Vitamin D levels in Indian systemic lupus erythematosus patients: association with disease activity index and interferon alpha
- Manamita Mandal†1,
- Rina Tripathy†2,
- Aditya K Panda3,
- Sarit S Pattanaik1,
- Simanchal Dakua1,
- Anjan Kumar Pradhan4,
- Soumen Chakraborty4,
- Balachandran Ravindran3Email author and
- Bidyut K Das1Email author
© Mandal et al.; licensee BioMed Central Ltd. 2014
Received: 12 May 2013
Accepted: 24 January 2014
Published: 10 February 2014
Low levels of vitamin D have been associated with several autoimmune disorders including multiple sclerosis, rheumatoid arthritis, type 1 diabetes and systemic lupus erythematosus (SLE). The major source of vitamin D is sunlight but exposure of SLE patients to UV rays has been shown to exacerbate disease pathology. Studies in various populations have shown an association between low vitamin D levels and higher SLE disease activity.
We enrolled 129 patients who fulfilled American College of Rheumatology criteria in the study. There were 79 treatment-naïve cases and 50 patients who were under treatment for underlying SLE. There were 100 healthy subjects from similar geographical areas included as controls. Plasma 25-OH vitamin D3 and interferon (IFN)-α levels were quantified by enzyme-linked immunosorbent assay (ELISA). The gene expression level of IFN-α was determined by quantitative real-time reverse transcriptase polymerase chain reaction (RT-PCR).
Plasma 25-OH vitamin D3 significantly correlated in an inverse manner with systemic lupus erythematosus disease activity index (SLEDAI) scores (P <0.0001, r = -0.42), anti-dsDNA (P <0.0001, r = -0.39), plasma IFN-α (P <0.0001, r = -0.43) and levels of IFN-α gene expression (P = 0.0009, r = -0.45). Further, plasma levels of IFN-α positively correlated with gene expression of IFN-α (P <0.0001, r = 0.84). Treatment-naïve SLE patients displayed significantly higher plasma levels of IFN-α compared to patients under treatment (P <0.001) and controls (P <0.001).
These results suggest an important role of vitamin D in regulating disease activity in SLE patients and the need to supplement vitamin D in their treatment.
Systemic lupus erythematosus (SLE) is an autoimmune disorder which appears in a group of individuals and which is related to several factors, including environmental and host genetics that contribute to the development of the disease. Patients with SLE develop an immune response against numerous, mostly intracellular self-antigens. This results in formation of immune complexes that get deposited in vascular beds in most organs of the body. Immune complex deposition causes local inflammation and tissue damage that probably amplify the autoimmune response. This has serious consequences on the outcome of the disease.
The importance of vitamin D in various autoimmune disorders has been reported. Vitamin D deficiency has been associated with multiple sclerosis (MS), rheumatoid arthritis (RA), type 1 diabetes mellitus, inflammatory bowel disease (IBD), mixed connective tissue disease, autoimmune thyroid disease, scleroderma and SLE[3–5]. Vitamin D supplementation improves disease outcome in various animal models of MS, RA, type 1 diabetes mellitus, IBD, autoimmune encephalomyelitis and SLE. The role of vitamin D in murine models of SLE has been investigated to a limited degree. Administration of vitamin D and its synthetic analogs to murine models has resulted in improved dermatological manifestations, reduced proteinuria and increased survival[12, 13]. An earlier report highlighted vitamin D3 insufficiency in two-thirds, and deficiency (<10 ng/ml) in approximately one-fifth of SLE patients. In addition, serum vitamin D3 (25-OH) levels have been found to correlate inversely with SLE disease activity index (SLEDAI) scores[15–17].
