Advances in the genetics of rheumatoid arthritis point to subclassification into distinct disease subsets
© BioMed Central Ltd 2008
Published: 31 March 2008
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© BioMed Central Ltd 2008
Published: 31 March 2008
In the past few years considerable advances have been made in the genetics of susceptibility to rheumatoid arthritis (RA). For decades the HLA-DRB1 alleles were the only extensively replicated genetic factor, but more genetic risk factors have now been identified that predispose to RA. Interestingly, several of the observed genetic variants conferred risk to anticitrulline-peptide antibody (ACPA)-positive RA and two variants may be restricted to ACPA-negative RA, pointing to the need for subclassification of RA. The current manuscript reviews recently identified genetic factors predisposing to ACPA-positive RA and ACPA-negative RA. Additionally, although being scarcely explored, genetic variants affecting the severity of disease course are discussed.
Rheumatoid arthritis (RA) is a chronic potentially destructive arthritis classified by the presence of four out of the seven criteria developed by the American College of Rheumatology (ACR) in 1987. The criteria were formulated by experts who compared characteristics of patients with longstanding classical RA (mean disease duration 8 years). These ACR criteria have been criticized during past years as they have a low discriminative ability in patients presenting with recent-onset arthritis [1–4]. This is not surprising considering the components of the ACR criteria. One of the criteria is the presence of erosions on the radiographs of hands and wrists. In the early phases of RA only 13% of the patients have erosive disease . Additionally, erosions often initially present in the small joints of the feet, and appear in the small joints of the hands at a later point in the disease course . Also, rheumatoid nodules are very rare in the early phases of RA, and rheumatoid factor is present in only 50% of the patients with early RA .
Conversely, the serological factor that has the strongest association with RA, anticitrulline-peptide antibody (ACPA), is not part of the classification criteria. A taskforce has therefore been formed by the European League Against Rheumatism to develop classification criteria for early inflammatory arthritis. This taskforce is guided by the European League Against Rheumatism Standing Committee on Epidemiology as well as the ACR Quality Measurement Committee. It was agreed that this was an appropriate goal and that a proposal outlining the work to be done should be submitted to the Executive Board of the European League Against Rheumatism and the ACR for consideration of support. This exercise should not be seen as an attempt to redefine criteria for established RA (as classifiable by the original 1987 ACR criteria), but as an attempt to develop criteria for early (actual or potential) RA.
Considering the classification of RA, several questions can be raised. Do we consider RA one disease or is it a disorder composed of several (sub)entities? Second, should classification be based on clinical features or also on pathophysiological characteristics? These questions are pressing, as current evidence indicates that the identified genetic risk factors do not predispose to all RA patients but only to a specific subset.
The present manuscript highlights the latest advances in the genetics of RA susceptibility in relation to subdivision of the disease based on autoantibodies, in particular ACPA. The genetic risk factors that predispose to ACPA-positive RA and ACPA-negative RA are reviewed. Additionally, the current knowledge on genetic variants involved in the severity of RA is evaluated.
The most important genetic risk factor for RA was identified three decades ago and consists of the human leucocyte antigen (HLA) class II molecules. There is extensive evidence showing that certain frequently occurring HLA-DRB1 alleles (HLA-DRB1*0101, HLA-DRB1*0102, HLA-DRB1*0401, HLA-DRB1*0404, HLA-DRB1*0405, HLA-DRB1*0408, HLA-DRB1*0410 HLA-DRB1*1001, HLA-DRB1*1402) are associated with susceptibility to RA. The indicated alleles share a conserved amino acid sequence (QKRAA, QRRAA or RRRAA) – also called the shared epitope (SE) – at position 70 to 74 in the third hypervariable region of the DRβ1 chain. These residues are part of an α-helical domain forming one side of the antigen-presenting binding site.
The SE hypothesis postulates that the SE motif itself is directly involved in the pathogenesis of RA by allowing the presentation of a peptide to arthritogenic T cells . No specific arthritogenic peptides that bind to the HLA-DRB1 proteins and subsequently activate T cells have so far been identified, hence the SE hypothesis is not functionally proven. Nevertheless, this hypothesis is robust because of its consistent association (although quantitatively varying between alleles and populations) among various ethnic populations. It is estimated that the heritability of susceptibility to RA is 50% to 60% and that the SE alleles account for at least 30% of the total genetic effect [9, 10].
