2013
DOI: 10.1016/j.clnu.2013.01.020
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Effect of high doses of vitamin D on arterial properties, adiponectin, leptin and glucose homeostasis in type 2 diabetic patients

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Cited by 137 publications
(159 citation statements)
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“…Of the 23 studies that were included in the systematic review, 13 reported fasting glucose as primary or secondary outcome measure (19,20,21,22,23,24,26,27,28,32,35,36,39). Three studies reported a significant reduction in fasting glucose level after vitamin D supplementation (21,28,39).…”
Section: The Effect On Fasting Glucosementioning
confidence: 99%
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“…Of the 23 studies that were included in the systematic review, 13 reported fasting glucose as primary or secondary outcome measure (19,20,21,22,23,24,26,27,28,32,35,36,39). Three studies reported a significant reduction in fasting glucose level after vitamin D supplementation (21,28,39).…”
Section: The Effect On Fasting Glucosementioning
confidence: 99%
“…Thirteen studies reported data on insulin resistance, of which twelve studies used the HOMA-IR to quantify insulin resistance (19,20,21,22,24,25,26,29,30,35,36,39), and one study measured insulin resistance through hyperinsulinaemic-euglycaemic clamp method (23). Two studies observed a significant reduction in insulin resistance after vitamin D supplementation (21,39), and one study found a negative effect of vitamin D supplementation on insulin resistance compared with placebo (35).…”
Section: The Effect On Insulin Resistancementioning
confidence: 99%
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“…Although the trial failed to meet endpoints for improved insulin and C-peptide secretion as well as HOMA-index, the correlation of BMI, HbA1c, insulin levels, and the vitamin D status suggests that glucose homeostasis may be positively regulated by vitamin D. The paradox observation that diff erences were more signifi cant at 6 months of therapy in the placebo group suggests that either the chosen dose is insuffi cient or that other factors regulate vitamin D's metabolic eff ects. A recent placebocontrolled trial with 47 diabetic patients and a lower daily dose (1 000 IU/d) demonstrated no metabolic eff ects but a nonsignificant increase in adiponectin and a signifi cant improvement of aortal stiff ness [ 42 ] . Physiologic and metabolic improvement may be due to direct or indirect VDR-mediated musculoskeletal, hepatic or eff ects on pancreatic β-cell secretion.…”
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confidence: 98%