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   <subfield code="a">10.1007/s10620-010-1544-3</subfield>
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   <subfield code="a">Vitamin D Deficiency in Children with Inflammatory Bowel Disease</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Alon Levin, Veena Wadhera, Steven Leach, Helen Woodhead, Daniel Lemberg, A. Czarina Mendoza-Cruz, Andrew Day]</subfield>
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   <subfield code="a">Background: Osteopenia and osteoporosis are commonly seen in inflammatory bowel disease (IBD). Vitamin D deficiency potentially contributes to diminished bone acquisition in childhood. Objectives: The objectives of this study were to assess vitamin D in a group of Australian children with IBD and to ascertain associations between vitamin D status and key clinical factors, for example disease location and severity. Methods: Data were obtained retrospectively from the records of children with IBD who had at least one measurement of serum 25-hydroxyvitamin D (25(OH)D) over a two-year period. Demographic variables, disease activity, inflammatory markers, disease location, duration, and therapy were recorded. Moderate and severe deficiency were defined as 25(OH)D &lt;51nmol/l and &lt;30nmol/l, respectively. Insufficiency was defined as 25(OH)D between 51 and 75nmol/l. Results: Overall, the mean 25(OH)D level in 78 children (104 measurements) was 71.2 (SD±26.5) nmol/l. Fifteen (19%) children were vitamin D deficient and 30 (38%) children were insufficient. Levels of 25(OH)D were not associated with disease location or use of immunosuppressive drugs. Children with vitamin D deficiency had greater corticosteroid exposure than those with normal status (P=0.001). The mean 25(OH)D of 38 children treated with nutritional therapy at diagnosis was higher than for 17 children initially treated with corticosteroids (P=0.04). Conclusions: A high proportion of these Australian children with IBD were vitamin D deficient. This emphasizes the importance of monitoring vitamin D status, and treating deficiency, in the management of pediatric IBD. The possible benefit of nutritional therapy in protection against vitamin D deficiency requires further prospective study.</subfield>
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   <subfield code="a">Springer Science+Business Media, LLC, 2011</subfield>
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   <subfield code="a">Inflammatory bowel disease</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Crohn's disease</subfield>
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   <subfield code="a">Vitamin D deficiency</subfield>
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   <subfield code="a">Corticosteroids</subfield>
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   <subfield code="a">Exclusive enteral nutrition</subfield>
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   <subfield code="a">Levin</subfield>
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   <subfield code="u">School of Women's &amp; Children's Health, The University of New South Wales, Sydney, NSW, Australia</subfield>
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   <subfield code="a">Czarina Mendoza-Cruz</subfield>
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