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Publication Date:
April 2012
ISSN:
2191-0251
DOI:
10.1515/jpem-2012-0048

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Editor-in-Chief: Zadik, Zvi

Editorial Board Member: Cassorla, Fernando / Cutfield, Wayne / de Muinck Keizer-Schrama, Sabine M.P.F. / Fideleff, Hugo L. / LaFranch, Stephen H. / Lanes M. D., Roberto / Levitsky, Lynne / Lippe, Barbara / Pfäffle, Roland / Root, Allen W. / Rosenfeld, Ron G. / Werther, George / Kiess, Wieland

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Is vitamin D deficiency a feature of pediatric celiac disease?

Jeffrey Villanueva1 / Louise Maranda2 / 2

1University of Massachusetts Medical School, Worcester, MA, USA

2University of Massachusetts Medical School – Pediatrics, Worcester, MA, USA

Corresponding author: Benjamin Udoka Nwosu, Division of Endocrinology, Department of Pediatrics, University of Massachusetts Medical School, 55 Lake Avenue North Worcester, MA 01655, USA Phone: +1-508-334-7872, Fax: +1-508-856-4287

Citation Information: Journal of Pediatric Endocrinology and Metabolism. Volume 25, Issue 5-6, Pages 607–610, ISSN (Online) 2191-0251, ISSN (Print) 0334-018X, DOI: 10.1515/jpem-2012-0048, April 2012

Publication History:
Received:
2012-01-15
Accepted:
2012-03-10
Published Online:
2012-04-21

Abstract

Background: Celiac disease (CD) is an autoimmune enteropathy characterized by villus atrophy and malabsorption of essential nutrients. Vitamin D deficiency has been described in autoimmune diseases, but its status in prepubertal children with CD has not been adequately studied.

Objective: To determine the vitamin D status of prepubertal children with CD.

Study design: A retrospective study of prepubertal children aged 3–12 years with CD (n=24) who were compared to prepubertal, non-CD children of the same age (n=50). Children were included in the study if they had a diagnosis of CD by intestinal biopsy, and were not on a gluten-free diet (GFD). Patients were excluded if they had diseases of calcium or vitamin D metabolism, or were receiving calcium or vitamin D supplementation or had other autoimmune diseases. All subjects had their serum 25-hydroxyvitamin D [25(OH)D] level measured.

Results: There was no difference in 25(OH)D level between the CD and non-CD children (27.58±9.91 vs. 26.20±10.45, p=0.59). However, when the patients were subdivided into obese and non-obese groups, the non-obese CD patients had a significantly higher 25(OH)D level than the obese normal children (28.39±10.26 vs. 21.58±5.67, p=0.009). In contrast, there was no difference in 25(OH)D level between non-obese CD patients and non-obese normal children (28.39±10.26 vs. 30.64±12.08, p=0.52). The season of 25(OH)D measurement was not a significant confounder (p=0.7).

Conclusions: Our data showed no difference in 25(OH)D levels between normal children and those with CD when adjusted for body mass index.

Keywords: celiac disease; children; prepubertal status; vitamin D

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