期刊论文详细信息
BMC Musculoskeletal Disorders
Early increase in serum-COMP is associated with joint damage progression over the first five years in patients with rheumatoid arthritis
Tore Saxne3  Dick Heinegård3  Kristina Forslind2  Kristina Albertsson4  Ingiäld Hafström4  Ingemar F Petersson3  Björn Svensson3  Maria L E Andersson1 
[1] R and D center, Spenshult Hospital, Oskarström, Sweden;Section of Rheumatology, Department of Internal medicine Helsingborgs Lasarett, Helsingborgs Lasarett, Helsingborg, Sweden;Department of Clinical Sciences, Lund, Section of Rheumatology, Lund University, Lund, Sweden;Department of Rheumatology, Karolinska Institutet, Karolinska University Hospital, Huddinge, Sweden
关键词: Radiographic joint damage progression;    Biomarkers;    Rheumatoid arthritis;    COMP;    Cartilage oligomeric matrix protein;   
Others  :  1130076
DOI  :  10.1186/1471-2474-14-229
 received in 2013-02-05, accepted in 2013-07-29,  发布年份 2013
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【 摘 要 】

Background

Currently available biomarkers for the early tissue process leading to joint damage in rheumatoid arthritis are insufficient and lack prognostic accuracy, possibly a result of variable activity of the disease over time. This study represents a novel approach to detect an altered activity of the disease process detected as increasing serum-COMP levels over a short time and whether this would correlate with joint damage progression over the first 5 years of disease.

Methods

In all, 349 patients from the Swedish BARFOT early RA study were examined. Serum-COMP was analysed by ELISA at diagnosis and after 3 months. Based on changes in serum-COMP levels, three subgroups of patients were defined: those with unchanged levels (change ≤ 20%) (N=142), decreasing levels (> 20%) (N=173) and increasing levels (> 20%) (N=34). Radiographs of hands and feet were obtained at inclusion, after 1, 2 and 5 years and scored according to Sharp van der Heijde (SHS). Radiographic progression was defined as increase in SHS by ≥5.8.

Results

The group of patients with increasing COMP levels showed higher median change in total SHS and erosion scores at 1, 2 and 5 year follow-up compared with the groups with stable or decreasing COMP levels. Furthermore, the odds ratio of radiographic progression was 2.8 (95% CI 1.26-6.38) for patients with increasing COMP levels vs. patients with unchanged levels.

The group of patients with increasing COMP levels had higher ESR at inclusion but there were no baseline differences between the groups for age, gender, disease duration, disease activity (DAS28), function (HAQ), CRP, nor presence of rheumatoid factor or anti-CCP. Importantly, neither did changes over the 3-month period in DAS28, HAQ, ESR nor CRP differ between the groups and these variables did not correlate to joint damage progression.

Conclusion

Increasing serum-COMP levels between diagnosis and the subsequent 3 months in patients with early RA represents a novel indicator of an activated destructive process in the joint and is a promising tool to identify patients with significant joint damage progression during a 5-year period.

