A case-control study of rheumatoid arthritis identifies an associated single nucleotide polymorphism in the NCF4 gene, supporting a role for the NADPH-oxidase complex in autoimmunity
© Olsson et al.; licensee BioMed Central Ltd. 2007
Received: 22 July 2007
Accepted: 26 September 2007
Published: 26 September 2007
Rheumatoid arthritis (RA) is a chronic inflammatory disease with a heritability of 60%. Genetic contributions to RA are made by multiple genes, but only a few gene associations have yet been confirmed. By studying animal models, reduced capacity of the NADPH-oxidase (NOX) complex, caused by a single nucleotide polymorphism (SNP) in one of its components (the NCF1 gene), has been found to increase severity of arthritis. To our knowledge, however, no studies investigating the potential role played by reduced reactive oxygen species production in human RA have yet been reported. In order to examine the role played by the NOX complex in RA, we investigated the association of 51 SNPs in five genes of the NOX complex (CYBB, CYBA, NCF4, NCF2, and RAC2) in a Swedish case-control cohort consisting of 1,842 RA cases and 1,038 control individuals. Several SNPs were found to be mildly associated in men in NCF4 (rs729749, P = 0.001), NCF2 (rs789181, P = 0.02) and RAC2 (rs1476002, P = 0.05). No associations were detected in CYBA or CYBB. By stratifying for autoantibody status, we identified a strong association for rs729749 (in NCF4) in autoantibody negative disease, with the strongest association detected in rheumatoid factor negative men (CT genotype versus CC genotype: odds ratio 0.34, 95% confidence interval 0.2 to 0.6; P = 0.0001). To our knowledge, this is the first genetic association identified between RA and the NOX complex, and it supports previous findings from animal models of the importance of reactive oxygen species production capacity to the development of arthritis.
Rheumatoid arthritis (RA) is a chronic inflammatory disease that leads to erosion and deformation of the joints. The prevalence in the general population is 0.5% to 1%, and women are at two to three times greater risk for developing the disease. Twin studies show a concordance rate of 12% to 15% in monozygotic twins and 4% in dizygotic twins, and the genetic heritability is estimated at 60% . Despite much effort to identify arthritis causing genes, only few genetic loci have been confirmed to be associated with RA, among which are the human leucocyte antigen (HLA) locus and the protein tyrosine phosphatase non-receptor 22 gene (PTPN22) [2–4].
RA is a heterogeneous disease with symptoms and disease progression that vary between patients. Classification of typical RA requires fulfilment of four out of seven criteria established by the American College of Rheumatology . The heterogeneity of the symptoms in RA probably mirrors the underlying genetic contribution; hence, the various combinations of symptoms observed in patients are probably caused by different combinations of risk alleles.
In the search for markers that can predict development of the disease before its onset, several autoantibodies, including rheumatoid factors (RFs) and antibodies against cyclic citrullinated peptides (anti-CCP antibodies), have been detected [6–8]. RFs, autoantibodies that recognize the Fc part of immunoglobulins , are present in 60% to 70% of RA patients and have been found to be associated with more severe clinical manifestations [10, 11]. Anti-CCP antibodies are present in 50% to 60% of RA patients and have also been shown to predict more severe disease [10, 12–14]. Interestingly, recent data suggest that the HLA-DRB1 locus, which has been shown to be associated with RA, is only associated with the presence of anti-CCP antibodies, and this association is independent of both RA development and the presence of RFs . Together with recent data describing the interaction between environmental factors and genetic predisposition [16, 17], these findings support the hypothesis that several independent disease mechanisms may lead to development of RA. They also emphasize the need to use relevant subgroups of RA patients in genetic association studies.
Various approaches have been used to identify genes that contribute to common diseases such as RA [18, 19]. Because of increasing knowledge of gene functions and immunological pathways, a candidate gene approach can be more efficient in terms of both cost and time than traditional linkage analysis or genome-wide approaches. The selection of genes in a candidate gene study can be based on previous knowledge of gene functions as well as on disease or immunological mechanisms. It can also be based on findings in animal models.
