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

被引:25
作者
El-Heis, Sarah [1 ]
D'Angelo, Stefania [1 ]
Curtis, Elizabeth M. [1 ]
Healy, Eugene [2 ]
Moon, Rebecca J. [1 ]
Crozier, Sarah R. [1 ,3 ]
Inskip, Hazel [1 ,4 ,5 ]
Cooper, Cyrus [1 ,4 ,5 ,6 ]
Harvey, Nicholas C. [1 ,4 ,5 ]
Godfrey, Keith M. [1 ,4 ,5 ,7 ]
机构
[1] Univ Southampton, Med Res Council, Lifecourse Epidemiol Ctr, Southampton, Hants, England
[2] Univ Southampton, Fac Med, Dermatopharmacol, Southampton, Hants, England
[3] Innovat Ctr, NIHR Appl Res Collaborat Wessex, Southampton Sci Pk, Southampton, Hants, England
[4] Univ Southampton, NIHR Nutr Biomed Res Ctr, Southampton, Hants, England
[5] Univ Hosp Southampton NHS Fdn Trust, Southampton, Hants, England
[6] Univ Oxford, NIHR Musculoskeletal Biomed Res Unit, Oxford, England
[7] Univ Southampton, Dev Sci, Southampton, Hants, England
基金
欧盟地平线“2020”; 英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
D DEFICIENCY; 25-HYDROXYVITAMIN D; IMMUNE-SYSTEM; PREGNANCY; ASTHMA; DERMATITIS; SEVERITY; DISEASES; WHEEZE; COPD;
D O I
10.1111/bjd.21721
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
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.
引用
收藏
页码:659 / 666
页数:8
相关论文
共 39 条
[21]   Vitamin D status in mothers and their newborns in Iran [J].
Maghbooli Z. ;
Hossein-Nezhad A. ;
Shafaei A.R. ;
Karimi F. ;
Madani F.S. ;
Larijani B. .
BMC Pregnancy and Childbirth, 7 (1)
[22]   Vitamin D deficiency in pregnancy - still a public health issue [J].
McAree, Trixie ;
Jacobs, Benjamin ;
Manickavasagar, Thubeena ;
Sivalokanathan, Suganthinie ;
Brennan, Lauren ;
Bassett, Paul ;
Rainbow, Sandra ;
Blair, Mitch .
MATERNAL AND CHILD NUTRITION, 2013, 9 (01) :23-30
[23]   Dairy food, calcium and vitamin D intake in pregnancy, and wheeze and eczema in infants [J].
Miyake, Y. ;
Sasaki, S. ;
Tanaka, K. ;
Hirota, Y. .
EUROPEAN RESPIRATORY JOURNAL, 2010, 35 (06) :1228-1234
[24]   Maternal Serum and Breast Milk Vitamin D Levels: Findings from the Universiti Sains Malaysia Pregnancy Cohort Study [J].
Mohamed, Hamid Jan Jan ;
Rowan, Angela ;
Fong, Bertram ;
Loy, See-Ling .
PLOS ONE, 2014, 9 (07)
[25]   Response to Antenatal Cholecalciferol Supplementation Is Associated With Common Vitamin D-Related Genetic Variants [J].
Moon, Rebecca J. ;
Harvey, Nicholas C. ;
Cooper, Cyrus ;
D'Angelo, Stefania ;
Curtis, Elizabeth M. ;
Crozier, Sarah R. ;
Barton, Sheila J. ;
Robinson, Sian M. ;
Godfrey, Keith M. ;
Graham, Nikki J. ;
Holloway, John W. ;
Bishop, Nicholas J. ;
Kennedy, Stephen ;
Papageorghiou, Aris T. ;
Schoenmakers, Inez ;
Fraser, Robert ;
Gandhi, Saurabh V. ;
Prentice, Ann ;
Inskip, Hazel M. ;
Javaid, M. Kassim .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2017, 102 (08) :2941-2949
[26]   Determinants of the Maternal 25-Hydroxyvitamin D Response to Vitamin D Supplementation During Pregnancy [J].
Moon, Rebecca J. ;
Harvey, Nicholas C. ;
Cooper, Cyrus ;
D'Angelo, Stefania ;
Crozier, Sarah R. ;
Inskip, Hazel M. ;
Schoenmakers, Inez ;
Prentice, Ann ;
Arden, Nigel K. ;
Bishop, Nicholas J. ;
Carr, Andrew ;
Dennison, Elaine M. ;
Eastell, Richard ;
Fraser, Robert ;
Gandhi, Saurabh V. ;
Godfrey, Keith M. ;
Kennedy, Stephen ;
Mughal, M. Zulf ;
Papageorghiou, Aris T. ;
Reid, David M. ;
Robinson, Sian M. ;
Javaid, M. Kassim .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2016, 101 (12) :5012-5020
[27]   Neonatal adiposity increases the risk of atopic dermatitis during the first year of life [J].
O'Donovan, Sinead M. ;
Hourihane, Jonathan O'B. ;
Murray, Deirdre M. ;
Kenny, Louise C. ;
Khashan, Ali S. ;
Chaoimh, Carol Ni ;
Irvine, Alan D. ;
Kiely, Mairead .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2016, 137 (01) :108-117
[28]   Maternal late-pregnancy serum 25-hydroxyvitamin D in relation to childhood wheeze and atopic outcomes [J].
Pike, Katharine C. ;
Inskip, Hazel M. ;
Robinson, Sian ;
Lucas, Jane S. ;
Cooper, Cyrus ;
Harvey, Nicholas C. ;
Godfrey, Keith M. ;
Roberts, Graham .
THORAX, 2012, 67 (11) :950-956
[29]   The vitamin D pathway: a new target for control of the skin's immune response? [J].
Schauber, Juergen ;
Gallo, Richard L. .
EXPERIMENTAL DERMATOLOGY, 2008, 17 (08) :633-639
[30]   Coincidence of immune-mediated diseases driven by Th1 and Th2 subsets suggests a common aetiology. A population-based study using computerized General Practice data [J].
Simpson, CR ;
Anderson, WJA ;
Helms, PJ ;
Taylor, MW ;
Watson, L ;
Prescott, GJ ;
Godden, DJ ;
Barker, RN .
CLINICAL AND EXPERIMENTAL ALLERGY, 2002, 32 (01) :37-42