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Prenatal vitamin D supplementation reduces risk of asthma/recurrent wheeze in early childhood: A combined analysis of two randomized controlled trials

  • Helene M. Wolsk ,

    Roles Data curation, Formal analysis, Investigation, Writing – original draft, Writing – review & editing

    ‡ These authors are co-first authors on this work.

    Affiliations COPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark, Channing Division of Network Medicine, Department of Medicine, Brigham and Women’s Hospital, Boston, MA, United States of America

  • Bo L. Chawes ,

    Roles Writing – original draft, Writing – review & editing

    ‡ These authors are co-first authors on this work.

    Affiliations COPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark, Channing Division of Network Medicine, Department of Medicine, Brigham and Women’s Hospital, Boston, MA, United States of America

  • Augusto A. Litonjua,

    Roles Conceptualization, Funding acquisition, Methodology, Project administration, Supervision, Writing – review & editing

    Affiliations Channing Division of Network Medicine, Department of Medicine, Brigham and Women’s Hospital, Boston, MA, United States of America, Harvard Medical School, Boston, MA, United States of America

  • Bruce W. Hollis,

    Roles Conceptualization, Funding acquisition, Methodology, Writing – review & editing

    Affiliation Department of Pediatrics, Medical University of South Carolina, Charleston, SC, United States of America

  • Johannes Waage,

    Roles Formal analysis, Writing – review & editing

    Affiliation COPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark

  • Jakob Stokholm,

    Roles Funding acquisition, Investigation, Writing – review & editing

    Affiliation COPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark

  • Klaus Bønnelykke,

    Roles Conceptualization, Funding acquisition, Investigation, Writing – review & editing

    Affiliation COPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark

  • Hans Bisgaard,

    Roles Conceptualization, Funding acquisition, Project administration, Resources, Supervision, Writing – review & editing

    Affiliation COPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark

  • Scott T. Weiss

    Roles Conceptualization, Funding acquisition, Project administration, Resources, Supervision, Writing – review & editing

    scott.weiss@channing.harvard.edu

    Affiliations Channing Division of Network Medicine, Department of Medicine, Brigham and Women’s Hospital, Boston, MA, United States of America, Harvard Medical School, Boston, MA, United States of America

Abstract

Background

We recently published two independent randomized controlled trials of vitamin D supplementation during pregnancy, both indicating a >20% reduced risk of asthma/recurrent wheeze in the offspring by 3 years of age. However, neither reached statistical significance.

Objective

To perform a combined analysis of the two trials and investigate whether maternal 25-hydroxy-vitamin D (25(OH)D) level at trial entry modified the intervention effect.

Methods

VDAART (N = 806) and COPSAC2010. (N = 581) randomized pregnant women to daily high-dose vitamin D3 (4,000 IU/d and 2,400 IU/d, respectively) or placebo. All women also received a prenatal vitamin containing 400 IU/d vitamin D3. The primary outcome was asthma/recurrent wheeze from 0-3yrs. Secondary end-points were specific IgE, total IgE, eczema and lower respiratory tract infections (LRTI). We conducted random effects combined analyses of the treatment effect, individual patient data (IPD) meta-analyses, and analyses stratified by 25(OH)D level at study entry.

Results

The analysis showed a 25% reduced risk of asthma/recurrent wheeze at 0-3yrs: adjusted odds ratio (aOR) = 0.74 (95% CI, 0.57–0.96), p = 0.02. The effect was strongest among women with 25(OH)D level ≥30ng/ml at study entry: aOR = 0.54 (0.33–0.88), p = 0.01, whereas no significant effect was observed among women with 25(OH)D level <30ng/ml at study entry: aOR = 0.84 (0.62–1.15), p = 0.25. The IPD meta-analyses showed similar results. There was no effect on the secondary end-points.

Conclusions

This combined analysis shows that vitamin D supplementation during pregnancy results in a significant reduced risk of asthma/recurrent wheeze in the offspring, especially among women with 25(OH)D level ≥ 30 ng/ml at randomization, where the risk was almost halved. Future studies should examine the possibility of raising 25(OH)D levels to at least 30 ng/ml early in pregnancy or using higher doses than used in our studies.

Trial registration

COPSAC2010: ClinicalTrials.gov NCT00856947; VDAART: ClinicalTrials.gov NCT00920621

Introduction

There are several reasons to hypothesize that low in utero vitamin D exposure increases risk of childhood asthma/recurrent wheeze: (1) Genetic studies have shown that polymorphisms in the vitamin D receptor are associated with childhood asthma susceptibility[1]. (2) Vitamin D has an impact on fetal developmental processes influencing both lung maturation[2] and the immune system[3]. (3) Epidemiological studies have shown that high dietary vitamin D intake during pregnancy reduces the risk of asthma/recurrent wheeze in the offspring[4,5]. (4) A meta-analysis of available observational cord blood studies showed decreased risk of asthma/recurrent wheeze by increasing cord blood 25-hydroxy-vitamin D (25(OH)D) level[6].

