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

Nutrient trials differ from drug trials because participants have varying circulating levels at entry into the trial. We sought to study the effect of a vitamin D intervention in pregnancy between subjects of different races and the association between 25-hydroxyvitamin D3 (25[OH]D) levels in pregna...

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Published inJournal of allergy and clinical immunology Vol. 140; no. 5; pp. 1423 - 1429.e5
Main Authors Wolsk, Helene M., Harshfield, Benjamin J., Laranjo, Nancy, Carey, Vincent J., O'Connor, George, Sandel, Megan, Strunk, Robert C., Bacharier, Leonard B., Zeiger, Robert S., Schatz, Michael, Hollis, Bruce W., Weiss, Scott T., Litonjua, Augusto A.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.11.2017
Elsevier Limited
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Abstract Nutrient trials differ from drug trials because participants have varying circulating levels at entry into the trial. We sought to study the effect of a vitamin D intervention in pregnancy between subjects of different races and the association between 25-hydroxyvitamin D3 (25[OH]D) levels in pregnancy and the risk of asthma/recurrent wheeze in offspring. The Vitamin D Antenatal Asthma Reduction Trial is a randomized trial of pregnant women at risk of having children with asthma randomized to 4400 international units/d vitamin D or placebo plus 400 international units/d vitamin D. Asthma and recurrent wheezing until age 3 years were recorded. African American (AA) women (n = 312) had lower initial levels of 25(OH)D (mean [SD], 17.6 ng/mL [8.3 ng/mL]) compared with non-AA women (n = 400; 27.1 ng/mL [9.7 ng/mL], P < .001). No racial difference was found from vitamin D supplementation in pregnancy on asthma/recurrent wheezing in offspring (P for interaction = .77). Having an initial level of greater than 30 ng/mL and being randomized to the intervention group was associated with the lowest risk for asthma/recurrent wheeze by age 3 years compared with having an initial level of less than 20 ng/mL and receiving placebo (adjusted odds ratio, 0.42; 95% CI, 0.19-0.91). We did not find differences between AA and non-AA mothers in the effect of maternal vitamin D supplementation and asthma/recurrent wheeze in offspring at 3 years. Maternal supplementation of vitamin D, particularly in mothers with initial 25(OH)D levels of greater than 30 ng/mL, reduced asthma/recurrent wheeze in the offspring through age 3 years, suggesting that higher vitamin D status beginning in early pregnancy is necessary for asthma/recurrent wheeze prevention in early life. [Display omitted]
AbstractList BACKGROUNDNutrient trials differ from drug trials because participants have varying circulating levels at entry into the trial.OBJECTIVEWe sought to study the effect of a vitamin D intervention in pregnancy between subjects of different races and the association between 25-hydroxyvitamin D3 (25[OH]D) levels in pregnancy and the risk of asthma/recurrent wheeze in offspring.METHODSThe Vitamin D Antenatal Asthma Reduction Trial is a randomized trial of pregnant women at risk of having children with asthma randomized to 4400 international units/d vitamin D or placebo plus 400 international units/d vitamin D. Asthma and recurrent wheezing until age 3 years were recorded.RESULTSAfrican American (AA) women (n = 312) had lower initial levels of 25(OH)D (mean [SD], 17.6 ng/mL [8.3 ng/mL]) compared with non-AA women (n = 400; 27.1 ng/mL [9.7 ng/mL], P < .001). No racial difference was found from vitamin D supplementation in pregnancy on asthma/recurrent wheezing in offspring (P for interaction = .77). Having an initial level of greater than 30 ng/mL and being randomized to the intervention group was associated with the lowest risk for asthma/recurrent wheeze by age 3 years compared with having an initial level of less than 20 ng/mL and receiving placebo (adjusted odds ratio, 0.42; 95% CI, 0.19-0.91).CONCLUSIONSWe did not find differences between AA and non-AA mothers in the effect of maternal vitamin D supplementation and asthma/recurrent wheeze in offspring at 3 years. Maternal supplementation of vitamin D, particularly in mothers with initial 25(OH)D levels of greater than 30 ng/mL, reduced asthma/recurrent wheeze in the offspring through age 3 years, suggesting that higher vitamin D status beginning in early pregnancy is necessary for asthma/recurrent wheeze prevention in early life.
