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Should We Assess Vitamin D Status in Pediatric Patients With Celiac Disease?
Author(s) -
Ahlawat Rajni,
Weinstein Toba,
Markowitz James,
Kohn Nina,
Pettei Michael J
Publication year - 2019
Publication title -
journal of pediatric gastroenterology and nutrition
Language(s) - English
Resource type - Journals
eISSN - 1536-4801
pISSN - 0277-2116
DOI - 10.1097/mpg.0000000000002417
Subject(s) - medicine , vitamin d and neurology , multivitamin , gastroenterology , vitamin , anthropometry , vitamin d deficiency , population , ingestion , physiology , environmental health
Objectives: Screening for vitamin D status in celiac disease (CD) has been recommended but the literature provides varying support. We sought to assess the vitamin D status in newly diagnosed children with CD and in a non‐CD control population and relate them to vitamin D intake. Methods: In a cross‐sectional study, s erum 25‐hydroxyvitamin D (25‐OHD) levels were drawn in children with newly diagnosed CD and compared with pediatric outpatients with functional abdominal complaints. Anthropometric data as well as vitamin D intake based on milk and multivitamin ingestion were collected. Results: Thirty‐eight newly diagnosed CD patients (10.4 ± 3.0 years old; 50% girls) and 82 controls (11.2 ± 4.2 years old; 58.5% girls) were studied. Both groups were similar except for average daily D intake and BMI. There was no statistical difference in mean 25‐OHD levels between CD (26.4 ± 8.0 ng/mL) and controls (23.5 ± 8.2 ng/mL) [ P  ≤ 0.07]. Both groups had high percentages of suboptimal D status (65.8% CD and 79.3% controls). 25‐OHD levels significantly correlated with age ( r  = −0.262; P  < 0.0038) and estimated vitamin D intake ( r  = 0.361; P  < 0.0001). Conclusions: No significant difference in 25‐OHD levels was noted between newly diagnosed CD and controls, but inadequate 25‐OHD levels were common in both. 25‐OHD levels were highly associated with vitamin D intake demonstrating similar vitamin D absorption between patients and controls. As CD is associated with bone disease and D status is frequently low, efforts at optimizing D, such as screening levels at diagnosis need to be conducted.

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