The role of the HLA-DRB1 SE alleles as well as of ACPA in RA susceptibility was recently studied in greater depth, and it was observed that the SE alleles associate only with RA patients who carry ACPA and not with ACPA-negative RA patients [11, 12]. This finding led to the hypothesis that the SE alleles confer risk to ACPA rather than to (ACPA-positive) RA. To investigate this hypothesis, the progression from recent-onset undifferentiated arthritis to RA was studied in relation to the SE alleles and autoantibodies [11, 13]. In patients who presented with undifferentiated arthritis, the presence of ACPA was associated with progression to RA, both in SE-positive undifferentiated arthritis patients and in SE-negative undifferentiated arthritis patients. In contrast, both in ACPA-positive undifferentiated arthritis patients and ACPA-negative undifferentiated arthritis patients, the association between the SE alleles and the development of RA was lost, indicating that the predictive value of the SE alleles is lost once the ACPA response has developed . These data indicate that the SE alleles particularly confer risk to ACPA and that these antibodies explain the association between the SE alleles and RA. Moreover, these observations provided the first evidence that the etiopathology of ACPA-positive RA is different from that of ACPA-negative RA.
The second risk factor for RA, identified in 2004, is non-HLA linked and concerns the C1858T single nucleotide polymorphism (SNP) in the gene encoding for the protein tyrosine phosphatase nonreceptor 22 (PTPN22) . An association between PTPN22 and RA has presently been demonstrated in several populations [15–17], and several studies have revealed that the PTPN22 T allele not only confers risk to RA but also to other autoimmune diseases such as lupus, type 1 diabetes and Graves disease. Intriguingly, PTPN22 is associated with ACPA-positive RA but not with ACPA-negative RA . Moreover, in three independent cohorts of RA patients a gene-gene interaction for the HLA SE alleles and PTPN22 was shown for ACPA-positive RA, but not for ACPA-negative RA . This observation strengthens the assumption that ACPA-positive RA and ACPA-negative RA have a different pathogenesis.
PTPN22 encodes for a lymphoid tyrosine phosphatase that affects the threshold for T-cell receptor signaling through binding to a Csk kinase. In vitro experiments have shown that the PTPN22 T-allele-encoded protein binds less efficiently to Csk, suggesting that the T cells expressing the T allele are hyperresponsive . Knocking out the murine homologue of PTPN22 resulted in lower thresholds of T-cell activation and induced an increased expansion and function of the effector/memory T-cell pool, which was associated with elevated levels of serum antibodies . Both of these studies indicate that the PTPN22 risk allele is associated with a reduced downregulation of T-cell activation. In contrast to this loss of function, a gain of function has also been described in carriers of the PTPN22 T allele . Hence the biological mechanisms underlying the association between PTPN22 and RA are incompletely understood.
Only very recently was the third genetic risk factor for RA identified. Interestingly, the observation was made in three countries at the same time using different approaches. In a study performed in the Netherlands, a candidate-gene approach showed an association between RA susceptibility and complement component 5-TNF receptor-associated factor 1 (C5-TRAF1) . In this study the complement C5 region on chromosome 9q33-34 was investigated as a candidate because mice studies revealed that mice deficient in complement factors are resistant to arthritis and that targeting C5 by antibodies prevents the onset of arthritis and reduces the clinical severity of arthritis in mice [22, 23]. Other studies showed that C5a receptor-deficient mice are resistant to arthritis induction . These data combined with the observation that high levels of C5a are found in synovial fluid of RA patients suggested these mediators play a central role in arthritis . Investigating the SNPs spanning this region revealed significant associations; the most significant SNP was not located within C5 but between C5 and TRAF1 . The protein encoded by TRAF1 is a member of the TNF receptor-associated factor 1 protein family, which mediates the signal transduction from various receptors of the TNF receptor superfamily, including the receptor for TNFα.
Interestingly, as this candidate gene study was completed an association between the C5-TRAF1 region was also demonstrated in two independent genome-wide association studies in the USA and Sweden . The demonstration of similar results in independent studies making use of different approaches provides strong evidence for the C5-TRAF1 region as a true RA-associated genetic variant. Moreover, additional evaluation in the Dutch study revealed that this genetic risk factor specifically predisposes to ACPA-positive RA and not to ACPA-negative RA . The two genome-wide association studies showing an association between C5-TRAF1 and RA only investigated ACPA-positive patients .
