The influence of vitamin D supplementation on the expression of mediators of inflammation in knee osteoarthritis

This trial aimed to determine the possible therapeutic and immunomodulatory effects of vitamin D3 in patients with knee OA. In this open-label clinical trial, symptoms were assessed over 3 months in patients with primary knee OA receiving oral vitamin D3 4000 IU/day. Clinical response was evaluated at baseline and 3 months using WOMAC subscores and VAS. Serum levels of cytokines IL-1 beta, TNF-alpha, IL-13, IL-17, IL-33, IL-4, and IL-10 were determined by ELISA method. Eighty patients with knee OA were included. All 80 completed the study; the median 25(OH)D3 level was 23.1 ng/ml at baseline and increased by 12.3 ng/ml after treatment. Vitamin D3 after 3 months of supplementation induced a significant reduction in VAS pain and WOMAC subscores. Using OMERACT-OARSI criteria, 86.7% of patients treated with vitamin D3 responded to treatment. At the end of 3 months, systemic values of IL-1 beta (p<0.01), IL-23 (p<0.01), and IL-33 (p<0.01) were significantly increased, values of TNF- (p<0.01), IL-13 (p<0.01), and IL-17 (p<0.01) were significantly decreased, while value of IL-4 was not significantly changed. No adverse events were detected. Treatment with vitamin D is associated with improvement in pain, as well as stiffness and physical function. Vitamin D supplementation increased systemic values of IL-33. Our results indicate that vitamin D3 supplementation may be used as a novel therapeutic in knee OA. Future studies are needed to investigate a potential role of IL-33 in the pathogenesis of knee OA.

Automated summary

This trial suggests that vitamin D3 has potential therapeutic and immunomodulatory effects in patients with knee osteoarthritis. Oral supplementation of vitamin D3 can significantly reduce pain and improve the quality of life in knee osteoarthritis patients. Vitamin D3 supplementation also increases systemic values of IL-33.