Research article | Open | Published:
Serum connective tissue growth factor is a highly discriminatory biomarker for the diagnosis of rheumatoid arthritis
Arthritis Research & Therapyvolume 19, Article number: 257 (2017)
Our previous proteomic study indicated that connective tissue growth factor (CTGF) may be a potential biomarker for rheumatoid arthritis (RA) diagnosis. The aim was to assess the performance of CTGF as a biomarker of RA.
Serum and synovial fluid CTGF was detected using a direct high sensitivity sandwich ELISA kit. Serum CTGF levels were tested for discriminatory capacity and optimal assay cutoffs determined in a training cohort of 98 cases of RA with 103 healthy controls. The assay performance was then validated in a further cohort of 572 patients (with RA (n = 217), ankylosing spondylitis (n = 92), gout (n = 74), osteoarthritis (n = 52), systemic lupus erythematosus (n = 72), or primary Sjögren’s syndrome (pSS) (n = 65)).
Significant elevation of synovial fluid CTGF concentration was found in RA patients, demonstrating excellent diagnostic ability to predict RA (area under the curve (AUC) = 0.97). Similar results were found in serum CTGF detection. At the optimal cutoff value 88.66 pg/mL, the sensitivity, specificity, and the AUC was 0.86, 0.92, and 0.92, respectively, in the training cohort. Similar performance was observed in the validation cohort, with sensitivity, specificity, positive likelihood, and negative likelihood of 0.82, 0.91, 5.74, and 0.12, respectively. Stronger discriminatory capacity was seen with the combination of CTGF and anti-citrullinated protein antibody (ACPA) (AUC = 0.96) than with either ACPA or rheumatoid factor (RF) alone (AUC = 0.80 or 0.79, respectively). The discriminatory performance of serum CTGF was consistent across all inflammatory conditions tested (AUC >0.92 in all cases), with the sole exception of pSS. Serum CTGF did not vary with symptom duration or disease activity.
Serum CTGF is a promising diagnostic biomarker for RA, with performance in the current study better than either ACPA or RF.
Rheumatoid arthritis (RA), which is the most common chronic inflammatory joint disease that affects approximately 1% of the world’s population , is characterized by synovial joint inflammation, progressive joint destruction, and disability . Currently, the clinical diagnosis of RA mainly relies on joint involvement, acute-phase reactants, duration of symptoms, and serological indices, including traditional rheumatoid factor (RF) and the presence of anti-citrullinated protein antibody (ACPA) .
However, in clinical use the 2010 criteria remain deficient, especially the serological indices. First, serological indices lack sensitivity or specificity. According to the meta-analysis of Nishimura et al., the sensitivity and specificity of a new serum index ACPA for the diagnosis of RA were 67% and 95%, respectively, and the sensitivity and specificity of the traditional index RF were even lower at 69% and 85% , respectively. As ACPA has high specificity, and RF has relatively higher sensitivity, the current recommendation is to combine RF and ACPA to detect RA. This combination truly improves the diagnostic value of these tests. However, studies have found that even the combination of these two markers is not perfect, with sensitivity of 78% and specificity of 82%  to detect RF-positive or ACPA-positive patients.
The second problem is the poor detection of early RA (ERA) by ACPA, with sensitivity as low as 57%. Similarly, the combination of ACPA and RF has limited performance benefits over either individual index [6, 7]. Therefore, the search for new serum biomarkers, especially those with high specificity and sensitivity to improve the current diagnostic tests for RA, retains great significance.
