Randomized Trial: Maternal Vitamin D Supplementation to Prevent Childhood Asthma (VDAART) (VDAART)

• ClinicalTrials.gov Identifier: NCT00920621
• Recruitment Status: Active, not recruiting
• First Posted: June 15, 2009
• Results First Posted: July 14, 2017
• Last Update Posted: July 20, 2023
• Sponsor: Brigham and Women's Hospital
• Collaborator: National Heart, Lung, and Blood Institute (NHLBI)
• Information provided by (Responsible Party): Scott T. Weiss, Brigham and Women's Hospital

Study Description

Brief Summary:

Vitamin D supplementation given to pregnant women will prevent asthma in their offspring and children.

Condition or disease	Intervention/treatment	Phase
Asthma	Dietary Supplement: Vitamin D 3 cholecalciferol; Dietary Supplement: Vitamin D3	Phase 3

Detailed Description:

Asthma is one of the leading causes of morbidity in children with 60% of all cases diagnosed by age 3. Thus, finding factors that can lead to prevention of this disease would be of great public health importance. Vitamin D deficiency is highly prevalent among pregnant women, and thus, represents a potentially modifiable factor for the prevention of disease. Due to the effect of vitamin D in modulating immune responses, we believe that vitamin D deficiency in pregnant mothers leads to faulty immune system development in the neonate, predisposing them to asthma and allergy. We have observational data from two independent birth cohort studies that higher maternal intakes of vitamin D during pregnancy are each independently associated with a 50% reduction in risk for recurrent wheezing and asthma in 3- and 5-yr old children. However, in order to recommend this as a universal treatment to prevent asthma, a randomized, controlled, clinical trial is necessary. Therefore, we propose a two arm, double-blind, placebo controlled, randomized, clinical trial of Vitamin D, to determine whether higher vitamin D intake and levels in the pregnant mother will prevent asthma and allergy in the child at age 3. We will identify pregnant women who have asthma or allergies or whose partner has asthma or allergies, from obstetric clinics in the three clinical centers participating in this trial. We will recruit 870 pregnant women during the first trimester of pregnancy and randomize them to one of two treatment arms of a 4-year clinical trial: 4000 IU of Vitamin D in addition to usual prenatal vitamins, n=435; and usual prenatal vitamins alone, n=435. Our primary specific aim is to determine whether adequate vitamin D supplementation in the pregnant mother is associated with reduced incidence of asthma in the child during the first 3 years of life. The sub-aims of the study will include (1) To determine whether adequate vitamin D supplementation in the pregnant mother is associated with reduced secondary outcomes in the child of (a) allergic sensitization, (b) doctor's diagnosis of eczema and (c) lower respiratory tract infections during the first 3 years of life; and (2) To determine whether adequate vitamin D supplementation in the pregnant mother is associated with improved vitamin D status in the mothers and their offspring through measurement of 25(OH)D levels in maternal plasma, cord blood, and children's blood at 1 and 3 yrs of age and (3)To determine whether sufficient vitamin D supplementation in the pregnant mother is associated with reduced incidence of preterm birth (birth <37 weeks gestation), preeclampsia, gestational hypertension, and/or Hemolytic anemia, Elevated Liver enzymes, Low Platelet count (HELLP syndrome) (PB/PE) compared to a usual care control group in VDAART.

VDAART Analysis Plan (Addendum to Protocol)

All analyses of primary and secondary outcomes stated in the VDAART Protocol will be performed using the intent-to-treat (ITT) paradigm, unless specifically stated.

I. Definition of outcomes.

A. Asthma and recurrent wheezing. The primary outcome of the trial will be development of a doctor's diagnosis of asthma and/or recurrent wheeze. While asthma is acknowledged to have its roots in early life, making a definite diagnosis is difficult until the child is older, and wheezing illnesses may be precursors of an asthma diagnosis. Thus, we will have a composite definition for the primary outcome.

• Asthma will be defined as a parent's report of physician's diagnosis at any time during the first three years of life, based on questionnaire responses. For time-to-event analyses, the time of incident asthma will be determined by the time of first positive questionnaire response.
• Recurrent wheezing will be defined as at least one report of wheezing in the third year of life plus any report of wheezing in any of the first two years of life.