The Pia4 locus in rats has been shown to reduce the severity of pristane-induced arthritis (an arthritis model) . A single nucleotide polymorphism (SNP) in the Ncf1 gene was found to be responsible for the protective effect . Ncf1 encodes the protein p47phox, which is part of the NADPH-oxidase (NOX) complex that produces reactive oxygen species (ROS) in response to infectious stimuli. Rats carrying the risk allele have reduced capacity to produce ROS, which is linked to increased risk for development of arthritis [21, 22]. Apart from NCF1, the NOX complex is composed of five other proteins encoded by the genes NCF2, NCF4, CYBB, CYBA and RAC2 [23, 24]. In phagocytes massive ROS production, called the oxidative burst, takes place in the phagosome or endosome (intracellular) or in the plasma membrane (extracellular) after ingestion of invading pathogens or after stimulation of innate immune receptors [25–27]. However, the ability to generate ROS extends to cells other than classical phagocytes, such as dendritic cells, suggesting that the NOX complex has additional functions in the immune system . Interestingly, recent findings from our group show that the redox balance of T-cell membranes has an important effect on the activation and proliferation of T cells .
Results obtain in animal models make NCF1 and the other genes of the NOX complex candidate genes for human RA. However, transferring animal data to the human setting is not straightforward in this case. In contrast to rats, the genomic organization of NCF1 in humans is very complex, which makes SNP-based association analysis difficult [30, 31]. However, because of the complex interplay between the proteins of the NOX complex, it is likely that genetic changes in any of the genes could have the same effect on ROS production, as is seen for Ncf1 in rats.
We used a candidate gene approach to study the association with RA of 51 SNPs in five genes included in the NOX complex. We found a SNP, located in intron 4 in NCF4, to be associated with RA in a Swedish case-control cohort. This supports the hypotheses that the NOX complex is involved in the development of RA and that ROS could be an important regulator of the immune system.
Materials and methods
Selection of single nucleotide polymorphism
The HapMap genome browser  was used as the primary source for selection of SNPs. Primarily, HapMap-validated SNPs were selected. However, in order to obtain evenly dispersed SNPs across the genes, SNPs were also selected from dbSNP . The selection was based on several criteria; the minor allele frequency should be more than 5% in the Centre d'Etude du Polymorphisme Humain (CEPH) or other European cohort, the SNP should be located in a nonrepetitive sequence, and the validation status at dbSNP should be at least two-hit. We also consulted the Linkage disequilibrium (LD) maps of the HapMap CEPH samples in order to disperse evenly the SNPs with respect to the LD structure. Sixty-seven SNPs were selected (see Additional file 1): six in CYBB, eight in CYBA, 22 in NCF2, 21 in NCF4 and 10 in RAC2. The number of SNPs selected in each gene reflects both the size of the gene and the availability of validated SNPs.
Samples from the Epidemiological Investigation of Rheumatoid Arthritis (EIRA), a population based case-control study, were analyzed. The study base comprised the population, aged 18 to 70 years, in a geographically defined area in the middle and southern parts of Sweden during the period from May 1996 to 2005. A case was defined as a person in the study base who, during the study period and for the first time, received a diagnosis of RA based on the American College of Rheumatology criteria of 1987 . All cases were examined and diagnosed by a rheumatologist at a participating centre. All public rheumatology units in the study area and almost all of the (very few) private units participated in the study. The present study includes data from 1,842 RA patients and 1,038 controls, randomly selected from the study base and matched on age, sex and residential area. Of the cases and controls, 71% and 72%, respectively, are female; the mean age was 51 ± 13 years in cases and 54 ± 12 in controls. Information about RF and anti-CCP antibody status was available for 1,315 of the patient samples; 63% of these were RF positive and 61% were anti-CCP positive.
Assay design, validation and genotyping were performed by Kbiosciences (London, UK) using a fluorescence resonance energy transfer based competitive allele-specific polymerase chain reaction system (KASPar).
Of the selected 67 SNPs, 51 were successfully turned into assays. Six SNPs failed to make good assays (rs1049255 [CYBA], rs699244, rs789180, rs4652813 and rs6667363 [NCF2], and rs2075938 [NCF4]), whereas 10 were monomorphic in the panel of 40 Caucasians used for validation or in the EIRA cohort (rs1804006 [CYBA], rs789183, rs13306581 and rs13306575 [NCF2], and rs13057803, rs1003501, rs12158689, rs9610595, rs2072706 and rs2072711 [NCF4]; Additional file 1). Fourteen of the SNPs were genotyped in all available samples (1,842 cases and 1,038 controls), whereas the other 37 SNPs were genotyped in a subset of the samples comprising 1,069 patients and 634 controls (Additional file 1).
