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Meta-analysis of serum C-reactive protein and cartilage oligomeric matrix protein levels as biomarkers for clinical knee osteoarthritis



The roles of C-reactive protein (CRP) and cartilage oligomeric matrix protein (COMP) in knee osteoarthritis (KOA) remain controversial, thus the present study is aimed to explore the relationships between CRP, COMP, and the incidence/progression of KOA.


A systematic search was conducted on PubMed and Embase until September, 2016 for all the relevant studies. The pooled mean difference (MD) with its 95% confidence interval (95% CI) based on fixed effects model or random effects model was calculated to assess the potential role of CRP and COMP in the incidence or progression of KOA. Heterogeneity was evaluated by Cochran’s Q and I2 tests. When P < 0.05 or I2 > 50%, a random effects model was chosen, otherwise, a fixed effects model was used. Moreover, the role of CRP in different degrees of pain was also analyzed. Sensitivity analysis was performed to evaluate the strength of the meta-analysis.


Fourteen studies were enrolled in the meta-analysis. No difference was found between baseline CRP and CRP levels in the last follow-up period of KOA (MD = − 0.09, 95% CI: -0.30, 0.13). Pooled data showed higher CRP concentration in patients with incident KOA when compared with controls (MD = 0.33, 95% CI: 0.04, 0.63). Moreover, higher serum COMP levels were found in patients with incident KOA (MD = 1.69, 95% CI: 0.61, 2.76) Additionally, significant higher CRP concentration was observed in KOA patients with highest degree of pain (MD = 1.60, 95% CI: 0.52, 2.67).


CRP and COMP serum levels were both associated with the incidence of KOA. Patients with a higher CRP and COMP concentration might have an increased probability of developing KOA. However, higher CRP serum levels was not related with KOA progression. Furthermore, KOA patients with more pain had higher CRP concentrations.


Osteoarthritis (OA), the most common type of arthritis, is characterized by joint space deterioration, pain, and loss of motion. Epidemiology studies have observed high prevalence of OA both in developed countries and developing countries. For example, the overall prevalence of knee OA was found to be 28.7% in India [1], the prevalence was highest (13.7%) in subjects living in the South-West region in China [2], and OA affected nearly 27 million Americans [3]. Additionally, the prevalence and incidence of the disease continue to increase. OA can become both a financial and health burden to patients and can affect their quality of life. Therefore, it is urgent to find an effective way to diagnosis and prevent the incidence or progression of OA in the early stage of disease.

Inflammation plays an important role in the pathogenesis of OA, although the specific correlations between biomarkers of inflammation and knee osteoarthritis (KOA) remain controversial. C-reactive protein(CRP) is a pentameric protein found in blood plasma associated with inflammation, infection, and injury. Studies demonstrated that CRP was correlated with complications, such as hypertension, cardiovascular disease, and diabetes [4, 5]. Studies have suggested that KOA was significantly related with CRP concentration [6, 7]. Other studies suggested that there were significant association between CRP concentration and KOA incidence [8,9,10]. Cartilage oligomeric matrix protein (COMP) is a 535-kDa non-collagen protein which has strong relation with the incidence of KOA. Some evidence has demonstrated that COMP serum levels in OA was different from healthy controls.

Because of these conflicting reports, the purpose of this study was to evaluate the association between CRP concentration, COMP serum levels and the incidence/progression of KOA. The relationship between CRP concentration and pain in KOA patients was also assessed.


Search strategy and study selection

A systematic search was performed on PubMed and Embase from database inception through September 2016. The following search terms were used: “osteoarthritis”, “knee osteoarthritis”, “C-reactive protein”, “CRP”, “cartilage oligomeric matrix protein”, “COMP”. Search terms were combined with OR and AND. All the reference list of retrieved studies and any additional publication were also searched and screened. The study was conducted based on the PRISMA guidelines [11].

Inclusion criteria

The included studies were in line with the following criteria: 1) subjects had clinical KOA; 2) investigated the association between KOA incidence and progression and the concentration of CRP or COMP serum levels; 3) parameter of CRP or COMP could be extracted or calculated; 4) published in English.

We excluded studies in which KOA patients were formerly treated by medication. In addition, repeated studies, reviews, comments, and letters were also excluded.

Data extraction and quality assessment

Data were extracted by two independent researchers following pre-designed form. The quality assessment was performed independently by two reviewers, and disagreement would be solved by the third reviewer.

