Horm Metab Res 2018; 50(01): 50-55
DOI: 10.1055/s-0043-119221
Endocrine Care

Clinical Trial on the Effects of Vitamin D Supplementation on Metabolic Profiles in Diabetic Hemodialysis

Autoren

  • Mohammad Reza Tamadon

    1   Department of Internal Medicine, School of Medicine, Semnan University of Medical Sciences, Semnan, Iran
  • Alireza Soleimani

    2   Department of Internal Medicine, School of Medicine, Kashan University of Medical Sciences, Kashan, Iran
  • Fariba Keneshlou

    3   Department of Urology, School of Medicine, Alborz University of Medical Sciences, Karaj, Iran
  • Malihe Zarrati Mojarrad

    4   Research Center for Biochemistry and Nutrition in Metabolic Diseases, Kashan University of Medical Sciences, Kashan, Iran
  • Fereshteh Bahmani

    4   Research Center for Biochemistry and Nutrition in Metabolic Diseases, Kashan University of Medical Sciences, Kashan, Iran
  • Afshin Naseri

    4   Research Center for Biochemistry and Nutrition in Metabolic Diseases, Kashan University of Medical Sciences, Kashan, Iran
  • Hamed Haddad Kashani

    5   Anatomical Sciences Research Center, Kashan University of Medical Sciences, Kashan, Iran
  • Elahe Seyed Hosseini

    5   Anatomical Sciences Research Center, Kashan University of Medical Sciences, Kashan, Iran
  • Zatollah Asemi

    4   Research Center for Biochemistry and Nutrition in Metabolic Diseases, Kashan University of Medical Sciences, Kashan, Iran

Abstract

The current study was conducted to assess the effects of vitamin D supplementation on insulin metabolism, lipid fractions, biomarkers of inflammation, and oxidative stress in diabetic hemodialysis (HD) patients. This randomized double-blind placebo-controlled clinical trial was carried out among 60 diabetic HD patients. Subjects were randomly allocated into two groups to intake either oral vitamin D3 supplements at a dosage of 50 000 IU (n=30) or placebo (n=30) every 2 weeks for 12 weeks. After 12 weeks of intervention, subjects who received vitamin D supplements compared with the placebo had significantly decreased serum insulin concentrations (–3.4±3.7 vs. +2.0±4.2 μIU/ml, p<0.001), homeostasis model of assessment-estimated insulin resistance (HOMA-IR) (–1.2±1.8 vs. +0.9±2.3, p<0.001), and improved quantitative insulin sensitivity check index (QUICKI) (+0.02±0.03 vs. –0.01±0.02, p<0.001). In addition, compared with the placebo, vitamin D supplementation led to significant reductions in serum high-sensitivity C-reactive protein (hs-CRP) (–1.4±2.5 vs. +1.4±4.8 mg/l, p=0.007), plasma malondialdehyde (MDA) (–0.1±0.2 vs. +0.1±0.2 μmol/l, p=0.009) and a significant increase in plasma total antioxidant capacity (TAC) concentrations (+33.8±56.7 vs. –2.0±74.5 mmol/l, p=0.04). We did not see any significant effect of vitamin D supplementation on lipid profiles and other biomarkers of inflammation and oxidative stress compared with the placebo. Overall, we found that vitamin D supplementation had beneficial effects on serum insulin, HOMA-IR, QUICKI, serum hs-CRP, plasma MDA, and TAC levels among diabetic HD patients for 12 weeks.

Clinical registration:

http://www.irct.ir: IRCT201611155623N92.

Supplementary Material



Publikationsverlauf

Eingereicht: 18. Juli 2017

Angenommen: 30. August 2017

Artikel online veröffentlicht:
28. September 2017

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