The Haploview software calculates P values for deviations from Hardy-Weinberg equilibrium (HWE) for each marker on the complete uploaded dataset . A significance threshold of P ≤ 0.001 was used. In order to obtain HWE P values for the case and control groups separately, each dataset was uploaded separately.
Single marker analysis
Contingency tables were created for each SNP using the JMP 5.0 software (SAS Institute, Cary, NC, USA), and P values for association with RA were calculated using χ2 tests for genotype frequencies. The sample set was stratified for sex in the initial analysis, and for sex and RF or anti-CCP status in the stratified analysis. Because CYBB is located on the X chromosome, allele frequencies were used to estimate association in the male samples.
To obtain a corrected α level in the stratified analysis, the Bonferroni correction method was applied, as implemented on the simple interactive statistical analysis website .
We also performed logistic regression analysis for the rs729749 SNP, in order to adjust for age, sex and living area. Logistic regression analysis was conducted for a subset of the material, in which all information regarding genetic factors, antibodies and matching variables was available. This same sample set was used for the frequency analysis of rs729749. We used the SAS software for Windows (version 9.1; SAS Institute, Cary, NC, USA) to perform logistic regression analysis.
Haplotype blocks were calculated using Haploview . SNPs that departed from HWE in both cases and controls were excluded from the analysis. The haplotype predictions were based on the CI method proposed by Gabriel and coworkers . However, the other available methods yielded the same result. Haplotypes were assessed using the WHAP software . Sub-haplotypes were investigated for associations based on the block structure predicted in Haploview. Because the haplotype block analysis is based on all genotyped SNPs, we used only the genotype information from the subset of the EIRA cohort comprising 1,069 cases and 634 controls. The permuted P values for the haplotypes are based on 5,000 permutations.
The region surrounding rs729749 was investigated for the presence of regulatory elements, transcription factor binding sites and conserved regions using the University of California, Santa Cruz (UCSC) Genome Browser . The ESPERR Regulatory potential (seven species), Conservation, and TFBS Conservation options were used.
P values and odds ratios (OR) with 95% CIs for the genetic models were calculated using the GraphPad Prism software (GraphPad Software, San Diego, CA, USA).
Fifty-one single nucleotide polymorphisms were successfully genotyped in a Swedish rheumatoid arthritis cohort
181,791,321 to 181,826,339
35,586,991 to 35,604,004
37,524,264 to 37,557,658
87,237,199 to 87,244,958
35,951,258 to 35,970,251
Genotype analysis indicates male-specific associations with rheumatoid arthritis in NCF2, NCF4 and RAC2
Associated SNPs in the initial genotype analysis
CC 0.69 (256)
CT 0.26 (95)
TT 0.05 (18)
CC 0.57 (141)
CT 0.40 (98)
TT 0.04 (9)
AA 0.81 (244)
AG 0.15 (46)
GG 0.03 (10)
AA 0.78 (146)
AG 0.22 (41)
GG 0.005 (1)
CC 0.77 (395)
CT 0.22 (115)
TT 0.01 (6)
CC 0.76 (229)
CT 0.20 (61)
TT 0.04 (11)
Stratification based on autoantibody status reveals a highly significant association of rs729749 with rheumatoid factor negative rheumatoid arthritis in men
Because RA is a heterogeneous disease, it is likely that the disease contributing genes differ in different subgroups of patients. Presence or absence of autoantibodies such as RF and anti-CCP antibodies might reflect different underlying disease mechanisms. In order to determine whether the detected associations are specific for a subclass of RA, we stratified the male cases by RF or anti-CCP antibody status and performed an analysis on genotype frequencies for the associated SNPs.
Stratified analysis of rs729749 in men
Logistic regression analysis of rs729749 in cases stratified for autoantibody status
Genotype CT versus CC
Genotype TT versus CC
0.66 to 0.97
0.67 to 1.62
0.75 to 1.17
0.60 to 1.71
0.35 to 0.73
0.52 to 2.81
0.69 to 1.04
0.56 to 1.53
0.75 to 1.23
0.58 to 1.84
0.39 to 0.88
0.26 to 2.12
0.54 to 0.90
0.71 to 2.14
0.65 to 1.18
0.47 to 1.90
0.20 to 0.60
0.88 to 5.29
0.70 to 1.07
0.61 to 1.71
0.80 to 1.31
0.63 to 2.00
0.36 to 0.83
0.28 to 2.24
0.54 to 0.89
0.62 to 1.84
0.61 to 1.10
0.43 to 1.73
0.2 to 0.7
0.7 to 4.6
To determine the validity of the P value, we estimated a corrected α value using the Bonferroni correction method. The corrected α level for the number of tests performed (159) was estimated at 0.0003. Hence, only the association detected for rs729749 in RF-negative males remained significant using the corrected α level.
