Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/38843
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dc.contributor.authorDe Courten M.P.J.en
dc.contributor.authorDe Courten B.en
dc.contributor.authorScragg R.en
dc.contributor.authorWalker K.en
dc.contributor.authorKellow N.en
dc.contributor.authorTeede H.en
dc.contributor.authorMousa A.en
dc.contributor.authorNaderpoor N.en
dc.date.accessioned2021-05-14T13:15:49Zen
dc.date.available2021-05-14T13:15:49Zen
dc.date.copyright2017en
dc.date.created20170623en
dc.date.issued2017-06-23en
dc.identifier.citationAmerican Journal of Clinical Nutrition. 105 (6) (pp 1372-1381), 2017. Date of Publication: 01 Jun 2017.en
dc.identifier.issn0002-9165en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/38843en
dc.description.abstractBackground: Vitamin D supplementation has been proposed as a potential strategy to prevent type 2 diabetes. Existing clinical trials have been limited by short duration, low doses of Vitamin D, variability in participants' Vitamin D-deficiency status, and the use of surrogate measures of body composition, insulin sensitivity, and insulin secretion. Objective(s): To address existing knowledge gaps, we conducted a double-blind, randomized, placebo-controlled trial to investigate whether Vitamin D supplementation that is provided in a sufficient dose and duration to Vitamin D-deficient individuals would improve insulin sensitivity or secretion as measured with the use of goldstandard methods. We hypothesized that Vitamin D supplementation would improve insulin sensitivity and secretion compared with placebo. Design(s): Sixty-five overweight or obese, Vitamin D-deficient (25-hydroxyVitamin D [25(OH)D] concentration <=50 nmol/L) adults were randomly assigned to receive either a bolus oral dose of 100,000 IU cholecalciferol followed by 4000 IU cholecalciferol/d or a matching placebo for 16 wk. Before and after the intervention, participants received gold-standard assessments of body composition (via dual X-ray absorptiometry), insulin sensitivity (via hyperinsulinemic-euglycemic clamps), and insulin secretion [via intravenous-glucose-tolerance tests (IVGTTs)]. Result(s): Fifty-four participants completed the study [35 men and 19 women; mean +/- SD age: 31.9 +/- 8.5 y; body mass index (in kg/m2): 30.9 +/- 4.4]. 25(OH)D increased with Vitamin D supplementation compared with placebo (57.0 +/- 21.3 compared with 1.9 +/- 15.1 nmol/L, respectively; P = 0.02). Vitamin D and placebo groups did not differ in change in insulin sensitivity (0.02 +/- 2.0 compared with 20.03 +/- 2.8 mg * kg-1 * min-1, respectively; P = 0.9) or firstphase insulin secretion (-21 +/- 212 compared with 24 +/- 184 mU/L, respectively; P = 0.9). Results remained nonsignificant after adjustment for age, sex, percentage of body fat, sun exposure, physical activity, and dietary Vitamin D intake (P>0.1). Conclusion(s): Vitamin D supplementation does not improve insulin sensitivity or secretion in Vitamin D-deficient, overweight or obese adults, despite using high-dose Vitamin D supplementation and robust endpoint measures. Therefore, it is unlikely that Vitamin D supplementation would be an effective strategy for reducing diabetes risk even in Vitamin D-deficient populations. This trial was registered at clinicaltrials.gov as NCT02112721. Am J Clin Nutr 2017;105:1372-81.Copyright © 2017 American Society for Nutrition.en
dc.languageenen
dc.languageEnglishen
dc.publisherAmerican Society for Nutrition (E-mail: staff@dues.faseb.org)en
dc.relation.ispartofAmerican Journal of Clinical Nutritionen
dc.titleVitamin D supplementation has no effect on insulin sensitivity or secretion in Vitamin D-deficient, overweight or obese adults: A randomized placebo-controlled trial.en
dc.typeArticleen
dc.type.studyortrialRandomised controlled trial-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.3945/ajcn.117.152736en
dc.publisher.placeUnited Statesen
dc.identifier.pubmedid28490514 [http://www.ncbi.nlm.nih.gov/pubmed/?term=28490514]en
dc.identifier.source616850920en
dc.identifier.institution(Mousa, Naderpoor, Teede, De Courten) Monash Center for Health Research and Implementation, School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia (Kellow, Walker, De Courten) Department of Nutrition and Dietetics, Be Active Sleep and Eat Facility, Monash University, Melbourne, Australia (Naderpoor, Teede) Diabetes and Vascular Medicine Unit, Monash Health, Melbourne, Australia (De Courten) Center for Chronic Disease, Victoria University, Melbourne, Australia (Scragg) School of Population Health, University of Auckland, Auckland, New Zealanden
dc.description.addressB. De Courten, Monash Center for Health Research and Implementation, School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia. E-mail: barbora.decourten@monash.eduen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2017 Elsevier B.V., All rights reserved.en
dc.subect.keywordsInsulin secretion Insulin sensitivity Obesity Randomized trial RCT Vitamin Den
dc.identifier.authoremailDe Courten B.; barbora.decourten@monash.eduen
dc.description.grantNo: 1047897 Organization: (NHMRC) *National Health and Medical Research Council* Country: Australiaen
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeArticle-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptInfection Prevention and Epidemiology-
crisitem.author.deptGeriatric Medicine-
crisitem.author.deptEmergency Medicine-
crisitem.author.deptDiabetes and Vascular Medicine-
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