Recognizing that wheezing symptoms may be modified by medication use, variable age of onset, and other variables, the following will be included in the composite outcome:

• children who had at least one wheezing episode (during the 1st 2 years of life), plus an asthma controller medication (defined as steroid inhalers or nebulizers OR steroid pills or liquids OR leukotriene modifiers) in the third year
• children who did not report any wheezing in the first 2 years but who report 2 separate episodes of wheezing in the third year OR are on controller medication (defined as above) on at least 2 separate reports in the third year OR at least 1 report of wheezing and at least 1 separate report of controller medication use in the third year

For recurrent wheezing (and the other wheezing phenotypes), the time of incident recurrent wheezing will be determined by the time of first report of wheezing, for time-to-event analyses. In the event that the child meets the definition based solely on the use of controller medication, the first report of use of this controller medication will be used to determine the time of onset of wheezing for time-to-event analyses.

For these outcomes, because the questions were asked every 3 months, and recognizing that missing questionnaires occurred, event times will be treated as interval-censored.

B. Eczema. Eczema will be defined as a positive response to parent's report of physician's diagnosis at any time during the first three years of life based on the questionnaire responses.

C. Lower respiratory tract infections (LRI). Lower respiratory tract infections (LRIs) will be defined based on parental responses to questionnaires. LRIs will be defined as a parental report of a physician's diagnosis of pneumonia, bronchiolitis, bronchitis, or croup (laryngotracheobronchitis). LRIs may occur multiple times over a three-year period in a child. Information on repeated episodes of LRI will be employed for rate estimation and comparison.

D. Total and specific IgE. Total and specific serum IgE will be measured from cord blood samples, and from year 3 samples from the children. Total IgE will be analyzed as a continuous outcome. Sensitization will be defined as any specific IgE ≥ 0.35 IU.

II. Secondary Analyses.

A. Analyses based on levels. Secondary analyses using baseline and follow-up maternal 25OHD levels will be performed. We will investigate the effect of baseline and follow-up maternal levels separately on the development of primary and secondary outcomes in the trial. Additionally, we will categorize mothers into categories based on joint baseline and follow-up levels. Mothers who have baseline levels and follow-up levels ≥ 40 mg/dl will be categorized in the HI-HI group; those who have baseline levels and follow-up levels < 40 mg/dl will be categorized in the LO-LO group; mothers who do not meet these definitions will be categorized either in the HI-LO or LO-HI groups based on their baseline and follow-up levels.

B. We also performed metabolomics on the children at age 1 and 3 and eventually age 6. We are assessing the association with vitamin D, asthma, and other phenotypes such as food allergies, IgE, and lung function with metabolites and genetic variants.

C. As an ancillary study, we have collected stool samples from the mothers in the 3rd trimester, and samples from the infants and children at 3-6 months, 1 year, and 3 years. We will sequence the stool samples for the microbiome, and we will assess the effects of the early life microbiome on the development of asthma, allergies (including food allergies and sensitization), growth and development, and obesity.

D. In a secondary analyses, we will determine the effect of 17q21 genotype on the efficacy of vitamin D supplementation in the prevention of asthma/wheeze. We will compute hazard ratios for the reduction in asthma/wheeze risk associated with prenatal supplementation, stratified by rs12936231. rs12936231 is a functional SNP influencing expression of ORMDL3, and given the role of ORMDL3 as a key sphingolipid biosynthesis regulator, we will subsequently investigate the relative abundance of sphingolipids between those in the vitamin D Intervention arm and those in the placebo group, stratified by 17q21 genotype. Relative abundance is quantified by normalizing the peak area of a metabolite to the median peak area of that metabolite within the same batch on the day the sample was run. The normalized peak area is then median scaled and imputed with the minimum across all samples. In this way, we can directly compare abundances relative to other samples for each metabolite. Relative abundance has no unit of measure. Finally we will identify interactions between prenatal vitamin D supplementation, rs12936231 genotype and sphingolipid metabolism in the risk of asthma/wheeze by age three. We will replicate this analysis in the COPSAC2010 population (ClinicalTrials.gov Identifier:NCT00856947).

VDAART Year 6 Analysis Plan

PRIMARY ANALYSIS: The null hypothesis of no treatment effect will be tested in a Cox Proportional Hazards Model of time to physician diagnosed asthma or onset of recurrent wheeze, adjusted for maternal levels of Vitamin D recorded at 10-18 weeks gestation, allowing for level by treatment interaction, and for any other relevant baseline covariates (race, maternal education, and clinical center), using the methods of Tsiatis et al. (Stat Med. 2008 October 15; 27(23): 4658-4677) to maximize precision of estimated treatment effect. The significance level for the test of no treatment effect will be 0.05.