Connective tissue growth factor (CTGF) was first discovered by Bradham in 1991  and belongs to the CCN family of growth factors, named CCN2. It is a 38 kD cysteine-rich protein made up of four domains, including insulin-like growth factor binding protein (IGFBP), von Willebrand factor type C repeat (VWC), thrombospondin type 1 repeat (TSP1), and C-terminal cystine-knot (CT) modules . CTGF plays an important role in many physiological and pathological activities , such as inflammation, angiogenesis, wound healing, fibrosis, carcinogenesis, and tumor development . There is some evidence that CTGF could also be involved in the onset of RA. Nozawa identified increased expression of CTGF in serum from 39 patients with RA when compared to patients with osteoarthritis (OA) and further confirmed that CTGF could enhance the activity of osteoclasts by stimulating integrin protein αvβ3 to aggravate bone destruction . Moreover, Fujishiro et al. found that inhibiting CTGF by neutralizing the anti-CTGF monoclonal antibody (mAb) significantly ameliorated arthritis in a murine model of RA . In addition, our previous proteomic study  and the subsequent validation tests using PCR and western blot found that CTGF was significantly elevated in the synovial fibroblasts of 50 patients with RA in comparison with 50 healthy controls, raising the possibility that it could be a potential diagnostic biomarker for RA. To evaluate the diagnostic value of CTGF, we performed a multicenter validation cohort study to determine the discriminatory value of CTGF in RA diagnosis.
Patients and samples
Cases and healthy controls were recruited from the First Affiliated Hospital of Wenzhou Medical University, the Central Hospital of Jiamusi City, and Shanghai Guanghua Hospital from 7 September 2010 to 31 September 2016. The sources and the numbers of samples are shown in Additional file 1. RA diagnosis was defined according to the 2010 American College of Rheumatology (ACR) criteria. A “training set” consisting of 98 patients with RA and synovial fluids from 70 patients with RA were collected. A validation cohort of 572 patients was also used; this included 217 patients (38%) diagnosed with RA (according to the 2010 ACR criteria for RA), 92 (16%) with ankylosing spondylitis (AS) (Modified New York criteria for AS), 74 (13%) with gouty arthritis (gout) (2015 ACR criteria for gout), 52 (9%) with OA (1986 ACR criteria for OA of the knee), 72 (13%) with systemic lupus erythematosus (SLE) (1997 ACR criteria for SLE), and 65 (11%) with primary Sjögren’s syndrome (pSS) (2012 ACR criteria for pSS). Detailed demographic and clinical characteristics of the different groups are shown in Table 1 and Additional file 2.
All patients were included in the study on the first day of clinical admission; serum was collected from the patients before they underwent any treatment. Synovial fluid was collected during joint arthroplasty surgery from both patients with RA and patients with femoral neck fracture or meniscus injury (control subjects) from Shanghai Guanghua Hospital. The Clinical Research Ethics Committees of the First Affiliated Hospital of Wenzhou Medical University (No. 2016157), the Central Hospital of Jiamusi City (No. 2012010), and Shanghai Guanghua Hospital (No. 200903) approved the study. All of the subjects provided written informed consent.
CTGF concentration detected by ELISA
CTGF concentrations were detected by direct high-sensitivity sandwich ELISA (Human CTGF ELISA Kit, GWB-SKR010, GenWay Biotech Inc., USA) in accordance with the manufacturer’s instructions. Absorption was determined at an optical density of 450 nm. The data were analyzed directly. ACPA and RF were measured in the clinical laboratory. All of the reactions were conducted in triplicate. Detailed kit information and specifications are provided in Additional file 3.
All data were calculated for quantitative variables in SPSS (version 19.0, IBM, USA). The Shapiro-Wilk method was used to test whether the data were normally distributed, and the Levene method was used to test the homogeneity of variance. Two sets of data that did not meet the criteria for normal distribution and homogeneity of variance were analyzed by the Mann-Whitney U test.
The discriminatory ability of CTGF was assessed by plotting the receiver operating characteristic (ROC) curve based on data from the training cohort. Detailed diagnostic performance of CTGF to identify RA was evaluated according to the area under the curve (AUC), sensitivity, and specificity. Confidence intervals (95%) for the AUC were performed in GraphPad Prism (version 5, GraphPad Software, USA), and the cutoff point of serum CTGF for predicting RA was chosen using Youden’s index.
Diagnostic performance of CTGF for detection of RA
In serum, CTGF concentrations in patients with RA were significantly higher compared to the controls (p < 0.05). (Fig. 1a and Table 1) Serum CTGF had high diagnostic value for RA in terms of sensitivity, specificity, and the AUC, which were 0.86, 0.92, and 0.92, respectively, at the cutoff value of 88.66 pg/mL (Youden’s index, 0.78; Fig. 1b).