Therefore, we recently conducted two independent randomized controlled trials (RCTs) of increased vitamin D supplementation during pregnancy to prevent childhood asthma/recurrent wheeze in the offspring by age 3 years: the Vitamin D Antenatal Asthma Reduction Trial (VDAART[7]) and the Copenhagen Prospective Studies on Asthma in Childhood 2010 (COPSAC2010[8]). Although both trials indicated a clinically important 20% or greater reduced risk of asthma/recurrent wheeze in the offspring, neither found this effect statistically significant in the primary intent-to-treat analyses[9,10].

A recent meta-analysis suggested that insufficient power due to an overestimation of the treatment effect may have been one of the issues for the non-significance of the findings[11], but we hypothesized that maternal 25(OH)D level at trial entry may also have influenced the effect of the vitamin D supplementation[12]. We therefore conducted a combined analysis of the two trials including the primary end-point asthma/recurrent wheeze by age 3 years as well as the secondary end-points specific IgE, total IgE, eczema and lower respiratory tract infections (LRTI) and did 25(OH)D level-based analyses to determine whether nutritional status at entry to the trials influenced the effect of vitamin D.

Methods

VDAART: Monitored by NHLBI and COPSAC: approved by the Ethics Committee for Copenhagen.

VDAART design (clinicaltrials.gov Identifier: NCT00920621)

Pregnant women were recruited from 3 clinical sites across the United States: (1) Boston Medical Center, Boston, MA; (2) Washington University at St. Louis, St. Louis, MO; and (3) Kaiser Permanente Southern California Region, San Diego, CA, as previously detailed[7]. Eligible participants were pregnant non-smoking women aged 18 to 39 years in estimated gestational age 10 to 18 weeks, who had a history of asthma, eczema, or allergic rhinitis or conceived the child with a man with a history of such diseases[7,9], excluding women with other chronic disorders.

The families were followed by telephone interviews every 3 months, capturing diagnoses, symptoms and the medication use of the child. In addition, the mother and child attended the clinics for yearly follow-up visits at age 1, 2 and 3 years. Content of VDAART prenatal and postnatal visits is previously reported[7].

VDAART vitamin D intervention.

The women were randomized 1:1, between 10–18 weeks of gestation, to a daily intake of 4,000 IU vitamin D3 plus a multivitamin containing 400 IU vitamin D3 or a matching placebo tablet plus a multivitamin containing 400 IU vitamin D3, i.e. 4,400 vs. 400 IU vitamin D3 supplement per day. The intervention was continued until delivery. Adherence was measured by MEMS® (Medication Events Monitoring Systems) caps, an electronic cap that recorded each time the tablet container was opened[7].

Blood was drawn from the mothers at entry to the trial and at the 3rd trimester visit (32 to 38 weeks of gestation) for measurement of circulating levels of 25(OH)D, determined by using the DiaSorin Liaison® chemiluminescence immunoassay[13].

COPSAC2010 design (COPSAC2010: clinicaltrials.gov identifier: NCT00856947)

Pregnant women were recruited from Zealand, Denmark between 2008–2010, by phone calls utilizing a monthly surveillance of reimbursement to general practitioners for the first pregnancy visit, as previously detailed[10]. Exclusion criteria were gestational age >26th week, any endocrine, cardiovascular, or nephrological disorders or vitamin D intake >600 IU/day[8].

The children were followed at the COPSAC research unit by the study pediatricians with scheduled visits at 1 week, 1, 3, 6, 12, 18, 24, 30, and 36 months, and with additional unscheduled visits at any respiratory, allergy or skin-related symptoms. In addition, symptoms between visits were captured with daily diary cards monitoring: (1) troublesome lung symptoms, including components of cough, wheeze, and dyspnea; (2) skin symptoms; and (3) respiratory infections. The COPSAC pediatricians acted as general practitioners for the cohort and were the sole responsible physicians for diagnosis and treatment of asthma, allergy, and eczema adhering to predefined algorithms[8].

COPSAC2010 vitamin D intervention.

The women were randomized 1:1 at gestational week 22–26 to a daily dose of 2,400 IU Vitamin D3 plus a multivitamin containing 400 IU vitamin D3 or matching placebo tablets plus a multivitamin containing 400 IU vitamin D3, i.e. 2,800 vs. 400 IU vitamin D3 supplement per day.

The 25(OH)D level of the mother was measured by isotope dilution liquid chromatography-tandem mass spectrometry (LC-MS/MS)[14,15] at time of randomization and at completion of the RCT at 1 week postpartum, allowing for assessment of adherence to the treatment plan, which was further scrutinized by counting returned tablets.

Additional RCTs.

In COPSAC2010 the pregnant women concomitantly participated in a nested, factorial designed, double-blind, RCT of 2.4 g/day n-3 LCPUFA (ClinicalTrials.gov: NCT00798226)[16]. There was no interaction between the vitamin D and PUFA interventions on risk of asthma/recurrent wheeze[16]. Furthermore, a smaller subgroup participated in a randomized, participant-blinded comparison of influenza A vaccines[8,17] (ClinicalTrials.gov: NCT01012557); and a minor sub-group of children participated in a double-blinded RCT of azithromycin vs. placebo during asthmatic episodes (ClinicalTrials.gov: NCT01233297)[18].

