less than 10 ng/mL and 2 participants had levels between 10 and 13 ng/mL at 2 visits during the trial; per protocol, all instances were referred to a pediatric endocrinologist for evaluation and management. There were no cases of hypercalcemia or vitamin D toxicity in either treatment group.

Discussion

In this randomized clinical trial of vitamin D₃ added to low-dose inhaled corticosteroids in school-aged children with vitamin D insufficiency and persistent asthma at high risk for severe exacerbations, vitamin D₃ supplementation did not lead to a significant improvement in the time to a severe asthma exacerbation. Moreover, vitamin D₃ supplementation had no significant beneficial effects on any of the trial’s secondary end points, including time to a viral-induced severe asthma exacerbation, the proportion of participants whose inhaled corticosteroid dose was reduced, or the mean or cumulative inhaled corticosteroid dose during the trial. At an observed event rate of approximately 38% in the control group, such effect maps to an HR of about 1.93, which is not included in the 95% CI of the estimate for the primary outcome.

While observational studies have reported associations between low vitamin D levels and childhood asthma outcomes,^2,3,4,5 randomized clinical trials have provided less encouraging evidence of a protective effect of vitamin D₃ supplementation against morbidity from asthma.¹³ Moreover, both the VDAART (Vitamin D Antenatal Asthma Reduction Trial) and the COPSAC 2010 (Copenhagen Prospective Studies on Asthma in Childhood 2010 cohort) trials have recently reported no significant effect of vitamin D₃ supplementation during pregnancy on asthma in the offspring by age 6 years, strongly suggesting that there is no role for such supplementation in the primary prevention of asthma.^23,24,25

The results from this trial cannot be attributed to failure to achieve vitamin D sufficiency after vitamin D₃ supplementation because most (>87%) of the participants in the treatment group had vitamin D levels of 30 ng/mL or greater during the trial. The placebo group had a relatively low proportion of participants in the control group achieving and sustaining vitamin D sufficiency (<40%), and participants in the vitamin D₃ group had consistently higher vitamin D levels than those in the placebo group throughout the trial. Thus, there was a low risk of a false-negative result due to failure of supplementation in producing a difference in vitamin D levels between treatment groups.

Daily vitamin D₃ supplementation at a dose of 4000 IU/d was well tolerated without significant adverse events, as no study participant developed vitamin D toxicity or hypercalcemia. Moreover, no study participant developed rickets, and only a small proportion of participants developed severe vitamin D deficiency (a vitamin D level <10 ng/mL) or had a vitamin D level between 10 and 13 ng/mL at 2 visits during the trial, supporting the appropriateness of the monitoring measures used in the trial. Although vitamin D₃ supplementation at 4000 IU/d appears effective in achieving vitamin D sufficiency in most children aged 6 to 16 years with vitamin D levels between 14 and 29 ng/mL, study findings cannot be generalized to settings with no or limited monitoring of vitamin D levels.

Limitations

This study has several limitations. First, the rate of severe asthma exacerbations in both the vitamin D₃ (37.5%) and placebo (34.4%) groups were lower than expected, and the study was not adequately powered to assess whether such a small difference was statistically significant. However, there was no evidence of a protective effect of vitamin D against severe asthma exacerbations or viral-induced severe asthma exacerbations, and vitamin D₃ supplementation did not lead to a reduction in the mean or cumulative dose of inhaled corticosteroids.

Second, there was limited statistical power to determine whether vitamin D₃ supplementation reduces severe asthma exacerbations in children with vitamin D levels less than 20 ng/mL because only a modest proportion of participants had such levels. However, most children with vitamin D levels less than 30 ng/mL in the US have levels greater than 20 ng/mL, and thus the findings from this study are applicable to most children with vitamin D insufficiency in this country.²⁶

Third, the findings cannot be extrapolated to other age groups, including preschool children, or to settings with limited ability to monitor vitamin D levels.

Conclusions

Supplement 1.

Trial Protocol

Click here for additional data file.^{(422.1KB, pdf)}

Supplement 2.

eTable. Vitamin D Levels in Nonsupplemented Participants in the Placebo group

eFigure. Time to First Viral-Induced Severe Asthma Exacerbation

Click here for additional data file.^{(258.5KB, pdf)}

Supplement 3.

