Iranian consensus on use of vitamin D in patients with multiple sclerosis

The link between vitamin D and multiple sclerosis was initially proposed after the discovery of higher disease prevalence in northern latitude that obtain lower amount of sunlight and consistently have lower vitamin D synthesis.

In-vitro and in-vivo studies have promoted the hypothesis of vitamin D and MS linkage. In-vitro studies showed that 1,25(OH)₂D shifts CD4 T-cells and MHC class II molecules to a more anti-inflammatory profile. 1,25(OH)₂D inhibits CD4 T-cells from developing to Th1 cytokine profile (TNF-α and IFN-γ). Also it promotes the expression of T-reg cells (secreting TGF-β and IL-10) and Th-2 (producing IL-13, IL-5, IL-4) [3].

Protective and/or therapeutic role of vitamin D was also reported in Experimental autoimmune encephalomyelitis (EAE)-the animal model of MS. Most of these studies started to feed mice with active form of vitamin D before EAE induction. Thus they mostly assessed the mechanism of protective role of vitamin D in EAE.

The proposed underling mechanisms for this relationship are: Inducing inflammatory cells apoptosis [4] i.e. CD4+ T-cells [5], suppressing immune cell infiltration into the CNS [4], i.e. CD 11b + monocytes [5], decreasing Inducible Nitric Oxide Synthase [4, 5], as well as, inhibiting proinflammatory cytokine secretion including IL-12 and IFN-γ [6, 7].

However, a number of studies proposed that vitamin D protective role might depend on its interaction with other factors such as inflammatory and anti-inflammatory cytokines. Inadequate IFN-γ may undermine vitamin D mediated inhibition of demyelinating disease. MS risk might increase in persons with insufficient IFN-γ expression, despite high sun exposure due to low Vitamin D Receptor gene expression and a high T-helper 1 and T-helper 17 cells in the CNS [8]. Vitamin D was failed to ameliorate EAE in mice with IL-10 and IL-10 receptor disrupted genes [9].

Strikingly, at least three studies revealed that serum vitamin D deficiency itself impairs the development of EAE. Deluca et al., maintained mice on vitamin D-deficient diet for two generations. EAE onset was postponed and the severity of EAE was ameliorated in D-deficient mice compared to controls [10]. Fermendes et al. reported that the offspring of vitamin D-deficient mice developed delayed and milder EAE. The over expression of TNF and osteopontin, as well as, the under expression of IFN were noted in the cerebellum and spinal cord of the second generation of vitamin D-deficient mice [11]. In Wang et al. study, VDR-knocks out mice with either sufficient or insufficient vitamin D intake, showed delayed onset and reduced severity of EAE. Wang et al. concluded that protective role of vitamin D against EAE is related to the accompanied hypercalcemia. Also, hypercalcemia induced by parathyroid hormones attenuated EAE in female mice [12].

As the absence of VDR and vitamin D deficiency inhibits the development of EAE, it is clear that the lack of the vitamin D signaling could not be a risk factor in EAE. More ever, a number of studies examined the role of UV light independent of vitamin D in protecting against EAE. The results revealed that UV itself attenuates EAE severity [13]. The observed discrepancy in the results of the animal studies raised the following questions: Does vitamin D alone has protective role against EAE? What is the cause and effect relationship between vitamin D-insufficiency and EAE?

Most frequently asked questions about vitamin D supplementation were discussed. The recommendations were scored using an agreement index ranging from 1 (not agree at all) to 5 (fully agree). The mean score is presented.

Although there is inconstancy in the results of cross-sectional studies that compare vitamin D status in MS patients and healthy subjects, the high prevalence of vitamin D deficiency in general population including MS patients is predominantly accepted. Thus, there was a general consensus of vitamin D assessment in all MS patients especially early after diagnosis and in first demyelinating event (agreement score: 4.9).