Baseline characteristics of the eligible studies included first author, publication year, patients’ demographic, study design, research area, the concentration of CRP and COMP serum levels, and the number of the number of KOA and control patients. The quality of the studies was assessed by Newcastle-Ottawa Scale (NOS) [12]. In brief, NOS contains 8 items, categorizes into three groups, and with a total score of 9 stars. Each eligible study was graded according to this tool. In the current study, a cohort study with a follow-up rate > 75% was assigned one star. If NOS score of the study reached more than 5, it was considered as high quality literature, and was suitable for the meta-analysis.

Statistical analysis

We extracted mean difference(MD) and standard deviation(SD) of CRP and COMP levels at baseline and at the end of the follow-up period of study subjects and controls. Heterogeneity among the included studies was calculated by Cochran’s Q-test and I2 test [13]. P < 0.05 or I2 > 50% was defined as significant heterogeneity between individual studies. Then, the random effects model was selected for pooling MD and SD of CRP and COMP levels to assess the association between CRP and COMP concentration and KOA incidence and progression. When P > 0.05 or I2 < 50%, a fixed effect model was chosen to pool MD and SD of CRP and COMP levels. Sensitivity analyses were performed by changing one study at a time, to see what effect this produces on the outcome. All statistical analysis was performed by Cochrane Collaboration Review Manager (version 5.3). We considered P < 0.05 as statistically significant.


Search results and study selection

As shown in Fig. 1, the initial search yielded a total of 982 articles. 537 remained after removing the duplicated articles. 392 studies were further excluded because they did not investigate the relationship between CRP or COMP concentration and the incidence/progression of KOA. A total of 145 articles were under full-text review, of which 131 studies were excluded. Among the 131 articles, 91 articles were reviews, comments or case reports, 25 studies did not provide sufficient data, 14 studies were not about KOA incidence or progression, and 1 duplicate population [9, 14]. Eventually, 14 articles were included in the meta-analysis [6, 7, 14,15,16,17,18,19,20,21,22,23,24,25].

Fig. 1

Flowchart of study selection for inclusion in the systematic review

All relevant baseline characteristics of the enrolled studies were summarized in Table 1. In general, nine studies were designed as case control, and five were designed as cohort studies. Four studies were conducted in Asia, seven were performed in Europe, one was in Australia, and two were in USA. Study sizes ranged from 15 to 5171 patients, and the follow-up period ranged from 2 weeks to 12.4 years. Furthermore, all the included studies were scored more than 5 stars based on the NOS criteria, suggesting all enrolled studies were suitable for meta-analysis.

Table 1 Baseline chacteristics of enrolled studies

Meta-analysis of the association between KOA progression and CRP levels

As shown in Fig. 2a, 5 studies including 836 KOA patients at baseline and 748 patients at the end of the follow-up period evaluated the association between KOA progression and CRP levels [6, 16,17,18, 21]. Significant heterogeneity was observed among the five studies (P < 0.00001, I2 = 93%). Therefore, a random effects model was used to pool data. No difference was found between baseline CRP and CRP levels at the last follow-up period in KOA patients (MD = 0.09, 95%CI: -0.30, 0.13). Because there was significant heterogeneity among the studies, sensitivity analysis was performed, and no discrepancy results were observed when we omitted one study at a time (Table 2).

Fig. 2

Pooled effect size of the relationship between C-reactive protein (CRP) concentration and knee osteoarthritis (KOA). a the association between CRP concentration and KOA progression; b the association between CRP concentration and KOA incidence

Table 2 Sensitivity analysis for the meta-analysis

Meta-analysis of the association between KOA incidence and CRP levels

Four studies including 557 KOA patients and 7417 controls were enrolled in the meta-analysis to assess the relation between KOA incidence and CRP levels (Fig. 2b) [7, 14, 17, 21]. A random effects model was selected due to significant heterogeneity among studies (P < 0.00001, I2 = 96%). The pooled MD with its 95% CI suggested that CRP concentration was somewhat higher in KOA patients when compared with healthy controls (MD = 0.33, 95% CI: 0.04, 0.63). High heterogeneity also existed in this subgroup. Therefore, sensitivity analysis was conducted by deducting one study at a time. When we removed the study by Engstrom et al., Hosnijeh et al., and Zhang et al., pooled data suggested no significant difference in CRP concentration between KOA patients and healthy controls (Table 2).

Meta-analysis of the association between COMP serum levels and KOA incidence

Figure 3 shows the association between KOA incidence and COMP serum levels from 5 studies containing 259 KOA patients and 137 healthy controls. Pooled data indicated that patients with clinical KOA had a higher serum COMP levels than controls (MD = 1.69, 95% CI: 0.61, 2.76). Sensitivity analysis was performed to evaluate the strength of this conclusion, and no inconsistent results were found when we omitted each study (Table 2).