Data Sharing Statement

Click here for additional data file.^{(19.7KB, pdf)}

References

1.Centers for Disease Control and Prevention Asthma: most recent asthma data. Updated March 24, 2020. Accessed June 18, 2020. https://www.cdc.gov/asthma/most_recent_data.htm
2.Brehm JM, Celedón JC, Soto-Quiros ME, et al. . Serum vitamin D levels and markers of severity of childhood asthma in Costa Rica. Am J Respir Crit Care Med. 2009;179(9):765-771. doi: 10.1164/rccm.200808-1361OC [DOI] [PMC free article] [PubMed] [Google Scholar]
3.Searing DA, Zhang Y, Murphy JR, Hauk PJ, Goleva E, Leung DY. Decreased serum vitamin D levels in children with asthma are associated with increased corticosteroid use. J Allergy Clin Immunol. 2010;125(5):995-1000. doi: 10.1016/j.jaci.2010.03.008 [DOI] [PMC free article] [PubMed] [Google Scholar]
4.Gupta A, Sjoukes A, Richards D, et al. . Relationship between serum vitamin D, disease severity, and airway remodeling in children with asthma. Am J Respir Crit Care Med. 2011;184(12):1342-1349. doi: 10.1164/rccm.201107-1239OC [DOI] [PMC free article] [PubMed] [Google Scholar]
5.Brehm JM, Acosta-Pérez E, Klei L, et al. . Vitamin D insufficiency and severe asthma exacerbations in Puerto Rican children. Am J Respir Crit Care Med. 2012;186(2):140-146. doi: 10.1164/rccm.201203-0431OC [DOI] [PMC free article] [PubMed] [Google Scholar]
6.Matheu V, Bäck O, Mondoc E, Issazadeh-Navikas S. Dual effects of vitamin D-induced alteration of TH1/TH2 cytokine expression: enhancing IgE production and decreasing airway eosinophilia in murine allergic airway disease. J Allergy Clin Immunol. 2003;112(3):585-592. doi: 10.1016/S0091-6749(03)01855-4 [DOI] [PubMed] [Google Scholar]
7.Huang Y, Wang L, Jia XX, Lin XX, Zhang WX. Vitamin D alleviates airway remodeling in asthma by down-regulating the activity of Wnt/β-catenin signaling pathway. Int Immunopharmacol. 2019;68:88-94. doi: 10.1016/j.intimp.2018.12.061 [DOI] [PubMed] [Google Scholar]
8.Heine G, Niesner U, Chang HD, et al. . 1,25-dihydroxyvitamin D(3) promotes IL-10 production in human B cells. Eur J Immunol. 2008;38(8):2210-2218. doi: 10.1002/eji.200838216 [DOI] [PubMed] [Google Scholar]
9.Jeffery LE, Burke F, Mura M, et al. . 1,25-Dihydroxyvitamin D3 and IL-2 combine to inhibit T cell production of inflammatory cytokines and promote development of regulatory T cells expressing CTLA-4 and FoxP3. J Immunol. 2009;183(9):5458-5467. doi: 10.4049/jimmunol.0803217 [DOI] [PMC free article] [PubMed] [Google Scholar]
10.Telcian AG, Zdrenghea MT, Edwards MR, et al. . Vitamin D increases the antiviral activity of bronchial epithelial cells in vitro. Antiviral Res. 2017;137:93-101. doi: 10.1016/j.antiviral.2016.11.004 [DOI] [PubMed] [Google Scholar]
11.Wang TT, Nestel FP, Bourdeau V, et al. . Cutting edge: 1,25-dihydroxyvitamin D3 is a direct inducer of antimicrobial peptide gene expression. Correction appears in J Immunol. 2004 Nov 15;173(10):following 6489. J Immunol. 2004;173(5):2909-2912. doi: 10.4049/jimmunol.173.5.2909 [DOI] [PubMed] [Google Scholar]
12.Jolliffe DA, Greenberg L, Hooper RL, et al. . Vitamin D supplementation to prevent asthma exacerbations: a systematic review and meta-analysis of individual participant data. Lancet Respir Med. 2017;5(11):881-890. doi: 10.1016/S2213-2600(17)30306-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
13.Stefanidis C, Martineau AR, Nwokoro C, Griffiths CJ, Bush A. Vitamin D for secondary prevention of acute wheeze attacks in preschool and school-age children. Thorax. 2019;74(10):977-985. doi: 10.1136/thoraxjnl-2019-213278 [DOI] [PubMed] [Google Scholar]