The normal range of 25(OH)D have been revised in recent years. Normality is currently between 30 and 100 ng/ml (75 and 250 nmol/l) [24]. Less than 10 ng/ml is considered as deficiency and a range between 11 and 30 ng/ml considered as insufficiency [24, 25]. However for many of the non-classic, extra-bone effect of vitamin D including MS prevention, 40 ng/ml (100 nmol/l) was suggested [24, 26, 27]. Previous studies recommended a threshold of 30 ng/ml for patients with hyperparathyroidism and renal disease stage 3–5 (including dialysis patients) [26].

A daily intake of 1000 IU vitamin D resulted in an approximately 10 ng/ml increases in 25(OH)D [28]. However, there are variations in individual response [28]. To reach a serum level of 30 ng/ml, a daily intake of 1000–4000 IU (average ~ 2000 IU) is required [26]. Most studies denoted that even a daily dose of 10,000 IU for several months is not resulted in adverse effects [28]. Sun bathing also could provide vitamin D dose equivalent to an oral consumption of up to 20,000 IU per day. However, in healthy individual who spend long times in sunny environment, serum level of 25(OH)D rarely exceed 100 ng/ml [26].

Although daily vitamin D is considered to be more physiologic, different studies reported that intermittently administered vitamin D has approximately equal effects on 25(OH)D level as cumulative daily dose [29]. A randomized controlled trial (RCT) performed by Ish-shalom reported adverse outcomes with one annual dose of 500,000 IU. According to previous studies daily, weekly, biweekly or monthly strategies are preferred [29]. The panel agreed on daily (agreement score: 3.3), weekly (agreement score: 3.3), biweekly (agreement score: 3.75) or monthly (agreement score: 4.1) strategies. A majority of experts believe that biweekly or monthly strategies resulted in better compliance.

As RCTs did not support the therapeutic effect of high-dose vitamin D, the panel recommended the currently prescribed doses of vitamin D in clinical practice to treat hypovitaminosis and prevent deficiency to MS patients [30]. Thus, in patients with vitamin D insufficiency or deficiency, a large replacing dose was proposed in initial phase (e.g. 50,000 IU pearl of vitamin D per week for 8–12 week [30]) (agreement score: 4.8). Checking the serum vitamin D level and patients’ compliance is recommended after initial phase (agreement score: 4.8).If the level of vitamin D does not reach normal level by 12 weeks, repeting the replacement phase for another 8–12 weeks is recommended (agreement score: 4.8) [30]. According to previous evidences, to maintain the 25(OH)D level above 30 ng/ml, 1500–2000 IU vitamin D/d is required [24]. The specialists suggested 2000 IU/d or equivalent intermittent (weekly, biweekly or monthly) Dose (agreement score: 4.9). The panel was disagreed with increasing the current recommended dose, before the release of the results of the ongoing large RCTs with agreement score of 5.

Up to the best of our knowledge, no high power trial compare vitamin D injection with oral therapy in MS patients. The results of the trials about intramascular vitamin D administration in Non-MS Patients are conflicting. A number of trials reported intra muscular to be more effective [31, 32], and some considered that oral supplementation as superior [33]. Further clinical trials are required to elucidate differences.

Bhargava et al. reported that MS patients have reduces serologic response to vitamin D supplementation. The results of their study proposed the idea that vitamin D pharmacokinetic may differ in MS patients compared to healthy subjects [34]. There is no drug interaction between disease modifying medications used for MS treatment and vitamin D [35].

Daily consumption of vitamin D2 and vitamin D3 seems to have almost similar effect on serum 25(OH)D level. When D3 is available, supplementation with D3 is preferred as it avoids problems with differences in 25(OH)D assay specificity [26] (agreement score: 4.6). More ever, when using intermittent regimen, D3 maintains serum 25(OH)D level consistent for a longer time.

