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Maternal 25-hydroxyvitamin D and its association with childhood atopic outcomes and lung function
BACKGROUND: It has been suggested that maternal vitamin D status in pregnancy influences the risk of asthma and atopy in the offspring. The epidemiological evidence to support these claims is conflicting and may reflect chance findings and differences in how vitamin D was assessed. OBJECTIVE: To exa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814422/ https://www.ncbi.nlm.nih.gov/pubmed/24074336 http://dx.doi.org/10.1111/cea.12172 |
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author | Wills, A K Shaheen, S O Granell, R Henderson, A J Fraser, W D Lawlor, D A |
author_facet | Wills, A K Shaheen, S O Granell, R Henderson, A J Fraser, W D Lawlor, D A |
author_sort | Wills, A K |
collection | PubMed |
description | BACKGROUND: It has been suggested that maternal vitamin D status in pregnancy influences the risk of asthma and atopy in the offspring. The epidemiological evidence to support these claims is conflicting and may reflect chance findings and differences in how vitamin D was assessed. OBJECTIVE: To examine the association between blood total maternal 25-hydroxy vitamin D (25(OH)D) concentrations in pregnancy and offspring asthma, atopy and lung function in the largest birth cohort study to date. METHODS: Participants were largely of white European origin and resident in the South West of England. We examined the associations of maternal 25(OH)D concentrations in pregnancy with the following outcomes in the offspring: wheeze, asthma, atopy, eczema, hayfever, at mean age 7.5 years (n = 3652–4696 depending on outcome), IgE at 7 years (n = 2915) and lung function and bronchial responsiveness at mean age 8.7 years (n = 3728–3784). RESULTS: Sixty-eight per cent of mothers had sufficient (> 50 nmol/L) concentrations of 25(OH)D, 27% were insufficient (27.5–49.99 nmol/L) and 5% were deficient (< 27.5 nmol/L). There was no evidence to suggest that maternal 25(OH)D concentration in pregnancy was associated with any respiratory or atopic outcome in the offspring. These findings remained after adjustment for season of measurement and for potential confounders. There was also no evidence that these relationships followed a non-linear form and no evidence that either deficient or high concentrations of maternal 25(OH)D were associated with atopic or respiratory outcomes. CONCLUSIONS: We found no evidence that maternal blood 25(OH)D concentration in pregnancy is associated with childhood atopic or respiratory outcomes. |
format | Online Article Text |
id | pubmed-3814422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38144222013-11-07 Maternal 25-hydroxyvitamin D and its association with childhood atopic outcomes and lung function Wills, A K Shaheen, S O Granell, R Henderson, A J Fraser, W D Lawlor, D A Clin Exp Allergy Original Articles BACKGROUND: It has been suggested that maternal vitamin D status in pregnancy influences the risk of asthma and atopy in the offspring. The epidemiological evidence to support these claims is conflicting and may reflect chance findings and differences in how vitamin D was assessed. OBJECTIVE: To examine the association between blood total maternal 25-hydroxy vitamin D (25(OH)D) concentrations in pregnancy and offspring asthma, atopy and lung function in the largest birth cohort study to date. METHODS: Participants were largely of white European origin and resident in the South West of England. We examined the associations of maternal 25(OH)D concentrations in pregnancy with the following outcomes in the offspring: wheeze, asthma, atopy, eczema, hayfever, at mean age 7.5 years (n = 3652–4696 depending on outcome), IgE at 7 years (n = 2915) and lung function and bronchial responsiveness at mean age 8.7 years (n = 3728–3784). RESULTS: Sixty-eight per cent of mothers had sufficient (> 50 nmol/L) concentrations of 25(OH)D, 27% were insufficient (27.5–49.99 nmol/L) and 5% were deficient (< 27.5 nmol/L). There was no evidence to suggest that maternal 25(OH)D concentration in pregnancy was associated with any respiratory or atopic outcome in the offspring. These findings remained after adjustment for season of measurement and for potential confounders. There was also no evidence that these relationships followed a non-linear form and no evidence that either deficient or high concentrations of maternal 25(OH)D were associated with atopic or respiratory outcomes. CONCLUSIONS: We found no evidence that maternal blood 25(OH)D concentration in pregnancy is associated with childhood atopic or respiratory outcomes. Blackwell Publishing Ltd 2013-10 2013-09-16 /pmc/articles/PMC3814422/ /pubmed/24074336 http://dx.doi.org/10.1111/cea.12172 Text en Copyright © 2013 John Wiley & Sons Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Articles Wills, A K Shaheen, S O Granell, R Henderson, A J Fraser, W D Lawlor, D A Maternal 25-hydroxyvitamin D and its association with childhood atopic outcomes and lung function |
title | Maternal 25-hydroxyvitamin D and its association with childhood atopic outcomes and lung function |
title_full | Maternal 25-hydroxyvitamin D and its association with childhood atopic outcomes and lung function |
title_fullStr | Maternal 25-hydroxyvitamin D and its association with childhood atopic outcomes and lung function |
title_full_unstemmed | Maternal 25-hydroxyvitamin D and its association with childhood atopic outcomes and lung function |
title_short | Maternal 25-hydroxyvitamin D and its association with childhood atopic outcomes and lung function |
title_sort | maternal 25-hydroxyvitamin d and its association with childhood atopic outcomes and lung function |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814422/ https://www.ncbi.nlm.nih.gov/pubmed/24074336 http://dx.doi.org/10.1111/cea.12172 |
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