14.Forno E, Celedón JC. Predicting asthma exacerbations in children. Curr Opin Pulm Med. 2012;18(1):63-69. doi: 10.1097/MCP.0b013e32834db288 [DOI] [PMC free article] [PubMed] [Google Scholar]
15.Nathan RA, Sorkness CA, Kosinski M, et al. . Development of the asthma control test: a survey for assessing asthma control. J Allergy Clin Immunol. 2004;113(1):59-65. doi: 10.1016/j.jaci.2003.09.008 [DOI] [PubMed] [Google Scholar]
16.Liu AH, Zeiger R, Sorkness C, et al. . Development and cross-sectional validation of the Childhood Asthma Control Test. J Allergy Clin Immunol. 2007;119(4):817-825. doi: 10.1016/j.jaci.2006.12.662 [DOI] [PubMed] [Google Scholar]
17.Bochkov YA, Grindle K, Vang F, Evans MD, Gern JE. Improved molecular typing assay for rhinovirus species A, B, and C. J Clin Microbiol. 2014;52(7):2461-2471. doi: 10.1128/JCM.00075-14 [DOI] [PMC free article] [PubMed] [Google Scholar]
18.Reddel HK, Taylor DR, Bateman ED, et al. ; American Thoracic Society/European Respiratory Society Task Force on Asthma Control and Exacerbations . An official American Thoracic Society/European Respiratory Society statement: asthma control and exacerbations: standardizing endpoints for clinical asthma trials and clinical practice. Am J Respir Crit Care Med. 2009;180(1):59-99. doi: 10.1164/rccm.200801-060ST [DOI] [PubMed] [Google Scholar]
19.Covar RA, Szefler SJ, Zeiger RS, et al. ; Childhood Asthma Research and Education Network . Factors associated with asthma exacerbations during a long-term clinical trial of controller medications in children. J Allergy Clin Immunol. 2008;122(4):741-747.e4. doi: 10.1016/j.jaci.2008.08.021 [DOI] [PMC free article] [PubMed] [Google Scholar]
20.Kuczmarski RJ, Ogden CL, Guo SS, et al. . 2000 CDC Growth Charts for the United States: methods and development. Vital Health Stat 11. 2002;(246):1-190. [PubMed] [Google Scholar]
21.Miller MR, Hankinson J, Brusasco V, et al. ; ATS/ERS Task Force . Standardisation of spirometry. Eur Respir J. 2005;26(2):319-338. doi: 10.1183/09031936.05.00034805 [DOI] [PubMed] [Google Scholar]
22.Hankinson JL, Odencrantz JR, Fedan KB. Spirometric reference values from a sample of the general US population. Am J Respir Crit Care Med. 1999;159(1):179-187. doi: 10.1164/ajrccm.159.1.9712108 [DOI] [PubMed] [Google Scholar]
23.Litonjua AA, Carey VJ, Laranjo N, et al. . Effect of prenatal supplementation with vitamin D on asthma or recurrent wheezing in offspring by age 3 years: the VDAART randomized clinical trial. JAMA. 2016;315(4):362-370. doi: 10.1001/jama.2015.18589 [DOI] [PMC free article] [PubMed] [Google Scholar]
24.Brustad N, Eliasen AU, Stokholm J, Bønnelykke K, Bisgaard H, Chawes BL. High-dose vitamin D supplementation during pregnancy and asthma in offspring at the age of 6 years. JAMA. 2019;321(10):1003-1005. doi: 10.1001/jama.2019.0052 [DOI] [PMC free article] [PubMed] [Google Scholar]
25.Litonjua AA, Carey VJ, Laranjo N, et al. . Six-year follow-up of a trial of antenatal vitamin D for asthma reduction. N Engl J Med. 2020;382(6):525-533. doi: 10.1056/NEJMoa1906137 [DOI] [PMC free article] [PubMed] [Google Scholar]
26.Mansbach JM, Ginde AA, Camargo CA Jr. Serum 25-hydroxyvitamin D levels among US children aged 1 to 11 years: do children need more vitamin D? Pediatrics. 2009;124(5):1404-1410. doi: 10.1542/peds.2008-2041 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplement 1.

