Multiple Sclerosis
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Treatment of Multiple Sclerosis – Relationship between Vitamin D and Interferon β-1b

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Published Online: Dec 23rd 2015 European Neurological Review, 2015;10(2):124–30 DOI:
Authors: Bruce Taylor, Harold Moses, Friedemann Paul, Gustavo Suarez, Mark Rametta
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There are many reports suggesting an association between vitamin D status and both the development of multiple sclerosis (MS) and its course. This relationship and the effects of vitamin D and interferon β-1b (IFNβ-1b) in the treatment of patients are reviewed in the BEtaferon/ Betaseron in Newly Emerging multiple sclerosis For Initial Treatment (BENEFIT) and the Betaferon/Betaseron Efficacy Yielding Outcomes of a New Dose in multiple sclerosis (BEYOND) studies. In the BENEFIT study the average serum 25-hydroxyvitamin D (25[OH]D) levels strongly predicted MS disease activity and progression. The probability of clinically definite MS (CDMS) and magnetic resonance imaging (MRI) activity was lower in these clinically isolated syndrome (CIS) patients with 25(OH)D levels ≥50 nmol/L and in those starting with IFNβ -1b. Furthermore, there was a beneficial effect on relapse rate, occurrence of new active MRI lesions and disease progression for a 50 nmol/L increase in 25(OH)D levels. Similarly, in relapsing-remitting (RR) MS patients from the BEYOND study serum 25(OH)D levels were inversely associated with MRI markers of MS activity. Genetic analysis of patients from these studies indicated that there may be a benefit in monitoring and managing vitamin D levels in early MS patients treated with IFNβ-1b and a cumulative number of risk alleles predict lower 25(OH)D levels in CIS and RRMS patients. Further studies have suggested that some of the IFNβ-1b therapeutic effects on relapse could be mediated through modulation of vitamin D metabolism. Thus, there seems to be a benefit on clinical and MRI measures if patients are treated with both vitamin D and IFNβ-1b. There is a need to further evaluate this effect in clinical trials. The relationship between vitamin D and MS disease activity along with the effects of vitamin D and IFNβ-1b in the treatment of MS patients is reviewed.


Vitamin D, 25-hydroxyvitamin D, multiple sclerosis, interferon β-1b


There is increasing evidence that vitamin D status is associated with both the development of multiple sclerosis (MS) and also the modulation of disease activity and possibly progression. Several publications have reported that the risk of MS is higher in patients with low vitamin D intake or serum 25-hydroxyvitamin D (25[OH]D) levels, for example due to low sun exposure.1,2 However, the findings of studies examining the relationship between vitamin D and MS disease activity are difficult to compare as the patients enrolled often had variable disease duration and it has been problematic to decide if low vitamin D levels were a consequence of MS activity (reverse causality) or if low levels early in the disease can predict long-term progression and disability.3,4

A recent publication analysed systematic reviews and meta-analyses to summarise the risk factors associated with MS.5 Of the 44 meta-analyses (416 primary studies), 11 had high significance (p<0.001). Anti-Epstein- Barr nuclear antigen (anti-EBNA) immunoglobulin (Ig)-G seropositivity, infectious mononucleosis and smoking showed the strongest consistent evidence of an association in these high significance studies. Vitamin D status did not reach significance as a risk factor. However, it is important to note that vitamin D measured at the onset of MS may not necessarily reflect vitamin D levels at other significant times in a person’s life, which may predispose them to later development of MS. Measure of prior sun exposure as potential, although not absolute, proxy for vitamin D levels in a Caucasian population have suggested that lifetime sun exposure, as well as sun exposure in the adolescent period, may be more important factors in MS risk than recent sun exposure.6,7 Effects of vitamin D levels on disease activity may be easier to assess as the exposure (vitamin D) is contemporaneous with the outcome (disease activity).

Here we review the relationship between vitamin D and MS disease activity and the effects of vitamin D and interferon β-1b (IFNβ-1b) in the treatment of MS in patients from the BEtaferon/Betaseron in Newly Emerging multiple sclerosis For Initial Treatment (BENEFIT) and the Betaferon/Betaseron Efficacy Yielding Outcomes of a New Dose in multiple sclerosis (BEYOND) studies. Furthermore, the molecular mechanisms underlying the impact of vitamin D on MS disease activity and the possible genetic component associated with vitamin D and MS are considered.

