Table 1.
Supplement | Study group | Effect | Side effect | References |
---|---|---|---|---|
100,000 IU of cholecalciferol per week for 4 weeks, followed by 100,000 IU of cholecalciferol per month for 6 months | 20 SLE patients with hypovitaminosis D | Vitamin D was induced: a preferential increase of naïve CD4+ T cells, an increase of regulatory T cells a decrease of effector Th1 and Th17 cells a decrease of memory B cells and anti-DNA antibodies |
Vitamin D was well tolerated | [86] |
50,000 units of vitamin D-2 weekly plus 200 units of calcium/vitamin D-3 twice daily | 1006 SLE patients with low levels of 25-hydroxyvitamin D (25[OH]D; < 40 ng/mL) | A 20-ng/mL increase in the 25(OH)D level was found that was associated with: A 21% decrease in the odds of having a high disease activity score and A 15% decrease in the odds of having clinically important proteinuria |
Vitamin D was well tolerated | [62] |
Oral cholecalciferol 2000 IU/day for 12 months | Patients with SLE and determined alterations in inflammatory and hemostatic markers and disease activity | At 12 months of therapy, there was a significant improvement in levels of inflammatory and hemostatic markers as well as disease activity in the treatment group | Vitamin D was well tolerated | [87] |
Oral vitamin D3 for a median period of 24 months | Sixty patients with SLE | Inverse significant correlations between 25(OH)D levels and the VAS and between changes in 25(OH)D levels and changes in the VAS in patients with baseline 25(OH)D levels < 30 ng/mL were found | Vitamin D was well tolerated | [52] |
Vitamin D supplementation for 6 months | SLE patients | The FoxP3+/IL-17A ratio in SLE patients after 6 months of vitamin D supplementation was higher than that in the baseline | Vitamin D was well tolerated | [88] |