Fig. 3

Pooled effect size of the relationship between cartilage oligomeric matrix protein (COMP) serum levels and knee osteoarthritis (KOA)

Meta-analysis of the association between CRP levels and pain in KOA patients

As shown in Fig. 4, three studies estimated the correlation between CRP levels and pain in KOA patients [15, 19, 20]. A total of 2291 patients were included, among them 1112 patients reported knee pain at baseline assessment, and 1179 patients without knee pain were set as controls. Higher mean concentrations of CRP were found in patients who self-reported the highest level of knee pain (MD = 1.60, 95% CI: 0.52, 2.67). When we removed the study by Nielsen et al. in the sensitivity analysis, the significant difference between groups disappeared.

Fig. 4

Pooled effect size of the relationship between C-reactive protein (CRP) concentration and pain in knee osteoarthritis (KOA)


For inflammatory diseases, C-reactive protein (CRP) concentration is recognized as the most common laboratory marker, several clinical studies put forward that CRP concentration was elevated in patients with KOA [26]. Additionally, COMP serum levels are also considered as a potential biomarker for the diagnosis of KOA. The present meta-analysis demonstrated that higher CRP concentration was associated with higher KOA incidence, however, CRP levels were not related to the progression of KOA. Moreover, CRP concentration was higher in KOA patients with higher degrees of knee pain. Higher serum COMP levels in patients with incident KOA were also observed. Thus, both CRP and COMP could serve as useful biomarkers of KOA.

The outcome of our study suggests that CRP as a biomarker plays a positive role in the diagnosis and prognosis of KOA. This finding is consistent with a previous study [27]. However, in sensitivity analysis, when removing the study by Engstrom et al. [6], Hosnijeh et al. [17], and Zhang et al. [21], the significant difference of CRP levels between KOA patients and control group diminished. Thus, further study enrolling larger sample size and balancing confounding factors such as patient’s backgrounds is needed. Although significantly higher COMP serum levels was observed in incident KOA, no stratified analysis based on severity of KOA was performed due to limited enrolled studies. Further investigation is required to determine if this marker can be utilized to assess the incidence OA. Given that both CRP and COMP levels were higher in patients with KOA, the two factors could be used in combination for the prognosis of KOA.

Significant heterogeneity existed in our study. Although we conducted sensitivity analysis to assess the strength of the meta-analysis using one-at-a-time method, heterogeneity did not reduce. In patients with early KOA, many factors could affect the concentration of CRP, such as life habit and the background of KOA. For example, a previous study indicated that cigarette smoking was positively associated with serum CRP levels [28]. In addition, experimental data suggested both dietary and serum Mg were inversely related with serum CRP in early radiographic KOA patients [29]. Moreover, serum CRP was associated with knee bone marrow lesions scores [30]. Thus, future study stratified by living habit and background of patients should be performed to verify the present conclusion.

There are some limitations should be noted in the meta-analysis. First, the number of enrolled subjects was small, which limited the subgroup analysis stratified by smoking status, and other confounding factors such as hyperlipidemia. Second, we did not restrict the timing of biomarker assessment, and exercise status of the patients, also the follow-up period ranged from 2 weeks to 12.4 years, which might be one of the reasons causing significant heterogeneity among individual studies. Third, a number of studies did not provide calculated data. Moreover, other chronic diseases might influence the CRP levels in patients, and we did not eliminate the effect of those factors. Our study was designed to evaluate the relationship between biamarkers and KOA. The association between CRP and other OA types, such as hand, hip, and spine OA was not considered.


The present meta-analysis indicated that both CRP and COMP could serve as biomarkers for KOA. Higher CRP and COMP serum levels might be associated with a higher incidence of KOA. However, higher CRP concentration was not associated with the progression of KOA. Further study is required verify the actual relationship between CRP and KOA incidence.



Confidence interval


Cartilage oligomeric matrix protein


C-reactive protein


Knee osteoarthritis


Mean difference




  1. 1.

    Pal CP, Singh P, Chaturvedi S, Pruthi KK, Vij A. Epidemiology of knee osteoarthritis in India and related factors. Indian J Orthop. 2016;50:518–22.

  2. 2.

    Tang X, Wang S, Zhan S, Niu J, Tao K, Zhang Y, Lin J. The prevalence of symptomatic knee osteoarthritis in China: results from the China health and retirement longitudinal study. Arthritis Rheumatol. 2016;68:648–53.

  3. 3.