Is Vitamin D Status an Early Predictor of Multiple Sclerosis Activity and Progression?
Clinically Isolated Syndrome Patients from the BENEFIT Study
The patients were assessed in order to determine if vitamin D status early in the MS disease process influenced the long-term disease course.8 BENEFIT was a randomised, placebo-controlled, double-blind trial that studied patients with a first event suggestive of MS treated with either IFNβ -1b or placebo. Recruited patients were mostly white of European ancestry. The BENEFIT study was originally set up to compare early and delayed treatment with IFNβ -1b. To fulfil the inclusion criteria, patients needed a minimum of two clinically silent magnetic resonance imaging (MRI) lesions. The placebo-randomised patients remained on placebo for 2 years or until a second clinical event occurred and a diagnosis of clinically definite MS (CDMS) could be made. All patients were eligible to enter a prospectively planned follow-up when they received open-label IFNβ-1b for up to 5 years after randomisation. Table 1 summarises selected characteristics of BENEFIT participants, the baseline characteristics were similar between patients with 25(OH)D levels <50 nmol/L and ≥50 nmol/L, except for the median number of T2 lesions, which were higher in the lower 25(OH)D group. Serum samples were collected at baseline, 6, 12 and 24 months for the measurement of 25(OH)D levels. Most statistical analyses were restricted to patients who had 25(OH)D measured at 6 and 12 months to reduce bias from seasonal variation, as the seasonally synchronous baseline, 12-month and 24-month samples could give a biased estimate of the year-round status of vitamin D. The clinical and MRI assessments of time to a definite diagnosis of MS, MS activity and MS progression were analysed. MS activity was assessed as the number of relapses and new active lesions on brain MRI, while percentage change in T2 lesion volume and the percentage change of brain volume represented MRI markers of progression. Clinically, progression was determined by the Expanded Disability Status Score (EDSS) score over time, with month 6 as the primary reference point. All analyses were adjusted for sex, age at baseline, treatment at randomisation, baseline T2 lesion score and type of clinically isolated syndrome (CIS) (monofocal versus multifocal).

Patients with higher 25(OH)D levels, were generally younger, with a lower BMI, smaller number of T2 lesions, smaller T2 lesion volume and higher brain volume at CIS. In total, 46.6 % of patients converted to CDMS and this was strongly related to serum 25(OH)D.

In the first 12 months after CIS, the average serum 25(OH)D level strongly predicted MS activity and progression in the subsequent 4 years. The

probability of CDMS was lower in the group of patients with levels of 25(OH)D ≥50 nmol/L and in the subgroup of patients starting with IFNβ- 1b from randomisation compared with those with levels <50 nmol/L (p=0.048 and p=0.0043 after 1 year for all patients and IFNβ-1b-treated patients, respectively). Furthermore, MRI activity, defined as the cumulative number of new active lesions (new or enlarging T2 lesions, new gadolinium-enhancing lesions), was significantly reduced in all patients and in the subgroup of patients treated with IFNβ-1b from randomisation with ≥50 nmol/L 25(OH)D levels versus those with levels <50 nmol/L (p=0.002; p=0.0055, respectively) (see Figures 1 and 2). In addition, the percent change in T2 lesion volume and brain volume were strongly inversely associated with 25(OH)D levels (p=0.008 and 0.005, respectively) and the subgroup of patients starting with early treatment with IFNβ-1b (p=0.016 and 0.0037, respectively). Furthermore, there was no difference in the number of patients with plasma 25(OH)D <50 nmol/L or ≥50 nmol/L reporting flu-like symptoms at 6 and 12 months.9,10

Patients were also assessed according to their 25(OH)D levels in increments of 50 nmol/L. Overall, there was also a non-significant 27 % decrease in relapse rate for a 50 nmol/L increment in 25(OH) D. This association was stronger among patients at both 6 and 12 months; in this group a significantly lower relapse rate with increasing serum 25(OH)D was observed after 12 months. The rate of occurrence of new active MRI lesions decreased with increasing serum 25(OH)D and a 50 nmol/L increase in the average 25(OH)D level significantly predicted a lower number of lesions. Measures of MS progression (change in brain volume, T2 lesion volume and EDSS score) were also inversely associated with increased 25(OH)D with each indicating a beneficial effect. For a 50 nmol/L increase in 25(OH)D, the rate of brain volume loss was lower by 0.27 % (p=0.12), T2 lesion volume decreased by 20 %/ year (p<0.001) and average EDSS score reduced by 0.16 steps (p=0.11).