【 授权许可】

   
2013 Andersson et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Katchamart W, Johnson S, Lin HJ, Phumethum V, Salliot C, Bombardier C: Predictors for remission in rheumatoid arthritis patients: A systematic review. Arthritis Care Res (Hoboken) 2010, 62:1128-1143.
  • [2]Scott DL, Smith C, Kingsley G: Joint damage and disability in rheumatoid arthritis: an updated systematic review. Clin Exp Rheumatol 2003, 21:S20-S27.
  • [3]Welsing PM, van Gestel AM, Swinkels HL, Kiemeney LA, van Riel PL: The relationship between disease activity, joint destruction, and functional capacity over the course of rheumatoid arthritis. Arthritis Rheum 2001, 44:2009-2017.
  • [4]Wick MC, Lindblad S, Klareskog L, Van Vollenhoven RF: Relationship between inflammation and joint destruction in early rheumatoid arthritis: a mathematical description. Ann Rheum Dis 2004, 63:848-852.
  • [5]Pincus T, Sokka T: Laboratory tests to assess patients with rheumatoid arthritis: advantages and limitations. Rheum Dis Clin North Am 2009, 35:731-734. vi-vii
  • [6]Pincus T, Yazici Y, Sokka T: Complexities in assessment of rheumatoid arthritis: absence of a single gold standard measure. Rheum Dis Clin North Am 2009, 35:687-697.
  • [7]Sokka T, Toloza S, Cutolo M, Kautiainen H, Makinen H, Gogus F, Skakic V, Badsha H, Peets T, Baranauskaite A, et al.: Women, men, and rheumatoid arthritis: analyses of disease activity, disease characteristics, and treatments in the QUEST-RA study. Arthritis Res Ther 2009, 11:R7.
  • [8]Schoels M, Bombardier C, Aletaha D: Diagnostic and prognostic value of antibodies and soluble biomarkers in undifferentiated peripheral inflammatory arthritis: a systematic review. J Rheumatol Suppl 2011, 87:20-25.
  • [9]Hedbom E, Antonsson P, Hjerpe A, Aeschlimann D, Paulsson M, Rosa-Pimentel E, Sommarin Y, Wendel M, Oldberg A, Heinegard D: Cartilage matrix proteins. An acidic oligomeric protein (COMP) detected only in cartilage. J Biol Chem 1992, 267:6132-6136.
  • [10]Saxne T, Heinegard D: Cartilage oligomeric matrix protein: a novel marker of cartilage turnover detectable in synovial fluid and blood. Br J Rheumatol 1992, 31:583-591.
  • [11]Larsson E, Erlandsson Harris H, Lorentzen JC, Larsson A, Mansson B, Klareskog L, Saxne T: Serum concentrations of cartilage oligomeric matrix protein, fibrinogen and hyaluronan distinguish inflammation and cartilage destruction in experimental arthritis in rats. Rheumatol (Oxford) 2002, 41:996-1000.
  • [12]Crnkic M, Mansson B, Larsson L, Geborek P, Heinegard D, Saxne T: Serum cartilage oligomeric matrix protein (COMP) decreases in rheumatoid arthritis patients treated with infliximab or etanercept. Arthritis Res Ther 2003, 5:R181-R185. BioMed Central Full Text
  • [13]de Jong Z, Munneke M, Vilim V, Zwinderman AH, Kroon HM, Ronday HK, Lems WF, Dijkmans BA, Breedveld FC, Vliet Vlieland TP, et al.: Value of serum cartilage oligomeric matrix protein as a prognostic marker of large-joint damage in rheumatoid arthritis–data from the RAPIT study. Rheumatol (Oxford) 2008, 47:868-871.
  • [14]Lindqvist E, Eberhardt K, Bendtzen K, Heinegard D, Saxne T: Prognostic laboratory markers of joint damage in rheumatoid arthritis. Ann Rheum Dis 2005, 64:196-201.
  • [15]Mansson B, Carey D, Alini M, Ionescu M, Rosenberg LC, Poole AR, Heinegard D, Saxne T: Cartilage and bone metabolism in rheumatoid arthritis. Differences between rapid and slow progression of disease identified by serum markers of cartilage metabolism. J Clin Invest 1995, 95:1071-1077.
  • [16]Morozzi G, Fabbroni M, Bellisai F, Pucci G, Galeazzi M: Cartilage oligomeric matrix protein level in rheumatic diseases: potential use as a marker for measuring articular cartilage damage and/or the therapeutic efficacy of treatments. Ann N Y Acad Sci 2007, 1108:398-407.
  • [17]Sharif M, Saxne T, Shepstone L, Kirwan JR, Elson CJ, Heinegard D, Dieppe PA: Relationship between serum cartilage oligomeric matrix protein levels and disease progression in osteoarthritis of the knee joint. Br J Rheumatol 1995, 34:306-310.
  • [18]Bruyere O, Collette JH, Ethgen O, Rovati LC, Giacovelli G, Henrotin YE, Seidel L, Reginster JY: Biochemical markers of bone and cartilage remodeling in prediction of longterm progression of knee osteoarthritis. J Rheumatol 2003, 30:1043-1050.
  • [19]Fex E, Eberhardt K, Saxne T: Tissue-derived macromolecules and markers of inflammation in serum in early rheumatoid arthritis: relationship to development of joint destruction in hands and feet. Br J Rheumatol 1997, 36:1161-1165.
  • [20]Syversen SW, Goll GL, van der Heijde D, Landewe R, Gaarder PI, Odegard S, Haavardsholm EA, Kvien TK: Cartilage and bone biomarkers in rheumatoid arthritis: prediction of 10-year radiographic progression. J Rheumatol 2009, 36:266-272.
  • [21]Conrozier T, Saxne T, Fan CS, Mathieu P, Tron AM, Heinegard D, Vignon E: Serum concentrations of cartilage oligomeric matrix protein and bone sialoprotein in hip osteoarthritis: a one year prospective study. Ann Rheum Dis 1998, 57:527-532.
  • [22]Georges C, Vigneron H, Ayral X, Listrat V, Ravaud P, Dougados M, Sharif M, Dieppe P, Saxne T: Serum biologic markers as predictors of disease progression in osteoarthritis of the knee. Arthritis Rheum 1997, 40:590-591.