At present it is not clear whether the most significant SNP in C5-TRAF1 is causative since other proxies in high-linkage disequilibrium with this SNP can also be responsible for the observed association. Additionally, the functional consequence of carrying the C5-TRAF1 polymorphism is as yet unknown.
A genetic risk factor that has been investigated frequently in relation to RA, providing inconsistent results, is a noncoding variant in the 3' end of the gene encoding for cytotoxic T lymphocyte antigen 4 (CTLA4) [27, 28]. Combined data from the USA and Sweden have more recently suggested that CTLA4 confers risk only to the subset of ACPA-positive RA patients and not to ACPA-negative disease . This association, however, was only found in the Swedish cohort and not in the American cohort. Although this may be seen as support for another genetic risk factor that mainly contributes to ACPA-positive disease, it may also be a false-positive finding or a population-specific effect.
The CTLA4 protein plays an important role in downregulation of T-cell activation. To be fully activated the T cell requires the recognition of an antigen bound to HLA and a costimulatory signal between CD80 or CD86 on the antigen-presenting cell and CD28 on the T cell. This costimulatory signal can be inhibited by CTLA4, which is expressed on T cells as CTLA4 binds to CD80/CD86 with higher affinity.
Very recently, a linkage peak on the long arm of chromosome 2 was investigated thoroughly. The study confirmed the association between CTLA4 and RA but also observed an association with an unlinked SNP in the region encoding for STAT4 . This finding was observed in a Swedish as well as an American case-control study. Although the majority of the RA patients of the American cohort were ACPA-positive, such data on the Swedish cohort were not provided. Based on this study, therefore, no information is available on whether STAT4 predisposes to ACPA-positive RA and/or ACPA-negative RA. Additionally, it cannot be excluded that this study provided false-positive results. Multiple replication studies are thus required before this polymorphism can be added to the list of identified risk factors for RA.
The Wellcome Trust Case Control Consortium performed a genome-wide association study in almost 2,000 RA patients. They reported moderately associated regions on chromosome 6 (6q23) located between the genes encoding for TNFAIP3-OLIG3, which were unequivocally replicated in a follow-up study . In total, combining the Wellcome Trust Case Control Consortium data with the validation cohort, 2,515 ACPA-positive RA patients and 1,039 ACPA-negative RA patients were compared with 6,629 healthy control individuals, revealing only significant results in the ACPA-positive patients .
Another SNP, located 3.8 kb from the abovementioned SNP, was found by an independent group that evaluated only ACPA-positive patients. The effects of this SNP on susceptibility to RA were reported to be statistically independent from the SNP initially described by the Wellcome Trust Case Control Consortium . Although the function of these intergenic SNPs as well as the definite haplotypes that predispose or protect to RA are not fully elucidated, these data do suggest that the gene(s) in the region encoding for TNFAIP3-OLIG3 are of importance for susceptibility to ACPA-positive RA.
A functional promoter polymorphism (-169T → T) in the Fc-receptor-like gene 3 at chromosome 1q21-23 was first demonstrated to be associated with RA in two independent Japanese case-control studies [33, 34]. Subsequently a number of studies evaluated this polymorphism, showing contrasting results. Two meta-analyses revealed recently that this SNP has a role in the risk for RA amongst East Asians, but there is no compelling evidence for an association of this SNP with RA in Caucasians [35, 36]. Similarly, although Kochi and colleagues suggested this SNP influences the level of autoantibodies, a recent study from Norway found no association between the Fc-receptor-like gene 3 genotype and the level of ACPA . These data demonstrate that associations between genetic variants and disease may differ in diverse ethnic populations.
Another genetic variant, the potency of which differs between populations, is peptidylarginine deiminase 4 (PADI4). Large-scale linkage disequilibrium studies and subsequent replication studies implicated a variant of PADI4 as a risk factor for RA in Japanese and Korean populations [38, 39]. This finding that was not observed in the majority of studies in populations of European descent. Intriguingly, the Japanese/Korean association is with a haplotype rather than with a SNP with a proposed function. Another SNP linked to this haplotype may therefore be the causative risk factor.