SECONDARY ANALYSES: Effect estimates from all secondary analyses will be reported as point estimates with nominal 95% confidence intervals. Estimates will be derived from models adjusted for baseline maternal levels of Vitamin D as noted above.

Current active asthma, late onset recurrent wheeze, allergic sensitization, any allergic rhinitis, MD-diagnosed food allergy, food allergy with symptoms, eczema: Analysis is confined to individuals who provide data after age 5. Loss to followup is reasonably balanced between arms. Logistic regression will be used to test the hypothesis that there is no effect of treatment on risk of current active asthma. Separate tests will be conducted for no treatment effect on risk of late onset recurrent wheeze, on risk of allergic sensitization defined using specific IgE greater than or equal to 0.35IU, and on risk of allergic rhinitis birth to age 6. Similar models will be used separately to assess treatment effect on risk of eczema, active eczema, and food allergies.

Lower respiratory infections: The count of LRI per unit time will be modeled using negative binomial regression with covariates including treatment arm.

Impulse oscillometry: Analysis of treatment effect on impulse oscillometry components will be based on data available for 6 year old children, and will use linear modeling with adjustment for maternal baseline Vitamin D. A secondary analysis will examine treatment effect on trends in these measures through ages 4-6. This test will be based on mixed effects modeling.

Spirometry: Spirometric outcomes will be analyzed using linear models with transformations as needed, adjusting for race, age, sex and height. Bronchodilator response will be dichotomized at 10% of pre-challenge values, analyzed with logistic regression.

VDAART Asthma and/or Recurrent Wheeze Definitions for Primary Analysis (Time-to-Event)

Physician-diagnosed asthma Report of physician-diagnosed asthma at any time in the first 6 years of life. The time of onset will be the first report of wheeze OR the first report of use of asthma medication.

Recurrent wheeze - no diagnosis of asthma Caregiver report of wheeze OR use of any asthma medication on two separate years over the first 6 years. The time of onset will be the first report of wheeze OR the first report of use of asthma medication.

VDAART Year 6 Analyses - Definitions for Secondary Outcomes

Current Active Asthma Report of physician-diagnosed asthma at any time in the first 6 years of life, PLUS after the 5th birthday a) report of child's use of any asthma medication (see below) OR b) report of wheeze.

Recurrent Wheeze at age 6 yrs - no diagnosis of asthma At least 1 caregiver report of wheeze OR use of any asthma medication prior to the 3rd birthday, PLUS a report of wheeze OR use of any asthma medication after the 3rd birthday.

Late onset Recurrent wheeze - no diagnosis of asthma, wheeze, or asthma medication use prior to 3rd birthday A report of wheezing OR use of any asthma medication after the 5th birthday PLUS either wheezing or use of any asthma medication after the 3rd birthday but before the 5th birthday (between 3yrs and 5 yrs).

Total and specific IgE. Total and specific serum IgE will be measured year 6 samples from the children.

1. Total IgE will be analyzed as a continuous outcome.
2. Sensitization will be defined as any specific IgE ≥ 0.35 IU to the panel of allergens.

Allergic Rhinitis. This will be a positive response to the question "Since the last time we talked has a health care provider said that [CHILD] has hay fever, allergic rhinitis, or allergies involving the eyes or nose?" Any positive response from birth through age 6.

Eczema.

1. Ever eczema - positive response to "…has a health care provider said that [CHILD] has eczema?" at any time from birth through age 6.
2. Persistent eczema. Ever eczema at any time in the 6 years plus positive response to "itchy rash which was coming and going but did not completely get better?" after the 3rd birthday.

Lower Respiratory Infections (LRI). Lower respiratory tract infections (LRIs) will be defined based on caregiver responses to questionnaires. LRIs will be defined as a caregiver report of a physician's diagnosis of pneumonia, bronchiolitis, bronchitis, or croup (laryngotracheobronchitis). LRIs may occur multiple times over a six-year period in a child. Information on repeated episodes of LRI will be employed for rate estimation and comparison.

Food Allergies.

