4.2 Article

Large Individual Differences in Serum 25-Hydroxyvitamin D Response to Vitamin D Supplementation: Effects of Genetic Factors, Body Mass Index, and Baseline Concentration. Results from a Randomized Controlled Trial

Journal

HORMONE AND METABOLIC RESEARCH
Volume 48, Issue 1, Pages 27-34

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0034-1398617

Keywords

serum 25-hydroxyvitamin D; vitamin D supplementation; genetic factors

Funding

  1. North Norway Regional Health Authority
  2. Norwegian Diabetes Association
  3. University of Tromso
  4. Research Council of Norway
  5. Novo Nordisk foundation
  6. Novo Nordisk Fonden [NNF12OC1016126] Funding Source: researchfish

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The main aim of the study was to determine the influence of genetic factors on the serum 25-hydroxyvitamin D response to vitamin D supplementation. The main outcome measure was an increase in serum 25-hydroxyvitamin D after vitamin D supplementation. The patients are part of a randomized controlled trial in individuals with prediabetes assigned to 20 000 IU of vitamin D-3 per week or placebo for 12 months. A total of 484 subjects were included in the analyses and geno-typed for single nucleotide polymorphisms in the DBP, DHCR7, CYP2R1, and CYP24A1 genes. Single nucleotide polymorphisms from all 4 selected genes were significantly related to baseline serum 25-hydroxyvitamin D concentrations with differences between major and minor homozygote genotypes ranging from 4.4 to 19.2 nmol/l. In the subjects given vitamin D, those with genotypes with the highest baseline 25-hydroxyvitamin D concentration also had the highest 25-hydroxyvitamin D concentration after 12 months, and the increase (delta) in 25-hydroxyvitamin D was significantly related to 3 of the single nucleotide polymorphisms. The increase in serum 25-hydroxyvitamin D was also higher in lean vs. obese subjects, and higher in those with low baseline 25-hydroxyvitamin D concentrations. When combining these 3 factors in a linear regression model, the predicted (and observed) difference in 25-hydroxyvitamin D increase between high and low responders to the supplementation was approximately 60 nmol/l. In conclusion, due to genetic, body mass, and baseline 25-hydroxyvitamin D differences, there are huge individual variations in the serum 25-hydroxyvitamin D response to vitamin D supplementation that could be of clinical importance. Supporting Information for this article is available online at http://www.thieme-connect. de/products

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