Role of Vitamin D in Systemic Sclerosis: A Systematic Literature Review
- PMID: 34881335
- PMCID: PMC8648450
- DOI: 10.1155/2021/9782994
Role of Vitamin D in Systemic Sclerosis: A Systematic Literature Review
Abstract
Background: Systemic sclerosis (SSc) is a chronic multisystem autoimmune condition defined by a complex pathobiology, comprising excessive fibrosis of skin and internal organs, peripheral vasculopathy with endothelial cell dysfunction, inadequate vascular repair and neovascularization, and aberrant immunity. Vitamin D is a steroid hormone with pleiotropic effects beyond its traditional role in calcium and bone homeostasis. Since vitamin D has immunomodulatory, cardioprotective, and antifibrotic properties, it could potentially interfere with SSc pathogenesis. Suboptimal vitamin D levels are classically recognized in scleroderma, irrespective of clinical and serological phenotype.
Aim: This systematic review is aimed at investigating and clarifying the role of vitamin D in SSc and emphasizing the association of vitamin D status with different clinical settings.
Methods and results: A systematic online search was performed, using PubMed databases to collect articles on the topic of vitamin D in SSc. The final analysis included 40 eligible articles.
Conclusions: Hypovitaminosis D is common in SSc patients and could be associated with clinical and serologic patterns of the disease. Intervention for low serum vitamin D levels in SSc pathogenesis remains controversial, as well as the significance of vitamin D supplementation in such patients.
Copyright © 2021 Alexandra-Diana Diaconu et al.
Conflict of interest statement
The authors declare that there is no conflict of interest regarding the publication of this paper.
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References
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- Hughes M., Allanore Y., Denton C. P., Matucci-Cerinic M. Systemic sclerosis. EMJ Rheumatology . 2020;7(1):100–109. doi: 10.33590/emjrheumatol/20-00073. - DOI
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- Orlandi M., Lepri G., Damiani A., et al. One year in review 2020: systemic sclerosis. Clinical and Experimental Rheumatology . 2020;38(125):3–17. - PubMed
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