Optimal Vitamin D Levels 2015 ~ Joanne Fine Strength

Optimal Vitamin D Levels 2015

Crohn's disease and ulcerative colitis are immune-mediated idiopathic diseases of the gastrointestinal tract. Crohn's disease can involve the entire gastrointestinal tract, while ulcerative colitis is isolated to the colon and rectum, both conditions are collectively referred to as inflammatory bowel disease (IBD)⁽ Reference Xavier and Podolsky ¹ ⁾. The key pathological mechanism in both cases is thought to be a dysregulated host immune response to commensal intestinal flora in genetically susceptible individuals⁽ Reference Abraham and Cho ² ^, Reference Khor, Gardet and Xavier ³ ⁾. Almost 100 genetic loci are currently associated with IBD, yet they incompletely explain the variance in disease incidence, suggesting a strong role for environmental factors, as supported by epidemiological data⁽ Reference Khor, Gardet and Xavier ³ ^– Reference Ananthakrishnan ⁵ ⁾.

Vitamin D has long been recognised as a major regulator of calcium and phosphorus metabolism and thus has key roles in bone formation and resorption⁽ Reference Holick ⁶ ^– Reference Rosen ⁸ ⁾. Low bone mineral density is a common manifestation in Crohn's disease⁽ Reference Leslie, Miller and Rogala ⁹ ^, Reference Laakso, Valta and Verkasalo ¹⁰ ⁾ and guidelines regarding supplementation are well established⁽ Reference Mowat, Cole and Windsor ¹¹ ⁾. Despite this vitamin D insufficiency remains common. With the discovery of the vitamin D receptor (VDR) in numerous tissues throughout the body beyond bone, including immune cells, a strong interest in understanding the role of vitamin D in disease pathogenesis and as a possible therapy in Crohn's disease has emerged⁽ Reference Ananthakrishnan, Khalili and Higuchi ¹² ^– Reference Jørgensen, Agnholt and Glerup ¹⁵ ⁾. The aim of the present review is to discuss vitamin D insufficiency in Crohn's disease, the potential benefits of supplementation and possible serum levels required to achieve the same.

Vitamin D physiology

Vitamin D metabolism

Vitamin D is a precursor of the active hormone calcitrol (1,25(OH)₂D) and is present in two forms; vitamin D₃ (cholecalciferol), which is the physiological form, and the synthetic analogue of vitamin D₂ (ergocalciferol). In human subjects, vitamin D can be obtained from two sources; diet and UVB exposure. Dietary sources of vitamin D₂ include irradiated yeast, plants and fungi, whereas vitamin D₃ is found in fish liver oils, oily fish, meat, eggs and some fortified produce. Sunlight is the major source of vitamin D₃ for human subjects. In the skin, UVB rays promote cleavage of 7-dehydrocholesterol (provitamin D₃) into previtamin D₃, which, in turn, is converted by a thermal process to vitamin D₃. Regardless of the source, vitamin D is hydroxylated twice, first in the liver, followed by the kidney. The latter hydroxylation generates 1,25(OH)₂D that exerts its actions by binding to a VDR⁽ Reference Raftery, O'Morain and O'Sullivan ¹⁶ ⁾. VDR are present on at least thirty different tissues throughout the body, including the intestinal and colonic tissues, circulating immune cells (such as activated lymphocyte T and B cells), monocytes, macrophages and muscle cells⁽ Reference Holick ⁷ ⁾. Importantly, many of these non-skeletal tissues also express vitamin D-activating enzymes, thereby permitting local production of 1,25(OH)₂D. Investigations into the role of the VDR and 1,25(OH)₂D in these extra-skeletal tissues has uncovered novel anti-proliferative, anti-inflammatory and immune-modulating effects, which may be relevant to Crohn's disease.

Optimal vitamin D status

The best measure of an individual's vitamin D status is serum 25-hydroxyvitamin D (25(OH)D)⁽ Reference Holick ⁶ ^, Reference Rosen ⁸ ⁾ which reflects both sunlight exposure and dietary vitamin D intake. The definition of vitamin D deficiency remains controversial. At present there is no target level set for people with Crohn's disease beyond recommendations for the general, healthy population. The US Institute of Medicine define deficiency as <30 nmol/l, and use 40 and 50 nmol/l to define the estimated average requirement and recommended daily allowance respectively with intakes of 15μg (600 IU) vitamin D₃/d recommended for adults and children, a tolerable upper intake level of 100μg (4000 IU)/d and a no observed adverse effect level of 250μg (10 000 IU) vitamin D₃/d⁽ ¹⁷ ⁾. The US Endocrine Society's Clinical Practice Guideline suggests 75 nmol/l as a cut-off for adequacy and intakes of 37·5–50μg (1500–2000 IU) vitamin D₃/d to achieve this concentration. Irrespective of the cut-off applied (30, 50 or 75 nmol/l), several studies have reported a high prevalence of vitamin D insufficiency and deficiency in established IBD cases (Table 1) and in 80 % of new Crohn's disease diagnoses⁽ Reference Leslie, Miller and Rogala ⁹ ⁾. In paediatric cases, 25 % of patients have severe deficient levels⁽ Reference Alkhouri, Hashmi and Baker ¹⁸ ⁾ (Table 1).