RA control subjects were mostly recruited at the First Affiliated Hospital of Wenzhou Medical University and Shanghai Guanghua Hospital. There were no significant differences in the CTGF concentrations in subject samples from the two centers (p > 0.05). ROC analysis showed similar predictive ability in subject samples from the two centers (Additional file 4).
As synovial fluid examinations could be supplements for serological tests, we measured CTGF in synovial fluid from patients with RA and control subjects. Compared to the healthy controls (23.87 (2.65, 166.8) pg/mL), patients with RA (534 (1.55, 2574) pg/mL) had a higher concentration of synovial fluid CTGF (Fig. 1c and Table 1). The diagnostic value of synovial fluid CTGF for RA was even higher (cutoff value, 104.2 pg/mL; Youden's index, 0.86), as the sensitivity, specificity, and AUC were 0.96, 0.91, and 0.97, respectively (Fig. 1d).
As both serum CTGF and synovial fluid CTGF could be good diagnostic indicators, the correlation between them was then calculated. Strong association was observed between serum CTGF and synovial fluid CTGF, with R = 0.81 (p < £0.01; Fig. 1e). This suggests that they are from the same source.
Validation of the high diagnostic value of CTGF in the validation cohort
We then sought to validate the serum CTGF threshold 88.66 pg/mL as a biomarker for RA, and test its discriminatory performance to distinguish between RA and various inflammatory conditions. Of the 572 patients in the validation study, 209 were CTGF-positive, and 178 of these had RA according to the ACR criteria. There were 39 patients with RA who were missed by the CTGF test. The positive and negative predictive values were 0.85 and 0.90, respectively. Other evaluation parameters demonstrated similarly high diagnostic value for CTGF, with sensitivity, specificity, positive likelihood ratio (+LR), and negative likelihood ratio (−LR) of 0.82, 0.91, 5.74, and 0.12, respectively (Table 2).
In the same validation cohort, ACPA had sensitivity and specificity of 67% and 97%, respectively. When used at its clinically utilized cutoff (>50 U/mL), a total of 82 patients were incorrectly classified. We then calculated the supplementary function of CTGF in detecting RA in ACPA-negative participants. The sensitivity, specificity, +LR, and –LR were 0.76, 0.91, 1.71, and 0.05, respectively. Similarly, the sensitivity, specificity, +LR, and –LR of CTGF in detecting RA from RF-negative participants were 0.79, 0.91, 2.46, and 0.06, respectively (Table 2).
Important differential diagnostic ability of CTGF
The performance of serum CTGF was tested to discriminate between patients with RA and the diagnostic subsets in the validation cohort. Based on the ROC analysis comparing patients with RA to patients in each subset of the non-RA group (Table 3), the optimum diagnostic cutoff was 73.35 pg/mL (Youden’s index, 0.80) for AS; 84.42 pg/mL (Youden’s index, 0.82) for gout; 46.75 pg/mL (Youden’s index, 0.79) for OA; 151 pg/mL (Youden’s index, 0.66) for PSS; and 79.64 pg/mL (Youden’s index, 0.82) for SLE. These results demonstrate the significant differential diagnostic ability of CTGF in distinguishing these diseases.
No significant correlation between serum CTGF and RA symptom duration or activity
Again in the pooled cases of RA from the training and validation cohorts, the correlation between serum CTGF and symptom duration or the disease activity score in 28 joints (DAS28) was calculated. No significance was observed, with R = 0.062, p > 0.05 and R = 0.10, p > 0.05, respectively (Fig. 2).
No association between serum CTGF and gender was observed in patients with RA (p > 0.05).
Addition of serum CTGF assay improves diagnostic performance of ACPA and RF
ROC analysis on a combination of serum indicators was then processed in the patients with RA from the validation cohorts (Fig. 3). While the AUC of single indicators of CTGF, ACPA, and RF was 0.93, 0.80, and 0.79 respectively, the AUC of the combination of CTGF and ACPA, CTGF and RF, ACPA and RF, and CTGF, ACPA, and RF were 0.96, 0.95, 0.86, and 0.97, respectively. The numbers of ACPA/CTGF-positive, RF/CTGF-positive, RF/ACPA-positive, triple-positive, and single-positive subjects vs all negative subjects are shown in Additional file 5.