Primary end-point.

The primary end-point for both trials was asthma/recurrent wheeze in the child's first three years of life.

In VDAART, this was diagnosed from parental reporting of a physician diagnosis of asthma or recurrent wheeze, defined by the occurrence of at least one of the following five conditions: (1) report of wheeze after the child's second birthday, preceded by at least one report of wheeze prior to the second birthday; (2) report of the child using asthma controller medication after the second birthday, preceded by a report of wheeze before the second birthday; (3) two or more reports of wheeze after the second birthday; (4) at least one report of wheeze and use of asthma controller medications at distinct visits after the second birthday; or (5) two distinct reports of use of asthma controller medications after the second birthday[7].

In COPSAC2010, the children were diagnosed during the clinical visits based on the daily symptom recordings, according to a previously validated quantitative symptom algorithm requiring all of the following criteria[19,20]: (1) five episodes of troublesome lung symptoms within 6 months, each lasting at least 3 consecutive days; (2) symptoms typical of asthma including exercise induced symptoms, prolonged nocturnal cough, and persistent cough outside common cold; (3) need for intermittent rescue use of inhaled β2-agonist; and (4) response to a 3-month course of inhaled corticosteroids and relapse upon ended treatment[19].

Secondary end-points.

Total IgE level was measured at age 3 years in VDAART and at age 6 and 18 months in COPSAC2010. Total IgE was analyzed as a dichotomized variable, using the median as the cut-off value.

Specific IgE levels were measured in VDAART at age 3 years, including Alternaria Alternata, Dermatophagoides farinae, Dermatophagoides pteronyssinus, German cockroach, cat and dog dander, egg, grass pollen mix, tree pollen mix, walnut tree, milk, peanut, soybean, and wheat. In COPSAC2010 specific IgE levels were measured at age 6 and 18 months, including milk, egg, dog and cat dander. In the meta-analysis we only included specific IgE levels of allergens analyzed in both cohorts (milk, egg, dog and cat) using specific IgE level ≥ 0.35 kU/l for any of the allergens as a dichotomized end-point.

Eczema (0–3 years): In VDAART eczema was defined by parental reporting of physician diagnosed eczema, medication usage, and itchy rash with classic localization. In COPSAC2010 the diagnosis was performed at clinical visits by the research pediatricians, based on Hannifin and Rajka’s criteria[21].

Lower respiratory tract infections (LRTI) (0–3 years): In VDAART LRTI was defined from parental reporting of physician diagnoses of bronchitis, bronchiolitis, pneumonia and croup. In COPSAC2010 LRTI included bronchiolitis and pneumonia, predominantly diagnosed by the COPSAC2010 pediatricians.

Statistics

We created logistic regression models for all endpoints, except for LRTI, which was analyzed using a Poisson regression model. Subsequently, we performed a combined analysis of the two trials results utilizing a random-effects meta-analysis model. Odds ratios (ORs) were pooled separately, weighing estimates by the inverse of the estimate variance. The heterogeneity between the studies was tested with a Cochran Q test with a significance level of 0.10 and quantified by using I2 statistics. We also created regression models for all end-points utilizing individual patient data from the two trials; i.e. a IPD meta-analysis. All presented estimates are adjusted for the same covariates as in the original intent-to-treat analyses: maternal educational level, and center for VDAART, and gender, birth season and the fish-oil intervention for COPSAC2010.

For the primary end-point asthma/recurrent wheeze at age 0–3 years, we first analysed the effect of the intervention (vitamin D vs. placebo). Second, to investigate the influence of nutritional status at entry to the trial, we conducted stratified analyses of the intervention among women with 25(OH)D ≥30ng/ml and <30 ng/ml at randomization. Third, we cross-classified the women using 25(OH)D level at randomization (above or below 30 ng/ml) combined with the assigned treatment (vitamin D or placebo). For the secondary end-points, we performed analyses of the effect of the intervention (vitamin D vs. placebo).

The main purpose of the study was to conduct a combined analysis of the effect estimates and individual patient data from our own two large RCTs (COPSAC2010 and VDAART), which are very aligned with respect to vitamin D dosage, time of intervention during pregnancy, number of enrolled women, and offspring outcome definition[9,10]. However, a literature search revealed one additional trial of vitamin D supplementation in pregnancy and subsequent asthma/recurrent wheeze performed by Goldring et al., which differed markedly from our trials by enrolling 180 women at pregnancy week 27 and randomizing them to either no vitamin D, 800 IU ergocalciferol daily until delivery or a single oral bolus of 200,000 IU cholecalciferol[22]. We only included this trial in an exploratory combined analysis of asthma/recurrent wheeze at age 3 years.

We used the statistical software R v. 3.2.3[23] and CRAN package meta v. 4.3.0[24].

Results

For details on included and excluded participants, see the CONSORT flow diagram for each cohort (Fig 1A and 1B).

