Role of the promoter polymorphism IL-6 -174G/C in dermatomyositis and systemic lupus erythematosus.

The promoter polymorphism -174G/C within the interleukin-6 gene (IL-6) has been reported to have a functional importance through the modulation of IL-6 gene expression in vitro and in vivo. IL-6 is thought to play an important role in autoimmune diseases and the effect of its receptor inhibitor-tocilizumab-has been recently studied. The aim of this case-control study was to investigate the association between the interleukin-6 -174G/C single nucleotide polymorphism and the susceptibility to dermatomyositis (DM) and systemic lupus erythematosus (SLE) in Bulgarian patients. Altogether, 87 patients-52 with SLE and 35 with DM-as well as 80 unrelated healthy controls were included in this study. All of them were analyzed by restriction fragment length polymorphism analysis (RFLP). The GG genotype and the G allele appeared to be associated with SLE, especially in women. None of the genotypes showed an association with DM. However, the G allele appeared to be associated with muscle weakness and it is a risk factor for elevated muscle enzymes. Our results indicate that IL-6 -174G/C polymorphism might be associated with the susceptibility to SLE especially in women. Although it is not associated with DM, it seems that IL-6 -174G/C polymorphism could modulate some clinical features in the autoimmune myopathies.

1. Introduction

Dermatomyositis (DM) and systemic lupus erythematosus (SLE) are diseases of unknown etiology. However, the dysregulation of cytokine production or action is thought to have an important role in their development [1]. The cytokine secretion was found to be under genetic control [2]. In our previous study, we have found association between TNF-α polymorphisms and the etiology of DM and SLE in Bulgarian patients [3].

TNF-α and IL-1 can induce IL-6 and IL-6 induces B-cell differentiation to plasma cells, hyperactivity, and secretion of antibodies and also promotes T-cell proliferation, cytotoxic T-cell differentiation, and local inflammation. According to Linker-Israeli et al. [4], elevated plasma levels of IL-6 messenger-RNA and protein could be detected in SLE patients. Serum TNF-α and IL-6 levels were reported to be sensitive markers for SLE activity [5, 6]. IL-6 is also considered to play a role in the development of DM, since it leads to reduced myogenesis [7]. Hagiwara et al. [8] have found that patients with DM and polymyositis have an increased number of IL-6 secreting cells compared to controls. Bilgic et al. [9] suggest that IL-6 serum level is a candidate biomarker for disease activity in both adult and juvenile DM.

The G allele of the IL-6 −174G/C polymorphism is associated with higher IL-6 expression [10]. The presence of the G allele has been associated with poor outcome in a variety of diseases including coronary artery disease [11], more severe manifestations of the Sjögren's syndrome [12] and systemic sclerosis [13], increased risk of juvenile rheumatoid arthritis [10], and growth retardation of children with Crohn's disease [14]. It was recently found that the IL-6 −174G/C gene promoter polymorphism predicts therapeutic response to TNF-α blockers [15].

The objective of our pilot study was to determine whether the IL-6 −174G/C polymorphism is a risk factor for the development of adult DM and SLE in Bulgarian patients and to define its contribution to the increased risk.

2. Materials and Methods

2.1. Clinical Material

Thirty-five patients with dermatomyositis who met the criteria of Bohan and Peter [16, 17] and Targoff et al. [18] and fifty-two with systemic lupus erythematosus who met the American College of Rheumatology (ACR) criteria were included in this study. The clinical and demographic data are presented in Table 1. In the DM group, 22 patients were females and 13 males. The mean age was 52 with a range of 18–82 years. In five patients, DM was associated with malignancy (breast and gastric carcinomas, myeloma and seminoma). In the SLE group, 43 were females and 9 males. The mean age was 40 with a range of 15–78 years. All of them showed renal involvement to a different extent. The patients have been followed for a mean of 10 years at the Department of Dermatology and Venereology, Medical University-Sofia, at the Department of Nephrology, Medical University-Sofia and at the Department of Nephrology, Ministry of Interior Hospital-Sofia.

Table 1

Demographic and clinical data.

Disease	DM		SLE
Demographic parameters	Female/male	22/13	Female/male	43/9
	Age, mean ± SD years	52 ± 14.7	Age, mean ± SD years	40 ± 12.4
Clinical parameters	Cutaneous disease	27 (77.1%)	Malar rash	34 (65.4%)
	Muscle weakness	28 (80.0%)	Discoid rash	9 (17.3%)
	Elevated muscle enzymes	19 (54.3%)	Arthritis	34 (65.4%)
	EMG findings	20 (57.1%)	Oral ulcer	3 (5.8%)
	Photosensitivity	21 (60.0%)	Photosensitivity	30 (57.7%)
	Immunological disease	9 (25.7%)	Serositis	11 (21.2%)
			Renal disease	52 (100%)
			Neurological disease	10 (19.2%)
			Haematological disease	20 (38.5%)
			Immunological disease	32 (61.5%)
			ANA	36 (69.2%)

The control group consisted of 80 anonymous healthy volunteers who did not show any clinical or laboratory signs of autoimmune skin diseases, as well as kinship with patients suffering from autoimmune skin diseases. They were randomly selected from the Biobank of the Molecular Medicine Center and the National Genetic Laboratory as to match the patients in age, gender, and ethnicity. The mean age was 45 ± 13.8 with a range of 19–76.