Table 1. Prevalence of suboptimal vitamin D status in inflammatory bowel disease in patients with active and quiescent disease

Vitamin D toxicity

Vitamin D toxicity is a rare clinical syndrome of both hypervitaminosis D and hypercalcaemia. Clinical symptoms of vitamin D toxicity include nausea, vomiting, dehydration, muscle weakness, lethargy and confusion⁽ Reference Blank, Scanlon and Sinks ¹⁹ ⁾. An upper toxic level of 250 nmol/l is frequently cited in the literature;⁽ Reference Souberbielle, Body and Lappe ²⁰ ^, Reference Vieth ²¹ ⁾ however, toxicity may not occur until 25(OH)D levels exceed 500 nmol/l⁽ Reference Vieth ²² ⁾ or even 750 nmol/l⁽ Reference Jones ²³ ⁾. Data on vitamin D toxicity derives mainly from studies involving healthy cohorts. A study in 340 healthy school children⁽ Reference Maalouf, Nabulsi and Vieth ²⁴ ⁾ showed that administration of 350μg (14 000 IU) vitamin D₃/week for 1 year was safe and brought the mean 25(OH)D concentrations to 90 (sd 55) nmol/l. Measurements conducted in adults with a constant sun exposure (Puerto-Rican farmers) revealed serum 25(OH)D levels which were often between 100 and 200 nmol/l, while their calcium status was normal⁽ Reference Haddock, Corcino and Vazques ²⁵ ⁾. In Crohn's disease, Jorgensen et al. ⁽ Reference Jørgensen, Agnholt and Glerup ¹⁵ ⁾ supplemented forty-six patients with 30μg (1200 IU) vitamin D₃/d and levels increased to 96 (sd 27) nmol/l without any side-effects such as hypercalcaemia after 12 months of treatment. In a smaller study (n 18), 125μg (5000 IU) vitamin D₃/d increased 25(OH)D concentrations to 112·5 (sd 47·5) nmol/l without safety concerns⁽ Reference Yang, Weaver and Smith ²⁶ ⁾. Currently 50μg (2000 IU) vitamin D₃/d is regarded as acceptable and can be taken without medical supervision⁽ Reference Hanley, Cranney and Jones ²⁷ ⁾, although most clinical trials in Crohn's disease do monitor patients tolerance to supplementation regardless of the dose used as part of the study protocol.

Factors influencing vitamin D levels in Crohn's disease

Several factors predict vitamin D deficiency in Crohn's disease including; longer disease duration, higher Crohn's disease activity index (CDAI) scores, C-reactive protein levels, poor nutrition status, smoking⁽ Reference Siffledeen, Siminoski and Steinhart ²⁸ ^– Reference Gilman, Shanahan and Cashman ³¹ ⁾, small bowel involvement⁽ Reference Gilman, Shanahan and Cashman ³¹ ⁾ and resection⁽ Reference Driscoll, Meredith and Sitrin ³² ⁾, non-Caucasian ethnicity⁽ Reference de Bruyn, van Heeckeren and Ponsioen ³³ ⁾, sunlight exposure, impaired conversion of vitamin D to its active metabolite, increased catabolism and increased excretion due to steatorrhoea.

In Crohn's disease dietary intakes and supplemental intakes appear inadequate for achieving sufficient 25(OH)D status. Less than half (43 %) of the patients are consumers of a vitamin D supplement, with multivitamin preparations being the most common form reported providing on average 5.6μg (5–10μg); 225 IU (200–400 IU) vitamin D daily. Moreover, for bone health, present guidelines suggest intakes of 20μg (800 IU)/d⁽ Reference Mowat, Cole and Windsor ¹¹ ⁾ which may or may not result in 25(OH)D concentrations ≥75 nmol/l. Studies have indicated intakes of 30, 50 or 125μg (1200, 2000 or 5000 IU)/d may be required to achieve levels ≥75 nmol/l, depending on baseline levels⁽ Reference Jørgensen, Agnholt and Glerup ¹⁵ ^, Reference Yang, Weaver and Smith ²⁶ ^, Reference Raftery, Lee and Cox ³⁴ ⁾.