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Fig 1.

A) The VDAART participants flow, B) The COPSAC2010 participants flow.

https://doi.org/10.1371/journal.pone.0186657.g001

The vitamin D intervention resulted in a significant increase in the mothers post-interventional 25(OH)D levels in both trials (Table 1): in VDAART an increase from 23ng/ml to 39ng/ml and in COPSAC2010 an increase from 31ng/ml to 43ng/ml, respectively.

In VDAART, 625 women (78%) had an initial 25(OH)D level <30 ng/ml (307 received vitamin D and 318 placebo) and 176 women (22%) had a level ≥30 ng/ml at trial entry (95 received vitamin D and 81 placebo). Correspondingly, in COPSAC, 276 women (48%) had an initial level <30 ng/ml (139 received vitamin D and 137 placebo) and 301 women (52%) had an initial level of 25(OH)D ≥30 ng/ml (153 received vitamin D and 148 placebo).

Primary end-point

Asthma/recurrent wheeze.

A total of 218 (29%) children were diagnosed with asthma/recurrent wheeze in the VDAART trial and 104 (18%) in COPSAC2010 during the first 3 years of life (Table 2).

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Table 2. End-points in the two trials at age 0–3 years.

https://doi.org/10.1371/journal.pone.0186657.t002

A combined analysis of the calculated odds-ratios from the separate trials showed a significant 26% reduced risk of asthma/recurrent wheeze in the vitamin D vs. control group: OR = 0.74 (95% CI, 0.57 to 0.96), p = 0.02 (Fig 2A and Table 3), with no heterogeneity among the trials: I2 = 0%, p = 0.89.

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Fig 2. Forest plots of the combined analyses of asthma/recurrent wheeze in COPSAC2010 and VDAART.

A) Combined analysis of the effect of randomization group, B) Combined analysis of women with initial 25(OH)D level ≥ 30 ng/ml, C) Combined analysis of women with initial 25(OH)D level < 30 ng/ml. All analyses are adjusted for gender, birth season and fish-oil intervention in COPSAC2010, and center and maternal education level in VDAART. All analyses of the average 25(OH)D level are also adjusted for intervention group. p<0.05 is shown in italic.

https://doi.org/10.1371/journal.pone.0186657.g002

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Table 3. Individual study results in VDAART and COPSAC2010 and the combined analyses of the primary end-point asthma/recurrent wheeze at age 0–3.

All analyses are adjusted for gender, birth season and fish-oil intervention in COPSAC2010, and center and maternal education level in VDAART. p<0.05 is shown in italic. *Random effects meta-analysis.

https://doi.org/10.1371/journal.pone.0186657.t003

In the analysis stratified for 25(OH)D level at trial entry, the offspring of women with 25(OH)D level ≥30ng/ml had a significantly reduced risk of asthma/recurrent wheeze: OR = 0.54 (0.33 to 0.88), p = 0.01, with little variation among the trials: I2 = 0% and p = 0.47, whereas no significant effect was observed among women with a level <30ng/ml: OR = 0.84 (0.62 to 1.15), p = 0.25, I2 = 0%, p = 0.79. However, no significant interaction between 25(OH)D level at trial entry (used as a dichotomized variable with ≥/< 30ng/ml as the cut-off) and randomization group was observed (p = 0.17), I2 = 0%, p = 0.66 (Fig 2B and 2C and Table 3).

An analysis of initial 25(OH)D level and randomization group, showed a lower risk of asthma/recurrent wheeze in women with 25(OH)D level ≥ 30ng/ml and randomized to vitamin D (women with initial 25(OH)D <30 ng/ml and randomized to placebo as reference), OR = 0.58 (0.37–0.91), p = 0.02, I2 = 0%, p = 0.35. There was no such association for women with 25(OH)D level ≥30ng/ml randomized to placebo or women with 25(OH)D level <30ng/ml randomized to vitamin D (Table 3).

An exploratory analysis of the primary end-point, asthma/recurrent wheeze, including the third vitamin D trial by Goldring et al. showed similar results with a significantly reduced risk of asthma/wheeze at 3 years of age in the vitamin D intervention group, compared to controls: OR = 0.76 (95% CI, 0.59–0.96), p = 0.02 (Fig 3), with little variation among the included studies: I2 = 0%, p = 0.97.

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Fig 3. Forest plots of the meta-analysis of asthma/recurrent wheeze in all three published randomized trials of vitamin D intervention in pregnancy and subsequent asthma/recurrent wheeze at age 3 years.

https://doi.org/10.1371/journal.pone.0186657.g003

Secondary end-points

Total IgE.

The median (interquartile range (IQR)) level of total IgE was 31.5 (11.5 to 103) kU/l in VDAART and 4.56 (2.50 to 8.79) kU/l in COPSAC2010 (Table 2). The combined analysis of the vitamin D intervention showed no effect on development of elevated total IgE level (above the median): OR = 0.90 (0.71 to 1.16), p = 0.46 (Table 4), I2 = 0%, p = 0.46. Analyzing total IgE level as a continuous variable yielded similar results (data not shown).