1. Doctor-diagnosis - any positive response from birth through age 6 to the question "In the last year, has a health care provider said that [CHILD] has food allergies?
2. Food allergy with symptoms - Doctor-diagnosis of food allergy PLUS any reaction to specific foods from the grid.

Lung Function.

1. Impulse oscillometry: R5, R20, AX, X5, R5-20, and R5-20% These variables will be used as continuous variables. The variables are measured at 4, 5, and 6 years of age. The primary analysis will look at values at 6 yrs of age, and a secondary analysis will investigate the trajectory (longitudinal analysis) from age 4 through 6 yrs.

2. Spirometry: pre- and post-bronchodilator FEV1, FVC, FEV1/FVC; Bronchodilator Response (BDR**). Analyses will adjust for race, age, sex, and height.

   • Asthma medication: rescue (inhaled beta-agonists or systemic corticosteroids) or controller medication (inhaled corticosteroids monotherapy, ICS/Long-acting beta-agonists, or leukotriene modifiers) ** A positive BDR will be defined as a change of 10% from the baseline FEV1 after inhalation of albuterol

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 876 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Double (Participant, Investigator)
• Primary Purpose: Prevention
• Official Title: Randomized Trial: Maternal Vitamin D Supplementation to Prevent Childhood Asthma (VDAART)
• Study Start Date: September 2009
• Actual Primary Completion Date: January 21, 2015
• Estimated Study Completion Date: February 2024

Arms and Interventions

Arm	Intervention/treatment
Experimental: Vitamin D treatment; vitamin D treatment plus prenatal multivitamins	Dietary Supplement: Vitamin D 3 cholecalciferol; Dosage form oral Dosage 4000IU Vitamin D 3 cholecalciferol; Other Names: vitamin D; vitamin D3; cholecalciferol; Dietary Supplement: Vitamin D3; 4000 IU of vitamin D3 administered orally once a day during pregnancy
Placebo Comparator: placebo; placebo plus prenatal multivitamins	Dietary Supplement: Vitamin D3; 4000 IU of vitamin D3 administered orally once a day during pregnancy

Outcome Measures

Primary Outcome Measures :

1. Asthma or Recurrent Wheeze in First 3 Years of Life [ Time Frame: First 3 years of life. ]

   Parental report of physician diagnosis of asthma or occurrence of recurrent wheeze in the child's first 3 years of life ascertained from questionnaires administered every 3 months.

   *For some variables the "negative" count incorporates "negative and indeterminate."

2. Achieved Maternal 25(OH)D Level of ≥ 30 ng/mL at Third Trimester Sampling. [ Time Frame: 32-38 weeks gestation ]
   Maternal serum 25-hydroxyvitamin D measurement at third trimester during pregnancy

Secondary Outcome Measures :

1. Child Positive-specific IgE Tests From Blood Collection at 3 Year Visit. [ Time Frame: 3 years ]
   Child positive-specific IgE tests from blood collection at 3 year visit.
2. Child Serum 25-hydroxyvitamin D Measurement From Blood Collection at 1 Year Visit. [ Time Frame: 1 year visit ]
   Child serum 25-hydroxyvitamin D measurement from blood collection at 1 year visit.
3. Parental Report of Physician Diagnosed Eczema (With Rash) in the Child's First 3 Years of Life. [ Time Frame: Child's first 3 years of life. ]

   Parental report of physician diagnosis of eczema with rash in typical distribution in the child's first 3 years of life ascertained from questionnaires administered every 3 months.

   *For some variables the "negative" count incorporates "negative and indeterminate."

4. Parental Report of Physician Diagnosis of Lower Respiratory Tract Infection in the Child's First 3 Years of Life. [ Time Frame: Child's first 3 years of life. ]
   Parental report of physician diagnosis of lower respiratory tract infection (LRI) in the child's first 3 years of life. LRI defined as physician diagnosed bronchitis, bronchiolitis, croup, or pneumonia ascertained from questionnaires administered every 3 months.
5. Child Serum 25-hydroxyvitamin D Measurement From Blood Collection at 3 Year Visit. [ Time Frame: Blood collection at childs' 3 year visit. ]
   Child serum 25-hydroxyvitamin D measurement from blood collection at 3 year visit.
6. Any Allergic Sensitization in the Child's First 3 Years of Life. [ Time Frame: Child's first 3 years of life. ]

   Any allergic sensitization in the child's first 3 years of life.