Diet in Crohn's disease provides approximately 1·0 μg/d (95 % CI 0·6, 1·9)⁽ Reference Suibhne, Cox and Healy ³⁵ ^, Reference Vogelsang, Klamert and Resch ³⁶ ⁾ with the main food sources being oily fish (38 %), followed by eggs (27 %)⁽ Reference Suibhne, Cox and Healy ³⁵ ⁾. Despite being low, dietary intakes in Crohn's disease are comparable with population intakes⁽ Reference McCarthy, Duggan and O'Brien ²⁹ ^, Reference Filippi, Al-Jaouni and Wiroth ³⁷ ^, Reference Bin, Flores and Alvares-da-Silva ³⁸ ⁾. Poor dietary intakes may also be hindered by reduced absorption. Vitamin D is absorbed in the proximal small intestine, particularly in the jejunum⁽ Reference Hollander and Truscott ³⁹ ⁾. The effect on vitamin D status due to small bowel involvement is uncertain. In a small study of twelve Crohn's disease patients with a terminal ileum resection a decline in vitamin D absorption correlating with the length of the resection was observed⁽ Reference Leichtmann, Bengoa and Bolt ⁴⁰ ⁾. Conversely Ulitsky et al.⁽ Reference Ulitsky, Ananthakrishnan and Naik ⁴¹ ⁾ reported no difference in vitamin D levels between those with a resection v. no resection.

Whereas most of the predictors of low serum 25(OH)D in Crohn's disease are consistent throughout the literature, the effect of Crohn's disease activity on the vitamin D status is not confirmed. Some studies have reported no difference in 25(OH)D-based disease activity,⁽ Reference Gilman, Shanahan and Cashman ³¹ ^, Reference Hassan, Hassan and Seyed-Javad ⁴² ⁾ whereas Jorgensen et al. reported low levels were associated with active disease⁽ Reference Jørgensen, Hvas and Agnholt ⁴³ ⁾. A clear trend of decreasing 25(OH)D from remission (64 nmol/l) to mild disease (49 nmol/l) and moderately active disease (21 nmol/l) (P < 0·01) was reported⁽ Reference Jørgensen, Hvas and Agnholt ⁴³ ⁾. A recent study confirmed these findings insofar as patients with active Crohn's disease had lower 25(OH)D levels than those in clinical remission; this measurement was independent of season or reported supplement use⁽ Reference Ham, Longhi and Lahiff ⁴⁴ ⁾. There also appears to be wide variation in the absorption of vitamin D in Crohn's disease; for example, Farraye et al.⁽ Reference Farraye, Nimitphong and Stucchi ⁴⁵ ⁾ reported that even in quiescent disease ability to absorb vitamin D is reduced by an average of 30 % in comparison with normal subjects after supplementation with 1250μg (50 000 IU) vitamin D₂. Whether or not the outcome would have been similar had vitamin D₃ been used remains to be seen.

In symptomatic/active disease cholestryamine may also be prescribed to reduce post-resectional diarrhoea. It also reduces bile acids, which are required for vitamin D absorption and may induce vitamin D malabsorption. Protein loosing enteropathy is a condition which can arise in severe disease and can result in the loss of vitamin D-binding protein along with the vitamin D bound to it⁽ Reference Mouli and Ananthakrishnan ⁴⁶ ⁾. Moreover, genetic variants in vitamin D hydroxylation and transport may also contribute substantially to both the development of vitamin D insufficiency and poor response to supplementation⁽ Reference Wang, Zhang and Richards ⁴⁷ ⁾.

Beyond diet, sunlight and casual UVB exposure is the main source of vitamin D for most of the population. However, in Crohn's disease immunosuppressive therapy, such as azathioprine and adalimumab, can increase the risk of skin cancer. For this reason patients prescribed such medications are counselled regarding the careful use of sunscreen, which also prevents UVB synthesis of vitamin D. Sun exposure may also have a link to Crohn's disease pre-diagnosis. UVB exposure is often reduced at higher latitudes and coincides with a higher prevalence of autoimmune diseases and colorectal cancer in these regions compared with those more southerly⁽ Reference Simpson, Blizzard and Otahal ⁴⁸ ^, Reference Peyrin-Biroulet, Oussalah and Bigard ⁴⁹ ⁾ suggesting a possible relationship between latitude and Crohn's disease.