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Table 4. Individual study results in VDAART and COPSAC2010 and combined analyses of the effect of vitamin D vs. placebo on the secondary end-points at age 0–3.

All analyses are adjusted for gender, birth season and fish-oil intervention in COPSAC2010, and center and maternal education level in VDAART. Lower respiratory tract infections (LRTI) are analyzed by Poisson regression model. *Random effects meta-analysis.

https://doi.org/10.1371/journal.pone.0186657.t004

Specific IgE.

A specific IgE level ≥0.35kU/l against milk, egg, cat and/or dog was present in 212(39%) children in the VDAART cohort at age 3 years; 61 children had elevated specific IgE against inhalant allergens and 193 against food allergens. In COPSAC2010, 39(8%) of the children had elevated specific IgE at ages 6 and/or 18 months; 10 had specific IgE against inhalant allergens and 31 against food allergens (Table 2). The combined analysis showed no effect of the vitamin D intervention on the risk of developing elevated specific IgE: OR = 1.08 (0.69 to 1.67), p = 0.78 (Table 4), I2 = 35%, p = 0.22.This also applied for analyses restricted to inhalant and food allergens (data not shown).

Eczema.

Eczema was diagnosed in 172 (23%) children in VDAART and 143 (25%) children in COPSAC2010, between 0-3yrs of age (Table 2). The combined analysis showed no effect of the vitamin D intervention on the risk of developing eczema: OR = 0.90 (0.70 to 1.17), p = 0.44 (Table 4), I2 = 0%, p = 0.88.

LRTI.

A total of 266 (39%) children in VDAART and 139 (24%) in COPSAC2010 developed one or more LRTI from 0–3 years of age (Table 2). Using a Poisson regression model, we found no effect on the risk of developing one or more LRTI in the combined analysis of the vitamin D intervention: OR = 0.94 (0.65 to 1.37), p = 0.76 (Table 4), I2 = 63%, p = 0.10.

Individual patient data meta-analysis.

Additionally, we conducted individual patient data meta-analysis for all end-points. These analyses yielded results similar as the random effects meta-analyses (Table 5), with OR = 0.75 (0.57 to 0.97), p = 0.03 for development of asthma/recurrent wheeze.

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Table 5. Meta-analyses of individual patient data (IPD), of vitamin D vs. placebo on the primary and secondary end-points at age 0–3.

All analyses are adjusted for gender, birth season, fish-oil intervention, center and maternal education level. Lower respiratory tract infections (LRTI) are analyzed by Poisson regression model.

https://doi.org/10.1371/journal.pone.0186657.t005

Discussion

In this combined analysis of the two largest RCTs to date of vitamin D supplementation during pregnancy, we showed that the supplementation resulted in a significant and clinically important 26% reduced risk of asthma/recurrent wheeze in the offspring until age 3, with a more pronounced 46% reduced risk if the women had 25(OH)D level ≥30ng/ml at trial entry. These results underline that vitamin D supplementation during pregnancy may be an important factor in the prevention of childhood asthma. The findings are suggestive that optimal effect from supplementation may be obtained by assuring baseline levels of at least 30 ng/ml in early pregnancy.

Strengths and limitations

The VDAART and COPSAC2010 RCTs both had asthma/recurrent wheeze at age 0–3 years as primary end-point and had a range of mutual secondary end-points including total IgE, specific IgE, eczema and LRTI. Thus, the aligned design with respect to follow-up length and predefined end-points is a major strength of this combined analysis. This resulted in more power to detect true effects of the vitamin D supplementation than the individual intent-to-treat analyses, illustrated by a similar overall effect estimate in the analyses, which now reached statistical significance.

The VDAART and COPSAC2010 trials used different doses of vitamin D, initiated the supplementation at different pregnancy stages ranging from 10 to 26 weeks of gestation, and enrolled pregnant women with divergent 25(OH)D levels at entry into the trials. Despite these differences, the trials similarly showed that the vitamin D supplementation resulted in significantly increased post-interventional 25(OH)D levels in the mothers. Furthermore, taking advantage of these differences in the combined analysis by utilizing the measured 25(OH)D levels at study entry, unmasked the most pronounced protective effect of the vitamin D intervention in women with 25(OH)D level ≥ 30 ng/ml.

VDAART is a high-risk cohort, with parental asthma or allergy as inclusion criteria. This is in contrast to the unselected COPSAC2010 cohort, which may explain the overall higher frequencies of the primary and secondary end-points in VDAART, compared to COPSAC2010. Particularly, total IgE levels were higher and elevated specific IgE was much more prevalent in VDAART (34%) vs. COPSAC2010 (8%), which can also be ascribed the different ages of measurement (3 years in VDAART vs. 6–18 months in COPSAC2010).

Finally, VDAART included a large group of African-American women in the trial, who are well-known to have a higher risk of developing asthma and allergy[25] and had lower vitamin D levels at randomization compared to the other ethnic groups[12]. In contrast, COPSAC2010 primarily recruited Caucasians to the trial. However, this unequal distribution of races in the trials did not affect the individual intent-to-treat analyses, which yielded very similar effect estimates.

