4.5 Article

Use of a Novel Vitamin D Bioavailability Test Demonstrates That Vitamin D Absorption Is Decreased in Patients with Quiescent Crohn's Disease

期刊

INFLAMMATORY BOWEL DISEASES
卷 17, 期 10, 页码 2116-2121

出版社

WILEY-BLACKWELL
DOI: 10.1002/ibd.21595

关键词

vitamin D; Crohn's disease; bioavailability test; IBD; malabsorption; 25-hydroxyvitamin D

资金

  1. CTSI [U54 RR025771]

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Background: Vitamin D deficiency is a common problem in patients with Crohn's disease (CD). The aim of this study was to determine the ability of normal subjects and patients with quiescent CD to absorb vitamin D(2) using a novel vitamin D bioavailability test. In addition, we evaluated whether the location of disease or previous surgery had any influence on the bioavailability of vitamin D(2) in CD patients. Methods: Ten normal subjects (50% female) and 37 CD patients with quiescent disease (51% female) were included in this study. Subjects who recently received any vitamin D(2) were excluded. The vitamin D bioavailability test was performed in all subjects. After a baseline blood draw, all subjects were then given a single 50,000 IU oral dose of vitamin D(2) in a capsule formulation and had their blood drawn 12 hours later to determine serum vitamin D(2), which reflected their vitamin D(2) absorption capacity. Results: Forty-two percent and 29% of CD patients were found to be either vitamin D-deficient (25-hydroxyvitamin D [25(OH) D] <= 20 ng/mL] or insufficient [25(OH) D 21-29 ng/mL], respectively. Twelve hours after ingesting 50,000 IU vitamin D2, vitamin D(2) levels rose from a baseline of 0.7 +/- 0.7 ng/mL (mean +/- SEM) to 49.8 +/- 3.0 ng/mL in normal subjects. In CD patients, baseline vitamin D(2) levels rose from 0 ng/mL to 34.8 +/- 2.8 ng/mL. CD patients had on average a 30% decrease in their ability to absorb vitamin D(2) (P = 0.01). Moreover, we found a wide variability of vitamin D(2) bioavailability in CD patients. Analysis of variance (ANOVA) revealed no statistical difference of vitamin D(2) bioavailability between patients in the CD subgroup stratified by the location of disease, the type of surgery, and receiving or not receiving surgery. Conclusions: More than 70% of the patients with quiescent CD were vitamin D-deficient or insufficient. The ability to absorb vitamin D(2) in CD patients is unpredictable and the only way to determine this is to perform a vitamin D bioavailability test. Use of this test may guide clinicians in administering the appropriate therapeutic dose of vitamin D for treating vitamin D deficiency in patients with CD.

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