More ever, vitamin D and calcium seemed to act together, such as in the pathogenesis of breast and colorectal cancer, oesteoprosis and probably autoimmune diseases [36]. Cantorna et al., reported that reduced lymphocyte count in the lymph nodes and enhanced IL-4 mRNA in response to 1,25(OH)₂D administration was occurred solely when calcium intake was sufficient [37]. In a study by Soliu Hänninen, MS patients have hypocalcemia [38]. More ever, proinflammatory cytokines such as IL1-α, IFN-γ and TNF-α which considered pathogenic in MS, also inhibits bone formation and stimulates bone resorption [38] Therefore, the panel recommended a combination of vitamin D and calcium (agreement score:2.8).

With daily or weekly dose, at least 3 months of supplementation is needed to reach a plateau [26, 39]. Thus, measurement of 25(OH)D is recommended after 3 months of therapy (agreement score: 4.9). In case of resolving the insufficiency and deficiency, the panel recommended routine check of serum vitamin D level at least two times a year especially the beginning of spring and autumn (agreement score: 4.9).

The panel also recommends monitoring of calcium level at baseline and after 3 months of supplementation in deficient patients (agreement score: 4.9).

Therefore, the panel recommended that further monitoring of PTH, and urinary and serum calcium be performed according to physician decision (agreement score: 4.9).

As the most of the people does not meet the minimum requirement of Ultraviolet B (UVB), vitamin D supplementation is recommended for the majority of general population. The risk of MS is only 0.2–0.4 % in first degree relatives. However, vitamin D supplementation is inexpensive and safe and also seems to be reasonable even from the general preventive medical point of view alone. However the panel did not reached the consensus about vitamin D level check for all family members of MS Patients. But the panel suggests serum vitamin D evaluation for first degree relatives of MS patients who are at high risk age. If serum level is <40 ng/ml, the panel recommended the currently prescribed doses of vitamin D in clinical practice (50,000 IU/week for 8–12 weeks) to treat hypovitaminosis [30]. The panel recommended the currently suggested maintenance dose of vitamin D (1000 IU/d for <18 year and 1500–2000 IU for adults) to maintain serum level of 25(OH) D above 30 ng/ml for the family memebers of MS patients [24] (agreement score: 4.2).

The vitamin D deficiency is highly prevalent in pregnant women worldwide [40, 41]. Results of a study showed that vitamin D level is significantly lower among pregnant MS patients compared to healthy controls [42]. Vitamin D deficiency might increase the risk of preeclampsia [43], bacterial vaginitis [44], low birth weight babies, gestational diabetes, obstructed labor, preterm delivery and miscarriage [45]. In 2011, the Institution of medicine (IOM) published new DRIs of vitamin D for pregnant women that increase from 400 to 600 IU (same as non-pregnant women). However, the new IOM report was based on the skeletal effect of vitamin D and not on other non-classical actions of vitamin D. The 2011 IOM increased the upper limit of vitamin D intake from 2000 to 4000 IU/d. The endocrine society recommended at least 600 IU/d for pregnant women and recommended that for pregnant individuals who are at increasing risk of deficiency, 1500–2000 IU might be needed to maintain vitamin D level above 30 ng/ml. Different studies evaluated the effective dose of vitamin D supplementation during pregnancy. The dose of vitamin D supplement varied widely in different studies (400–4000 IU per day or equivalent single dose). The minimum effective dose which improve pregnancy outcome, but not induce toxicity is still unclear [45]. Also no significant association between vitamin D level and postpartum relapse rate was observed [42]. The panel suggests vitamin D level check and supplementation in case of deficiency/insufficiency before becoming pregnant (agreements score: 4.75). During pregnancy, the panel suggested a daily dose of 1500–2000 IU or equivalent biweekly intake in second and third trimesters (agreement score: 4.75). The panel also suggested 25(OH)D check every 3 months (agreement score: 4.75). In case of serum levels greater than 100 ng/ml, the supplementation should be ceased (agreement score: 5).

Like other essential micronutrients, vitamin D intake has a U curve regarding adverse effects due to deficiency and toxicity. Vitamin D toxicity from dietary source is unusual. However, signs of toxicity might appear as a result of high dose vitamin D supplementation [45].