   *For some variables the "negative" count incorporates "negative and indeterminate."

7. Mass Spec Vitamin D Value From Cord Blood at Delivery [ Time Frame: Blood collection at delivery ]
   Mass Spec Vitamin D value from cord blood at delivery
8. Sphingolipid Profile [ Time Frame: 1 year ]
   Mass spec measured relative abundance of five metabolites of the sphingolipid metabolism pathway in plasma samples extracted at the year one visit.
9. Sphingolipid Profile [ Time Frame: 3 years ]
   Mass spec measured relative abundance of five metabolites of the sphingolipid metabolism pathway in plasma samples extracted at the year three visit.
10. Child 17q21 Genotype [ Time Frame: 3 years ]
    Genotype at the rs12936231 SNP
11. Fecal Microbiome Profile [ Time Frame: Mother at 32-38 weeks gestation, Child's first 6 years of life ]
    We extracted DNA and sequenced the bacterial 16S V4 hyper-variable region. The average number of 16S region reads sequenced per participant is provided here. Prior evidence suggests that read counts of at least 1,000 are adequate for 16S fecal microbiome profiling (Reference: Momozawa Y, et cal. Characterization of bacteria in biopsies of colon and stools by high throughput sequencing of the V2 region of bacterial 16S rRNA gene in human. PLoS One. 2011 Feb 10;6(2):e16952.)

Eligibility Criteria

• Ages Eligible for Study: 18 Years to 39 Years (Adult)
• Sexes Eligible for Study: Female
• Accepts Healthy Volunteers: Yes

Criteria

Inclusion Criteria:

• Personal history of asthma, eczema, allergic rhinitis or a history of asthma, eczema, allergic rhinitis in the biological father of the child
• Gestational age between 10 and 18 weeks at the time of randomization
• Maternal age between 18 and 39 years
• Not a current smoker
• English or Spanish speaking
• Intent to participate for the full 4 years (through Pregnancy and then until the 3rd birthday of the child)

Exclusion Criteria:

• Not meeting inclusion criteria
• Gestational age greater than 18 weeks
• Presence of chronic medical conditions
• Taking vitamin D supplements containing more than 2000 IU/day of vitamin D3
• Multiple gestation pregnancy (twins, triplets)
• Pregnancy achieved by assisted reproduction techniques (e.g., IUI, IVF)

Contacts and Locations

Locations

United States, California

Robert Zeiger, MD

San Diego, California, United States

United States, Massachusetts

George O'Connor, MD

Boston, Massachusetts, United States

United States, Missouri

Leonard Bacharier, MD

Saint Louis, Missouri, United States

Sponsors and Collaborators

Brigham and Women's Hospital

National Heart, Lung, and Blood Institute (NHLBI)

Investigators

• Principal Investigator: Scott T Weiss; Brigham and Women's Hospital

More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Knihtila HM, Kelly RS, Brustad N, Huang M, Kachroo P, Chawes BL, Stokholm J, Bonnelykke K, Pedersen CT, Bisgaard H, Litonjua AA, Lasky-Su JA, Weiss ST. Maternal 17q21 genotype influences prenatal vitamin D effects on offspring asthma/recurrent wheeze. Eur Respir J. 2021 Sep 23;58(3):2002012. doi: 10.1183/13993003.02012-2020. Print 2021 Sep.

Litonjua AA, Carey VJ, Laranjo N, Stubbs BJ, Mirzakhani H, O'Connor GT, Sandel M, Beigelman A, Bacharier LB, Zeiger RS, Schatz M, Hollis BW, Weiss ST. Six-Year Follow-up of a Trial of Antenatal Vitamin D for Asthma Reduction. N Engl J Med. 2020 Feb 6;382(6):525-533. doi: 10.1056/NEJMoa1906137.

Lu M, Hollis BW, Carey VJ, Laranjo N, Singh RJ, Weiss ST, Litonjua AA. Determinants and Measurement of Neonatal Vitamin D: Overestimation of 25(OH)D in Cord Blood Using CLIA Assay Technology. J Clin Endocrinol Metab. 2020 Apr 1;105(4):e1085-92. doi: 10.1210/clinem/dgz299.

