Biomarkers in Rheumatoid ArthritisView this Special Issue
Research Article | Open Access
Jeng-Hsien Yen, Che-Mai Chang, Yu-Wen Hsu, Chih-Hung Lee, Mei-Shin Wu, Daw-Yang Hwang, Ben-Kuen Chen, Hsien-Tzung Liao, Man-Tzu Marcie Wu, Wei-Chiao Chang, "A Polymorphism of ORAI1 rs7135617, Is Associated with Susceptibility to Rheumatoid Arthritis", Mediators of Inflammation, vol. 2014, Article ID 834831, 5 pages, 2014. https://doi.org/10.1155/2014/834831
A Polymorphism of ORAI1 rs7135617, Is Associated with Susceptibility to Rheumatoid Arthritis
Rheumatoid arthritis (RA), a chronic inflammatory disease usually occurring in synovial tissues and joints, is highly associated with genetic and environmental factors. ORAI1, a gene related to cellular immune system, has been shown to be involved in the pathogenesis of chronic inflammatory diseases and immune diseases. To identify whether ORAI1 gene contributes to RA susceptibility, we enrolled 400 patients with RA and 621 healthy individuals for a case-control genetic association study. Five tagging single nucleotides polymorphisms (tSPNs) within ORAI1 gene were selected for genotyping. An SNP, rs7135617, showed a significant correlation with the risk of RA. Our results indicated that genetic polymorphism of ORAI1 gene is involved in the susceptibility of RA in a Taiwanese population.
Rheumatoid arthritis (RA) is an autoimmune disease that affects joints in the body. RA is also a chronic inflammatory disease that can lead to long-term joint damage, chronic pain, and loss of motor function in the hands. RA frequently affects smaller joints . Symptoms caused by RA include joint stiffness, a low-grade fever, rheumatoid nodules, and lumps of tissue under the skin. The prevalence of RA is 0.5%~1%, which is relatively constant in many populations . A high prevalence of RA was reported in Indians; in contrast, a low prevalence of RA was observed in Chinese and Japanese populations . Differences of RA prevalence among populations reveal the importance of genetic factors in the risk of RA.
The cause of RA is still unclear. The immune system plays an important role in RA. Several genetic regions were reported to be associated with RA. The major histocompatibility complex (MHC) is a well-known region . HLA DRB1 alleles were shown to be significant markers of RA in several populations [3–8]. In addition, using a genome-wide association study, Kochi et al. identified a polymorphism in a gene encoding chemokine (C-C motif) receptor 6 (CCR6) at 6q27, which was associated with RA . The contribution of this region is estimated to be about 30% of the total genetic effects on RA susceptibility. This regulatory variant in CCR6 was further confirmed in Taiwanese RA patients .
The store-operated calcium channel plays an important role in activation of T-lymphocytes. Orai1 is the pore-forming subunit of the store-operated calcium channel . A loss of functional mutation of ORAI1 was found to cause severe combined immunodeficiency (SCID) . Genetic polymorphisms of ORAI1 were reported to be associated with a risk of HLA-B27-positive ankylosing spondylitis . However, the role of ORAI1 in RA is still unclear. In this study, we assessed whether genetic variations in ORAI1 contribute to RA susceptibility in the Taiwanese population.
2. Materials and Methods
2.1. Study Subjects
In total, 1021 Taiwanese individuals including 400 patients with rheumatoid arthritis (RA) and 621 healthy subjects were enrolled at Kaohsiung Medical University Hospital. Patients with RA were diagnosed to fulfill the revised criteria of the American Rheumatism Association for RA. This study was approved by the Institutional Review Board of Kaohsiung Medical University Hospital. All participants were provided with sufficient information and a consent form for the study before clinical data and samples were collected.
2.2. DNA Extraction and Genotyping
Patients’ genomic DNAs were isolated from whole blood samples using a Gentra extraction kit and ethanol precipitation as described in our previous study . Genotyping for single-nucleotide polymorphisms (SNPs) of Orai1 was conducted using a TaqMan Allelic Discrimination Assay (Applied Biosystems, Foster City, CA). A polymerase chain reaction (PCR) was performed in a 96-well microplate with an ABI 9700 thermal cycler (Applied Biosystems, Foster City, CA). After the PCR, the fluorescence was measured and analyzed using system SDS software version 1.2.3 (Applied Biosystems, Foster City, CA).
2.3. Statistical Analysis
JMP 8.0 software for Windows (SAS Institute, Cary, NC) was used for the statistical analysis of genotyping results. Statistical differences in genotypes and allelic frequencies between cases and controls were assessed using a χ2 test. A linkage disequilibrium (LD) map used to define the haplotype blocks was constructed using Haploview software (version 4.2; http://www.broad.mit.edu/mpg/haploview/). The haplotype analysis was performed to compare distributions of haplotype frequencies of ORAI1 between cases (RA) and controls.