RA is a chronic autoimmune disease with symmetric polyarthritis as one of its main manifestations. Diagnosis can be challenging, particularly in early disease and in patients with atypical presentation . Thus, much research and effort have gone into the development of RA diagnosis criteria in order to improve the diagnosis and classification of RA. The 1987 ACR criteria for RA, comprising morning stiffness, arthritis, rheumatoid nodules, serum RF, and radiographic changes, were in use for many years . However, these criteria are not very efficient, in that the criteria only help to diagnose those patients who already have serious structural damage. In addition, some of the criteria, like radiographic changes, are not accurate quantitative indicators and mainly depend on the subjective judgment of rheumatologists . These weaknesses stimulated the development of the current gold standard, the 2010 ACR criteria for RA. Compared to the previous version, the new criteria did not include the subjective and inaccurate criterion of radiographic changes, but included a more specific and objective biomarker, ACPA. A systematic literature review shows that the 2010 criteria help to diagnose more patients in the earlier stages of RA. The sensitivity of these criteria has risen by 11%, at the cost of a decline in specificity of only 4% .
There remains a need for improved diagnostic tests and criteria in RA, in particular for identifying the disease and to assist in distinguishing RA from other rheumatic diseases. In the current study, we demonstrated that CTGF could partially solve this problem.
One of the most important problems in RA diagnosis is a lack of sensitivity or specificity of the current indicators, ACPA and RF. ACPA is a good clinical indicator of RA (high predictability values and high diagnostic accuracy) and has moderate sensitivity of approximately 67% [4, 19]. However, the sensitivity of ACPA is lower in early RA. RF fares even worse, with a range of specificity from 38% to 85%, indicating that positive IgM-RF has modest diagnostic value [4, 20]. In the current study, we demonstrated that serum CTGF was an excellent serum indicator, with better performance than either of these widely used assays. As an independent biomarker, the sensitivity, specificity, and AUC of CTGF appeared high at 0.86, 0.92, and 0.92, which was much better than for RF, and CTGF had similar specificity but better sensitivity when compared with ACPA. The fact that ACPA is part of the ACR 2010 classification criteria would be expected to inflate its performance to diagnose RA using these criteria, and the relative superiority of serum CTGF in the current study is notable. Furthermore, approximately 30% of patients with RA who have clinical manifestations of the disease may have negative ACPA results . Therefore, we tested the diagnostic ability of CTGF in the ACPA-negative population, and found that serum CTGF was able to identify more patients with RA, with sensitivity and specificity of 76% and 91%, respectively.
The combination of RF and ACPA performs significantly better than either marker alone in the diagnosis of RA [5, 22]. However, researchers also reported that a model including ACPA and RF can correctly identify only 54–57% of patients with RA . In our study, a combination of CTGF, ACPA, and RF had the best diagnostic efficiency, better than single indicators, the combination of RF and CTGF, or even the recommended assay of combined ACPA and RF, with an AUC of 0.97. However, as the AUC of the combination of CTGF and ACPA was not significantly weaker than the combination of the three, we recommend the use of the combination of CTGF and ACPA.
Biomarkers are also of clinical utility in distinguishing RA from other rheumatic diseases. Matsui et al.  reported a relatively high frequency of ACPA in patients with other rheumatic diseases, including SLE (15%), pSS (14%), polymyositis/dermatomyositis (23%), and scleroderma (16%). In the present study, we found serum CTGF has good discriminatory capacity in distinguishing RA from other rheumatic diseases, with the AUC for serum CTGF detection greater than 0.92 for all diseases tested except for pSS. The discriminatory capacity of serum CTGF is extremely high in distinguishing SLE from RA and OA from RA.
Synovial proliferation and joint erosion are characteristic features of RA [24, 25]. CTGF has been shown to stimulate hyperproliferation of fibroblast-like synoviocytes in RA , and to act as an angiogenesis factor in the formation of pannus. These roles may explain why CTGF discriminates well between RA and other inflammatory arthropathies, and demonstrates face validity for the biomarker.
