Evidence map›Paper›PMID 35763390›Full record

Trial reportThe British journal of dermatology2022

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

Sarah El-Heis, Stefania D'Angelo, Elizabeth M Curtis, Eugene Healy, Rebecca J Moon, Sarah R Crozier, Hazel Inskip, Cyrus Cooper, Nicholas C Harvey, Keith M Godfrey and 1 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The British journal of dermatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 6 pooled it
8.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 6 syntheses or guidelines pooled it, 42 citations in OpenAlex.

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  6. Vitamin D supplementation for women during pregnancy.The Cochrane database of systematic reviews · 2024
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  7. Pregnancy vitamin D supplementation and bone mineral density of the mother: a post hoc analysis of the MAVIDOS randomised placebo-controlled trial.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2025
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  18. Prevention of Atopic Dermatitis: What Are We Missing?Allergy, asthma & immunology research · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Sarah El-HeisMedical Research Council Lifecourse Epidemiology Centre, University of Southampton, Southampton, UK.ORCID 0000-0003-4277-7187
Stefania D'AngeloMedical Research Council Lifecourse Epidemiology Centre, University of Southampton, Southampton, UK.
Elizabeth M CurtisMedical Research Council Lifecourse Epidemiology Centre, University of Southampton, Southampton, UK.
Eugene HealyDermatopharmacology, Faculty of Medicine, University of Southampton, Southampton, UK.
Rebecca J MoonMedical Research Council Lifecourse Epidemiology Centre, University of Southampton, Southampton, UK.
Sarah R CrozierMedical Research Council Lifecourse Epidemiology Centre, University of Southampton, Southampton, UK.
Hazel InskipMedical Research Council Lifecourse Epidemiology Centre, University of Southampton, Southampton, UK.
Cyrus CooperMedical Research Council Lifecourse Epidemiology Centre, University of Southampton, Southampton, UK.
Nicholas C HarveyMedical Research Council Lifecourse Epidemiology Centre, University of Southampton, Southampton, UK.
Keith M GodfreyMedical Research Council Lifecourse Epidemiology Centre, University of Southampton, Southampton, UK.
MAVIDOS Trial Group
MRC Lifecourse Epidemiology Unit · GBUniversity Hospital Southampton NHS Foundation Trust · GBNIHR Southampton Biomedical Research Centre · GBUniversity of Southampton · GB

Funding

Medical Research Council G0400491Medical Research Council MC_PC_15015Medical Research Council MC_PC_21001Medical Research Council MC_PC_21002Medical Research Council MC_PC_21003Medical Research Council MC_U147585819Medical Research Council MC_U147585824Medical Research Council MC_U147585827Medical Research Council MC_UP_A620_1014Medical Research Council MC_UU_12011/1Medical Research Council MC_UU_12011/4Versus Arthritis 17702Versus Arthritis 21231Wellcome Trust 201222/Z/16/Z
6 · The paper itself

Abstract

backgroundEvidence linking prenatal maternal vitamin D supplementation with the offspring's risk of atopic eczema is inconsistent, with most data coming from observational studies.

objectivesTo 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.

methodsWithin 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).

resultsThe 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 0·55, 95% confidence interval (CI) 0·32-0·97, P = 0·04]; this effect weakened and was not statistically significant at ages 24 months (OR 0·76, 95% CI 0·47-1·23) or 48 months (OR 0·75, 95% CI 0·37-1·52). The statistical interaction of intervention and breastfeeding duration in relation to eczema at age 12 months was not significant (P = 0·41), but stratification showed reduced infantile eczema risk in the intervention group for infants breastfed for ≥ 1 month (OR 0·48, 95% CI 0·24-0·94, P = 0·03) but not in those breastfed for < 1 month (OR 0·80, 95% CI 0·29-2·17, P = 0·66).

conclusionsOur 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.

Indexed as

Dermatitis, AtopicOsteoporosisChildChild, PreschoolCholecalciferolDietary SupplementsDouble-Blind MethodFemaleHumansInfantInfant, NewbornPregnancyVitamin DVitaminsCholecalciferolVitamin DVitamins

Identifiers

PMID35763390
PMCPMC9804289
OpenAlexW4283692918

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.