Epidemiological evidence: low vitamin D status and Crohn's disease

Environmental triggers for IBD have been difficult to identify⁽ Reference Frolkis, Dieleman and Barkema ⁵⁰ ⁾. A German twin cohort study confirmed the strong genetic element to IBD, yet concordance rates between monozygotic twins are nonetheless low (35 % for Crohn's disease and 16 % for ulcerative colitis). This suggests important environmental interactions with disease-inducing genes⁽ Reference Spehlmann, Begun and Burghardt ⁵¹ ⁾. One potential environmental risk factor is the UVB exposure. Recently a link between latitude and incidence rates of Crohn's disease has been identified in a large prospective study⁽ Reference Khalili, Huang and Ananthakrishnan ⁵² ⁾. By tracking the location and lifestyle information of approximately 175 000 female American nurses biennially over 20 years, the authors detected a greater increase in the incidence rates of Crohn's disease and ulcerative colitis the farther subjects lived from the equator. At age 30 years, living in southern latitudes was associated with a roughly halved risk of developing Crohn's disease and approximately a 40 % reduced risk of developing ulcerative colitis. Similarly Ananthakrishnan et al.⁽ Reference Ananthakrishnan, Khalili and Higuchi ¹² ⁾ found that women with a higher serum vitamin D level had a significantly reduced risk of Crohn's disease (hazard ratio: 0·38) suggesting a protective effect of vitamin D sufficiency.

In Europe an evident north–south gradient of incidence and prevalence also exists⁽ Reference Shivananda, Lennard-Jones and Logan ⁵³ ^– Reference Schultz and Butt ⁵⁵ ⁾. For example, low sunlight exposure was associated with an increased incidence of Crohn's disease in France and no association with ulcerative colitis⁽ Reference Burisch, Pedersen and Cukovic-Cavka ⁵⁶ ⁾. Migration of populations who live near the equator to countries of greater latitude also increases the rate of Crohn's disease⁽ Reference Pinsk, Lemberg and Grewal ⁵⁷ ^, Reference Sewell, Yee and Inadomi ⁵⁸ ⁾. More recently, Limketkai et al.⁽ Reference Limketkai, Bayless and Brant ⁵⁹ ⁾ reported that lower UV exposure is associated with greater rates of hospitalisation, prolonged hospitalisation and the need for bowel surgery in IBD. Further studies are needed to determine if this association is causal and also the role of other environmental factors that might explain these findings such as pollutants, diet and commensal or pathogenic microorganisms.

Vitamin D and immune function in Crohn's disease: experimental data

Vitamin D appears to have an important role in innate immunity⁽ Reference Cantorna, Zhu and Froicu ¹⁴ ^, Reference Cantorna and Mahon ⁶⁰ ⁾. For example, human cathelicidin antimicrobial peptide and beta defensins are antimicrobial peptides of the innate immune system, which are expressed by the gastrointestinal epithelium⁽ Reference Jäger, Stange and Wehkamp ⁶¹ ⁾. Antimicrobial peptides protect against bacterial invasion⁽ Reference Tollin, Bergman and Svenberg ⁶² ⁾ and human cathelicidin antimicrobial peptide is important in maintaining and re-establishing intestinal barrier integrity⁽ Reference Otte, Zdebik and Brand ⁶³ ⁾ and in the healing of human intestinal epithelial cells⁽ Reference Otte, Zdebik and Brand ⁶³ ⁾. Moreover in vitro studies have shown that 1,25(OH)₂D can induce the expression of the gene encoding human cathelicidin antimicrobial peptide⁽ Reference Gombart, Borregaard and Koeffler ⁶⁴ ⁾. However, the largest body of experimental evidence for an immunoregulatory role for vitamin D in IBD concerns the adaptive T-cell response. Several types of T-cells are important for the regulation of homeostasis in the gastrointestinal tract and either induce or suppress IBD. The VDR and 1,25(OH)₂D inhibit Th1 and Th17 functions by suppressing the production of particular cytokines⁽ Reference Cantorna and Mahon ¹³ ^, Reference Daniel, Sartory and Zahn ⁶⁵ ^, Reference Tang, Zhou and Luger ⁶⁶ ⁾ which restores gastrointestinal homeostasis post infection or chemical injury. In addition, 1,25(OH)₂D stimulates dendritic cell production of IL-10, and T-cell levels of CTLA-4 (an inhibitory co-stimulatory signal), which further enhances its anti-inflammatory effect⁽ Reference Jeffery, Burke and Mura ⁶⁷ ⁾.