3.1. Clinical Characteristics of Subjects
To investigate whether SNPs of ORAI1 contribute to the susceptibility to RA, we performed a case and control association study. As shown in the Table 1, 400 rheumatoid arthritis patients and 621 healthy controls were recruited. Of the RA patients, 82.2% were female. The mean age was 62.4 years. In the healthy controls, 57.5% individuals were female and the overall mean age was 51.2 years.
3.2. A Significant Association between rs7135617 and Susceptibility of RA
In this study, five tagged SNPs (tSNPs) of ORAI1 (rs12320939, rs12313273, rs7135617, rs6486795, and rs712853) with minor allele frequencies (MCFs) of >10% were selected from the HapMap Han Chinese database. Differences in genotypic and allelic frequencies of SNPs between cases and controls were compared. As shown in Table 2, rs7135617 revealed a significant association with RA in both the genotypic () and recessive models (odds ratio (95% CI): 1.58 (1.14~2.19); ).
|Significant () values are in bold.|
3.3. Haplotype Analysis of ORAI1 Genetic Polymorphisms in the Susceptibility to RA
To further identify whether haplotypes of ORAI1 were correlated with RA, we created an LD map (Figure 1) and analyzed haplotype frequency differences between RA patients and controls. The haplotype analysis showed that no association was observed in pairwise allelic comparisons of rs12313273/rs7135617 (Table 3) or rs7135617/rs6486795 (Table 4).
|Haplotype frequency less than 1% was excluded.|
|Haplotype frequency less than 1% was excluded.|
In this study, we screened SNPs of ORAI1 and performed a case-control association study. In this study, 1021 subjects (400 cases and 621 controls) were recruited. Five genetic polymorphisms were selected for genotyping. Our results indicated a significant association between rs7135617 and susceptibility to RA. Previous studies reported significant associations between genetic polymorphisms of ORAI1 and inflammatory diseases such as ankylosing spondylitis, calcium nephrolithiasis, and atopic dermatitis [13, 15, 16]. In this study, we found an SNP (rs7135617) located in the intron of ORAI1 associated with a risk of RA in the Taiwanese population.
ORAI1-mediated calcium signaling was reported to be involved in a variety of human diseases. Feske et al. identified a mutation in ORAI1 from SCID patients . A missense mutation resulted in the dysfunction of store-operated calcium entry that in turn attenuated immune responses . Our previous studies indicated that ORAI1 was highly expressed in the spleen, an organ involved in immune system . The rs7135617 within ORAI1 was associated with an autoimmune disease, ankylosing spondylitis. Consistent with a previous report, this study also confirmed an important role of ORAI1 polymorphism rs7135617 in RA. However, functional role of “intronic splicing regulatory elements of ORAI1” underlying RA susceptibility is not clear. Therefore, we further applied Human Splicing Finder version 2.4.1 (HSF)  to analyze the possible functions of rs7135617G>T. Results indicated that rs7135617 was predicted as a potential target binding site of SR SC35 protein. SR SC35 protein is an important splicing factor which can influence selection of splice site . The consensus value of rs7135617 wild-type (G) motif is 75.97 whereas the mutant-type (T) motif is 91.09. The variation of the consensus value (ΔCV) is +19.9%. A higher consensus value indicates higher strength and more possibility to be the splicing enhancer binding motif of SC35 protein. Combined with bioinformatics findings and genotyping data, our results imply that ORAI1 polymorphism rs7135617 may influence splicing process which further affects calcium signaling.
This study has some limitations. First, the collection of samples did not contain clinical biochemical data of RA patients. Therefore, this study was only able to detect associations between SNPs and the risk of RA. Second, rs7135617 is located in the intron. The T allele is a risk allele for RA. However, further functional role of ORAI1 polymorphism rs7135617 requires experimental validation in order to clarify the mechanism underlying calcium signaling and susceptibility of RA.
Third, the study was limited by the modest sample size (1021 subjects); however, we believe this might be partly overcome by the fact that our samples are homogeneous and well defined in terms of phenotype assessment.
Given the polygenic nature of immune diseases such as RA, the susceptibility gene ORAI1 could provide new clues to the pathogenesis of RA. Although a larger-scale population study is needed, our results, at least in part, indicated an important role of ORAI1 gene in the susceptibility to RA. Further study of the relationship between ORAI1 genotypes and the downstream functional relevance during chronic inflammation of the joints should be conducted in order to understand the etiology of RA.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
Jeng-Hsien Yen, Che-Mai Chang, and Yu-Wen Hsu contributed equally to this work
This work was supported by the funding from Taipei Medical University (Grant no. TMU101-AE1-B14 for Dr. Wei-Chiao Chang) and Grants from the National Science Council, Taiwan (NSC101-2628-B038-001-MY2; NSC101-2320-B038-029-MY3).
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