No Effect of High-Dose Vitamin D Supplementation on Glycemic Status or Cardiovascular Risk Factors in Subjects With Prediabetes

In observational studies, low serum 25-hydroxyvitamin D [25(OH)D] concentrations have been associated with insulin resistance and other risk factors for cardiovascular disease. We present 1-year data from an ongoing 5-year trial in 511 individuals with impaired fasting glucose (IFG) and/or impaired...

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Published inDiabetes care Vol. 37; no. 8; pp. 2123 - 2131
Main Authors Sollid, Stina Therese, Hutchinson, Moira Y.S., Fuskevåg, Ole M., Figenschau, Yngve, Joakimsen, Ragnar M., Schirmer, Henrik, Njølstad, Inger, Svartberg, Johan, Kamycheva, Elena, Jorde, Rolf
Format Journal Article
LanguageEnglish
Published Alexandria, VA American Diabetes Association 01.08.2014
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ISSN0149-5992
1935-5548
1935-5548
DOI10.2337/dc14-0218

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Summary:In observational studies, low serum 25-hydroxyvitamin D [25(OH)D] concentrations have been associated with insulin resistance and other risk factors for cardiovascular disease. We present 1-year data from an ongoing 5-year trial in 511 individuals with impaired fasting glucose (IFG) and/or impaired glucose tolerance (IGT) randomly assigned to 20,000 IU/week vitamin D3 or placebo. An oral glucose tolerance test was performed at baseline and after 1 year. Mean baseline serum 25(OH)D was 59.9 nmol/L and 61.1 nmol/L in the vitamin D and placebo groups, respectively, and increased by 45.8 nmol/L and 3.4 nmol/L, respectively. With adjustment for baseline concentrations, no differences in measures of glucose metabolism, insulin secretion or sensitivity, blood pressure, or hs-CRP were found after 1 year. There was a slight, but significant decrease in total and LDL cholesterol in the vitamin D group compared with the placebo group, but as there was also a decrease in HDL cholesterol, the change in the total/HDL cholesterol ratio did not differ significantly. Only analyzing subjects with 25(OH)D <50 nmol/L did not change the results. This study shows that vitamin D supplementation does not improve glycemic indices, blood pressure, or lipid status in subjects with IFG and/or IGT.
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ISSN:0149-5992
1935-5548
1935-5548
DOI:10.2337/dc14-0218