Interestingly, a German study revealed an association between PADI4 and RA but the haplotypes providing this association were different to the haplotypes that conferred risk in the Asian populations . This may indicate that PADI4 or a factor linked to PADI4 may predispose to RA but that the actual causing genetic variant is not elucidated. Possible other explanations for this discrepancy are the presence of other genetic or environmental factors that interact with the genetic factor in a specific population, thereby affecting disease susceptibility or enrichment of genetic variants in one population but not in the other population. Although the peptidylarginine deiminases are implicated in the generation of ACPA, there is no compelling evidence supporting PADI4 genotypes correlating with ACPA levels – or ACPA-positive disease in particular.
The assumption that the etiopathology of ACPA-positive RA is different from that of ACPA-negative RA is strengthened when genetic risk factors are found that exclusively associate with RA characterized by the absence of ACPA. Two independent studies showed that the HLA-DR3 alleles predispose only to ACPA-negative RA but not to ACPA-positive RA [12, 41]. Whether this association is attributable to the HLA-DR3 gene itself or to genes linked to this locus is not known, however, as HLA-DR3 is part of a conserved ancestral haplotype (A1;B8;DRB1*03). The major histo-compatibility complex class III region – encoding for, amongst others, TNF and lymphotoxin α – is also part of this ancestral haplotype and has been described to influence the susceptibility to RA.
Recently described in a Swedish cohort and a Dutch cohort of patients was a second risk factor for ACPA-negative RA – interferon regulatory factor 5 (IRF5) . Whereas IRF5 is consistently associated with susceptibility to lupus, the correlation of IRF5 with RA is less clear as French and Spanish studies observed no association between IRF5 and RA [43, 44]. Nevertheless these two studies did not investigate the effect of this risk factor on ACPA-negative RA separately, and thus these findings may be false negative. Future studies may further increase comprehension of the role of IRF5 in RA.
The fact that more genetic risk factors for ACPA-positive disease have thus far been identified than for ACPA-negative RA does not necessarily indicate that the contribution of genetic factors to the etiopathology of ACPA-positive RA is larger than that to the etiopathology of ACPA-negative RA. In contrast, many important studies that revealed new genetic risk factors used cohorts constituting of mainly ACPA-positive RA patients [14, 30–32]. Part of the research conducted is thus biased towards locating genetic variants predisposing to ACPA-positive RA.
The reports demonstrating dissimilar genetic risk factors for ACPA-positive RA and ACPA-negative RA strongly suggest that ACPA-positive RA and ACPA-negative RA are separate subsets of RA with pathophysiological differences. Nonetheless, the effects of the described polymorphisms on gene function are still uncertain. Although the first structural difference between ACPA-positive RA and ACPA-negative RA – a difference in synovial tissue infiltrates between ACPA-positive RA patients and ACPA-negative RA-patients with active arthritis – was recently observed , the complete spectrum of pathophysiologic differences between ACPA-positive RA and ACPA-negative RA is as yet incompletely identified.
Altogether the genetics of RA susceptibility has made enormous progress during the past years, several more genetic risk factors will be recognized – considering the enormous efforts that are currently being made for RA susceptibility. In contrast, the field of the genetics of RA severity is relatively unexplored. Radiological joint damage is conceived as the most objective measure to determine the severity of RA. The number of studies investigating the relation between joint destruction and genetic variants is limited. Some SNPs are observed to associate with the disease outcome, but none of these associations are convincingly replicated in independent cohorts. Moreover, although a recent twin study indicated that genetic factors play a role in determining the severity of RA , the heritability of the level of joint destruction (the variance of joint destruction that can be ascribed to genetic factors) is still unknown.
Joint damage in RA is highly variable between patients and the cumulative level is associated with the level of (persistent) inflammation. Nonetheless, several studies have provided evidence for incomplete coupling between inflammation and destruction, which suggests that other individual factors also play a role. This suggestion leads to the hypothesis that candidate genes for the severity of RA are, on the one hand, genes that regulate the level of (local) inflammation and, on the other, genes that mediate the process of bone/cartilage destruction or bone regeneration. The contemporary data on genetics of RA severity are summarized below.