We conducted both random effects meta-analyses and individual patient data (IPD) analysis. These yielded similar results, increasing the confidence in our findings. Furthermore, including a third trial of vitamin D supplementation in the meta-analysis, which intervened at a later pregnancy stage (week 27) and with a much lower dose (800 IU/day) [22] also showed an overall protective effect of vitamin D on development of asthma/recurrent wheeze.

Interpretation

This combined analysis of our two vitamin D RCTs showed a significant 26% reduced risk of the primary end-point asthma/recurrent wheeze during the first 3 years of life, which suggests that the non-significant/borderline significant trial responses observed in the individual intent-to-treat analyses were partly due to lack of power caused by an overestimation of the treatment effect, rather than lack of an intervention effect.

A recent meta-analysis supports our finding of a significant reduction in asthma/wheeze from prenatal vitamin D supplementation[11]. However, unlike drug trials, in nutrient trials, participants have varying levels of the nutrient in the body when entering the trial[26]. Thus, 25(OH)D level in the pregnant mother at enrollment into the trial could be an important effect modifier, which was not accounted for in the earlier reported individual intent-to-treat analyses[9,10]. To explore that issue, we performed the combined analyses stratified for the women’s 25(OH)D level at trial entry, which showed that the vitamin D supplement resulted in a significantly reduced risk of asthma/recurrent wheeze in the offspring of women with 25(OH)D ≥ 30 ng/ml, but a much smaller and statistically non-significant effect among women with 25(OH)D < 30 ng/ml. This finding is contrary to what many have suggested that only those who are deficient in vitamin D would benefit from supplementation. This finding suggests that the level of deficiency may be different for non-bone outcomes compared with bone outcomes, and that the level needed for optimal prevention of childhood asthma lies above 30 ng/ml, higher that what is needed for bone health[27].

When the two trials were initiated, it was thought that the effects of vitamin D were confined to the alveolar stage of lung development, occurring in the third trimester of pregnancy[28]. However, emerging evidence arising from lung gene expression data from our own lab have subsequently shown that vitamin D already has effects at the stage of branching morphogenesis of the fetal lung occurring in the first trimester of pregnancy prior to randomization in both these trials[2]. Therefore, initiating the supplementation at 10–18 weeks’ gestation in VDAART and in particular at 22–26 weeks’ gestation in COPSAC2010 was presumably too late to achieve a maximal effect of vitamin D on fetal lung development. In addition, as human fertility is also influenced by vitamin D[29,30], it may even be worthwhile to target supplementation before conception to optimize implantation of the fertilized egg and assure sufficient vitamin D for lung and immune development from the very beginning of life.

Our combined analysis also suggests that we may have used an insufficient dosage of vitamin D in both the trials. The Institute of Medicine has recently redefined the cut-off for sufficient 25(OH)D level from 30 ng/ml to 20 ng/ml or higher based on the effect on optimal bone health[27], but the sufficient 25(OH)D level in a mother during pregnancy for optimal immune and lung development in the fetus is unknown and might be as high as 40–60 ng/ml. We observed that the vitamin D supplement resulted in a significant increase in post-interventional maternal 25(OH)D level in both trials, but levels ≥ 30 ng/ml were only achieved in 75% of the supplemented mothers in VDAART and 82% in COPSAC2010 underscoring that too low a dose may have attenuated the trial results in both trials but to a greater extent in VDAART possibly because of the increased African American enrollment. The lack of effect of the vitamin D supplement among women with low 25(OH)D levels at trial entry also suggests that the dose might have been too low to reverse developmental changes caused by insufficient vitamin D exposure before the supplementation was initiated.

The secondary end-point combined analysis of total IgE confirmed the non-significant effect of the intervention reported in the individual trials[9,10]. The analysis showed also no overall effect on specific IgE levels towards the food and aeroallergens measured in both trials (egg, milk, cat and dog). This is consistent with a recent RCT showing no effect on cat specific IgE levels, whereas decreased house-dust mite specific IgE was shown in the offspring of mothers supplemented with vitamin D during pregnancy[31]. The combined analyses did not show a reduction in eczema risk or occurrence of LRTI, which is in line with previous observational studies[4,32,33].

It has already been shown that maternal vitamin D status is associated with other immune-mediated diseases such as pre-eclampsia[34] and Type I diabetes in the offspring[35]. Combining this knowledge with our findings from this combined analysis, showing that vitamin D supplementation has a protective effect on childhood asthma/recurrent wheeze, makes vitamin D a very promising nutrient for future prevention of immune-mediated disorders. Future studies should explore the optimal timing and level of vitamin D supplementation during pregnancy.

Conclusion

This combined analysis shows a significant and clinically important 26% protective effect of vitamin D supplementation during pregnancy on the risk of asthma/recurrent wheeze in the offspring, with a more pronounced risk reduction of 46% in women with 25(OH)D level ≥ 30 ng/ml at trial entry. Prenatal care strategies targeted at raising vitamin D levels in pregnant women should therefore be considered.