Although associations were generally stronger for MRI than for clinical outcomes, the latter were still remarkable considering the overall low rate of relapses (0.2 per year) and small EDSS score change (median change, 0.0) in BENEFIT. The results emphasise the importance of identifying and correcting 25(OH)D insufficiency early in the course of MS and also indicate that early treatment with IFNβ-1b has an additive effect with 25(OH)D to reduce disease severity and progression in both clinical and imaging outcomes without impacting tolerability to IFNβ-1b.

Relapsing-remitting Multiple Sclerosis Patients from the BEYOND Study
The BEYOND study included patients from Western and Eastern Europe, North America and the Southern hemisphere who had been diagnosed with relapsing-remitting MS (RRMS) using the McDonald 2001 criteria and were treatment naïve. The regional subgroup baseline characteristics are summarised in Table 2.11 The three study arms were treatment with IFNβ-1b (either 500 μg or 250 μg) or glatiramer acetate (GA) 20 mg and the mean time on study was 2.3 years.11 Blood samples from the two IFNβ-1b arms were analysed to determine the impact of averaged vitamin D levels on MS disease course. The GA group was not included in the analysis. In total, 1,482 patients had at least two 25(OH)D measurements 6 months apart. For 25(OH)D status, the primary exposure variable was the cumulative average of season-adjusted 25(OH)D values up to 12 months with the adjustment performed within each region. Season adjustment was completed as described previously.2 The 50 nmol/L increments and also the <37.5, 37.5–49.9, 50–<74.9, 75–99.9 and ≥100 nmol/L were compared.

The multivariate statistical analysis was adjusted for age, gender, disease duration, region of residence, baseline EDSS and treatment dose. Crosssectional analysis compared season-adjusted 25(OH)D versus baseline MRI and versus 12-month MRI. Finally, longitudinal analysis compared the season-adjusted 25(OH)D levels in first year with clinical/MRI disease course during the study.

The 25(OH)D levels were lowest in Eastern Europe and highest in Australia, Brazil and North America – as expected levels reflected the seasonal variation in sunlight for each region. Significant differences were also observed in several clinical parameters. Younger age, higher volume of T2 hyperintense lesions and longer disease duration were seen in Eastern Europe and Russia compared with Western Europe and North America. In the cross-sectional analyses adjusted for age, sex, treatment group (IFNβ-1b 250 versus 500 μg), baseline EDSS score, disease duration, region of residence, baseline 25(OH) D levels, reported as estimates (95 % confidence interval [CI]) were inversely associated with T2 lesion volume with a 50 nmol/L higher level corresponding to a difference of -0.11 cm3 (log T2 lesion volume) -0.20 to -0.02; p=0.02, and the total number of T1-enhancing lesions -0.24, -0.45 to -0.02; p=0.03 at baseline. The association between 25(OH)D and MRI parameters at 12 months gave similar results, with a difference in log T2 lesion volume of -0.19 cm3, -0.31 to 0.07; p=0.003. The difference at 12 months for log T1 hypointense lesion volume was -0.07 cm3, -0.14 to 0.00; p=0.055 and during year 1 the rate of T2 lesion count 0.78, 0.62 to 0.99; p=0.04. Furthermore, 25(OH) D levels were also inversely associated with the cumulative number of new active lesions (the sum of new T2 lesions and T1-enhancing lesions) between baseline and 12 months (0.76, 0.60 to 0.98; p=0.03). In longitudinal analysis, the relative rate (RR) of cumulative new active lesions was reduced by 31 % (RR 0.69, 95% CI, 0.55–0.86; p=0.001) for each 50 nmol/L increase in 25(OH)D level in all patients. This inverse association was also strong and significant in analyses restricted to patients with 25(OH)D levels greater than 50 nmol/L (RR 0.62; 95 % CI, 0.46–0.84; p=0.002), and was consistently observed in each of the four regions (see Figure 3).

In the cross-sectional analysis between baseline 25(OH)D levels and the number of relapses in the previous 2 years, no significant association was observed. However, baseline 25(OH)D level was inversely associated with EDSS scores at baseline with a 50 nmol/L higher level of 25(OH)D corresponding to a mean difference of 0.28 in EDSS scores (95 % CI, -0.40 to -0.16; p<0.001).