There were some negative results in our study that might contribute to the application of CTGF in diagnosing RA. No correlation was observed between serum concentrations of CTGF and the duration of RA symptoms. This indicated that the diagnostic efficiency of CTGF may not decrease in early RA, whereas there could be a significant decline in the sensitivity of ACPA when diagnosing patients with ERA rather than patients with established RA . Interestingly, almost no association of CTGF with DAS28 was found in our study, indicating that CTGF might be used without too much consideration of different disease activities.
Synovial fluid detection could also give some clues in distinguishing RA from diseases that are difficult to identify. We quantified CTGF in synovial fluid from patients with RA and the control subjects, and we found that this was a better biomarker than CTGF in serum, with a higher AUC for diagnosing RA. Additionally, the RA-to-control ratio of the concentration of CTGF in synovial fluid and serum are 60 and 10, respectively, and in synovial tissue, according to our previous proteomic study the ratio was 2.54 . Furthermore, there is strong correlation between serum CTGF and synovial fluid CTGF, indicating the same sources of CTGF production. Thus, we surmised that rather than the chondrocytes , the synovial tissue or the synovial fibroblasts  in the tissue was the initial source of CTGF, and CTGF was then secreted into the synovial fluid, participating in pannus formation as an angiogenesis factor , and later diffused into the blood. This hypothesis needs further validation.
Our study has several limitations. Although we have carried out a multicenter study, our participating centers were all from eastern or northern areas of China, and therefore further studies in different ethnic groups are warranted. We also have not tested the performance of CTGF in a specific cohort of patients with early arthritis, nor in preclinical disease, which are situations where ACPA has demonstrated diagnostic or predictive utility. Further testing of the impact of treatment on CTGF levels is also indicated.
In summary, in a multicenter study we identified an excellent and stable biomarker for RA. Serum CTGF concentration has much better diagnostic ability than RF, and is not weaker than ACPA. The combination of CTGF and ACPA could further improve diagnostic efficiency. In addition, it is a better biomarker to distinguish RA from other rheumatic diseases. Thus, we recommend CTGF for clinical use in diagnosing RA and distinguishing RA from other rheumatic diseases.
Anti-citrullinated protein antibody
American College of Rheumatology
Area under the curve
Connective tissue growth factor
Disease activity score in 28 joints
Enzyme-linked immunosorbent assay
Early rheumatoid arthritis
Insulin-like growth factor binding protein
Primary Sjögren’s syndrome
Receiver operating characteristic
Systemic lupus erythematosus
Thrombospondin type 1 repeat
von Willebrand factor type C repeat
Lee DM, Weinblatt ME. Rheumatoid arthritis. Lancet. 2001;358(9285):903–11. doi: 10.1016/S0140-6736(01)06075-5.
Lawrence RC, Helmick CG, Arnett FC, Deyo RA, Felson DT, Giannini EH, et al. Estimates of the prevalence of arthritis and selected musculoskeletal disorders in the United States. Arthritis Rheum. 1998;41(5):778–99. doi: 10.1002/1529-0131(199805)41:5<778::AID-ART4>3.0.CO;2-V.
Aletaha D, Neogi T, Silman AJ, Funovits J, Felson DT, Bingham 3rd CO, et al. 2010 Rheumatoid arthritis classification criteria: an American College of Rheumatology/European League Against Rheumatism collaborative initiative. Arthritis Rheum. 2010;62(9):2569–81. doi: 10.1002/art.27584.
Nishimura K, Sugiyama D, Kogata Y, Tsuji G, Nakazawa T, Kawano S, et al. Meta-analysis: diagnostic accuracy of anti-cyclic citrullinated peptide antibody and rheumatoid factor for rheumatoid arthritis. Ann Intern Med. 2007;146(11):797–808.
Sun J, Zhang Y, Liu L, Liu G. Diagnostic accuracy of combined tests of anti cyclic citrullinated peptide antibody and rheumatoid factor for rheumatoid arthritis: a meta-analysis. Clin Exp Rheumatol. 2014;32(1):11–21.
Infantino M, Manfredi M, Meacci F, Sarzi-Puttini P, Ricci C, Atzeni F, et al. Anti-citrullinated peptide antibodies and rheumatoid factor isotypes in the diagnosis of rheumatoid arthritis: an assessment of combined tests. Clin Chim Acta. 2014;436:237–42. doi: 10.1016/j.cca.2014.05.019.