Lee-Sarwar KA, Kelly RS, Lasky-Su J, Zeiger RS, O'Connor GT, Sandel MT, Bacharier LB, Beigelman A, Rifas-Shiman SL, Carey VJ, Harshfield BJ, Laranjo N, Gold DR, Weiss ST, Litonjua AA. Fecal short-chain fatty acids in pregnancy and offspring asthma and allergic outcomes. J Allergy Clin Immunol Pract. 2020 Mar;8(3):1100-1102.e13. doi: 10.1016/j.jaip.2019.08.036. Epub 2019 Sep 5. No abstract available.

Yu B, Zanetti KA, Temprosa M, Albanes D, Appel N, Barrera CB, Ben-Shlomo Y, Boerwinkle E, Casas JP, Clish C, Dale C, Dehghan A, Derkach A, Eliassen AH, Elliott P, Fahy E, Gieger C, Gunter MJ, Harada S, Harris T, Herr DR, Herrington D, Hirschhorn JN, Hoover E, Hsing AW, Johansson M, Kelly RS, Khoo CM, Kivimaki M, Kristal BS, Langenberg C, Lasky-Su J, Lawlor DA, Lotta LA, Mangino M, Le Marchand L, Mathe E, Matthews CE, Menni C, Mucci LA, Murphy R, Oresic M, Orwoll E, Ose J, Pereira AC, Playdon MC, Poston L, Price J, Qi Q, Rexrode K, Risch A, Sampson J, Seow WJ, Sesso HD, Shah SH, Shu XO, Smith GCS, Sovio U, Stevens VL, Stolzenberg-Solomon R, Takebayashi T, Tillin T, Travis R, Tzoulaki I, Ulrich CM, Vasan RS, Verma M, Wang Y, Wareham NJ, Wong A, Younes N, Zhao H, Zheng W, Moore SC. The Consortium of Metabolomics Studies (COMETS): Metabolomics in 47 Prospective Cohort Studies. Am J Epidemiol. 2019 Jun 1;188(6):991-1012. doi: 10.1093/aje/kwz028.

Lee-Sarwar KA, Kelly RS, Lasky-Su J, Zeiger RS, O'Connor GT, Sandel MT, Bacharier LB, Beigelman A, Laranjo N, Gold DR, Weiss ST, Litonjua AA. Integrative analysis of the intestinal metabolome of childhood asthma. J Allergy Clin Immunol. 2019 Aug;144(2):442-454. doi: 10.1016/j.jaci.2019.02.032. Epub 2019 Mar 23.

Mirzakhani H, Carey VJ, Zeiger R, Bacharier LB, O'Connor GT, Schatz MX, Laranjo N, Weiss ST, Litonjua AA. Impact of parental asthma, prenatal maternal asthma control, and vitamin D status on risk of asthma and recurrent wheeze in 3-year-old children. Clin Exp Allergy. 2019 Apr;49(4):419-429. doi: 10.1111/cea.13320. Epub 2019 Jan 3.

Savage JH, Lee-Sarwar KA, Sordillo JE, Lange NE, Zhou Y, O'Connor GT, Sandel M, Bacharier LB, Zeiger R, Sodergren E, Weinstock GM, Gold DR, Weiss ST, Litonjua AA. Diet during Pregnancy and Infancy and the Infant Intestinal Microbiome. J Pediatr. 2018 Dec;203:47-54.e4. doi: 10.1016/j.jpeds.2018.07.066. Epub 2018 Aug 30.

Mirzakhani H, Carey VJ, McElrath TF, Qiu W, Hollis BW, O'Connor GT, Zeiger RS, Bacharier L, Litonjua AA, Weiss ST. Impact of Preeclampsia on the Relationship between Maternal Asthma and Offspring Asthma. An Observation from the VDAART Clinical Trial. Am J Respir Crit Care Med. 2019 Jan 1;199(1):32-42. doi: 10.1164/rccm.201804-0770OC.

Mirzakhani H, Al-Garawi AA, Carey VJ, Qiu W, Litonjua AA, Weiss ST. Expression network analysis reveals cord blood vitamin D-associated genes affecting risk of early life wheeze. Thorax. 2019 Feb;74(2):200-202. doi: 10.1136/thoraxjnl-2018-211962. Epub 2018 Jul 18.

Kelly RS, Sordillo JE, Lasky-Su J, Dahlin A, Perng W, Rifas-Shiman SL, Weiss ST, Gold DR, Litonjua AA, Hivert MF, Oken E, Wu AC. Plasma metabolite profiles in children with current asthma. Clin Exp Allergy. 2018 Oct;48(10):1297-1304. doi: 10.1111/cea.13183. Epub 2018 Jul 3.