Vitamin D and intestinal permeability in Crohn's disease: experimental data

Animal studies have shown that vitamin D may be linked to Crohn's disease severity and the function of the epithelial barrier. Vitamin D deficiency increased symptoms of several experimental models of IBD⁽ Reference Cantorna ⁶⁸ ⁾ and VDR deficiency increased susceptibility of mice to colitis⁽ Reference Froicu and Cantorna ⁶⁹ ^, Reference Froicu, Weaver and Wynn ⁷⁰ ⁾. Conversely treatment with 1,25(OH)₂D improves IBD symptoms and blocks the progression of colitis in mice⁽ Reference Daniel, Sartory and Zahn ⁶⁵ ^, Reference Froicu, Weaver and Wynn ⁷⁰ ^, Reference Cantorna, Munsick and Bemiss ⁷¹ ⁾

Vitamin D may also function on the epithelial barrier. Epithelial cells are connected by intercellular junctions, comprising tight junctions and adherens junctions⁽ Reference Henderson and van Limbergen ⁷² ⁾. Patients with Crohn's disease have increased small intestine permeability⁽ Reference Marchiando, Graham and Turner ⁷³ ⁾ resulting in part from defects in these junctions. Compromised barrier function in Crohn's disease has been associated with inflammation, dysbiosis⁽ Reference Cantorna, McDaniel and Bora ⁷⁴ ⁾, disease pathogenesis and as a predictor of clinical relapse⁽ Reference D'Incà, Di Leo and Corrao ⁷⁵ ^, Reference Wyatt, Vogelsang and Hübl ⁷⁶ ⁾. Evidence suggests that vitamin D increases tight junction proteins and enhances gut mucosal healing post-injury⁽ Reference Kong, Zhang and Musch ⁷⁷ ⁾. For example, following exposure to dextran sulphate sodium, a chemical which induces colitis, the VDR knock out mice were unable to maintain the integrity of the epithelial barrier⁽ Reference Froicu and Cantorna ⁶⁹ ^, Reference Ooi, Li and Rogers ⁷⁸ ⁾ and had lower expression of tight junction proteins than in wild-type mice⁽ Reference Kong, Zhang and Musch ⁷⁷ ^– Reference Zhang, Leung and Richers ⁷⁹ ⁾. As a result of reduced tight junction proteins, vitamin D-deficient and VDR knock out mice had increased gut permeability compared with vitamin D-sufficient wild-type mice⁽ Reference Ooi, Li and Rogers ⁷⁸ ⁾. Whilst the basic science supports a role for vitamin D in Crohn's disease as reviewed elsewhere⁽ Reference Hewison ⁸⁰ ⁾, further work is required to establish if this translates to human studies.

Observational studies: association between vitamin D levels, disease activity and surgery in Crohn's disease

Whilst epidemiological, animal and experimental data are promising the full possible range of effects of vitamin D in Crohn's disease are unknown, as are the optimal level(s) for inducing them. Observational studies which have focused on vitamin D and its effect on clinical markers such as CDAI (a research tool used to quantify the symptoms of patients with Crohn's disease) and inflammatory markers have been inconclusive. In cross-sectional IBD cohort studies El-Matary et al.⁽ Reference El-Matary, Sikora and Spady ⁸¹ ⁾ and Hassan et al.⁽ Reference Hassan, Hassan and Seyed-Javad ⁴² ⁾ reported no association between 25(OH)D and CDAI. CDAI levels <150 are indicative of remission, whereas levels above that suggest active disease. The mean 25(OH)D in these two studies were 66·7 (sd 27·3) nmol/l and 32·7 (sd 28·3) nmol/l, respectively. The cohorts included both Crohn's disease and ulcerative colitis patients and the sample sizes were small. Another cross-sectional study exclusive to Crohn's disease (n 34) reported a significant inverse association between 25(OH)D and CDAI with mean concentrations of 53·5 (sd 27) nmol/l⁽ Reference Joseph, George and Pulimood ⁸² ⁾. Similar findings were reported by Ulitsky et al.⁽ Reference Ulitsky, Ananthakrishnan and Naik ⁴¹ ⁾ who observed greater disease activity in those with lower 25(OH)D levels (Table 2).

