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Multiple Sclerosis and Vitamin D
by Janet Drissen
 

       There is convincing scientific evidence that vitamin D plays a role in controlling autoimmunity and MS. Vitamin D status affects chemicals called cytokines that modulate the immune system and this modulation may benefit persons with MS.  

       Vitamin D, calciferol (kal-SIF-er-ol) is a fat soluble vitamin that is found in milk products, butter, cereals, veal, beef, egg yolks, liver and fatty fish although most of the world’s population relies on sunlight to maintain adequate amounts of vitamin D. Exposure to sunlight is an important source of vitamin D. Ultraviolet rays from sunlight trigger vitamin D synthesis in the skin. Exposing the face and arms to the sun for fifteen minutes three times a week is a way of ensuring adequate (200-400 IU) amounts of vitamin D although optimal levels (1000 IU) are required in MS. Season, sunscreens (SPF 8 or higher), time of day, latitude, cloud cover, smog and clothing effect UV ray exposure. North 
American adults receive no vitamin D from sunlight four to six months of the year. Those of us with MS rarely get sufficient sun exposure and cover up for the occasion.  

       Vitamin D exists in several forms, each with a different activity. The animal version is D3 or cholecalciferol (KO-lee-kal-SIF-er-ol), it is synthesized in the skin with exposure to ultraviolet radiation and is also present in fish liver oils. The plant version is D2 or ergocalciferol (er-go-kal-SIF-er-ol). D5 is a synthetic form. Of the three, vitamin D3 is considered the natural form and is the most active. Some forms are relatively inactive in the body and have a limited ability to function as a vitamin. The kidney and liver convert vitamin D to its active hormone form, calcitriol.  

       MS, Sjogren’s syndrome, rheumatoid arthritis, thyroiditis and Crohn’s disease have all been linked to low levels of vitamin D. Deficiency depresses calcium absorption, blood calcium, and bone mineralization, whereas an excess does the opposite. Vitamin D is the most likely of the vitamins to have toxic side effects when consumed in amounts above recommendations on a continuous basis. The importance of discussing this supplement with your physician cannot be overstressed and all sources must be considered. Also magnesium and calcium should accompany vitamin D.  

       Several researchers have noted that MS is far more common in northerly countries and almost non-existent near the equator. Goldberg (1974) was the first of many to postulate that low sunlight areas had increased MS due to low vitamin D production. Goldberg proposed that genetically susceptible individuals may need higher doses of vitamin D during myelin formation and that insufficient amounts during childhood might result in defective myelin that is susceptible to breakdown.  

       In the early 80’s it was found that immune cells carry a receptor for the active hormone of vitamin D and that this hormone likely regulates immune functions (Bhalla et al, 1983). It has been shown that injections of calcitriol hormone form of vitamin D) could protect against or arrest EAE (animal form of MS) in mice. (Lemire and Archer, 1991) Furthermore, immunological analyses and further experiments revealed the following immune regulating actions of calcitriol. (the following points from Vitamin D Supplementation in the Fight Against Multiple Sclerosis, an essay by Ashton F. Embry)  

               1.Suppresses antibody production by B cells and the proliferation of T cells in the thymus (Yang et al, 1993)  
               2.Upregulates cytokines TGF-beta and IL-4. These proteins, which are produced by immune cells, act as suppressants of inflammatory T cells (Cantorna et al, 1998b).  
               3.Inhibits production of pro-inflammatory cytokines such as IL-1, IL-2, TNF and IFN gamma (Muller and  Bendtzen, 1996) which also reduces inflammatory reactions.  
               4.Interferes with T helper functions and inhibits the passive transfer of cellular immunity by these cells by Th in vivo (Thomasset, 1994)  
               5.Inhibits the production of NO (nitric oxide) by immune cells (Garrison et al, 1997) NO has been identified as one of the most destructive products of the immune system and is an important factor in demyelination.  
               6.Inhibits the proliferation of activated and memory T cells (Muller and Bendtzen, 1992) Such cells are the main mediators the inflammatory autoimmune reactions of MS.  
               7.Exerts immunomodulating effects in the central nervous system by producing a profound 
downregulation of antigen expression by both infiltrating and resident antigen presenting cells(eg. 
Macrophages) (Nataf et al, 1996)  

       Note that some of these actions are what Betaseron, Rebif and Avonex do while Copaxone is thought to decoy the immune system and in the US Novantrone suppresses it.  

       Since the vitamin D hormone has proven to reduce inflammatory autoimmune reactions, the reduction of disease activity during pregnancy may be easier to explain. There is a natural increase in the production of calcitriol during pregnancy and a rapid decline afterward.  

       The evidence goes on with genetic data (Fukazaet al 1999) and associations between vitamin D receptor genes and MS.  

       Then there are inarguable evidences like Norway where the rate of MS is higher inland where fish consumption is less than coastal areas. In Switzerland, the rate of MS is high at low altitudes but low at high altitudes where the sun is closer.  

       The Canadian Compendium of Pharmaceuticals recommends 200-400 IU of vitamin D daily although a small study at Penn state and Helen Hayes hospital in New York has shown that 2.5 times the recommended dose for adults causes blood chemistry changes that indicate positive effects for MS patients.  

       Vitamin D is contraindicated when there is decreased renal function so alfacalcidol, calcitriol or dihydrotachysterol is useful for patients with renal failure. When used concurrently, vitamin D interacts with magnesium-containing antacids and with thiazide diuretics. Drug interactions are reported with phenytoin, phenobarbitol and digoxin.  

       Remember, don’t ever get sunburned and if you already have significant sun exposure then you should not take cod liver oil or vitamin D for those months. The safest way to ensure optimal levels of vitamin D is to do so under the supervision of your doctor.  
  
REFERENCES 

               1.Whitney, Elanor Noss and Rolfes, Sharon Rady. Understanding Nutrition,  
8th Edition pg.348-349  
               2.Embry, Ashton F., Vitamin D Supplementation In The Fight Against Multiple Sclerosis.  
An essay pg. 1-4 http://www.direct-ms.org/vitamind.html  
               3.Canadian Compendium of Pharmaceuticals ans Specialties 2001, pg. 1698  
 

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