Trial Protocol

Click here for additional data file.^{(422.1KB, pdf)}

Supplement 2.

eTable. Vitamin D Levels in Nonsupplemented Participants in the Placebo group

eFigure. Time to First Viral-Induced Severe Asthma Exacerbation

Click here for additional data file.^{(258.5KB, pdf)}

Supplement 3.

Data Sharing Statement

Click here for additional data file.^{(19.7KB, pdf)}

[joi200079r1] 1.Centers for Disease Control and Prevention Asthma: most recent asthma data. Updated March 24, 2020. Accessed June 18, 2020. https://www.cdc.gov/asthma/most_recent_data.htm

[joi200079r2] 2.Brehm JM, Celedón JC, Soto-Quiros ME, et al. . Serum vitamin D levels and markers of severity of childhood asthma in Costa Rica. Am J Respir Crit Care Med. 2009;179(9):765-771. doi: 10.1164/rccm.200808-1361OC [DOI] [PMC free article] [PubMed] [Google Scholar]

[joi200079r3] 3.Searing DA, Zhang Y, Murphy JR, Hauk PJ, Goleva E, Leung DY. Decreased serum vitamin D levels in children with asthma are associated with increased corticosteroid use. J Allergy Clin Immunol. 2010;125(5):995-1000. doi: 10.1016/j.jaci.2010.03.008 [DOI] [PMC free article] [PubMed] [Google Scholar]

[joi200079r4] 4.Gupta A, Sjoukes A, Richards D, et al. . Relationship between serum vitamin D, disease severity, and airway remodeling in children with asthma. Am J Respir Crit Care Med. 2011;184(12):1342-1349. doi: 10.1164/rccm.201107-1239OC [DOI] [PMC free article] [PubMed] [Google Scholar]

[joi200079r5] 5.Brehm JM, Acosta-Pérez E, Klei L, et al. . Vitamin D insufficiency and severe asthma exacerbations in Puerto Rican children. Am J Respir Crit Care Med. 2012;186(2):140-146. doi: 10.1164/rccm.201203-0431OC [DOI] [PMC free article] [PubMed] [Google Scholar]

[joi200079r6] 6.Matheu V, Bäck O, Mondoc E, Issazadeh-Navikas S. Dual effects of vitamin D-induced alteration of TH1/TH2 cytokine expression: enhancing IgE production and decreasing airway eosinophilia in murine allergic airway disease. J Allergy Clin Immunol. 2003;112(3):585-592. doi: 10.1016/S0091-6749(03)01855-4 [DOI] [PubMed] [Google Scholar]

[joi200079r7] 7.Huang Y, Wang L, Jia XX, Lin XX, Zhang WX. Vitamin D alleviates airway remodeling in asthma by down-regulating the activity of Wnt/β-catenin signaling pathway. Int Immunopharmacol. 2019;68:88-94. doi: 10.1016/j.intimp.2018.12.061 [DOI] [PubMed] [Google Scholar]

[joi200079r8] 8.Heine G, Niesner U, Chang HD, et al. . 1,25-dihydroxyvitamin D(3) promotes IL-10 production in human B cells. Eur J Immunol. 2008;38(8):2210-2218. doi: 10.1002/eji.200838216 [DOI] [PubMed] [Google Scholar]

[joi200079r9] 9.Jeffery LE, Burke F, Mura M, et al. . 1,25-Dihydroxyvitamin D3 and IL-2 combine to inhibit T cell production of inflammatory cytokines and promote development of regulatory T cells expressing CTLA-4 and FoxP3. J Immunol. 2009;183(9):5458-5467. doi: 10.4049/jimmunol.0803217 [DOI] [PMC free article] [PubMed] [Google Scholar]