Table 2. Observational studies of the association between 25-hyroxyvitamin D (25(OH)D) status and disease related outcomes in inflammatory bowel disease (IBD)

Almost two-thirds of patients with Crohn's disease will eventually require surgery as part of their clinical course. Ananthakrishnan et al.⁽ Reference Ananthakrishnan, Cagan and Gainer ⁸³ ⁾ reported that 25(OH)D levels >50 nmol/l in Crohn's disease were associated with fewer surgeries and hospitalisations compared with those with levels below this threshold. A more aggressive disease course and need for surgery among those with vitamin D deficiency was also seen in a South Asian cohort⁽ Reference Boyd and Limdi ⁸⁴ ⁾. Overall, despite limitations inherent in cross-sectional studies, such as mixed cohorts of ulcerative colitis and Crohn's disease, a reduced spread of vitamin D levels, different methods of data analysis, role of causality and various primary outcome measures, most of these studies suggest positive correlations between vitamin D and Crohn's disease-related outcomes (Table 2).

Clinical studies; association between 25-hyroxyvitamin D levels, disease activity and relapse in Crohn's disease

Only a small number of intervention studies have examined the effects of vitamin D supplementation in a clinical trial setting in IBD (Table 3). Two studies have reported positive associations with disease activity. The first, a prospective open label study compared supplementation with active vitamin D (alfacalcidiol) to 25μg (1000 IU) vitamin D₃ (cholecalciferol) in Crohn's disease⁽ Reference Miheller, Muzes and Hritz ⁸⁵ ⁾. After 6 weeks alfacalcidiol treatment resulted in a significant decrease in CDAI scores and C-reactive protein levels, as well as improvement in quality of life (QoL) scores. In spite of this at 12 months there were no significant differences between the groups with respect to these variables⁽ Reference Miheller, Muzes and Hritz ⁸⁵ ⁾. The primary aim of the present study was to examine the effects on bone metabolism and not disease activity; moreover, the paper did not report the 25(OH)D levels obtained by the groups, which may have not been in the therapeutic range at 12 months. Yang et al.⁽ Reference Yang, Weaver and Smith ²⁶ ⁾ titrated vitamin D₃ intake until such a point serum levels were ≥100 nmol/l (commonly requiring 125μg (5000 IU)/d) and reported significant improvements in CDAI with a mean reduction in CDAI from 230 (sd 74) to 118 (sd 66; P < 0·0001). This may suggest a minimum level of 100 nmol/l is required to exert a significant effect on disease severity but further research is warranted. Whilst promising these studies were open label trials and therefore have their inherent limitations. A double-blind randomised placebo-controlled study assessed the effectiveness of vitamin D₃ supplementation in preventing clinical relapse. In comparison with the placebo group, oral vitamin D₃ supplementation of 30μg (1200 IU)/d for 12 months reduced the risk of relapse from 29 to 13 % at 1 year (P = 0·056)⁽ Reference Jørgensen, Agnholt and Glerup ¹⁵ ⁾. This difference in relapse was not statistically significant and merits further work (Table 3).

Table 3. Intervention studies; relationship between 25-hyroxyvitamin D (25(OH)D) and outcomes in Crohn's disease

The current authors previously examined the effects of vitamin D supplementation on intestinal permeability as measured by the lactulose : mannitol ratio and sucrose excretion which indicates small bowel permeability⁽ Reference Raftery, Martineau and Greiller ⁸⁶ ⁾. In a double-blind placebo-controlled study 27 Crohn's disease patients were randomised to 50μg (2000 IU)/d vitamin D₃ or placebo. At follow-up (3 months) mean (95 % CI) 25(OH)D levels were as expected significantly higher in the vitamin D group 91·6 (75·5–107·6) nmol/l than in the placebo group 40·4 (30·4–50·4) nmol/l (P < 0·001). At 3 months, there was a significant increase in lactulose : mannitol ratio (P = 0·010) and sucrose excretion (P = 0·030) in the controls, but these parameters were unchanged in the vitamin D group, suggesting that 25(OH)D levels ≥75 nmol/l may preserve intestinal integrity.

Clinical studies; association between 25-hyroxyvitamin D levels and muscle function