The major source of vitamin D is the conversion of 7-dehydrocholesterol to previtamin D3 in the skin when exposed to solar ultraviolet radiation. Previtamin D3 then gets converted to vitamin D3 (cholecalciferol) through a heat-mediated process in the skin. A lesser amount of vitamin D3 (25-OH) is obtained from foods that supply less than 20% of the body’s requirements. Vitamin D3 undergoes two hydroxylations to achieve its functional form. The first hydroxylation occurs in the liver resulting in 25-hydroxyvitamin D (25(OH)D3) or calcidiol, which is normally quantified for evaluating vitamin D status, and the second hydroxylation takes place in the kidney to its active form 1,25-dihydroxyvitamin D3 (1, 25(OH)2D). In addition to the liver and kidney, hydroxylation of vitamin D3 also occurs in the lymph nodes and skin.
Several studies worldwide have investigated the role of vitamin D3 in the pathogenesis of SLE. However, to date, there have been no reports from an Indian population. Although the prevalence of SLE in India is rare (3 per 100,000), the survival rates of these patients (5-year: 70%; 10-year: 50%) are low compared to Western cohorts[21, 22]. Interestingly, vitamin D3 insufficiency or deficiency appears to be widespread in the Indian subcontinent, which makes it important to analyze its role in the background of SLE from an Indian cohort. We have addressed this issue in a tertiary-care, hospital-based, case-control study, to assess the role of vitamin D3 in SLE in a cohort from eastern India.
Clinical characteristics of SLE patients and healthy controls
SLE (n = 129)
Healthy controls (n = 100)
Age in years (mean ± SD)
28.14 ± 8.43
31.18 ± 5.32
Duration of disease years (mean ± SD)
2.90 ± 2.66
SLEDAI scores (mean ± SD)
18.36 ± 6.73
Treatment details of patients under therapy at the time of recruitment to the study (n = 50)
Number of patient treated (%)
Prednisolone; mean (range)
18.99 mg (5-50 mg)
6.5 mg/kg body weight
25-OH vitamin D quantification in plasma
The plasma levels of 25-OH Vitamin D were quantified by enzyme-linked immunosorbent assay (ELISA) kit (CPC, Euroimmun, Lübeck, Germany) according to the manufacturer’s instructions. Vitamin D deficiency was defined as plasma levels of 25-OH vitamin D <10 ng/ml and insufficiency as 10 to 30 ng/ml.
Quantification of plasma interferon alpha
Plasma levels of interferon (IFN)-α were measured by ELISA kit (Bender MedSystems Inc., Burlingame, CA, USA) according to the manufacturer’s protocol.
RNA extraction and reverse transcription
According to the manufacturer’s instructions, total RNA was isolated from 250 μl of whole blood by TRIzol LS reagent (Invitrogen, Carlsbad, CA, USA). RNA concentration was determined by spectrophotometry using an Implen NanoPhotometer (Implen, Munich, Germany). To remove any traces of genomic DNA, 1 μg of total RNA was then treated with 2U DNase (Sigma-Aldrich, St Louis, MO, USA) for 30 min at 37°C. DNase-treated RNA was reverse transcribed with a hexamer primer using a First Strand cDNA Synthesis kit (Thermo Fisher Scientific, Waltham, MA, USA), according to the manufacturer’s instructions. Once the cDNA was synthesized, its fidelity was tested by PCR and stored at -70°C.
Real-time PCR assay
Real-time PCR assay of IFN-α was carried out as described earlier. Briefly, reactions were set up in a total volume of 20 μl using 2 μl of cDNA, 10 μl of MESA GREEN qPCR MasterMix Plus (Eurogentec, Seraing, Belgium) and 10 picomole each of gene-specific primer (IFN-α (sense: 5′-TTCCTCCTGYYTGAWGGACAGA-3; antisense: 5′-GATCTCATGATTTCTGCTCTGACA-3′), glyceraldehyde-3 phosphate dehydrogenase (G3PDH) was taken as control (sense: 5′-GGTATCGTGGAAGGACTCATGAC-3′; antisense: 5′-ATGCCAGTGAGCTTCCCGTTCAGC-3′)) and performed in the MJ Research DNA Engine Opticon Real-Time Thermal Cycler (MJ Research, Waltham, MA, USA).The cycling conditions were: 95°C for 4 min; 35 cycles of 95°C for 30 s, 55°C for 30 s and 72°C for 30 s with a single fluorescence measurement; a final elongation step was carried out at 72°C for 10 min. Specificity of the PCR products was confirmed by analysis of the dissociation curve. The melting curve program consisted of temperatures between 55 and 95°C with a heating rate of 0.1°C/s and a continuous fluorescence measurement. Additionally, the amplicons’ expected size and the absence of nonspecific products were confirmed by analysis of the real-time PCR products in 1% agarose gel in 1 × TBE, stained with ethidium bromide and visualized under ultraviolet light (expected product size of IFN-α: 375 bp and G3PDH: 187 bp). IFN-α gene expression in each sample was calculated by the 2-ΔCt method (ΔCt = Ct of IFN-α – Ct of GAPDH).
