Meta-analysis of the association of HLA-DRB1 with rheumatoid arthritis in Chinese populations

RA is an autoimmune disease characterized by chronic inflammation of the joints, which may lead to joint destruction and disability. It is the common chronic inflammatory rheumatic disease in the world, with prevalence estimates of 0.25% to 0.5% [1]. Previous literature suggests that people with rheumatoid arthritis may live 10–15 years less than their healthy counterparts [2]. RA is a complex polygenic disease of unknown etiology. However, genetic variation is believed to be important in determining the susceptibility of RA. It was proven to be associated with (histocompatibility locus antigen) HLA region strongly, especially with HLA-DRB1 alleles [3].

HLA-DRB1 alleles encode (70Q(R)K(R)RAA74) encoding the shared epitope (SE) (RAA amino acid pattern in positions 72 to 74 of the third hypervariable region of the DRβ1 chain) are associated with RA susceptibility [4]. SE contains HLA-DRB1 alleles representing significant genetic risk factor for RA. Many studies have attempted to clarify the relationship between HLA-DRB1 and RA, but there has been no definite consensus to date in Chinese populations. Due to the relatively small numbers of patients or the ethnic and clinical heterogeneity of the patients, the results are different in many studies. Well-designed meta-analyses of Caucasian and American populations showed that there was a strong association between HLA-DRB1 and RA susceptibility and severity [5].

Individual studies have reported different results regarding the association of HLA alleles with RA in Chinese populations. Some have reported that the frequency of the HLA-DRB1*0401 and *0405 alleles are significantly increased in RA patients, whereas others have found no associations [6, 7]. Moreover, there were controversial results about differences of clinical and laboratory parameters between the DR4+ and DR4- in RA patients [8, 9].

This study was performed to systematically summarize the association between Chinese with RA and HLA-DRB1 alleles. It was also performed to investigate the differences of clinical and laboratory parameters between the DR4+ and DR4- in RA patients. The frequency of HLA-DRB1 alleles varies according to ethnic and racial background, with some alleles being extremely rare. Therefore, articles were not required to identify all alleles for inclusion.

With our inclusion criteria, a total of 489 references were retrieved for initial review using search strategies as described. 239 citations were excluded from analysis after the first screening based on abstracts or titles. After exclusion of the articles that did not meet the inclusion criteria, we identified 40 potential studies for detail evaluation. Upon further review, 18 articles were eliminated due to the following reasons: 3 studies overlapped with others; 15 studies didn’t provide sufficient data about HLA-DRB1 alleles frequency on cases and/or controls or lacked clinical feature or laboratory indexes data to create for meta-analysis. Finally, 22 studies performed on the association of HLA-DRB1 with rheumatoid arthritis in Chinese populations were included and analyzed. Selection process for the studies included in the meta-analysis is summarized in Figure 1. The main features of eligible studies in our meta-analysis are summarized in Tables 1.

In this meta-analysis, 12 HLA-DRB1 polymorphisms were addressed and evaluated. Our meta-analysis results showed that there was a positive association between HLA-DRB1*04, *0401, *0404, *0405 and *0410 and susceptibility to RA, which indicated that they may be potential risk factors for RA in Chinese populations. The SE hypothesis indicated that these genes encoding the third hypervariable region of the DR antigen amino acid and the sequence are QKRAA, or QRRAA or RRRAA [31]. It is based on the assumption that class II molecules are directly involved in the etiology and pathogenesis of autoimmune disease. The initiation of an immune response requires T cell activation, and such activation requires the presence of both antigen and HLA-DRB1 on antigen presenting cells. Many current studies assume that some direct physical interaction between class II molecules and T cell receptor or antigen is involved in this process. The SE hypothesis assumes that structural differences between class II molecules can influence the interaction, either at the level of antigen presentation or during T cell differentiation in the thymus [32].