    Issa SN, Sharma L. Epidemiology of osteoarthritis: an update. Curr Rheumatol Rep. 2006;8:7–15.

  4. 4.

    Ablij H, Meinders A. C-reactive protein: history and revival. Eur J Intern Med. 2002;13:412.

  5. 5.

    Dalton RR, Hoffman WH, Passmore GG, Martin SL. Plasma C-Reactive protein levels in severe diabetic ketoacidosis. Ann Clin Lab Sci. 2003;33:435–42.

  6. 6.

    Engstrom G, Gerhardsson de Verdier M, Rollof J, Nilsson PM, Lohmander LS. C-reactive protein, metabolic syndrome and incidence of severe hip and knee osteoarthritis. A population-based cohort study. Osteoarthr Cartil. 2009;17:168–73.

  7. 7.

    Kerkhof HJ, Bierma-Zeinstra SM, Castano-Betancourt MC, de Maat MP, Hofman A, Pols HA, Rivadeneira F, Witteman JC, Uitterlinden AG, van Meurs JB. Serum C reactive protein levels and genetic variation in the CRP gene are not associated with the prevalence, incidence or progression of osteoarthritis independent of body mass index. Ann Rheum Dis. 2010;69:1976–82.

  8. 8.

    Garnero P, Piperno M, Gineyts E, Christgau S, Delmas PD, Vignon E. Cross sectional evaluation of biochemical markers of bone, cartilage, and synovial tissue metabolism in patients with knee osteoarthritis: relations with disease activity and joint damage. Ann Rheum Dis. 2001;60:619–26.

  9. 9.

    Sanchez-Ramirez DC, van der Leeden M, van der Esch M, Roorda LD, Verschueren S, van Dieen J, Lems WF, Dekker J. Increased knee muscle strength is associated with decreased activity limitations in established knee osteoarthritis: two-year follow-up study in the Amsterdam osteoarthritis cohort. J Rehabil Med. 2015;47:647–54.

  10. 10.

    Conrozier T, Chappuis-Cellier C, Richard M, Mathieu P, Richard S, Vignon E. Increased serum C-reactive protein levels by immunonephelometry in patients with rapidly destructive hip osteoarthritis. Rev Rhum Engl Ed. 1998;65:759–65.

  11. 11.

    Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Int J Surg. 2010;8:336–41.

  12. 12.

    Lo CK, Mertz D, Loeb M. Newcastle-Ottawa scale: comparing reviewers' to authors' assessments. BMC Med Res Methodol. 2014;14:45.

  13. 13.

    Lau J, Ioannidis JP, Schmid CH. Quantitative synthesis in systematic reviews. Ann Intern Med. 1997;127:820–6.

  14. 14.

    Sanchez-Ramirez DC, van der Leeden M, van der Esch M, Roorda LD, Verschueren S, van Dieen JH, Dekker J, Lems WF. Elevated C-reactive protein is associated with lower increase in knee muscle strength in patients with knee osteoarthritis: a 2-year follow-up study in the Amsterdam osteoarthritis (AMS-OA) cohort. Arthritis Res Ther. 2014;16:R123.

  15. 15.

    Arendt-Nielsen L, Eskehave TN, Egsgaard LL, Petersen KK, Graven-Nielsen T, Hoeck HC, Simonsen O, Siebuhr AS, Karsdal M, Bay-Jensen AC. Association between experimental pain biomarkers and serologic markers in patients with different degrees of painful knee osteoarthritis. Arthritis Rheumatol. 2014;66:3317–26.

  16. 16.

    Khadem Haghighian M, Alipoor B, Malek Mahdavi A, Eftekhar Sadat B, Asghari Jafarabadi M, Moghaddam A. Effects of sesame seed supplementation on inflammatory factors and oxidative stress biomarkers in patients with knee osteoarthritis. Acta Med Iran. 2015;53:207–13.

  17. 17.

    Saberi Hosnijeh F, Siebuhr AS, Uitterlinden AG, Oei EH, Hofman A, Karsdal MA, Bierma-Zeinstra SM, Bay-Jensen AC, van Meurs JB. Association between biomarkers of tissue inflammation and progression of osteoarthritis: evidence from the Rotterdam study cohort. Arthritis Res Ther. 2016;18:81.

  18. 18.

    Scorei R, Mitrut P, Petrisor I, Scorei I. A double-blind, placebo-controlled pilot study to evaluate the effect of calcium fructoborate on systemic inflammation and dyslipidemia markers for middle-aged people with primary osteoarthritis. Biol Trace Elem Res. 2011;144:253–63.

