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Diabetic Hemodialysis: Vitamin D Supplementation and its Related Signaling Pathways Involved in Insulin and Lipid Metabolism.

Current molecular medicine
January 1, 2019
Elahe S Hosseini et al. (7 authors)
Journal ArticleRandomized Controlled TrialResearch Support, Non-U.S. Gov'tHuman StudyClinical
Study Details

Study Goal

The researchers aimed to determine the effects of vitamin D supplementation on gene expressions related to insulin and lipid metabolism, including pyruvate dehydrogenase kinase 1 (PDK1), in diabetic hemodialysis patients.

Results Summary

The study found no significant effects of vitamin D supplementation on the expression of PDK1 (P=0.37) in diabetic hemodialysis patients.

Population

Diabetic hemodialysis patients (n=55)

Effective Dosage

50,000 IU every 2 weeks

Duration

12 weeks

Interactions

None mentioned

Extracted Claims (10)
InterventionDirectionEndpointPopulationDosageImpactClaim #
vitamin D supplementation
increase
peroxisome proliferation-activated receptor gamma (PPAR-γ)
diabetic hemodialysis (HD) patients
-
enables to overexpress
#1
vitamin D supplementation
increase
AKT
diabetic hemodialysis (HD) patients
-
enables to overexpress
#2
vitamin D supplementation
increase
PI3K
diabetic hemodialysis (HD) patients
-
enables to overexpress
#3
vitamin D supplementation
increase
insulin receptor substrate-1 (IRS1)
diabetic hemodialysis (HD) patients
-
enables to overexpress
#4
vitamin D supplementation
increase
glucose transporter type 4 (GLUT-4)
diabetic hemodialysis (HD) patients
-
enables to overexpress
#5
vitamin D supplementation
decrease
protein kinase C (PKC)
diabetic hemodialysis (HD) patients
-
downregulate
#6
vitamin D supplementation
decrease
low-density lipoprotein receptor (LDLR)
diabetic hemodialysis (HD) patients
-
downregulated
#7
vitamin D supplementation
no change
pyruvate dehydrogenase kinase 1 (PDK1)
diabetic hemodialysis (HD) patients
-
did not show any effects
#8
vitamin D supplementation
no change
IRS2
diabetic hemodialysis (HD) patients
-
did not show any effects
#9
vitamin D supplementation
no change
lipoprotein (a) [Lp(a)]
diabetic hemodialysis (HD) patients
-
did not show any effects
#10
Abstract

BACKGROUND: This study was conducted to determine the effects of vitamin D supplementation on some of the gene expressions related to insulin and lipid metabolism in diabetic hemodialysis (HD) patients. METHODS: A double-blind, randomized, placebo-controlled clinical trial was carried out in 55 patients with diabetic HD. The current project used two groups in which each subject received vitamin D supplements (50,000 IU, n=28) or placebo (50,000 IU, n=27) every 2 weeks for 12 weeks. Gene expression analyses (RT-PCR) were included to obtain the rate of gene expression of the related insulin and lipid metabolism genes in peripheral blood mononuclear cells (PBMCs) of patients with diabetic HD. RESULTS: Our data revealed that consumption of vitamin D supplementation enables to overexpress the peroxisome proliferation-activated receptor gamma (PPAR-γ) (P=0.001), AKT (P=0.04), PI3K (P=0.02), insulin receptor substrate-1 (IRS1) (P0.008) and glucose transporter type 4 (GLUT-4) (P=0.01) and downregulate the expression of protein kinase C (PKC) (P=0.001) in patients with diabetic HD than control group following the 12-week intervention. In addition, vitamin D supplementation downregulated low-density lipoprotein receptor (LDLR) (P=0.03) expression in the subjects with diabetic HD than the control group. Vitamin D supplementation did not show any effects on the expression of pyruvate dehydrogenase kinase 1 (PDK1) (P=0.37), IRS2 (P=0.90) and lipoprotein (a) [Lp(a)] (P=0.05). CONCLUSION: Our findings confirmed that diabetic HD subjects who received the vitamin D supplementation (for 12 weeks), showed a significant overexpression in the PPAR-γ, AKT, PI3K, IRS1 and GLUT4 genes, and also showed a significant downregulation in the PKC and LDLR genes. Moreover, no effects on PDK1, IRS2 and Lp(a) expression were observed.

Medical Subject Headings (MeSH)
Adaptor Proteins, Signal TransducingAdolescentAdultAgedAged, 80 and overDiabetic NephropathiesDietary SupplementsDouble-Blind MethodEnzyme InductionFemaleGene Expression RegulationGlucose Transporter Type 4HumansInsulinInsulin Receptor Substrate ProteinsLipid MetabolismLipoprotein(a)MaleMiddle AgedPPAR gammaPhosphatidylinositol 3-KinasesProtein Kinase CPyruvate Dehydrogenase Acetyl-Transferring KinaseRenal DialysisSignal TransductionVitamin DYoung Adult
Study Links
Quality Scores
SafetyNot Assessed
Efficacy20/10
Quality75/10
Citation Metrics
Total Citations3
Citations/Year0.5
Relative Citation Ratio0.20
NIH Percentile10.3%
Research Impact Scores
APT Score0.05
Weight Score1.91
Normalized Score0.43
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