In summary, in these RRMS patients, serum 25(OH)D levels were inversely associated with MRI markers of MS activity and there was a similar magnitude across geographic regions despite differences in average levels. Furthermore, the association was similar in different patient subgroups according to demographic or clinical characteristics. The associations between 25(OH)D and relapses or clinical progression were not significant, which may be due to the low relapse rate as well as a relatively short follow-up.

Another study investigated whether higher levels of 25(OH)D were protective in patients treated with GA compared with IFNβ (Comprehensive Longitudinal Investigation of Multiple Sclerosis at the Brigham and Women’s Hospital, Partners MS Center [CLIMB] study).12 Levels of 25(OH)D were determined in 247 RRMS patients treated with either GA or IFNβ as their first disease-modifying drug (DMD). Higher 25(OH)D significantly predicted longer time to first event (clinical and MRI endpoint) in the IFN group (p=0.013), but not with GA (p=0.38).

Molecular Mechanisms Underlying the Impact of Vitamin D on Multiple Sclerosis Disease Activity
A global gene expression analysis of the patients from BENEFIT showed that 25(OH)D regulates the expression dynamics of a large gene–gene interaction system, which primarily regulates immune modulatory processes modulating MS activity.13 A decrease in MS activity was observed with increasing 25(OH)D levels. A number of known targets of IFNβ-1b and a regulator of sphingosine-1-phosphate bioavailability were identified in the complex network of genes regulated by 25(OH) D. These results indicate a possible benefit in early MS patients treated with IFNβ-1b, of monitoring and managing vitamin D levels.

Genetic Modification of 25(OH)D Levels in Multiple Sclerosis
Candidate single nucleotide polymorphisms (SNPs) were analysed by genome-wide association studies (GWAS) to assess their impact on 25(OH)D levels in IFNβ-1b-treated CIS and RRMS patients from the BENEFIT and BEYOND trials (n= 815).14

All assessed candidate SNPs in DHCR7 (7-dehydrocholesterol reductase), GC (vitamin D binding protein) and CYP2R1 (cytochrome P450, family 2, subfamily R, polypeptide 1) genes were significantly associated with 25(OH)D levels (p≤0.05). Furthermore, a 25(OH)D risk score to indicate the odds ratio of being 25(OH)D deficient was derived from the cumulative count of risk alleles per patient. As the number of risk alleles increased, levels of 25(OH)D decreased (see Figure 4). The findings indicated that the effects of multiple risk alleles are additive and may be used to develop a 25(OH)D genetic risk score in MS patients (higher score represents a higher possibility of low 25(OH) D). This vitamin D risk score could increase awareness of the risk of deficiency in MS patients in the absence of 25(OH)D measurement. The results indicated that the cumulative number of risk alleles predict lower 25(OH)D levels in CIS/RRMS patients.

Vitamin D and Interferon β
Studies in animal models of MS, randomised clinical trials and cohort studies have assessed whether there is an association between vitamin D and IFNβ. The 1,25[OH][2]D[3] analogue, TX527 (19-nor- 14,20-bisepi-23-yne-1-1,25[OH][2]D[3]) has diminished calcemic effects but enhanced anti-proliferative and pro-differentiating properties on normal and malignant cell types in vivo compared with 1,25[OH][2]D[3].15 Studies in an experimental autoimmune encephalomyelitis (EAE) animal model demonstrated that TX527 attenuates EAE.16 Further studies evaluated combinations of TX527, IFNβ and cyclosporine A in this model and showed that the combination of TX527 and IFNβ was significantly more effective in ameliorating the disease than either treatment alone. In addition, there was no effect with IFNβ and cyclosporine A but when TX527 was added to this combination virtually complete protection occurred. The authors suggested that the effect of IFNβ and TX527 should be evaluated in a clinical trial of MS.16

The safety and efficacy of adding vitamin D3 to IFNβ-1b treatment was assessed in a double-blind, placebo-controlled, randomised trial in 66 MS patients over 1 year.17 In treated patients, the median change in T2 burden of disease was reduced in treated patients (83 mm3 versus 287 mm3 in the placebo group). Levels of 25(OH)D in serum increased with 84 % of patients achieving >85 nmol/L in the IFNβ-1b group compared with placebo (p<0.0001). In addition, there was a trend towards a reduction in disability accumulation and improved timed tandem walk in the treatment group with no significant difference in annual relapse rate or adverse events.17

