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. 2014 May 29;7:69–87. doi: 10.2147/JIR.S63898

Table 3.

Summary of interventional studies evaluating the effect of vitamin D supplements on cardiovascular disease (CVD) risk

Source Study design Condition Population (cases) Main outcome(s)
Harris et al72 Randomized, placebo-controlled trial Vitamin D (2,000 IU/day) for 16 weeks 57 African American adults Vitamin D supplements (2,000 IU/day) for 16 weeks were effective at improving vascular endothelial function in African American adults
Zittermann et al73 Randomized, placebo-controlled trial Vitamin D (83 μg/day) for 1 year 200 overweight subjects (mean 25[OH]D3 levels =12 ng/mL) Vitamin D supplements enhanced the beneficial effects of weight loss on CVD risk, including decreasing lipid levels and inflammation
Sun et al74 Cross-sectional (prospective study) Vitamin D (≥600 IU/day) or vitamin D (<100 IU/day) 2,280,324 person-years of follow-up Higher intake of vitamin D was associated with a lower risk of CVD in men but not in women
Cauley et al75 Cross-sectional (prospective study) Calcium plus vitamin D supplementation 29,862 postmenopausal women There was no difference in CVD morbidity between groups
Ponda et al77 Randomized, placebo-controlled trial Vitamin D (50,000 IU/week) for 8 weeks 151 vitamin D-deficient (25[OH]D levels <20 ng/mL) patients Correcting vitamin D deficiency in the short term did not improve the lipid profile
Yiu et al78 Randomized, placebo-controlled trial Vitamin D (5,000 IU/day) for 12 weeks 100 type 2 diabetes mellitus patients 12 weeks of oral supplementation with vitamin D did not significantly affect vascular function or serum biomarkers of inflammation and oxidative stress
Stricker et al168 Randomized, placebo-controlled trial Vitamin D (100,000 IU/single oral dose) 76 patients with peripheral arterial disease Vitamin D supplementation did not influence endothelial function, arterial stiffness, coagulation, or inflammation parameters
Gepner et al76 Randomized, placebo-controlled trial Vitamin D (2,500 IU/day) for 4 months 114 subjects Vitamin D supplementation did not improve endothelial function, arterial stiffness, or inflammation