All statistical analysis was performed by GraphPad prism 5.01 (GraphPad Software, San Diego, CA, USA). Distribution of plasma 25-OH vitamin D3 and IFN-α in treatment-naïve SLE patients, controls and treated patients were assessed by D’Agostino-Pearson omnibus normality test. Based on the results of the normality test, the association of 25-OH vitamin D3 and IFN-α with clinical disease was analyzed by analysis of variance (ANOVA) or Kruskal-Wallis test followed by an appropriate post test. Correlation of 25-OH vitamin D3 with double-stranded (ds)DNA, SLEDAI scores and IFN-α was analyzed by Spearman’s correlation test. Further correlation of IFN-α gene expression with plasma IFN-α and 25-OH vitamin D3 levels was analyzed by Spearman’s correlation test. A P value <0.05 was considered as significant.
Clinical characteristics of SLE patients
One hundred and twenty-nine patients were enrolled in the current study. Baseline characteristics are shown in Table 1. There were 125 (97%) females and 4 (3%) males with a mean age (standard deviation) of 28.14 (8.43) years. The mean duration of disease (standard deviation) was 2.90 years (2.66). Out of the 129 SLE patients, 50 patients included in the study were already on treatment for SLE and were also receiving supplements of oral calcium and vitamin D3 at the time of blood collection (Table 1). The other 79 patients were treatment-naive cases, undiagnosed earlier and the details of the treatment received for their complaints before hospitalization were not known since the patients had not maintained any records. The clinical profiles of patients were as follows: photosensitivity rash (26%), malar rash (57%), discoid rash (11%), oral ulcer (59%), arthritis (60%), neuropsychiatric disease (9%), myocarditis (2%), serositis (5%), nephritis (37%) and vasculitis (13%) (Table 1).
Plasma 25-OH vitamin D3 levels in SLE patients and healthy controls
Vitamin D3 levels negatively correlated with SLEDAI scores and anti-dsDNA
Correlation between 25-OH vitamin D3 and IFN-α
Correlation of IFN-α gene expression with plasma IFN-α and 25-OH vitamin D3 levels
Association of plasma IFN-α with SLE disease severity
The role of vitamin D3 in autoimmune disorders has been the subject of several studies with regard to its importance as an immune regulator. This is the first study from India to demonstrate an association between vitamin D3 and SLE, highlighting its significant inverse correlation with SLEDAI scores, anti-dsDNA and IFN-α. These are markers of disease activity and IFN-α is closely associated with disease pathogenesis.
Low levels of vitamin D3 in SLE patients have been reported compared to healthy controls in different populations. Interestingly, mean plasma levels of 25-OH vitamin D3 were not significantly different among treatment-naïve SLE cases (11.61 ng/ml), healthy medical students (9.55 ng/ml) and other healthy controls from same locality (13.36 ng/ml). Vitamin D3 insufficiency has been reported to be widely prevalent in the Indian subcontinent irrespective of the social class. Two groups of healthy controls were analyzed, which included medical students (HCA), who led a lifestyle marked by poor exposure to sunlight and irregular dietary habits, and a group of healthy subjects from the same locality (HCB). Interestingly, 63% of healthy medical students were deficient and 37% were insufficient of vitamin D3. Furthermore, 94% of the other groups of healthy controls were either deficient or insufficient of vitamin D3. This was an important observation considering India being a tropical country with lots of sunshine. However, the facts were contrary and several hypotheses have been discussed to explain the discrepancy. Higher melanin concentration in the skin, current lifestyle changes, avoidance of sunlight and poor food habits are some of the causes attributed to the widespread prevalence of low vitamin D3 among Indians. Low vitamin D3 may not be cause for development of SLE but persons with low serum levels are likely to suffer from severe disease. The current cross-sectional study does not address the issue of cause and effect relationship between vitamin D3 and SLE.
