4.6 Article

Cholecalciferol Supplementation Does Not Influence β-Cell Function and Insulin Action in Obese Adolescents: A Prospective Double-Blind Randomized Trial

期刊

JOURNAL OF NUTRITION
卷 145, 期 2, 页码 284-290

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OXFORD UNIV PRESS
DOI: 10.3945/jn.114.202010

关键词

vitamin D supplementation; insulin action; insulin secretion; obese adolescents; disposition index

资金

  1. Thrasher Research Foundation

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Background: There is increasing interest in the extraskeletal effects of vitamin D, particularly in the obese state with regard to the development of insulin resistance and diabetes. Objective: The objective of the study was to determine the effect of 2 doses of cholecalciferol (vitamin D-3) supplementation on insulin action (S) and pancreatic p-cell function in obese adolescents. Methods: We performed a 12-wk double-blind, randomized comparison of the effect of vitamin D-3 supplementation on Si and p-cell function in obese Caucasian adolescents (body mass index > 95th percentile). The subjects were randomly assigned to receive either 400 IU/d (n = 25) or 2000 IU/d (n = 26) of vitamin D-3. Each subject underwent a 7-sample 75 g oral glucose tolerance test, with glucose, insulin, and C-peptide measurements, to calculate Si and p-cell function as assessed by the disposition index (DI), with use of the oral minimal model before and after supplementation. A total of 51 subjects aged 15.0 +/- 1.9 y were enrolled. Included for analysis at follow-up were a total of 46 subjects 120 male and 26 female adolescents), 23 in each group. Results: Initial serum 25-hydroxyvitamin D [25(OH)D] was 24.0 +/- 8.1 mu g/L. There was no correlation between 25(OH)D concentrations and Si or DI. There was a modest but significant increase in 25(OH)D concentration in the 2000 IU/d group (3.1 +/- 6.5 g/L, P = 0.04) but not in the 400 IU/d group (P = 0.39). There was no change in Si or DI following vitamin D-3 supplementation in either of the treatment groups (all P > 0.10). Conclusions: The current study shows no effect from vitamin D-3 supplementation, irrespective of its dose, on p-cell function or insulin action in obese nondiabetic adolescents with relatively good vitamin D status. Whether obese adolescents with vitamin D deficiency and impaired glucose metabolism would respond differently to vitamin D-3 supplementation remains unclear and warrants further studies. This trial was registered at clinicaltrials.gov as NCT00858247.

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