Role of gene polymorphisms in vitamin D metabolism and in multiple sclerosis

Authors

  • Aylin Elkama Gazi University, Faculty of Pharmacy, Department of Toxicology, Ankara
    • Bensu Karahalil Gazi University, Faculty of Pharmacy, Department of Toxicology

      DOI:

      https://doi.org/10.2478/aiht-2018-69-3065

      Keywords:

      cytochrome P, HLA-DRB1, vitamin D receptor

      Abstract

      Multiple sclerosis (MS) is a complex inflammatory disease of the central nervous system (CNS) resulting in neurological impairment and disability. There is evidence that adequate vitamin D levels may lower the risk of MS development. The aetiology of MS is complex and involves both genetic and environmental factors. In fact, not one but several genes are believed to lead to the disease. As for environmental factors, one of the most important risk factors is vitamin D deficiency, which, in turn, is closely related to gene polymorphisms that play a role in vitamin D metabolism and regulation. However, information about these gene polymorphisms is quite contradictory. The aim of this review is to discuss the association between some of the vitamin D-related gene variants and MS.

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      Published

      12 March, 2018

      Issue

      Section

      Review

      How to Cite

      1.
      Elkama A, Karahalil B. Role of gene polymorphisms in vitamin D metabolism and in multiple sclerosis. Arh Hig Rada Toksikol [Internet]. 2018 Mar. 12 [cited 2026 Sep. 13];69(1). Available from: https://arhiv.imi.hr/index.php/arhiv/article/view/866

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