A1 Refereed original research article in a scientific journal
25(OH)D Levels in Infancy Is Associated With Celiac Disease Autoimmunity in At-Risk Children: A Case–Control Study
Authors: Aronsson Carin Andrén, Liu Xiang, Norris Jill M., Uusitalo Ulla, Butterworth Martha D., Koletzko Sibylle, Virtanen Suvi M., Erlund Iris, Kurppa Kalle, Hagopian William A., Rewers Marian J., She Jin-Xiong, Toppari Jorma, Ziegler Anette-G., Akolkar Beena, Krischer Jeffrey P., Agardh Daniel; on behalf of the TEDDY Study Group
Publisher: FRONTIERS MEDIA SA
Publication year: 2021
Journal: Frontiers in Nutrition
Journal name in source: FRONTIERS IN NUTRITION
Journal acronym: FRONT NUTR
Article number: ARTN 720041
Volume: 8
Number of pages: 10
ISSN: 2296-861X
DOI: https://doi.org/10.3389/fnut.2021.720041
Self-archived copy’s web address: https://research.utu.fi/converis/portal/detail/Publication/67653008
Objectives: An observed variation in the risk of celiac disease, according to the season of birth, suggests that vitamin D may affect the development of the disease. The aim of this study was to investigate if vitamin D concentration is associated with the risk of celiac disease autoimmunity (CDA) in genetically at-risk children.
Study Design: Children prospectively followed in the multinational The Environmental Determinants of Diabetes in the Young study, conducted at six centers in Europe and the US, were selected for a 1-to-3 nested case-control study. In total, 281 case-control sets were identified. CDA was defined as positivity for tissue transglutaminase autoantibodies (tTGA) on two or more consecutive visits. Vitamin D was measured as 25-hydroxyvitamin D [25(OH)D] concentrations in all plasma samples prior to, and including, the first tTGA positive visit. Conditional logistic regression was used to examine the association between 25(OH)D and risk of CDA.
Results: No significant association was seen between 25(OH)D concentrations (per 5 nmol/L increase) and risk for CDA development during early infancy (odds ratio [OR] 0.99, 95% confidence interval [CI] 0.95-1.04) or childhood (OR 1.02, 95% CI 0.97-1.07). When categorizing 25(OH)D concentrations, there was an increased risk of CDA with 25(OH)D concentrations < 30 nmol/L (OR 2.23, 95% CI 1.29, 3.84) and > 75 nmol/L (OR 2.10, 95% CI 1.28-3.44) in early infancy, as compared with 50-75 nmol/L.
Conclusion: This study indicates that 25(OH)D concentrations 75 nmol/L during early infancy were associated with an increased risk of developing CDA in genetically at-risk children. The non-linear relationship raises the need for more studies on the possible role of 25(OH)D in the relation to celiac disease onset.
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