Background Nutrient trials differ from drug trials because participants have varying circulating levels at entry into the trial. Objective We sought to study the effect of a vitamin D intervention in pregnancy between subjects of different races and the association between 25-hydroxyvitamin D3 (25[OH]D) levels in pregnancy and the risk of asthma/recurrent wheeze in offspring. Methods The Vitamin D Antenatal Asthma Reduction Trial is a randomized trial of pregnant women at risk of having children with asthma randomized to 4400 international units/d vitamin D or placebo plus 400 international units/d vitamin D. Asthma and recurrent wheezing until age 3 years were recorded. Results African American (AA) women (n = 312) had lower initial levels of 25(OH)D (mean [SD], 17.6 ng/mL [8.3 ng/mL]) compared with non-AA women (n = 400; 27.1 ng/mL [9.7 ng/mL], P  < .001). No racial difference was found from vitamin D supplementation in pregnancy on asthma/recurrent wheezing in offspring ( P for interaction = .77). Having an initial level of greater than 30 ng/mL and being randomized to the intervention group was associated with the lowest risk for asthma/recurrent wheeze by age 3 years compared with having an initial level of less than 20 ng/mL and receiving placebo (adjusted odds ratio, 0.42; 95% CI, 0.19-0.91). Conclusions We did not find differences between AA and non-AA mothers in the effect of maternal vitamin D supplementation and asthma/recurrent wheeze in offspring at 3 years. Maternal supplementation of vitamin D, particularly in mothers with initial 25(OH)D levels of greater than 30 ng/mL, reduced asthma/recurrent wheeze in the offspring through age 3 years, suggesting that higher vitamin D status beginning in early pregnancy is necessary for asthma/recurrent wheeze prevention in early life.
Nutrient trials differ from drug trials because participants have varying circulating levels at entry into the trial. We sought to study the effect of a vitamin D intervention in pregnancy between subjects of different races and the association between 25-hydroxyvitamin D3 (25[OH]D) levels in pregnancy and the risk of asthma/recurrent wheeze in offspring. The Vitamin D Antenatal Asthma Reduction Trial is a randomized trial of pregnant women at risk of having children with asthma randomized to 4400 international units/d vitamin D or placebo plus 400 international units/d vitamin D. Asthma and recurrent wheezing until age 3 years were recorded. African American (AA) women (n = 312) had lower initial levels of 25(OH)D (mean [SD], 17.6 ng/mL [8.3 ng/mL]) compared with non-AA women (n = 400; 27.1 ng/mL [9.7 ng/mL], P < .001). No racial difference was found from vitamin D supplementation in pregnancy on asthma/recurrent wheezing in offspring (P for interaction = .77). Having an initial level of greater than 30 ng/mL and being randomized to the intervention group was associated with the lowest risk for asthma/recurrent wheeze by age 3 years compared with having an initial level of less than 20 ng/mL and receiving placebo (adjusted odds ratio, 0.42; 95% CI, 0.19-0.91). We did not find differences between AA and non-AA mothers in the effect of maternal vitamin D supplementation and asthma/recurrent wheeze in offspring at 3 years. Maternal supplementation of vitamin D, particularly in mothers with initial 25(OH)D levels of greater than 30 ng/mL, reduced asthma/recurrent wheeze in the offspring through age 3 years, suggesting that higher vitamin D status beginning in early pregnancy is necessary for asthma/recurrent wheeze prevention in early life. [Display omitted]