In a prospective cohort comprising 178 patients with clinically definite MS (CDMS), Stewart et al. measured 25(OH)D levels in serum twice a year together with a direct patient review and a questionnaire regarding sun exposure and relapse information in order to determine if IFNβ treatment was associated with vitamin D levels and if they interact with respect to relapse rate.18 Patients treated with IFNβ had significantly higher mean 25(OH)D levels than non-treated patients (p<0.001). This was mediated by an interaction between a patient’s sun exposure and IFNβ therapy, with treated patients achieving approximately three times the amount of 25(OH)D for each hour of sun exposure than those not on therapy. Furthermore, there was an association between 25(OH)D and reduced relapse risk only in treated patients (p<0.001). The reduction in relapse rate was only seen in IFNβ-treated patients with higher 25(OH)D levels whereas in those with insufficiency the relapse rate increased. These findings suggest that some of the therapeutic effects of IFNβ on relapse may be mediated through modulation of vitamin D metabolism. It could therefore be beneficial to monitor vitamin D status and supplement if necessary in patients treated with IFNβ.18

Reder et al. investigated whether vitamin D enhanced IFNβ signalling by studying in vitro intracellular IFNβ response to combinations of vitamin D and IFNβ in treatment-naïve RRMS and progressive MS patients and those receiving IFNβ or GA.19 Vitamin D enhanced IFNβ activation of STAT1 by 30–70 % in untreated patients and by 30–150 % in those treated with IFNβ, but with only modest effects with GA. This increase in IFN signaling may provide a mechanism for the benefits of vitamin D in preventing and ameliorating MS, both before and during IFNβ- 1b treatment. Vitamin D may also help overcome the effects of low intrinsic serum IFN-α and β levels in MS.20

A study of RRMS patients treated with IFNβ and given vitamin D at either 800 or 4,370 IU/day assessed for the post-injection cytokine surge that is associated with flu-like symptoms.21 In the low-dose group, serum IL- 17 increased significantly (p=0.037) but the response was inconsistent in the high-dose group with 40 % having decreased IL-17 levels and 45 % increased levels. No significant changes occurred in the serum concentration of IL-10 and IFN-α. These results showed no benefit of vitamin D supplementation on flu-like symptoms but illustrate its immunomodulatory properties.

Vitamin D status was assessed in patients who participated in the BENEFIT and BEYOND studies in order to explore the relationship between serum vitamin D level and the disease course. In the BENEFIT patients, serum 25(OH)D level predicted MS activity and progression. There appeared to be a correlation with serum 25(OH) D levels ≥50 nmol/L and a positive benefit. The findings indicate the potential benefit of identifying patients with vitamin D insufficiency and correcting it. Furthermore, results from the BENEFIT cohort suggest that vitamin D and IFNβ-1b have an additive effect on disease activity.8,9

Similarly in the BEYOND study cohort, serum 25(OH)D levels had an inverse association with MRI markers of MS disease activity, which was similar in those from different locations and with various demographic and clinical characteristics. There was a non-significant association with relapses possibly as a result of the low relapse rate and relatively short follow-up period.

Preliminary results in EAE suggest that vitamin D has a synergistic effect with IFNβ. Furthermore IFNβ has an additive effect with 25(OH)D on changes in gene expression known to reduce gadolinium-enhancing lesion counts, which suggests that improving vitamin D levels in such MS patients may be beneficial. 25(OH)D also shows systemic gene expression regulation on 25(OH)D target gene sets. Moreover, GWAS studies have identified candidate SNPs that were significantly associated with 25(OH)D levels.

Many studies of vitamin D and MS have caveats, which potentially cast doubts on their validity. There is a general consensus that betterdesigned trials are needed to establish more robust evidence – especially multicentre, randomised, controlled, clinical trials using clinical, immunological and MRI outcomes. To address this problem Efficacy of Vitamin D Supplementation in Multiple Sclerosis (EVIDIMS), a German, multicentre, stratified, randomised, controlled, double-blind, phase II trial was initiated.22 This trial aimed to randomise 80 CIS or RRMS patients treated with IFNβ-1b to 20, 400 or 400 IU 25(OH)D every other day for 18 months. The primary endpoint is the cumulative number of new T2 lesions on cranial MRI during the treatment period. Secondary endpoints include other MRI parameters, such as progression of brain atrophy over the study period and number and volume of T1-hypointense and T2-hyperintense lesions. As retinal thinning is increasingly recognised