[joi200079r10] 10.Telcian AG, Zdrenghea MT, Edwards MR, et al. . Vitamin D increases the antiviral activity of bronchial epithelial cells in vitro. Antiviral Res. 2017;137:93-101. doi: 10.1016/j.antiviral.2016.11.004 [DOI] [PubMed] [Google Scholar]

[joi200079r11] 11.Wang TT, Nestel FP, Bourdeau V, et al. . Cutting edge: 1,25-dihydroxyvitamin D3 is a direct inducer of antimicrobial peptide gene expression. Correction appears in J Immunol. 2004 Nov 15;173(10):following 6489. J Immunol. 2004;173(5):2909-2912. doi: 10.4049/jimmunol.173.5.2909 [DOI] [PubMed] [Google Scholar]

[joi200079r12] 12.Jolliffe DA, Greenberg L, Hooper RL, et al. . Vitamin D supplementation to prevent asthma exacerbations: a systematic review and meta-analysis of individual participant data. Lancet Respir Med. 2017;5(11):881-890. doi: 10.1016/S2213-2600(17)30306-5 [DOI] [PMC free article] [PubMed] [Google Scholar]

[joi200079r13] 13.Stefanidis C, Martineau AR, Nwokoro C, Griffiths CJ, Bush A. Vitamin D for secondary prevention of acute wheeze attacks in preschool and school-age children. Thorax. 2019;74(10):977-985. doi: 10.1136/thoraxjnl-2019-213278 [DOI] [PubMed] [Google Scholar]

[joi200079r14] 14.Forno E, Celedón JC. Predicting asthma exacerbations in children. Curr Opin Pulm Med. 2012;18(1):63-69. doi: 10.1097/MCP.0b013e32834db288 [DOI] [PMC free article] [PubMed] [Google Scholar]

[joi200079r15] 15.Nathan RA, Sorkness CA, Kosinski M, et al. . Development of the asthma control test: a survey for assessing asthma control. J Allergy Clin Immunol. 2004;113(1):59-65. doi: 10.1016/j.jaci.2003.09.008 [DOI] [PubMed] [Google Scholar]

[joi200079r16] 16.Liu AH, Zeiger R, Sorkness C, et al. . Development and cross-sectional validation of the Childhood Asthma Control Test. J Allergy Clin Immunol. 2007;119(4):817-825. doi: 10.1016/j.jaci.2006.12.662 [DOI] [PubMed] [Google Scholar]

[joi200079r17] 17.Bochkov YA, Grindle K, Vang F, Evans MD, Gern JE. Improved molecular typing assay for rhinovirus species A, B, and C. J Clin Microbiol. 2014;52(7):2461-2471. doi: 10.1128/JCM.00075-14 [DOI] [PMC free article] [PubMed] [Google Scholar]

[joi200079r18] 18.Reddel HK, Taylor DR, Bateman ED, et al. ; American Thoracic Society/European Respiratory Society Task Force on Asthma Control and Exacerbations . An official American Thoracic Society/European Respiratory Society statement: asthma control and exacerbations: standardizing endpoints for clinical asthma trials and clinical practice. Am J Respir Crit Care Med. 2009;180(1):59-99. doi: 10.1164/rccm.200801-060ST [DOI] [PubMed] [Google Scholar]

[joi200079r19] 19.Covar RA, Szefler SJ, Zeiger RS, et al. ; Childhood Asthma Research and Education Network . Factors associated with asthma exacerbations during a long-term clinical trial of controller medications in children. J Allergy Clin Immunol. 2008;122(4):741-747.e4. doi: 10.1016/j.jaci.2008.08.021 [DOI] [PMC free article] [PubMed] [Google Scholar]

[joi200079r20] 20.Kuczmarski RJ, Ogden CL, Guo SS, et al. . 2000 CDC Growth Charts for the United States: methods and development. Vital Health Stat 11. 2002;(246):1-190. [PubMed] [Google Scholar]