Nutrient trials differ from drug trials because participants have varying circulating levels at entry into the trial. We sought to study the effect of a vitamin D intervention in pregnancy between subjects of different races and the association between 25-hydroxyvitamin D (25[OH]D) levels in pregnancy and the risk of asthma/recurrent wheeze in offspring. The Vitamin D Antenatal Asthma Reduction Trial is a randomized trial of pregnant women at risk of having children with asthma randomized to 4400 international units/d vitamin D or placebo plus 400 international units/d vitamin D. Asthma and recurrent wheezing until age 3 years were recorded. African American (AA) women (n = 312) had lower initial levels of 25(OH)D (mean [SD], 17.6 ng/mL [8.3 ng/mL]) compared with non-AA women (n = 400; 27.1 ng/mL [9.7 ng/mL], P < .001). No racial difference was found from vitamin D supplementation in pregnancy on asthma/recurrent wheezing in offspring (P for interaction = .77). Having an initial level of greater than 30 ng/mL and being randomized to the intervention group was associated with the lowest risk for asthma/recurrent wheeze by age 3 years compared with having an initial level of less than 20 ng/mL and receiving placebo (adjusted odds ratio, 0.42; 95% CI, 0.19-0.91). We did not find differences between AA and non-AA mothers in the effect of maternal vitamin D supplementation and asthma/recurrent wheeze in offspring at 3 years. Maternal supplementation of vitamin D, particularly in mothers with initial 25(OH)D levels of greater than 30 ng/mL, reduced asthma/recurrent wheeze in the offspring through age 3 years, suggesting that higher vitamin D status beginning in early pregnancy is necessary for asthma/recurrent wheeze prevention in early life.
Background Nutrient trials differ from drug trials because participants have varying circulating levels at entry into the trial. Objective We sought to study the effect of a vitamin D intervention in pregnancy between subjects of different races and the association between 25-hydroxyvitamin D3(25[OH]D) levels in pregnancy and the risk of asthma/recurrent wheeze in offspring. Methods The Vitamin D Antenatal Asthma Reduction Trial is a randomized trial of pregnant women at risk of having children with asthma randomized to 4400 international units/d vitamin D or placebo plus 400 international units/d vitamin D. Asthma and recurrent wheezing until age 3 years were recorded. Results African American (AA) women (n = 312) had lower initial levels of 25(OH)D (mean [SD], 17.6 ng/mL [8.3 ng/mL]) compared with non-AA women (n = 400; 27.1 ng/mL [9.7 ng/mL],P< .001). No racial difference was found from vitamin D supplementation in pregnancy on asthma/recurrent wheezing in offspring (Pfor interaction = .77). Having an initial level of greater than 30 ng/mL and being randomized to the intervention group was associated with the lowest risk for asthma/recurrent wheeze by age 3 years compared with having an initial level of less than 20 ng/mL and receiving placebo (adjusted odds ratio, 0.42; 95% CI, 0.19-0.91). Conclusions We did not find differences between AA and non-AA mothers in the effect of maternal vitamin D supplementation and asthma/recurrent wheeze in offspring at 3 years. Maternal supplementation of vitamin D, particularly in mothers with initial 25(OH)D levels of greater than 30 ng/mL, reduced asthma/recurrent wheeze in the offspring through age 3 years, suggesting that higher vitamin D status beginning in early pregnancy is necessary for asthma/recurrent wheeze prevention in early life.
Author Zeiger, Robert S.
Laranjo, Nancy
O'Connor, George
Sandel, Megan
Schatz, Michael
Harshfield, Benjamin J.
Bacharier, Leonard B.
Hollis, Bruce W.
Wolsk, Helene M.
Weiss, Scott T.
Strunk, Robert C.
Carey, Vincent J.
Litonjua, Augusto A.