Teller found that the “shared” DRB1 amino acid sequence was relatively infrequent in the Hispanic American patients with RA which may not be useful in other ethnic groups [33]. This study may supplement data of association of DRB1 in Chinese populations.

In the subgroup analysis by geographic distribution, results showed that DRB1*0404 might be a potential risk factor for RA in the northerners of China rather than southerners. It showed that there was a higher susceptibility of DRB1*04,*0401,*0405 in the southerners than in the northerners of China. However as to DRB1*0404, it had an opposite result. All these may suggest a possible role of geographic differences in genetic backgrounds and the environment they lived in.

Summary of the meta-analysis findings of the association between DR4+ and DR4-in RA patients was shown in Table 3. As to laboratory parameters, ESR, CRP, RF, Anti-CCP in patients with DR4+ were higher which indicate the serious condition, poor prognosis and difficulty to alleviate in patients with DR4+. As to clinical features, there was no difference in duration of morning stiffness, number of swollen joints, joint function and number of joint tenderness between the DR4+ and DR4- in RA patients, the mechanism about it should be further explored.

Results of subgroup analysis show that there was a positive association between DRB1*0404 and X-ray phases to RA in phases I~II, but not in the phases III~IV. It suggests that the DR4+ patients with bone erosion may occur at an early stage.

We also found that the most common polymorphism was DRB1*0405 in Chinese population. While DRB1*0401 and DRB1*0402 were the most common polymorphismss in white population and Jews [34]. The role of the various subtypes in RA susceptibility were different in different populations and the constitute of susceptibility and non-susceptibility subsets were also different. Therefore, studies of RA-related genes should be on the basis of region, nationality and the sample should be expanded and more associated genes should be tested at the same time. We should also improve the typing technology, making a comprehensive analysis of the patients with RA. This will benefit to the revealment of the pathogenesis, early diagnosis and the prevention and control of RA.

Several limitations of the current studies could not be ignored. First, although we did not detect significant publication bias except for ESR between studies, it is uncertain whether the cases are comparably representative, and they are observational studies, more prone to many biases than prospective randomized controlled studies [35]. We found publication bias for ESR, there may be missing information which reflected “negative” or more conservative association of ESR with DR4.It need more samples to validate the reliability of our conclusions. Secondly, we distinguish the geographical populations into N-Han and S-Han with the Yangtze River serving as a geographical boundary, however the way to distinguish them is complicated which may lead to an inflated rate of false-positive results [36]. Thirdly, we were not able to perform subgroup for each polymorphism due to the limited number of published studies. Fourthly, our systematic review was based on unadjusted data, as the alleles information stratified for the main confounding variables was not available in the original papers. Although we actively contacted with the authors, we did not got a comprehensive set of data. Fifthly, we were not able to stratify our analyses according to the presence of anti-CCP antibodies. Chun-Lai found that different DRB1 SE alleles are common in Asian patients. These alleles confer a significant risk of developing ACPA-positive RA, but not ACPA-negative RA (i.e., in three Asian populations from Malaysia) [37]. Fisher et al. found that HLA-DRB1 SE was associated with both ACPA positive and negative RA, in a Korean population, but that there was a particularly strong interaction of smoking and HLA- DRB1 SE alleles that associated with ACPA fine-specificity [38, 39]. Finally, although all cases and controls of each study were well defined with similar inclusion criteria, there may be potential factors that were not taken into account that may have influenced our results.

As not enough studies were available in this field and current evidence remains limited. Therefore, it should be emphasised the necessity to conduct more studies with an adequate methodological quality, properly controlling for possible confounds in order to obtain a more valid result.

Our meta-analysis shows that HLA-DRB1*04, *0401, *0404, *0405 and *0410 are associated with RA, while DRB1*0405 is the most common polymorphism in Chinese populations. ESR, CRP, RF, Anti-CCP in patients with DR4+ were higher than DR4-, whereas there’s no difference for indexes of clinical features.