Compared with healthy controls in Crohn's disease skeletal muscle mass and strength are reduced⁽ Reference Schneider, Al-Jaouni and Filippi ⁸⁷ ^– Reference Geerling, Badart-Smook and Stockbrügger ⁸⁹ ⁾ and muscle fatigue is increased⁽ Reference van Langenberg, Della Gatta and Warmington ⁹⁰ ⁾. Fatigue is a major concern in Crohn's disease⁽ Reference Jelsness-Jorgensen, Bernklev and Henriksen ⁹¹ ^– Reference Maunder, de Rooy and Toner ⁹⁴ ⁾ with two of five patients reporting that it negatively impacts their QoL, even in remission⁽ Reference Minderhoud, Oldenburg and van Dam ⁹⁵ ⁾. Reasons for this may include elevated pro-inflammatory factors such as TNFα and IL-6⁽ Reference Reimund, Wittersheim and Dumont ⁹⁶ ^, Reference Cominelli ⁹⁷ ⁾ which are associated with lower muscle mass and strength in elderly populations⁽ Reference Visser, Pahor and Taaffe ⁹⁸ ^, Reference Schaap, Pluijm and Deeg ⁹⁹ ⁾, poor nutrition, physical inactivity and prolonged corticosteroid therapy⁽ Reference Geerling, Badart-Smook and Stockbrügger ⁸⁹ ⁾. The underlying mechanisms of how vitamin D might improve muscle are poorly understood; however, several lines of evidence support a role of vitamin D in muscle health. First, proximal muscle weakness is a prominent feature of vitamin D deficiency⁽ Reference Al-Shoha, Qiu and Palnitkar ¹⁰⁰ ⁾ in addition to diffuse muscle pain and gait impairments such as a waddling way of walking⁽ Reference Schott and Wills ¹⁰¹ ⁾. Secondly, skeletal muscle is a major reservoir of 25(OH)D⁽ Reference Mawer, Backhouse and Holman ¹⁰² ⁾; however, whilst it was previously thought that VDR were abundantly expressed in muscle cells with roles myogenesis and contractility this is currently under debate⁽ Reference Boillon, Gielen and Vanderschueren ¹⁰³ ⁾. Although vitamin D supplementation increases muscle strength and balance in some populations for example in the elderly⁽ Reference Pfeifer, Begerow and Minne ¹⁰⁴ ⁾ data in Crohn's disease are not as widely available. In a cross-sectional study, van Landenberg et al. ⁽ Reference van Langenberg, Gatta and Hill ¹⁰⁵ ⁾ reported that high 25(OH)D and physical activity may protect against reduced muscle mass⁽ Reference van Langenberg, Della Gatta and Warmington ⁹⁰ ⁾. Conversely Salacinski et al.⁽ Reference Salacinski, Regueiro and Broeder ¹⁰⁶ ⁾ were unable to show a relationship between 25(OH)D levels and muscle strength in Crohn's disease. Although they did show that those with higher 25(OH)D levels (≥100 nmol/l) exhibited greater muscle strength (normalised to body weight) than those with lower levels (≤80 nmol/l) suggesting perhaps optimal effects on muscle function with levels ≥100 nmol/l; however, this is tentative data.

The current authors previously reported the results of a 3-month randomised, double-blind intervention study in quiescent Crohn's disease (n 27)⁽ Reference Raftery, Lee and Cox ³⁴ ⁾. Patients were randomised to either 50μg (2000 IU)/d vitamin D₃ or placebo and the primary outcome measures included changes in hand-grip strength, a proxy measure for muscle strength. Post-intervention, both dominant and non-dominant hand-grip strength were significantly higher in the vitamin D-treated group compared with the controls. In the same study group, we also assessed changes in fatigue and QoL⁽ Reference Raftery, Lee and Cox ³⁴ ⁾. At 3 months, patients who achieved 25(OH)D levels ≥75 nmol/l had significantly higher QoL compared with patients below this cut-off (P = <0·0001)]. In line with this, significantly less fatigue was experienced in those with 25(OH)D levels ≥75 nmol/l compared with those below this cut-off, as assessed by question 2 of the IBD questionnaire.

In a cross-sectional study of 504 IBD patients (403 Crohn's disease patients and 101 ulcerative colitis patients) vitamin D deficiency (<50 nmol/l) was associated with lower QoL in Crohn's disease but not ulcerative colitis;⁽ Reference Ulitsky, Ananthakrishnan and Naik ⁴¹ ⁾ however, muscle function and fatigue were not measured in the present study. Another intervention study⁽ Reference Yang, Weaver and Smith ²⁶ ⁾ also showed improved QoL scores following vitamin D supplementation (P < 0·0004), particularly when serum concentrations were ≥100 nmol/l⁽ Reference Yang, Weaver and Smith ²⁶ ⁾. This was paralleled with significant improvements in CDAI scores; however, muscle strength was not measured in this study.