[joi200079r21] 21.Miller MR, Hankinson J, Brusasco V, et al. ; ATS/ERS Task Force . Standardisation of spirometry. Eur Respir J. 2005;26(2):319-338. doi: 10.1183/09031936.05.00034805 [DOI] [PubMed] [Google Scholar]

[joi200079r22] 22.Hankinson JL, Odencrantz JR, Fedan KB. Spirometric reference values from a sample of the general US population. Am J Respir Crit Care Med. 1999;159(1):179-187. doi: 10.1164/ajrccm.159.1.9712108 [DOI] [PubMed] [Google Scholar]

[joi200079r23] 23.Litonjua AA, Carey VJ, Laranjo N, et al. . Effect of prenatal supplementation with vitamin D on asthma or recurrent wheezing in offspring by age 3 years: the VDAART randomized clinical trial. JAMA. 2016;315(4):362-370. doi: 10.1001/jama.2015.18589 [DOI] [PMC free article] [PubMed] [Google Scholar]

[joi200079r24] 24.Brustad N, Eliasen AU, Stokholm J, Bønnelykke K, Bisgaard H, Chawes BL. High-dose vitamin D supplementation during pregnancy and asthma in offspring at the age of 6 years. JAMA. 2019;321(10):1003-1005. doi: 10.1001/jama.2019.0052 [DOI] [PMC free article] [PubMed] [Google Scholar]

[joi200079r25] 25.Litonjua AA, Carey VJ, Laranjo N, et al. . Six-year follow-up of a trial of antenatal vitamin D for asthma reduction. N Engl J Med. 2020;382(6):525-533. doi: 10.1056/NEJMoa1906137 [DOI] [PMC free article] [PubMed] [Google Scholar]

[joi200079r26] 26.Mansbach JM, Ginde AA, Camargo CA Jr. Serum 25-hydroxyvitamin D levels among US children aged 1 to 11 years: do children need more vitamin D? Pediatrics. 2009;124(5):1404-1410. doi: 10.1542/peds.2008-2041 [DOI] [PMC free article] [PubMed] [Google Scholar]

PERMALINK

Effect of Vitamin D3 Supplementation on Severe Asthma Exacerbations in Children With Asthma and Low Vitamin D Levels

Erick Forno, MD, MPH

Leonard B Bacharier, MD

Wanda Phipatanakul, MD, MS

Theresa W Guilbert, MD, MS

Michael D Cabana, MD, MPH

Kristie Ross, MD, MS

Ronina Covar, MD

James E Gern, MD

Franziska J Rosser, MD, MPH

Joshua Blatter, MD, MPH

Sandy Durrani, MD

Yueh-Ying Han, PhD

Stephen R Wisniewski, PhD

Juan C Celedón, MD, DrPH

Key Points

Question

Findings

Meaning

Abstract

Importance

Objective

Design, Setting, and Participants

Interventions

Main Outcomes and Measures

Results

Conclusions and Relevance

Trial Registration

Introduction

Methods

Participants

Study Design and Treatment

Figure 1. Selection of Study Participants.

Viral Polymerase Chain Reaction

Outcome Measures

Prespecified Power Calculations

Statistical Analysis

Results

Early Termination

Enrollment and Study Completion

Baseline Characteristics

Table 1. Baseline Characteristics of Randomized Participants.

Serum Vitamin D Levels

Figure 2. Vitamin D Levels During Trial Period by Treatment Group.

Primary Outcome: Time to Severe Asthma Exacerbation

Table 2. VDKA Trial Outcomes and Serious Adverse Events for Vitamin D3 Supplementation vs Placebo.

Figure 3. Results of the Analysis of Time to a First Severe Asthma Exacerbation.

Secondary Outcomes

Exploratory Outcomes

Adverse Events

Discussion

Limitations

Conclusions

References

Associated Data

Supplementary Materials

ACTIONS

PERMALINK

RESOURCES

Similar articles

Cited by other articles

Links to NCBI Databases

Effect of Vitamin D₃ Supplementation on Severe Asthma Exacerbations in Children With Asthma and Low Vitamin D Levels

Table 2. VDKA Trial Outcomes and Serious Adverse Events for Vitamin D₃ Supplementation vs Placebo.