Haplotype analysis reveals an associated haplotype in NCF4caused by the rs729749 single nucleotide polymorphism
Homozygosity could explain the genetic risk associated with rs729749
The rs726749 SNP is noncoding and located in the beginning of intron 4 in NCF4. Analysis of the region using the UCSC genome browser (March 2006 assembly)  revealed that it is not located at any known transcription factor binding site or regulatory element; however, there is a conserved regulatory region (as predicted by the ESPERR regulatory potential option) approximately 300 base pairs downstream of rs729749. Nonetheless, the genetic effect of this SNP is not obvious.
Genetic models of rs729749 in RF negative males
Frequency of risk variant
CC + TT versus CT
1.60 to 4.46
CC versus CT
1.50 to 4.24
TT versus CT
1.86 to 13.4
CC versus CT + TT
1.18 to 3.01
TT versus CC + CT
1.06 to 6.53
Here we report an association of the SNP rs729749, located in the gene NCF4, with RA in Swedish RF/anti-CCP antibody negative male patients. NCF4 is part of the NOX complex, and our results support recent findings that ROS play a role in the development of RA. However, because this is the first report of an association between a gene in the NOX complex and RA, genetic replication as well as functional studies will be required before it is possible to determine conclusively whether NCF4 is an RA susceptibility gene. Furthermore, the results from this study do not exclude the possibility that the other genes in the NOX complex could affect RA susceptibility. There could, for example, be epistatic effects between the different genes in the complex.
There is a lack of consensus in the field about statistical significance levels in association studies. In this study we initially used an α level of 0.05 to reduce the risk for overlooking associations that are specific for a subgroup of RA patients. There are strong medical and biological arguments in favour of subgrouping RA patients, and an analysis of nonstratified samples might conceal a true association. In the initial analysis of the genotype frequencies we found indications of association with three SNPs, and stratification of the samples indicates that the association for rs729749 is male specific and predominates in RF-negative disease. We also found a weaker association in anti-CCP antibody negative disease, but at this stage it is not possible to say whether this is due to the fact that the presence of RFs and anti-CCP antibodies is dependent  or whether the anti-CCP antibodies independently influence genetic risk.
The detected association of rs729749 is strongest in RF-negative males, and therefore it is possible that this particular SNP modulates the affected disease pathway so that it mainly influences the clinical disease in RF-negative RA, specifically in men. However, it is not impossible that this pathway play a role also in other subtypes of RA. The results from this study strengthen the view that different combinations of genes are involved in the disease progression in different RA subclasses defined, for instance, by sex or autoantibody status. The most striking aspect of the identified association of the rs729749 SNP is the clear sex specificity, indicating that the disease pathway affected by the rs729749 SNP is specific to men. The fact that RA is three times more common in women than in men suggests that men and women respond differently to factors that trigger the onset of RA and that some disease pathways could be sex specific. The RF-negative specificity of the association is not as striking as the sex specificity, but it might still point toward which RA subgroup is affected by the rs729749 SNP. Because both RFs and anti-CCP antibodies can be detected before the appearance of any disease symptoms [7, 42], they might reflect or be part of initial disease mechanisms that are only present in anti-CCP antibody or RF positive patients. Furthermore, it has repeatedly been shown that patients who are negative for these autoantibodies have a less severe disease outcome than do anti-CCP antibody or RF positive RA patients [10–12]. This further supports the view that autoantibody negative RA is another variant of RA. Also, the few genes confirmed to be associated with RA have been shown mainly to affect subclasses of RA.
