4.6 Article

Maternal antenatal vitamin D supplementation and offspring risk of atopic eczema in the first 4 years of life: evidence from a randomized controlled trial

Journal

BRITISH JOURNAL OF DERMATOLOGY
Volume 187, Issue 5, Pages 659-666

Publisher

OXFORD UNIV PRESS
DOI: 10.1111/bjd.21721

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Funding

  1. Arthritis Research UK [17702]
  2. Medical Research Council [4050502589]
  3. Bupa Foundation
  4. National Institute for Health Research (NIHR) Southampton Biomedical Research Centre
  5. University of Southampton
  6. University Hospital Southampton NHS Foundation Trust
  7. NIHR Musculoskeletal Biomedical Research Unit, University of Oxford
  8. MRC [U105960371]
  9. UK Medical Research Council [MC_UU_12011/4]
  10. National Institute for Health Research [NF-SI-051510042]
  11. NIHR Southampton 1000DaysPlus Global Nutrition Research Group [17/63/154]
  12. NIHR Southampton Biomedical Research Centre [IS-BRC-1215-20004]
  13. European Union [598488-EPP-1-2018-1-DEEPPKA2-CBHE-JP]
  14. British Heart Foundation [RG/15/17/3174]
  15. European Union's Seventh Framework Programme (FP7/2007-2013) [289346, 613977]
  16. BBSRC [BB/P028179/1]
  17. ERA-Net on Biomarkers for Nutrition and Health (ERA HDHL), Horizon 2020 grant [696295]

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This study provides evidence from a randomized controlled trial that prenatal maternal cholecalciferol supplementation can reduce the risk of infantile atopic eczema, potentially through increased breast milk cholecalciferol levels.
Background Evidence linking prenatal maternal vitamin D supplementation with the offspring's risk of atopic eczema is inconsistent, with most data coming from observational studies. Objectives To examine the influence of maternal cholecalciferol supplementation during pregnancy on the risk of atopic eczema in the offspring at ages 12, 24 and 48 months. Methods Within the UK Maternal Vitamin D Osteoporosis Study (MAVIDOS) double-blind, randomized placebo-controlled trial, we examined the relationship of maternal vitamin D supplementation during pregnancy with offspring atopic eczema at ages 12, 24 and 48 months. In MAVIDOS, pregnant women were allocated to either cholecalciferol 1000 IU per day or matched placebo, taken from around 14 weeks' gestation until delivery, with the primary outcome of neonatal whole-body bone mineral content. The prevalence of atopic eczema in the offspring was ascertained at ages 12 (n = 635), 24 (n = 610) and 48 (n = 449) months, based on the UK Working Party criteria for the definition of atopic dermatitis. The trial was registered with ISRCTN (82927713) and EudraCT (2007-001716-23). Results The characteristics of mothers and offspring were similar between the intervention and placebo groups, apart from longer breastfeeding duration in the intervention group. Adjusting for breastfeeding duration, offspring of mothers who received cholecalciferol 1000 IU daily had a lower odds ratio (OR) of atopic eczema at age 12 months [OR 0 center dot 55, 95% confidence interval (CI) 0 center dot 32-0 center dot 97, P = 0 center dot 04]; this effect weakened and was not statistically significant at ages 24 months (OR 0 center dot 76, 95% CI 0 center dot 47-1 center dot 23) or 48 months (OR 0 center dot 75, 95% CI 0 center dot 37-1 center dot 52). The statistical interaction of intervention and breastfeeding duration in relation to eczema at age 12 months was not significant (P = 0 center dot 41), but stratification showed reduced infantile eczema risk in the intervention group for infants breastfed for >= 1 month (OR 0 center dot 48, 95% CI 0 center dot 24-0 center dot 94, P = 0 center dot 03) but not in those breastfed for < 1 month (OR 0 center dot 80, 95% CI 0 center dot 29-2 center dot 17, P = 0 center dot 66). Conclusions Our data provide the first randomized controlled trial evidence of a protective effect of antenatal cholecalciferol supplementation on the risk of infantile atopic eczema, with the effect potentially being via increased breast milk cholecalciferol levels. The findings support a developmental influence on atopic eczema, and point to a potentially modifiable perinatal influence on atopic eczema. What is already known about this topic? There are currently no antenatal interventions proven to reduce the incidence of infantile atopic eczema in the general population. However, observational studies have led to speculation that antenatal vitamin D supplementation may be beneficial.

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