as a promising surrogate marker of tissue loss and neurodenegeration in MS, retinal nerve fibre layer thickness and macular volume measured by optical coherence tomography are additional secondary outcome parameters.23–25 The study has completed recruitment, however, results have not been published to date. Another such trial is the Supplementation of VigantOL® Oil (Merck KGaA, Darmstadt, Germany) versus placebo as add-on in patients with RRMS receiving Rebif® (Merck Serono S.A. – Geneva, Switzerland) treatment (SOLAR) study.26 This 96-week, three-arm, multicentre, double-blind, randomised, placebo-controlled phase II trial will assess vitamin D3 (7,000 IU daily for 4 weeks then 14,000 daily for a further 92 weeks) as add-on therapy to subcutaneous IFNβ-1a 44 μg three times weekly in RRMS patients. The study aimed to randomise 348 patients with RRMS and 25(OH)D serum levels <150 nmol/l in a 1:1 ratio to high-dose vitamin D3 versus placebo. A composite of clinical and MRI parameters was chosen as primary endpoint. The primary MRI endpoint is the mean number of combined unique active lesions at week 48 and the primary clinical endpoint the proportion of relapse-free patients at week 96.26 Several additional clinical and MRI endpoints will be assessed. This study has been completed, however, data have not yet been presented. The investigators anticipate that these studies will provide additional insights into the effect of vitamin D on IFN treatment. There is a lack of consensus concerning the definition of vitamin D deficiency and sufficiency both in the general population and in disorders such as MS. Until the results of the EVIDIMS and SOLAR studies are available, it would seem prudent that people with MS, regardless of their treatment status, have sufficient levels of vitamin D, according to local guidelines. There is growing evidence that this should be at least 50 nmol/L for those on IFNβ.

It seems likely that there is an association between vitamin D levels and IFNβ treatment in MS patients with an additive benefit for the combination.27 Many studies have identified benefits on clinical and MRI measures in treating patients with both therapies. Ongoing clinical trials may provide more definitive evidence for this potentially beneficial combination.

Whether there may be a beneficial effect of a combination therapy of vitamin D3 with GA is under investigation in the Vitamin D to Ameliorate Multiple Sclerosis (VIDAMS) trial (NCT01490502).28 One hundred and seventy-two patients with RRMS are randomised in a 1:1 ratio to 5,000 IU or 600 IU oral vitamin D3 add on to GA over 96 weeks. The primary endpoint is the proportion of patients with a relapse at 2 years. Secondary and tertiary endpoints include additional clinical and MRI parameters. The study had not yet completed enrolment in spring 2015.29

Article Information:

Bruce Taylor receives research support from the National Health and Medical Research Council (NHMRC) Australia, MS Research Australia and the Royal Hobart Hospital Research Foundation. He has served on advisory boards for Novartis Biogen and Genzyme and has received travel assistance from Novartis, Biogen and Teva. Harold Moses has served as a consultant to Biogen, Teva, Serono, Medimmune, Novartis, Genzyme, NIH (Neuronext) and Bayer. Friedemann Paul receives funding from Deutsche Forschungsgemeinschaft (Exc 257), Bundesministerium für Bildung und Forschung (BMBF Competence Network Multiple Sclerosis KKNMS), EU FP7 (, Guthy Jackson Charitable Foundation, National Multiple Sclerosis Society of the USA, research support and personal compensation for activities with Alexion, Bayer, Biogen, MerckSerono, Chugai, MedImmune, Novartis, SanofiGenzyme and Teva. Gustavo Suarez is an employee of Bayer HealthCare Pharmaceuticals. Mark Rametta is an employee of Bayer HealthCare Pharmaceuticals.


Bruce Taylor, Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia. E:


The publication of this article was supported by Bayer HealthCare Pharmaceuticals Inc. The views and opinions expressed in the article are those of the authors
and not necessarily those of Bayer HealthCare Pharmaceuticals Inc.


This article is published under the Creative Commons Attribution Noncommercial License, which permits any non-commercial use, distribution, adaptation and reproduction provided the original author(s) and source are given appropriate credit.


Medical writing support was provided by Ray Ashton, Richmond Medical Communications, which was funded by Bayer HealthCare Pharmaceuticals Inc. All named authors meet the ICMJE criteria for authorship for this manuscript, take responsibility for the integrity of the work as a whole and have given final approval for the version to be published.




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