Genetic polymorphisms related to vitamin D and the therapeutic potential of vitamin D in multiple sclerosis

被引:5
作者
Niino, Masaaki [1 ]
Miyazaki, Yusei [1 ,2 ]
机构
[1] Hokkaido Med Ctr, Dept Clin Res, Sapporo, Hokkaido, Japan
[2] Hokkaido Med Ctr, Dept Neurol, Sapporo, Hokkaido, Japan
关键词
genetics; cytokine; risk factor; vitamin D receptor; therapy; D-RECEPTOR GENE; PLACEBO-CONTROLLED TRIAL; GENOME-WIDE ASSOCIATION; D-BINDING PROTEIN; 1,25-DIHYDROXYVITAMIN D-3; 25-HYDROXYVITAMIN D; RELAPSE RISK; DOUBLE-BLIND; 1-ALPHA; 25-DIHYDROXYVITAMIN D-3; SERUM; 25-HYDROXYVITAMIN-D;
D O I
10.1139/cjpp-2014-0374
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Vitamin D receptors (VDRs), which are responsible for most vitamin D functions, are expressed on various immune cells. Vitamin D is considered to be a potent immunomodulator. A variety of cells in the central nervous system (CNS) also express VDRs; thus, vitamin D may play a role in the regulation of neurodegeneration and repair processes within the CNS. Considered together with epidemiological studies, low vitamin D status is reckoned to be one of the risk factors for multiple sclerosis (MS). Further, vitamin D is considered to be a possible treatment for MS. However, previous clinical trials with small cohorts have not demonstrated significant effects of vitamin D in MS. Current ongoing clinical trials with large cohorts could provide answers with respect to the clinical effects of vitamin D in MS. However, genetic studies have suggested that genes associated with vitamin D, including VDRs, are susceptible genes for MS. Vitamin D needs to be considered from the perspective of the interaction between vitamin-D-related genetic factors and environmental factors affecting vitamin D levels.
引用
收藏
页码:319 / 325
页数:7
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