According to endocrine society guideline maintenance dose of <4000 IU/day does not resulted in any notable adverse effects [24]. Consumption of maintenance dose of ≥4000 IU per day might increase the likelihood of hypercalcemia [46‐48]. According to the results of Burton et al. study, large replacing dose for short duration did not result in hypercalcemia. As shown in Table 1 they prescribed 40,000 IU/d for 28 weeks to MS patients [49]. Also studies recommended 50,000 IU vitamin D/week for 8–12 to treat hypovitaminosis [30]. Only annual large dose exceeding 300,000 IU vitamin D2 was reported to be associated with an increased risk of hip/femur/wrist fracture in elderly women [48] and greater number of falls [49].

The sign and symptoms of vitamin D intoxication might include: anorexia, nausea and vomiting, abdominal pain, constipation, dehydration, polyuria, polydipsia, nephrocalcinosis, nephrolithiasis, chronic interstitial nephritis, nephrogenic diabetes insipidus and chronic renal failure, paresthesia, hypotonia, seizure, confusion, apathy, coma, hypertension, arrhythmia, bradycardia, cardiomyopathy, calcification, muscle weakness, conjunctival calcification and osteoporosis. The signs of toxicity mostly observed when very large single dose was used. For example IOM reported that >50–60 ng/ml should raise concerns about possible adverse effects (Tolerable Upper Intake Levels: Calcium and Vitamin D). In the “endocrine society guidline” and “practical guideline for central Europe”, >100 ng/ml was considered as the intoxicated level [24, 27]. The panel was agreed with the safety serum level of 100 ng/ml (agreement score: 5). The panel suggest the discontinuation of vitamin D supplementation if the circulating level is above 100 ng/ml and recheck after 6 months regarding vitamin D reserve (agreement score: 5). If the blood level is more than 150 ng/ml, the panel recommended urinalysis because of the risk of hypercalcuria and renal stones [50].

RCTs have previously revealed that vitamin D supplementation can significantly improve muscle function and physical performance in vitamin D-deficit individuals [51]. Low 25(OH)D level might indirectly affect physical performance by inducing hyperparathyroidism. PTH has been shown to stimulate IL-6 secretion. IL-6 increment is associated with poor physical function and reduced muscle strength [51].

Previous RCTs recommended 1000 IU vitamin D/day in older individuals with low physical performance [52]. The panel suggests 1000 IU or its intermittent equivalents in MS patients with limited physical activity (agreement score: 4.75).

CIS is defined as first demyelinating event indicating high risk for MS (i.e., one clinical event involving the spinal cord, the optic nerve, the brainstem or cerebellum or occasionally the hemispheres) and at least 2 silent T2 bright areas on a brain or spinal cord MRI (at least one must be in the brain). Previous studies reported that severe vitamin D deficiency is more common among clinically isolated syndrome patients [53]. Also, according to previous studies low serum vitamin D is correlates with increased MS risk in CIS patients [54]. On the other hand, in CIS patients, higher total cholesterol level was associated with an increment in the number of contrast enhancing lesions on brain-MRI and consequently the first clinical event. Brown et al. conducted a study on the relationship between vitamin D metabolits’ level and serum lipoprotein status. They reported that a higher 25(OH)D3 level was associated with higher HDL biomarkers (HDL-c, Apo AII, Apo AI, arylesterase and paroxanase activity) and LDL biomarkers (LDL-c and Apo B). Though, the relationship between HDL-biomarkers and 25(OH)D3 was stronger. Therefore, they proposed that the effect of hypovitaminosis D on lipid profile in CIS patients, might be one of the susceptible cause of its adverse effect on CIS course of disease [55]. The panel suggests vitamin D level check and 8–12 weeks of supplementation in case of insufficiency and deficiency (25(OH)D below 40 ng/ml) for all CIS patients (agreement score: 4).

The study was approved by local ethical committee of Multiple Sclerosis Research Center (IR.MSRC.rec.1393.324, March 2014).