The well established association of the HLA-DRB1 alleles, which encode the so-called shared epitope (SE), was recently suggested to be restricted to anti-CCP antibody but not RF positive RA [15, 16, 41]. However, it has also been shown that SE alleles are associated with higher titres of autoantibodies against type II collagen . Interestingly, the HLA-DR3 locus, which does not encode the SE, appears to be associated only with anti-CCP negative RA [41, 44]. The recently discovered PTPN22 risk allele has been shown to be associated with both RF and anti-CCP antibody positive RA [43, 45, 46], but there are conflicting data regarding the autoantibody restriction of this association . Furthermore, the reported association of the PD-1.2A allele of the PDCD1 gene is restricted to RF negative as well as SE negative RA . Hence, even though little is known about the precise disease mechanisms in RA, it is obvious that the symptoms can be caused by several different distinct disease pathways.
Because of the lack of certain autoantibodies, it is tempting to speculate that RF or anti-CCP antibody negative RA patients have a lesser B-cell component, and reports indicating that B-cell depleting therapy is a less effective treatment for RF-negative RA supports such a view [49, 50]. Several recent clinical studies, however, have yielded conflicting results on B-cell depletion efficiency , and more extensive studies are required before any conclusions can be drawn about the B-cell dependence in RF and anti-CCP antibody negative RA. In addition, it is fair to assume that the autoantibody negative forms of RA, in themselves, represent a heterogeneous collection of pathways related, for example, to osteoarthritis, arthropathies, or lupus.
The rodent arthritis models are heterogeneous as well but they may relate to more defined arthritis conditions than the human disease. Interestingly, the pristane-induced arthritis model used to identify the polymorphism in Ncf1 in rats is B-cell independent. Studies have shown that transfer of T-cells from genetically susceptible and immunized rats into genetically resistant and un-immunized rats is enough to induce arthritis in the resistant rat .
Both the HLA-DRB1 locus and PTPN22 are believed to affect T-cell activation. HLA-DRB1 is expressed by antigen-presenting cells and restricts the presentation of antigens to T cells. PTPN22 on the other hand has an intracellular effect, and the amino acid shift to the disease-associated tryptophan impairs the function of the Lyp protein, encoded by PTPN22, rendering it a less potent negative regulator of T-cell activation . Studies in animal models as well as recent findings suggest that the NOX complex could also be involved in T-cell activation [29, 54]. ROS production has been found in antigen-presenting cells, and it has also been shown that T-cell receptor signalling is affected by oxidation of the T-cell membrane as well as by intracellular levels of ROS [55, 56]. Interestingly, hydrogen peroxide generated from •O2- produced by the NOX complex can readily cross the cell membrane and inactivate protein tyrosine phosphatases, including that encoded by PTPN22, through oxidation of a specific cysteine residue . ROS production of antigen-presenting cells, such as dendritic cells, has been found to be crucial for the activation of T-cells  and could therefore determine the immune response to an antigen. Furthermore, recent work from our group highlights the importance of the redox balance on the surface of T cells for activation. T-cells originating from the Ncf1 mutated rat DA have an increased number of reduced thiol groups on the cell surface, which increases proliferation and activation . Gelderman and coworkers  showed that T-cells originating from the nonmutated E3 rats could be made arthritogenic by increasing the number of reduced thiol groups on the cell surface. Because NOX production could not be detected in T-cells, it was concluded that the redox balance of T-cell surfaces is determined by other cells, such as macrophages or dendritic cells.
In the rat a clear difference in the capacity to produce oxidative burst is the result of a single SNP in Ncf1, resulting in the shift from threonine to the disease-promoting methionine at position 153 in the p47phox protein . The consequences of the amino acid shift have not yet been identified, although position 153 does not coincide with any critical binding sites. It is most likely that the shift affects the three-dimensional structure of the protein, impairing the binding capabilities to the other proteins in the complex. The activation of the NOX complex is initiated through phosphorylation of the three cytoplasmic proteins p47phox (NCF1), p67phox (NCF2) and p40phox (NCF4) [23, 26, 57]. The phosphorylations lead to conformational changes of p47phox, and subsequent translocation of the three proteins to the membrane, where it interacts with and activates the membrane bound complex flavocytochrome b558, which is composed of gp91phox (CYBB) and p22phox (CYBA) [24, 58]. RAC2 also translocates to the membrane after dissociation from Rho-guanine nucleotide dissociation inhibitor and interacts with flavocytochrome b558 [23, 59]. Studies show that p67phox and Rac2 are critical for the function of the complex [25, 60], whereas p40phox and p47phox function as adaptor proteins and are responsible for the assembly of the complex . The precise role of p40phox is still debated, and there is evidence of both positive and negative regulation of the NOX complex [61–63]. Recent studies have suggested that p40phox, as well as p47phox, functions by 'carrying' p67phox to the membrane through the interaction with phospholipids [62, 64]. Studies of mutations causing human chronic granulomatous disease show that mutations in NCF1, CYBB, CYBA, or NCF2 lead to a complete lack of function of the NOX complex [65, 66]. However, SNPs in less critical regions, like the 153 SNP in Ncf1 found in rat, apparently reduce but do not completely abolish ROS production, which leads to an increased susceptibility to arthritis . These facts indicate that the SNPs of interest for examination in an RA association study of the NOX complex will probably be located at noncritical positions and will not completely abolish but only slightly modify binding to the other proteins.