Vitamin D and cancer in Crohn's disease

More recently, associations between vitamin D status and cancer have been examined. Epidemiological studies suggest an increased risk of and mortality from cancer in northern latitudes with reduced UVB exposure, an association possibly mediated by vitamin D⁽ Reference Wacker and Holick ¹⁰⁷ ⁾. Furthermore, prospective cohorts have demonstrated an inverse association between 25(OH)D and cancers of the colon, breast and prostate⁽ Reference Feskanich, Ma and Fuchs ¹⁰⁸ ^– Reference Giovannucci, Liu and Rimm ¹¹¹ ⁾ with one intervention study reporting a reduced risk of cancer by 60 %⁽ Reference Lappe, Travers-Gustafson and Davies ¹¹² ⁾ with levels >80 nmol/l. Ananthakrishnan et al. ⁽ Reference Ananthakrishnan, Khalili and Higuchi ¹² ⁾ looked at data from 2809 patients with IBD and a median plasma 25(OH)D level of 65 nmol/l. During a median follow-up period of 11 years, 196 patients (7 %) developed cancer, excluding nonmelanoma skin cancer (forty-one cases of colorectal cancer). Patients with vitamin D deficiency had an increased risk of cancer (adjusted OR, 1·82; 95 % CI 1·25, 2·65) compared with those with sufficient levels. Each 1–2·5 nmol/l increase in plasma 25(OH)D was associated with an 8 % reduction in risk of colorectal cancer (OR, 0·92; 95 % CI 0·88, 0·96). The mean plasma 25(OH)D in patients who subsequently developed cancer was 12·5 nmol/l lower than in those who did not develop cancer (57 v. 69 nmol/l; P < 0·0001). They also reported a statistically significant inverse association for lung cancer (OR, 0·95; 95 % CI 0·90, 0·99). However, the study has its limitations; for example, the confounding impact of inflammation and low BMI on low 25(OH)D status was not reported and there was a lack of information on screening practices and on smoking.

Conclusion

Vitamin D insufficiency in IBD remains common. Consensus expert opinion has suggested 25(OH)D levels of 75–100 nmol/l may provide optimal benefits for musculoskeletal and cancer outcomes⁽ Reference Souberbielle, Body and Lappe ²⁰ ⁾ and levels of 100–175 nmol/l for optimal immune effects⁽ Reference Cannell and Hollis ¹¹³ ⁾. The data reviewed here show evidence of positive associations with levels ≥75 nmol/l in Crohn's disease, and further possible associations with levels ≥100 nmol/l but such associations need validation with well-designed randomised controlled trials. These include associations with CDAI, muscle function, fatigue, QoL, maintenance of epithelial barrier function, decreased hospitalisations, reduced risk of surgery and cancer. In terms of dosage required to achieve these levels 20–25μg (800–1000 IU)/d vitamin D₃ appears sufficient to achieve a serum level of 50 nmol/l, and between 25 and 100μg (1000 and 4000 IU)/d to bring levels beyond 75 nmol/l (on average 50μg (2000 IU)/d is required for this purpose⁽ Reference Heaney, Davies and Chen ¹¹⁴ ^– Reference Holick ¹²³ ⁾). In the present study of Crohn's disease patients, we found that 50μg (2000 IU)/d increased mean 25(OH)D levels to 91·6 (95% CI 75·5, 107·6) nmol/l over winter months, which was significantly higher than levels in the placebo group 40·4 (95% CI 30·4, 50·4) nmol/l (P < 0·001)⁽ Reference Raftery, Lee and Cox ³⁴ ⁾. To obtain 25(OH)D status ≥100 nmol/l in Crohn's disease, 125μg (5000 IU)/d may be required⁽ Reference Yang, Weaver and Smith ²⁶ ⁾. This is the lower end of what is considered the 'physiological' zone of 75–200 nmol/l, the range which corresponds to the serum levels observed in outdoor workers⁽ Reference Haddock, Corcino and Vazques ²⁵ ^, Reference Barger-Lux and Heaney ¹²⁴ ^, Reference Azizi, Pavlotsky and Kudish ¹²⁵ ⁾ as well as in traditionally living populations in East Africa⁽ Reference Luxwolda, Kuipers and Kema ¹²⁶ ⁾. This zone is far below the toxic zone, which appears to be located above the 400 nmol/l serum level⁽ Reference Hathcock, Shao and Vieth ¹²⁷ ⁾. To conclude there are many unanswered clinical questions regarding the role of vitamin D in Crohn's disease such as: (1) what is the optimal role of vitamin D supplementation as a therapeutic modality in Crohn's disease; (2) what is the effect of disease activity and resection on circulating 25(OH)D concentrations; (3) what is the level with which a plateau effect is observed in terms of relapse prevention/immune augmentation, if any. Additional well-designed and executed randomised double-blind placebo-controlled trials which investigate 25(OH)D levels are required to address these questions.

Optimal Vitamin D Levels 2015

Source: https://www.cambridge.org/core/journals/proceedings-of-the-nutrition-society/article/optimal-vitamin-d-levels-in-crohns-disease-a-review/E041A64165B65124937A5652A55E62EE