Acknowledgments

We gratefully express our gratitude to the children and families of the VDAART and COPSAC2010 trials for all their support and commitment.

References

  1. 1. Raby BA, Lazarus R, Silverman EK, Lake S, Lange C, Wjst M, et al. Association of Vitamin D Receptor Gene Polymorphisms with Childhood and Adult Asthma. Am J Respir Crit Care Med. 2004;170: 1057–1065. pmid:15282200
  2. 2. Kho AT, Sharma S, Qiu W, Gaedigk R, Klanderman B, Niu S, et al. Vitamin D related genes in lung development and asthma pathogenesis. BMC Med Genomics. 2013;6: 47. pmid:24188128
  3. 3. Litonjua AA. Childhood asthma may be a consequence of vitamin D deficiency. Curr Opin Allergy Clin Immunol. 2009;9: 202–207. pmid:19365260
  4. 4. Camargo CA, Rifas-Shiman SL, Litonjua AA, Rich-Edwards JW, Weiss ST, Gold DR, et al. Maternal intake of vitamin D during pregnancy and risk of recurrent wheeze in children at 3 y of age. Am J Clin Nutr. 2007;85: 788–795. pmid:17344501
  5. 5. Devereux G, Litonjua AA, Turner SW, Craig LC, McNeill G, Martindale S, et al. Maternal vitamin D intake during pregnancy and early childhood wheezing. The American Journal of Clinical Nutrition. 2007;85: 853–859. pmid:17344509
  6. 6. Feng H, Xun P, Pike K, Wills AK, Chawes BL, Bisgaard H, et al. In utero exposure to 25(OH) D and risk of childhood asthma, wheeze and respiratory tract infections: a meta-analysis of birth cohort studies. J Allergy Clin Immunol. 2016; pmid:27639938
  7. 7. Litonjua AA, Lange NE, Carey VJ, Brown S, Laranjo N, Harshfield BJ, et al. The Vitamin D Antenatal Asthma Reduction Trial (VDAART): rationale, design, and methods of a randomized, controlled trial of vitamin D supplementation in pregnancy for the primary prevention of asthma and allergies in children. Contemp Clin Trials. 2014;38: 37–50. pmid:24614387
  8. 8. Bisgaard H, Vissing NH, Carson CG, Bischoff AL, Følsgaard NV, Kreiner-Møller E, et al. Deep phenotyping of the unselected COPSAC2010 birth cohort study. Clin Exp Allergy. 2013;43: 1384–1394. pmid:24118234
  9. 9. Litonjua AA, Carey VJ, Laranjo N, Harshfield BJ, McElrath TF, O’Connor GT, 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: 362–370. pmid:26813209
  10. 10. Chawes BL, Bønnelykke K, Stokholm J, Vissing NH, Bjarnadóttir E, Schoos A- MM, et al. Effect of Vitamin D3 Supplementation During Pregnancy on Risk of Persistent Wheeze in the Offspring: A Randomized Clinical Trial. JAMA. 2016;315: 353–361. pmid:26813208
  11. 11. Vahdaninia M, Mackenzie H, Helps S, Dean T. Prenatal Intake of Vitamins and Allergic Outcomes in the Offspring: A Systematic Review and Meta-Analysis. J Allergy Clin Immunol Pract. 2016; pmid:27888033
  12. 12. Wolsk HM, Harshfield BJ, Laranjo N, Carey VJ, O’Connor G, Sandel M, et al. Vitamin D supplementation in pregnancy, prenatal 25(OH)D levels, race, and subsequent asthma or recurrent wheeze in offspring: Secondary analyses from the Vitamin D Antenatal Asthma Reduction Trial. J Allergy Clin Immunol. 2017; pmid:28285844
  13. 13. Ersfeld DL, Rao DS, Body J-J, Sackrison JL Jr., Miller AB, Parikh N, et al. Analytical and clinical validation of the 25 OH vitamin D assay for the LIAISON® automated analyzer. Clinical Biochemistry. 2004;37: 867–874. pmid:15369717
  14. 14. Højskov CS, Heickendorff L, Møller HJ. High-throughput liquid-liquid extraction and LCMSMS assay for determination of circulating 25(OH) vitamin D3 and D2 in the routine clinical laboratory. Clin Chim Acta. 2010;411: 114–116. pmid:19850018
  15. 15. Maunsell Z, Wright DJ, Rainbow SJ. Routine Isotope-Dilution Liquid Chromatography-Tandem Mass Spectrometry Assay for Simultaneous Measurement of the 25-Hydroxy Metabolites of Vitamins D2 and D3. Clinical Chemistry. 2005;51: 1683–1690. pmid:16020493
  16. 16. Bisgaard H, Stokholm J, Chawes BL, Vissing NH, Bjarnadóttir E, Schoos A- MM, et al. Fish Oil-Derived Fatty Acids in Pregnancy and Wheeze and Asthma in Offspring. N Engl J Med. 2016;375: 2530–2539. pmid:28029926