2.2. Genetic Analysis

The scientific investigation presented in this paper has been carried out in accordance with The Code of Ethics of the World Medical Association (Declaration of Helsinki) for experiments involving humans. The study was approved by the local ethics committee at the Medical University—Sofia. All participants signed an informed consent and venous blood was drawn for DNA isolation. Genomic DNA was extracted from the peripheral blood with the Chemagen DNA purification kit, using Chemagic Magnetic Separation Module I (Chemagen AG).

The analysis of IL-6 −174G/C polymorphism was performed as previously described by Libra et al. [19].

2.3. Statistical Analysis

Allele and genotype frequencies were compared between DM and SLE cases and controls, using Fisher's exact test to calculate P values for 2 × 2 tables. Where significant, data were expressed as P value and odds ratios (OR) with exact 95% confidence intervals (CI). Bonferroni correction was applied with a threshold significance level of 0.01. The test for Hardy-Weinberg equilibrium was done by χ 2 statistics.

3. Results

The single nucleotide polymorphism (SNP) was found to be in Hardy-Weinberg equilibrium. The observed allele and genotype frequencies of the IL-6 −174G/C polymorphism among the patients with DM and SLE and the healthy controls are summarized in Table 1.

The frequency of the GG genotype was higher among SLE patients (55.8%) compared to controls (40.0%) and it is associated with an increased OR (P = 0.055, after Bonferroni correction P = 0.28, OR 1.9; 95% CI 0.9–3; Table 2). Stratification by gender led to a stronger association of the GG genotype with SLE in women (P = 0.008, after Bonferroni correction P = 0.04, OR 2.9, 95% CI 1.3–6.6; Table 3). No difference was found in the genotype distribution between DM patients and controls. Stratification by gender did not lead to any statistically significant results.

Table 2

Genotype and allele frequencies of IL-6 −174G/C polymorphism in dermatomyositis and systemic lupus erythematosus patients and controls.

Genotype	DM	SLE	Controls
N = number of patients	N = 35	N = 52	N = 80
−174G/C
GG	14 (40.0%)	29 (55.8%)	32 (40.0%)
GC	11 (31.4%)	13 (25.0%)	21 (26.3%)
CC	10 (28.6%)	10 (19.2%)	27 (33.7%)
G	55.7%	68.3%	53.1%
C	44.3%	34.6%	46.9%
P value	NS*	G—P = 0.01

*Not significant.

Table 3

Allele and genotype frequency of the IL-6 −174G/C polymorphism in females with dermatomyositis and systemic lupus erythematosus and in controls.

Genotype	DM	SLE	Controls
N = number of females	N = 22	N = 43	N = 58
−174G/C
GG	8 (36.4%)	26 (60.5%)	20 (34.5%)
GC	6 (27.2%)	10 (23.2%)	14 (24.1%)
CC	8 (36.4%)	7 (16.3%)	24 (41.4%)
G	50.0%	72.1%	46.6%
C	50.0%	27.9%	53.4%
P value	NS*	GG—0.008; G—0.0002

*Not significant.

The G allele showed an association with SLE (P = 0.01, after Bonferroni correction P = 0.05, OR 1.9, 95% CI 1.1–3.2; Table 2). Stratification by gender led to a stronger association of the G allele with SLE in women (P = 0.0002, after Bonferroni correction P = 0.001, OR = 3, 95% CI 1.6–5.4; Table 3). No significant increase of the G allele was found in the DM group versus controls (Table 2), and stratification by gender did not lead to any statistically significant results (Table 3).

No association was found between the −174G/C polymorphism and SLE clinical features (Table 4).

Table 4

Comparison between the genotypes and ACR criteria.

Genotype	GG (n = 29)	GC (n = 13)	CC (n = 10)	P value
Malar rash	20 (69.0%)	5 (38.5%)	9 (90.0%)	NS*
Discoid rash	6 (20.7%)	3 (23.1%)	0 (0.0%)	NS
Photosensitivity	17 (58.6%)	8 (61.5%)	5 (50.0%)	NS
Oral ulcer	1 (3.4%)	2 (15.4%)	0 (0.0%)	NS
Arthritis	18 (56.5%)	9 (69.2%)	7 (70.0%)	NS
Serositis	6 (20.7%)	4 (30.8%)	1 (10.0%)	NS
Renal disease	29 (100.0%)	13 (100.0%)	10 (100.0%)	—
Neurological disease	6 (26.1%)	2 (15.4%)	2 (20.0%)	NS
Haematological disease	11 (37.9%)	4 (30.8%)	5 (50.0%)	NS
Immunological disease (anti-dsDNA, anti-Sm, and antiphospholipid Ab)	20 (69.0%)	6 (46.2%)	6 (60.0%)	NS
ANA	22 (75.9%)	7 (53.8%)	7 (70.0%)	NS

*Not significant.