Author_xml – sequence: 1
  givenname: Helene M.
  surname: Wolsk
  fullname: Wolsk, Helene M.
  organization: Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Mass
– sequence: 2
  givenname: Benjamin J.
  surname: Harshfield
  fullname: Harshfield, Benjamin J.
  organization: Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Mass
– sequence: 3
  givenname: Nancy
  surname: Laranjo
  fullname: Laranjo, Nancy
  organization: Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Mass
– sequence: 4
  givenname: Vincent J.
  surname: Carey
  fullname: Carey, Vincent J.
  organization: Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Mass
– sequence: 5
  givenname: George
  surname: O'Connor
  fullname: O'Connor, George
  organization: Pulmonary Center, Department of Medicine, Boston University School of Medicine, Boston, Mass
– sequence: 6
  givenname: Megan
  surname: Sandel
  fullname: Sandel, Megan
  organization: Department of Pediatrics, Boston Medical Center, Boston, Mass
– sequence: 7
  givenname: Robert C.
  surname: Strunk
  fullname: Strunk, Robert C.
  organization: Division of Pediatric Allergy, Immunology and Pulmonary Medicine, Department of Pediatrics, Washington University School of Medicine and St Louis Children's Hospital, St Louis, Mo
– sequence: 8
  givenname: Leonard B.
  surname: Bacharier
  fullname: Bacharier, Leonard B.
  organization: Division of Pediatric Allergy, Immunology and Pulmonary Medicine, Department of Pediatrics, Washington University School of Medicine and St Louis Children's Hospital, St Louis, Mo
– sequence: 9
  givenname: Robert S.
  surname: Zeiger
  fullname: Zeiger, Robert S.
  organization: Department of Allergy and Research evaluation, Kaiser Permanente Southern California, San Diego and Pasadena, Calif
– sequence: 10
  givenname: Michael
  surname: Schatz
  fullname: Schatz, Michael
  organization: Department of Allergy and Research evaluation, Kaiser Permanente Southern California, San Diego and Pasadena, Calif
– sequence: 11
  givenname: Bruce W.
  surname: Hollis
  fullname: Hollis, Bruce W.
  organization: Department of Pediatrics, Medical University of South Carolina, Charleston, South Carolina
– sequence: 12
  givenname: Scott T.
  surname: Weiss
  fullname: Weiss, Scott T.
  organization: Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Mass
– sequence: 13
  givenname: Augusto A.
  surname: Litonjua
  fullname: Litonjua, Augusto A.
  email: augusto.litonjua@channing.harvard.edu
  organization: Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Mass
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28285844$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright 2017 American Academy of Allergy, Asthma & Immunology
American Academy of Allergy, Asthma & Immunology
Copyright © 2017 American Academy of Allergy, Asthma & Immunology. All rights reserved.
Copyright Elsevier Science Ltd. Nov 1, 2017
Copyright_xml – notice: 2017 American Academy of Allergy, Asthma & Immunology
– notice: American Academy of Allergy, Asthma & Immunology
– notice: Copyright © 2017 American Academy of Allergy, Asthma & Immunology. All rights reserved.
– notice: Copyright Elsevier Science Ltd. Nov 1, 2017
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Issue 5
Keywords AA
OR
Vitamin D
prenatal
25(OH)D
allergy
asthma
IU
VDAART
randomized controlled trial
Vitamin D Antenatal Asthma Reduction Trial
25-hydroxyvitamin D 3
International units
Odds ratio
African American
Language English
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Snippet Nutrient trials differ from drug trials because participants have varying circulating levels at entry into the trial. We sought to study the effect of a...
Background Nutrient trials differ from drug trials because participants have varying circulating levels at entry into the trial. Objective We sought to study...
BACKGROUNDNutrient trials differ from drug trials because participants have varying circulating levels at entry into the trial.OBJECTIVEWe sought to study the...
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SubjectTerms Adolescent
Adult
African Americans
Age
Allergies
allergy
Allergy and Immunology
Asthma
Asthma - epidemiology
Asthma - prevention & control
Birthdays
Calcifediol - blood
Child, Preschool
Children
Children & youth
Dietary Supplements
Female
Humans
Male
Offspring
Pregnancy
prenatal
Prenatal experience
Prenatal Exposure Delayed Effects - epidemiology
Prenatal Exposure Delayed Effects - prevention & control
randomized controlled trial
Recurrence
Respiratory Sounds
Risk
Supplements
United States - epidemiology
Vitamin D
Vitamin D - administration & dosage
Vitamin deficiency
Wheezing
Womens health
Young Adult
Title 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
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