Whiting PF, Smidt N, Sterne JA, Harbord R, Burton A, Burke M, et al. Systematic review: accuracy of anti-citrullinated peptide antibodies for diagnosing rheumatoid arthritis. Ann Intern Med. 2010;152(7):456–64. doi: 10.7326/0003-4819-152-7-201004060-00010. W155-66.
Bradham DM, Igarashi A, Potter RL, Grotendorst GR. Connective tissue growth factor: a cysteine-rich mitogen secreted by human vascular endothelial cells is related to the SRC-induced immediate early gene product CEF-10. J Cell Biol. 1991;114(6):1285–94. PubMed PMID: 1654338, PubMed Central PMCID: PMC2289134.
Kubota S, Takigawa M. The role of CCN2 in cartilage and bone development. J Cell Commun Signal. 2011;5(3):209–17. PubMed PMID: 21484188, PubMed Central PMCID: PMC3145877, doi: 10.1007/s12079-011-0123-5.
Klaassen I, van Geest RJ, Kuiper EJ, van Noorden CJ, Schlingemann RO. The role of CTGF in diabetic retinopathy. Exp Eye Res. 2015;133:37–48. doi: 10.1016/j.exer.2014.10.016.
Kubota S, Takigawa M. Cellular and molecular actions of CCN2/CTGF and its role under physiological and pathological conditions. Clin Sci. 2015;128(3):181–96. doi: 10.1042/CS20140264.
Nozawa K, Fujishiro M, Kawasaki M, Kaneko H, Iwabuchi K, Yanagida M, et al. Connective tissue growth factor promotes articular damage by increased osteoclastogenesis in patients with rheumatoid arthritis. Arthritis Res Ther. 2009;11(6):R174. PubMed PMID: 19922639, PubMed Central PMCID: PMC3003536, doi: 10.1186/ar2863.
Nozawa K, Fujishiro M, Kawasaki M, Yamaguchi A, Ikeda K, Morimoto S, et al. Inhibition of connective tissue growth factor ameliorates disease in a murine model of rheumatoid arthritis. Arthritis Rheum. 2013;65(6):1477–86. doi: 10.1002/art.37902.
Wang JG, Xu WD, Zhai WT, Li Y, Hu JW, Hu B, et al. Disorders in angiogenesis and redox pathways are main factors contributing to the progression of rheumatoid arthritis: a comparative proteomics study. Arthritis Rheum. 2012;64(4):993–1004. doi: 10.1002/art.33425.
Matsuo K, Xiang Y, Nakamura H, Masuko K, Yudoh K, Noyori K, et al. Identification of novel citrullinated autoantigens of synovium in rheumatoid arthritis using a proteomic approach. Arthritis Res Ther. 2006;8(6):R175. PubMed PMID: 17125526, PubMed Central PMCID: PMC1794520, doi: 10.1186/ar2085.
Silman AJ. The 1987 revised American Rheumatism Association criteria for rheumatoid arthritis. Br J Rheumatol. 1988;27(5):341–3.
Johnson SR, Goek ON, Singh-Grewal D, Vlad SC, Feldman BM, Felson DT, et al. Classification criteria in rheumatic diseases: a review of methodologic properties. Arthritis Rheum. 2007;57(7):1119–33. doi: 10.1002/art.23018. PubMed PMID: WOS:000250265200004.
Radner H, Neogi T, Smolen JS, Aletaha D. Performance of the 2010 ACR/EULAR classification criteria for rheumatoid arthritis: a systematic literature review. Ann Rheum Dis. 2014;73(1):114–23. doi: 10.1136/annrheumdis-2013-203284. PubMed PMID: WOS:000327835100022.
Besada E, Nikolaissen C, Nossent H. Should rheumatoid factor in rheumatoid arthritis be sent to Davy Jones’s Locker? Scand J Rheumatol. 2012;41(2):85–8. doi: 10.3109/03009742.2011.617316. PubMed PMID: WOS:000301539900001.