Wolsk HM, Chawes BL, Litonjua AA, Hollis BW, Waage J, Stokholm J, Bonnelykke K, Bisgaard H, Weiss ST. Prenatal vitamin D supplementation reduces risk of asthma/recurrent wheeze in early childhood: A combined analysis of two randomized controlled trials. PLoS One. 2017 Oct 27;12(10):e0186657. doi: 10.1371/journal.pone.0186657. eCollection 2017.

Blighe K, Chawes BL, Kelly RS, Mirzakhani H, McGeachie M, Litonjua AA, Weiss ST, Lasky-Su JA. Vitamin D prenatal programming of childhood metabolomics profiles at age 3 y. Am J Clin Nutr. 2017 Oct;106(4):1092-1099. doi: 10.3945/ajcn.117.158220. Epub 2017 Aug 23.

Mirzakhani H, O'Connor G, Bacharier LB, Zeiger RS, Schatz MX, Weiss ST, Litonjua AA. Asthma control status in pregnancy, body mass index, and maternal vitamin D levels. J Allergy Clin Immunol. 2017 Nov;140(5):1453-1456.e7. doi: 10.1016/j.jaci.2017.03.053. Epub 2017 Jun 9.

Hornsby E, Pfeffer PE, Laranjo N, Cruikshank W, Tuzova M, Litonjua AA, Weiss ST, Carey VJ, O'Connor G, Hawrylowicz C. Vitamin D supplementation during pregnancy: Effect on the neonatal immune system in a randomized controlled trial. J Allergy Clin Immunol. 2018 Jan;141(1):269-278.e1. doi: 10.1016/j.jaci.2017.02.039. Epub 2017 May 26.

Mirzakhani H, Litonjua AA, McElrath TF, O'Connor G, Lee-Parritz A, Iverson R, Macones G, Strunk RC, Bacharier LB, Zeiger R, Hollis BW, Handy DE, Sharma A, Laranjo N, Carey V, Qiu W, Santolini M, Liu S, Chhabra D, Enquobahrie DA, Williams MA, Loscalzo J, Weiss ST. Early pregnancy vitamin D status and risk of preeclampsia. J Clin Invest. 2016 Dec 1;126(12):4702-4715. doi: 10.1172/JCI89031. Epub 2016 Nov 14.

Al-Garawi A, Carey VJ, Chhabra D, Mirzakhani H, Morrow J, Lasky-Su J, Qiu W, Laranjo N, Litonjua AA, Weiss ST. The Role of Vitamin D in the Transcriptional Program of Human Pregnancy. PLoS One. 2016 Oct 6;11(10):e0163832. doi: 10.1371/journal.pone.0163832. eCollection 2016.

Litonjua AA, Carey VJ, Laranjo N, Harshfield BJ, McElrath TF, O'Connor GT, Sandel M, Iverson RE Jr, Lee-Paritz A, Strunk RC, Bacharier LB, Macones GA, Zeiger RS, Schatz M, Hollis BW, Hornsby E, Hawrylowicz C, Wu AC, Weiss ST. 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 Jan 26;315(4):362-70. doi: 10.1001/jama.2015.18589.

• Responsible Party: Scott T. Weiss, Principal Investigator, Brigham and Women's Hospital
• ClinicalTrials.gov Identifier: NCT00920621
• Other Study ID Numbers: 655; 5U01HL091528-03 ( U.S. NIH Grant/Contract ); HL091528-01A1
• First Posted: June 15, 2009
• Results First Posted: July 14, 2017
• Last Update Posted: July 20, 2023
• Last Verified: June 2023

Keywords provided by Scott T. Weiss, Brigham and Women's Hospital:

Asthma; Vitamin D; Randomized Control Trial

Additional relevant MeSH terms:

Asthma; Bronchial Diseases; Respiratory Tract Diseases; Lung Diseases, Obstructive; Lung Diseases; Respiratory Hypersensitivity; Hypersensitivity, Immediate; Hypersensitivity; Immune System Diseases; Vitamin D; Ergocalciferols; Cholecalciferol; Vitamins; Micronutrients; Physiological Effects of Drugs; Bone Density Conservation Agents; Calcium-Regulating Hormones and Agents