The HLA-SE alleles, and the DR4 alleles in particular, are known to predispose to a destructive disease course. It is now also known that the SE alleles primarily associate with the presence of ACPA and that these autoantibodies are a strong predictor for a severe disease outcome. This knowledge results in the question of whether the SE alleles contribute to a destructive disease course independent of the disease's effect on ACPA; a question that remains unsolved.
The HLA-DRB1 alleles not only encode for risk factors but are also protective factors. The HLA-DRB1 alleles encoding for the amino acids DERAA protect against a destructive disease course, an effect that is independent of the presence/absence of SE alleles but is most evident in the ACPA-positive group .
Within a number of cytokines such as TNFα, IL1, IL4, IL-1α, IL-1β or IL-1RN, variations have been reported and associations have been found only in small studies that are not independently replicated [48–50]. Future studies will reveal whether the observed associations will be observed in replication studies.
The SNPs located in the region encoding for C5 and TRAF1 observed to associate with susceptibility to RA in three different cohorts [21, 26] were evaluated for their correlation with disease severity in one study . This provided the first indication that carrying the C5-TRAF1 risk allele relates to a destructive disease course. This association is not yet replicated, however, and it has not been investigated whether the correlation with a severe disease course was independent of ACPA.
The destruction of bone and cartilage in RA is mediated by proteolytic enzymes that belong to the family of matrix metalloproteinases (MMPs). The most intensively studied proteinases are MMP3 (stromelysin) and MMP1 (collagenase). The levels of these MMPs are increased in both serum and synovial fluid of patients with RA, and the serum levels of MMP3 have been correlated with joint destruction in RA. Studies assessing polymorphism within the MMP3 gene promoter region revealed correlations between MMP3 haplotypes and joint damage; however, the results on which haplotypes conferred an increased risk were inconsistent [51–53]. Further evaluation of the effect of genetic variation in MMP3 on the level of joint damage in RA is therefore required.
The increasing comprehension of the role of genetics in disease outcome in RA may promote the development of personalized medicine. Although the prospects of RA patients on a group level have improved dramatically due to the growing arsenal of new aggressive antirheumatic drugs and recent data demonstrating that combination therapy is more effective than monotherapy, these developments do not automatically lead to benefit on the individual level. At present, > 95% of newly diagnosed RA patients start with methotrexate monotherapy, which is ineffective in 66% of patients . Subsequently, methotrexate is switched to another disease-modifying antoretroviral drug or a disease-modifying antoretroviral drug is added to the methotrexate therapy; if this strategy also fails, targeted therapies such as TNF blockers may be prescribed. The disease course in RA is highly variable and this commonly used step-up therapeutic strategy implies that a proportion of newly diagnosed RA patients are insufficiently treated for a specific time, resulting in the development of erosions that might have been prevented if a more vigorous treatment strategy had been applied. Clinical and serological characteristics solely are insufficient to predict the disease outcome in individual patients . Additional knowledge on genetic variants will increase the predictive ability.
Genetic factors confirmed for or suggestive of association with anticitrulline-peptide antibody (ACPA)-positive and ACPA-negative rheumatoid arthritis
ACPA-positive rheumatoid arthritis
ACPA-negative rheumatoid arthritis
Human leucocyte antigen shared epitope alleles
Human leucocyte antigen DR3
Protein tyrosine phosphatase nonreceptor 22 (PTPN22)
Complement component 5-TNF receptor-associated factor 1 (C5-TRAF1)
TNFα-induced protein 3-oligodendrocyte lineage transcription factor 3 (TNFAIP3-OLIG3)
Cytotoxic T lymphocyte antigen 4 (CTLA4)
Interferon regulatory factor 5 (IRF5)
Signal transducer and activator of transcription 4 (STAT4)
In contrast to the recent advances in the field of susceptibility to RA, genetic variants affecting the severity of the disease course in RA are scarcely explored. It is hoped that future studies will identify genetic risk factors that predict a severe disease course and that these result will allow personalized medicine in RA, thereby reducing avoidable joint destruction due to undertreatment and also lessening complications due to overtreatment.
American College of Rheumatology
complement component 5-TNF receptor-associated factor 1
cytotoxic T lymphocyte antigen 4
human leucocyte antigen
interferon regulatory factor 5
peptidylarginine deiminase 4
protein tyrosine phosphatase nonreceptor 22
single nucleotide polymorphism
tumor necrosis factor