Besada E, Nikolaisen C, Nossent H. Diagnostic value of antibodies against mutated citrullinated vimentin for rheumatoid arthritis. Clin Exp Rheumatol. 2011;29(1):85–8.
Shmerling RH. Testing for anti-cyclic citrullinated peptide antibodies: is it time to set this genie free? Arch Intern Med. 2009;169(1):9–14. doi: 10.1001/archinternmed.2008.522.
Ajeganova S, van Steenbergen HW, Verheul MK, Forslind K, Hafstrom I, Toes REM, et al. The association between anti-carbamylated protein (anti-CarP) antibodies and radiographic progression in early rheumatoid arthritis: a study exploring replication and the added value to ACPA and rheumatoid factor. Ann Rheum Dis. 2017;76(1):112–8. doi: 10.1136/annrheumdis-2015-208870. PubMed PMID: WOS:000392425200016.
Matsui T, Shimada K, Ozawa N, Hayakawa H, Hagiwara F, Nakayama H, et al. Diagnostic utility of anti-cyclic citrullinated peptide antibodies for very early rheumatoid arthritis. J Rheumatol. 2006;33(12):2390–7. PubMed PMID: WOS:000243317900006.
Benito MJ, Murphy E, Murphy EP, van den Berg WB, FitzGerald O, Bresnihan B. Increased synovial tissue NF-kappa B1 expression at sites adjacent to the cartilage-pannus junction in rheumatoid arthritis. Arthritis Rheum. 2004;50(6):1781–7. doi: 10.1002/art.20260.
Miller MC, Manning HB, Jain A, Troeberg L, Dudhia J, Essex D, et al. Membrane type 1 matrix metalloproteinase is a crucial promoter of synovial invasion in human rheumatoid arthritis. Arthritis Rheum. 2009;60(3):686–97. PubMed PMID: 19248098, PubMed Central PMCID: PMC2819053, doi: 10.1002/art.24331.
Ding S, Duan H, Fang F, Shen H, Xiao W. CTGF promotes articular damage by increased proliferation of fibroblast-like synoviocytes in rheumatoid arthritis. Scand J Rheumatol. 2016;45(4):282–7. doi: 10.3109/03009742.2015.1092581.
Andreas K, Haupl T, Lubke C, Ringe J, Morawietz L, Wachtel A, et al. Antirheumatic drug response signatures in human chondrocytes: potential molecular targets to stimulate cartilage regeneration. Arthritis Res Ther. 2009;11(1):R15. PubMed PMID: 19192274, PubMed Central PMCID: PMC2688247, doi: 10.1186/ar2605.
Liu SC, Chuang SM, Hsu CJ, Tsai CH, Wang SW, Tang CH. CTGF increases vascular endothelial growth factor-dependent angiogenesis in human synovial fibroblasts by increasing miR-210 expression. Cell Death Dis. 2014;5:e1485. PubMed PMID: 25341039, PubMed Central PMCID: PMC4649533, doi: 10.1038/cddis.2014.453.
This project was supported by the Public Technology Applied Research Foundation of Zhejiang Province (Grant No. 2016C33183); the National Natural Science Foundation (Grant No. 81472055 and 81672129) and the National and Zhejiang College Students Innovative Entrepreneurial Training Program (Grant No. 201610343001 and 2017R413063) of China. MAB is supported by a National Health and Medical Council (Australia) Senior Principal Fellowship and a 1000 Talents Program fellowship from the Government of Zhejiang Province.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
The study protocol was approved by the Clinical Research Ethics Committees of the First Affiliated Hospital of Wenzhou Medical University (No. 2016157), the Central Hospital of Jiamusi City (No. 2012010), and Shanghai Guanghua Hospital (No. 200903).
Consent for publication
All of the subjects provided written informed consent for publication.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Sample numbers and sources in the training and validation cohort. (DOCX 14 kb)
Detailed demographic and clinical characteristics of patients in the validation cohort with conditions other than RA (not-RA). (DOCX 15 kb)
Detailed kit information for assays of CTGF, ACPA, and RF. (DOCX 14 kb)
ROC analysis showed the similar predictive performance at the two centers. (DOCX 230 kb)
The diagnosis value of ACPA, RF, and CTGF in the validation cohort. (DOCX 13 kb)