The rs729749 SNP is located in the middle part of intron 4 in NCF4. By studying the genome maps using the UCSC genome browser, we could not find any evidence of it affecting a transcription factor binding site or a known regulatory element. However, there is a conserved regulatory region predicted approximately 300 base pairs downstream of rs729749. The haplotype analysis indicates that rs729749, or a SNP in very high LD, is responsible for the association detected for the haplotype. Also, because the predicted regulatory region is very close to rs729749, it could very well contain the causative SNP.
The genetic analysis of the association shows that the homozygous model gives the best significance, indicating that this could be the genetic effect. However, the low number of samples in the subgroup of RF-negative males together with the low frequency of the T allele make this assumption somewhat uncertain. Furthermore, it is not obvious what the functional consequences of a homozygous effect would be. We therefore chose to present all models tested in order to provide the full picture.
In the logistic regression analysis, weak associations were also detected for RF and anti-CCP antibody positive disease. One possible explanation for these findings is that some patients could have been 'misdiagnosed' regarding autoantibody status. The diagnosis is made by measuring the autoantibody titres, and certain threshold are used to determine positive versus negative status. However, sometimes autoantibody status changes as the disease progresses, and therefore there is a degree of uncertainty regarding autoantibody status.
A method or a strategy to apply multiple testing corrections accurately in a case-control candidate gene association study has not yet been established [67, 68]. The conventional multiple correction methods, such as Bonferroni, are considered by some to be too stringent for large-scale studies [69, 70]. The Bonferroni correction method is used to correct for the number of independent tests performed. However, in an association analysis neither the SNPs tested nor the different stratified analyses are truly independent. The allele frequencies of the SNPs are affected by the LD of the region, and the stratified analyses are based on the same SNPs and samples as the initial analysis and can therefore not be considered to be independent from each other. Nonetheless, in order to obtain an indication of the validity of the P values obtained in these analyses, we used the Bonferroni correction method to estimate an α level correcting for the number of tests (159) performed in the frequency analysis. The 159 tests reflect the sex-stratified analysis of all 51 SNPs (153) plus the stratified analysis of RF and anti-CCP antibody status performed for rs729749, rs789181 and rs1476002 in the male subset (6). Correcting for 159 tests gives a new α level of 0.0003, which means that only the association of rs729749 in RF-negative males passed the significance threshold using this stringent method.
The EIRA study included mainly individuals born in Sweden. Taking those born outside Sweden into consideration also, 97% were of Caucasian origin. In order to minimize potential bias resulting from population stratification, we performed logistic regression analyses in which ORs were adjusted for age and residential area.
We found evidence of an RA-associated SNP in the NCF4 gene of the NOX complex. The association is specific for male patients, with the strongest association found in RF-negative RA. This finding supports the notion of RA being a heterogeneous disease caused by a variety of disease pathways that are regulated by a variety of contributing risk genes. The detected association with a component of the NOX complex also strengthens previous evidence obtained in animal models that suggests that the NOX complex and ROS have a major impact on inflammation and autoimmunity. It is hoped that this finding will help to elucidate the complex genetics that underlie RA and autoimmunity.
= cyclic citrullinated peptide
= Centre d'Etude du Polymorphisme Humain
= confidence interval
= Epidemiological Investigation of Rheumatoid Arthritis
= Hardy-Weinberg equilibrium
= NADPH oxidase
= odds ratio
= rheumatoid arthritis
= rheumatoid factor
= reactive oxygen species
= shared epitope
= single nucleotide polymorphism.
This work was supported by the Swedish Research Council, the Strategic Science foundation, the Foundations of Craaford, Kock, Österlunds and the European Union Grants Autocure (LSHB-2006-018661) and Neuropromise (LSHM-LT-018637).
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