An association was found between the GG and GC genotypes and the G allele with muscle weakness (GG + GC—P = 0.012, after Bonferroni correction P = 0.06, OR 11.5, 95% CI 1.7–77.2; G—P = 0.023, after Bonferroni correction P = 0.12, OR 4.2, 95% CI 1.2–15; Table 5) and the elevated muscle enzymes (GG + GC—P = 0.013, after Bonferroni correction P = 0.065, OR 8.5, 95% CI 1.5–49.5; G—P = 0.054, after Bonferroni correction P = 0.27, OR 2.5, 95% CI 0.9–6.5; Table 5) in DM patients.

Table 5

Comparison between the genotypes and DM clinical parameters.

Genotype	GG (n = 14)	GC (n = 11)	CC (n = 10)	P value
Muscle weakness	12 (85.7%)	11 (100.0%)	5 (50.0%)	GG + GC—P = 0.012, G—P = 0.023
Elevated muscle enzymes	8 (57.1%)	9 (81.8%)	2 (20.0%)	GG + GC—P = 0.013, G—P = 0.054
EMG findings	7 (50.0%)	8 (72.7%)	5 (50.0%)	NS*
Cutaneous disease	11 (78.6%)	9 (81.8%)	7 (70.0%)	NS
Photosensitivity	10 (71.4%)	6 (54.5%)	5 (50.0%)	NS
Immunological disease (anti-myositis-specific antibodies)	3 (21.4%)	4 (36.4%)	2 (20.0%)	NS

*Not significant.

4. Discussion

From all polymorphisms within the IL-6 gene, the promoter polymorphism −174G/C seems to be of greatest significance for the development of autoimmune diseases. However, the results published so far in the literature are rather conflicting.

In our study, no association was found between the GG genotypes and DM but its frequency was higher among the SLE patients compared to the controls and it is associated with an increased OR. Stratification by gender led to a stronger association of the GG genotype with SLE in women. The association remained statistically significant after the application of Bonferroni correction. The GG genotype was earlier found to be increased in Egyptian [20] and Malaysian [21] patients with SLE but no significant differences in the genotype frequencies were found between German patients and healthy controls [22]. There were no significant differences in the genotype frequencies between Portuguese [23] and Chinese [24] patients with SLE either. Probably such differences could be explained with population variations [25]. In our study, no marked increase of the GC genotype was observed among the controls but such elevation was earlier found among Egyptian [20] and Malaysian [21] controls. Chua et al. [21] suggested that the C allele might have a masking effect on the G allele when both alleles are present in heterozygous individuals. However, they have not observed any significant association of the homozygous C allele with the onset of SLE or with protection from the disease.

In our study, the G allele showed an association with SLE. Stratification by gender led to a stronger association of the G allele with SLE in women. The associations remained significant after the application of Bonferroni correction. No significant increase of the G allele was found in the DM group versus controls, and stratification by gender did not lead to any statistically significant results. Earlier studies showed no significant differences in allele frequencies between German SLE patients and healthy controls [22]. There were no significant differences in the allele frequencies between Portuguese [23] and Chinese [24] patients with SLE either. However, our results are in line with the results of a recent meta-analysis which proved that the −174G allele is associated with SLE mainly in the European populations and less with SLE in the Asian ones [26].

Earlier study of the relationship between −174G/C polymorphism and clinical manifestations and laboratory parameters showed an association between the G allele and the presence of anti-nuclear antibodies in all patients and rash and hematuria in male patients with SLE [27]. By comparing patients with various disease manifestations, Schotte et al. [22] found an association of the −174G allele with discoid skin lesions and anti-histone antibodies. Hamdy et al. [20] reported a statistically significant increase of the GG genotype with pulmonal affection, nephritis, and arthritis. The SLE patients with GG genotype showed significantly higher frequencies and increased risk of constitutional manifestations at disease onset, photosensitivity, hematological disorders, and positivity of ANA and anti-dsDNA [27]. Quite surprisingly, Santos et al. [23] found the −174CC genotype but not the GG genotype to be independently associated with renal disease and the C allele with the presence of irreversible damage. Huang et al. [24] did not detect any association between the IL-6 genotype and clinical or laboratory profiles in SLE patients. Similarly to the results of Huang et al. [24], we found no relationship between the −174G/C polymorphism and ACR criteria. Although the statistical significance was lost when Bonferroni correction was applied, an increased frequency of the GG and GC genotypes and the G allele was found in DM patients with muscle weakness and elevated muscle enzymes which is in line with the role of IL-6 as a myokine. Our results confirm other authors' findings that the elevated levels of IL-6 lead to muscle weakness [28, 29]. To the best of our knowledge, this is the first study that investigates the IL-6 −174G/C polymorphism in patients with DM.

The major limitation of our study is the small sample size which could affect the statistical power of the results. Obviously, more studies in a larger cohort are needed to clarify the role of this polymorphism for the susceptibility and clinical manifestations of SLE and DM.

In conclusion, our results show that the IL-6 −174G/C polymorphism might be associated with SLE mainly in women. The GG genotype and G allele might be associated with DM clinical features.