Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/124863
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorde Courten, B.-
dc.contributor.authorMousa, A.-
dc.contributor.authorNaderpoor, N.-
dc.contributor.authorTeede, H.-
dc.contributor.authorde Courten, M.P.J.-
dc.contributor.authorScragg, R.-
dc.date.issued2015-
dc.identifier.citationTrials, 2015; 16(1):1-12-
dc.identifier.issn1745-6215-
dc.identifier.issn1745-6215-
dc.identifier.urihttp://hdl.handle.net/2440/124863-
dc.description.abstractDespite Australia's sunny climate, low vitamin D levels are increasingly prevalent. Sun exposure is limited by long working hours, an increase in time spent indoors, and sun protection practices, and there is limited dietary vitamin D fortification. While the importance of vitamin D for bone mineralization is well known, its role as a protective agent against chronic diseases, such as type 2 diabetes and cardiovascular disease, is less understood. Observational and limited intervention studies suggest that vitamin D might improve insulin sensitivity and secretion, mainly via its anti-inflammatory properties, thereby decreasing the risk of development and progression of type 2 diabetes. The primary aim of this trial is to investigate whether improved plasma concentrations of 25-hydroxyvitamin D (25(OH)D), obtained through vitamin D supplementation, will increase insulin sensitivity and insulin secretion. A secondary aim is to determine whether these relationships are mediated by a reduction in underlying subclinical inflammation associated with obesity.Fifty overweight but otherwise healthy nondiabetic adults between 18 and 60 years old, with low vitamin D levels (25(OH)D < 50 nmol/l), will be randomly assigned to intervention or placebo. At baseline, participants will undergo a medical review and anthropometric measurements, including dual X-ray absorptiometry, an intravenous glucose tolerance test, muscle and fat biopsies, a hyperinsulinemic euglycemic clamp, and questionnaires assessing diet, physical activity, sun exposure, back and knee pain, and depression. The intervention group will receive a first dose of 100,000 IU followed by 4,000 IU vitamin D (cholecalciferol) daily, while the placebo group will receive apparently identical capsules, both for a period of 16 weeks. All measurements will be repeated at follow-up, with the primary outcome measure expressed as a change from baseline in insulin sensitivity and secretion for the intervention group compared with the placebo group. Secondary outcome measures will compare changes in anthropometry, cardiovascular risk factors, and inflammatory markers.The trial will provide much needed clinical evidence on the impact of vitamin D supplementation on insulin resistance and secretion and its underlying mechanisms, which are relevant for the prevention and management of type 2 diabetes.Clinicaltrials.gov ID: NCT02112721 .-
dc.description.statementofresponsibilityBarbora de Courten, Aya Mousa, Negar Naderpoor, Helena Teede, Maximilian P J de Courten and Robert Scragg-
dc.language.isoen-
dc.publisherBMC-
dc.rights© 2015 de Courten et al. Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.-
dc.source.urihttp://dx.doi.org/10.1186/s13063-015-0851-6-
dc.subject25(OH)D; inflammation; insulin secretion;, insulin sensitivity; type 2 diabetes; vitamin D-
dc.titleVitamin D supplementation for the prevention of type 2 diabetes in overweight adults: study protocol for a randomized controlled trial-
dc.typeJournal article-
dc.identifier.doi10.1186/s13063-015-0851-6-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1047897-
pubs.publication-statusPublished-
dc.identifier.orcidTeede, H. [0000-0001-7609-577X]-
Appears in Collections:Aurora harvest 8
Medicine publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.