There are several interesting observations in the current study that points to an important role for vitamin D3 in disease modulation. One of them being a significant inverse correlation between vitamin D3 and SLEDAI scores and the other association is between vitamin D3 and anti-dsDNA. Association between plasma vitamin D3 and SLEDAI scores has not been uniform across observations: several studies have reported a negative correlation[15–17], while others have found none[36–39].
One of the important functions of vitamin D3 is maintenance of homeostasis of B cells. Low levels of vitamin D3 contribute to hyperactivity of B cells and enhanced production of autoantibodies. Furthermore, vitamin D3 is known to modulate various immunological pathways and thus could have a defining role in the development, progression and pathogenesis of SLE. Vitamin D3 also inhibits differentiation of dendritic cells (DCs) and T-helper cells (CD4+), enhances T regulatory cell proliferation and suppresses release of inflammatory mediators, which collectively help in control of autoimmune disorders.
In recent years, the role of interferon in the pathogenesis of lupus has been widely investigated. Higher levels of IFN-α were observed in our SLE patients compared to healthy controls, corroborating earlier observations[32, 44–46]. The interferon levels were significantly low in patients under treatment compared to treatment-naïve cases, supporting its possible role in disease modulation. Furthermore, IFN-α could be a marker of disease activity and low levels in treated patients could indicate response to therapy.
Interestingly, our study revealed a strong negative correlation of vitamin D3 with IFN-α (P <0.0001, r = -0.52). The robustness of the assay was validated by assessment of IFN-α gene expression, which corroborated with the earlier observations on the association between plasma IFN-α and vitamin D3. There are no reports in the literature assessing the association between IFN-α and vitamin D3.
In active SLE overexpression of interferon-inducible genes (IFN signature) has been reported. The major source of IFN-α in SLE patients are activated DCs. Maturation/activation of DCs and production of IFN-α has been observed to be inhibited by vitamin D in in vitro studies[48, 49]. A direct role for vitamin D3 in modulating lupus activity has been demonstrated in animal models[11–13]. Our observations, although cross-sectional, and studies on experimental models, provide evidence for a disease-modulating role for vitamin D3, which could be a promising therapeutic adjunct in the treatment of SLE. In view of the limited number of drugs available for the treatment of lupus and the low cost of vitamin D3 therapy, there is a strong case for its use routinely.
To conclude, vitamin D deficiency is prevalent among healthy Indians as well as among SLE patients. The significant inverse correlation of vitamin D3 with SLEDAI scores, anti-dsDNA and IFN-α highlights its immune-modulatory role contributing to disease outcome. Although the present study indicates a necessity for vitamin D3 supplementation in the management of SLE patients, larger randomized controlled trials would be necessary to define the daily requirement and optimum blood levels of vitamin D3 that are effective in influencing disease outcome.
American College of Rheumatology
complement component 3
complement component 4
enzyme-linked immunosorbent assay
inflammatory bowel disease
neuropsychiatric systemic lupus erythematosus
real-time polymerase chain reaction
systemic lupus erythematosus
systemic lupus erythematosus disease activity index.
The work was partly supported by intramural grants from the Department of Biotechnology, Government of India to the Institute of Life Sciences, Bhubaneswar. We would like to thank all patients and controls included in this study. We also thank to Mr. Subrat K. Mohanty for collection of blood from patients and healthy controls.
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