  19. 19.

    Sowers M, Jannausch M, Stein E, Jamadar D, Hochberg M, Lachance L. C-reactive protein as a biomarker of emergent osteoarthritis. Osteoarthr Cartil. 2002;10:595–601.

  20. 20.

    Stannus OP, Jones G, Blizzard L, Cicuttini FM, Ding C. Associations between serum levels of inflammatory markers and change in knee pain over 5 years in older adults: a prospective cohort study. Ann Rheum Dis. 2013;72:535–40.

  21. 21.

    Zhang Q, Li H, Zhang Z, Yang F, Chen J. Serum metabolites as potential biomarkers for diagnosis of knee osteoarthritis. Dis Markers. 2015;2015:684794.

  22. 22.

    Fernandes FA, Pucinelli ML, da Silva NP, Feldman D. Serum cartilage oligomeric matrix protein (COMP) levels in knee osteoarthritis in a Brazilian population: clinical and radiological correlation. Scand J Rheumatol. 2007;36:211–5.

  23. 23.

    Li H, Wang D, Wu ZQ, Zhong JM, Yuan YJ. Serum levels of cartilage oligomeric matrix protein in the diagnosis of knee osteoarthritis. Zhongguo Gu Shang. 2012;25:380–3.

  24. 24.

    Senolt L, Braun M, Olejarova M, Forejtova S, Gatterova J, Pavelka K. Increased pentosidine, an advanced glycation end product, in serum and synovial fluid from patients with knee osteoarthritis and its relation with cartilage oligomeric matrix protein. Ann Rheum Dis. 2005;64:886–90.

  25. 25.

    Wakitani S, Nawata M, Kawaguchi A, Okabe T, Takaoka K, Tsuchiya T, Nakaoka R, Masuda H, Miyazaki K. Serum keratan sulfate is a promising marker of early articular cartilage breakdown. Rheumatology (Oxford). 2007;46:1652–6.

  26. 26.

    Takahashi M, Naito K, Abe M, Sawada T, Nagano A. Relationship between radiographic grading of osteoarthritis and the biochemical markers for arthritis in knee osteoarthritis. Arthritis Res Ther. 2004;6:R208–12.

  27. 27.

    Hurter K, Spreng D, Rytz U, Schawalder P, Ott-Knusel F, Schmokel H. Measurements of C-reactive protein in serum and lactate dehydrogenase in serum and synovial fluid of patients with osteoarthritis. Vet J. 2005;169:281–5.

  28. 28.

    Zhang Y, Zeng C, Wei J, Li H, Yang T, Yang Y, Deng ZH, Ding X, Lei G. Associations of cigarette smoking, betel quid chewing and alcohol consumption with high-sensitivity C-reactive protein in early radiographic knee osteoarthritis: a cross-sectional study. BMJ Open. 2016;6:e010763.

  29. 29.

    Li H, Zeng C, Wei J, Yang T, Gao SG, Luo W, Li YS, Xiong YL, Xiao WF, Lei GH. Associations of dietary and serum magnesium with serum high-sensitivity C-reactive protein in early radiographic knee osteoarthritis patients. Mod Rheumatol. 2016:1–6.

  30. 30.

    Zhu Z, Jin X, Wang B, Wluka A, Antony B, Laslett LL, Winzenberg T, Cicuttini F, Jones G, Ding C. Cross-sectional and longitudinal associations between serum levels of high-sensitivity C-reactive protein, knee bone marrow lesions, and knee pain in patients with knee osteoarthritis. Arthritis Care Res (Hoboken). 2016;68:1471–7.

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I would like to thank Dr. Liu Shaolong for his valuable guidance in every stage of the writing of this thesis.

Also, I shall extend my thanks to Haiyuan Dong from General Office of Shanxi Medical Journal and Qianqian He from Shanxi Medical University for their kind help in the data extraction and quality assessment processes.


This study was sponsored by the National Natural Science Foundation of China (No. 81573245); Shanxi provincial health and Family Planning Commission projects (No. 2014169).

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All data generated or analysed during this study are included in this published article.

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Only ZJF conceived this study, participated in the experiments and finally wrote the paper. ZJF approved the final manuscript.

Correspondence to Junfeng Zhang.

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Zhang, J. Meta-analysis of serum C-reactive protein and cartilage oligomeric matrix protein levels as biomarkers for clinical knee osteoarthritis. BMC Musculoskelet Disord 19, 22 (2018) doi:10.1186/s12891-018-1932-y

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  • C-reactive protein
  • Knee osteoarthritis
  • Pain
  • Meta-analysis