  17. 17. Bischoff AL, Følsgaard NV, Carson CG, Stokholm J, Pedersen L, Holmberg M, et al. Altered Response to A(H1N1)pnd09 Vaccination in Pregnant Women: A Single Blinded Randomized Controlled Trial. PLoS ONE. 2013;8: e56700. pmid:23637733
  18. 18. Stokholm J, Chawes BL, Vissing NH, Bjarnadóttir E, Pedersen TM, Vinding RK, et al. Azithromycin for episodes with asthma-like symptoms in young children aged 1–3 years: a randomised, double-blind, placebo-controlled trial. The Lancet Respiratory Medicine. 2016;4: 19–26. pmid:26704020
  19. 19. Bisgaard H, Hermansen MN, Loland L, Halkjaer LB, Buchvald F. Intermittent inhaled corticosteroids in infants with episodic wheezing. N Engl J Med. 2006;354: 1998–2005. pmid:16687712
  20. 20. Bisgaard H, Bønnelykke K, Sleiman PMA, Brasholt M, Chawes B, Kreiner-Møller E, et al. Chromosome 17q21 gene variants are associated with asthma and exacerbations but not atopy in early childhood. Am J Respir Crit Care Med. 2009;179: 179–185. pmid:19029000
  21. 21. Hanifin J, Rajka G. Diagnostic features of atopic dermatitis. Acta Derm Venereol Suppl. 1980;92: 44–47.
  22. 22. Goldring ST, Griffiths CJ, Martineau AR, Robinson S, Yu C, Poulton S, et al. Prenatal vitamin d supplementation and child respiratory health: a randomised controlled trial. PLoS ONE. 2013;8: e66627. pmid:23826104
  23. 23. R Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. [Internet]. Vienna, Austria; 2015. Available: http://www.R-project.org/
  24. 24. Guido Schwarzer (2015). meta: General Package for Meta-Analysis. R package version 4.3–0. https://CRAN.R-project.org/package=meta.
  25. 25. Wegienka G, Havstad S, Joseph CL, Zoratti E, Ownby D, Woodcroft K, et al. Racial Disparities in Allergic Outcomes in African Americans Emerge as Early as Age 2 Years. Clin Exp Allergy. 2012;42: 909–917. pmid:22909162
  26. 26. Heaney RP. Guidelines for optimizing design and analysis of clinical studies of nutrient effects. Nutrition Reviews. 2014;72: 48–54. pmid:24330136
  27. 27. Ross AC, Manson JE, Abrams SA, Aloia JF, Brannon PM, Clinton SK, et al. The 2011 Report on Dietary Reference Intakes for Calcium and Vitamin D from the Institute of Medicine: What Clinicians Need to Know. J Clin Endocrinol Metab. 2011;96: 53–58. pmid:21118827
  28. 28. Zosky GR, Berry LJ, Elliot JG, James AL, Gorman S, Hart PH. Vitamin D deficiency causes deficits in lung function and alters lung structure. Am J Respir Crit Care Med. 2011;183: 1336–1343. pmid:21297070
  29. 29. Abadia L, Gaskins AJ, Chiu Y- H, Williams PL, Keller M, Wright DL, et al. Serum 25-hydroxyvitamin D concentrations and treatment outcomes of women undergoing assisted reproduction. Am J Clin Nutr. 2016;104: 729–735. pmid:27465382
  30. 30. Boisen IM, Bøllehuus Hansen L, Mortensen LJ, Lanske B, Juul A, Blomberg Jensen M. Possible influence of vitamin D on male reproduction. J Steroid Biochem Mol Biol. 2016; pmid:27693423
  31. 31. Grant CC, Crane J, Mitchell EA, Sinclair J, Stewart A, Milne T, et al. Vitamin D supplementation during pregnancy and infancy reduces aeroallergen sensitization: a randomized controlled trial. Allergy. 2016;71: 1325–1334. pmid:27060679
  32. 32. Chawes BL, Bønnelykke K, Jensen PF, Schoos A- MM, Heickendorff L, Bisgaard H. Cord blood 25(OH)-vitamin D deficiency and childhood asthma, allergy and eczema: the COPSAC2000 birth cohort study. PLoS ONE. 2014;9: e99856. pmid:24925304
  33. 33. Magnus MC, Stene LC, Håberg SE, Nafstad P, Stigum H, London SJ, et al. Prospective Study of Maternal Mid-pregnancy 25-hydroxyvitamin D Level and Early Childhood Respiratory Disorders. Paediatr Perinat Epidemiol. 2013;27: 532–541. pmid:24134527
  34. 34. Agarwal S, Kovilam O, Agrawal DK. Vitamin D and its impact on maternal-fetal outcomes in pregnancy: A critical review. Crit Rev Food Sci Nutr. 2016; 0. pmid:27558700
  35. 35. Sørensen IM, Joner G, Jenum PA, Eskild A, Torjesen PA, Stene LC. Maternal Serum Levels of 25-Hydroxy-Vitamin D During Pregnancy and Risk of Type 1 Diabetes in the Offspring. Diabetes. 2012;61: 175–178. pmid:22124461