  • [23]Petersson IF, Boegard T, Svensson B, Heinegard D, Saxne T: Changes in cartilage and bone metabolism identified by serum markers in early osteoarthritis of the knee joint. Br J Rheumatol 1998, 37:46-50.
  • [24]Williams FM, Andrew T, Saxne T, Heinegard D, Spector TD, MacGregor AJ: The heritable determinants of cartilage oligomeric matrix protein. Arthritis Rheum 2006, 54:2147-2151.
  • [25]Arnett FC, Edworthy SM, Bloch DA, McShane DJ, Fries JF, Cooper NS, Healey LA, Kaplan SR, Liang MH, Luthra HS, et al.: The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum 1988, 31:315-324.
  • [26]Svensson B, Schaufelberger C, Teleman A, Theander J: Remission and response to early treatment of RA assessed by the Disease Activity Score. BARFOT study group. Better Anti-rheumatic Farmacotherapy. Rheumatol (Oxford) 2000, 39:1031-1036.
  • [27]Prevoo ML, Hof MA V 't, Kuper HH, Van Leeuwen MA, Van de Putte LB, Van Riel PL: Modified disease activity scores that include twenty-eight-joint counts. Development and validation in a prospective longitudinal study of patients with rheumatoid arthritis. Arthritis Rheum 1995, 38:44-48.
  • [28]Fransen J, van Riel PL: DAS remission cut points. Clin Exp Rheumatol 2006, 24:29-32.
  • [29]Landewe R, van der Heijde D, van der Linden S, Boers M: Twenty-eight-joint counts invalidate the DAS28 remission definition owing to the omission of the lower extremity joints: a comparison with the original DAS remission. Ann Rheum Dis 2006, 65:637-641.
  • [30]Felson DT, Smolen JS, Wells G, Zhang B, van Tuyl LH, Funovits J, Aletaha D, Allaart CF, Bathon J, Bombardieri S, et al.: American college of rheumatology/european league against rheumatism provisional definition of remission in rheumatoid arthritis for clinical trials. Ann Rheum Dis 2011, 70:404-413.
  • [31]Ekdahl C, Eberhardt K, Andersson SI, Svensson B: Assessing disability in patients with rheumatoid arthritis. Use of a Swedish version of the Stanford Health Assessment Questionnaire. Scand J Rheumatol 1988, 17:263-271.
  • [32]Brescia V, Tampoia M: Biological variation of Cartilage Oligomeric Matrix Protein (COMP): A proposal to interpret laboratory serial testing. Clin Chim Acta 2007.
  • [33]Ricos C, Alvarez V, Cava F, Garcia-Lario JV, Hernandez A, Jimenez CV, Minchinela J, Perich C, Simon M: Integration of data derived from biological variation into the quality management system. Clin Chim Acta 2004, 346:13-18.
  • [34]Ricos C, Cava F, Garcia-Lario JV, Hernandez A, Iglesias N, Jimenez CV, Minchinela J, Perich C, Simon M, Domenech MV, Alvarez V: The reference change value: a proposal to interpret laboratory reports in serial testing based on biological variation. Scand J Clin Lab Invest 2004, 64:175-184.
  • [35]Ricos C, Iglesias N, Garcia-Lario JV, Simon M, Cava F, Hernandez A, Perich C, Minchinela J, Alvarez V, Domenech MV, et al.: Within-subject biological variation in disease: collated data and clinical consequences. Ann Clin Biochem 2007, 44:343-352.
  • [36]van der Heijde D: How to read radiographs according to the Sharp/van der Heijde method. J Rheumatol 2000, 27:261-263.
  • [37]Svensson B, Boonen A, Albertsson K, van der Heijde D, Keller C, Hafstrom I: Low-dose prednisolone in addition to the initial disease-modifying antirheumatic drug in patients with early active rheumatoid arthritis reduces joint destruction and increases the remission rate: a two-year randomized trial. Arthritis Rheum 2005, 52:3360-3370.
  • [38]Hetland ML, Stengaard-Pedersen K, Junker P, Ostergaard M, Ejbjerg BJ, Jacobsen S, Lottenburger T, Hansen I, Tarp U, Andersen LS, et al.: Radiographic progression and remission rates in early rheumatoid arthritis - MRI bone oedema and anti-CCP predicted radiographic progression in the 5-year extension of the double-blind randomised CIMESTRA trial. Ann Rheum Dis 2010, 69:1789-1795.
  • [39]Heinegard D: Proteoglycans and more–from molecules to biology. Int J Exp Pathol 2009, 90:575-586.
  • [40]Smolen JS, van der Heijde DM, Aletaha D, Xu S, Han J, Baker D, St Clair EW: Progression of radiographic joint damage in rheumatoid arthritis: independence of erosions and joint space narrowing. Ann Rheum Dis 2009, 68:1535-1540.
  • [41]Graudal N, Tarp U, Jurik AG, Galloe AM, Garred P, Milman N, Graudal HK: Inflammatory patterns in rheumatoid arthritis estimated by the number of swollen and tender joints, the erythrocyte sedimentation rate, and hemoglobin: longterm course and association to radiographic progression. J Rheumatol 2000, 27:47-57.
  • [42]Plant MJ, Williams AL, O'Sullivan MM, Lewis PA, Coles EC, Jessop JD: Relationship between time-integrated C-reactive protein levels and radiologic progression in patients with rheumatoid arthritis. Arthritis Rheum 2000, 43:1473-1477.
  • [43]Hafstrom I, Albertsson K, Boonen A, van der Heijde D, Landewe R, Svensson B: Remission achieved after 2 years treatment with low-dose prednisolone in addition to disease-modifying anti-rheumatic drugs in early rheumatoid arthritis is associated with reduced joint destruction still present after 4 years: an open 2-year continuation study. Ann Rheum Dis 2009, 68:508-513.
  • [44]Larsson E, Erlandsson Harris H, Larsson A, Mansson B, Saxne T, Klareskog L: Corticosteroid treatment of experimental arthritis retards cartilage destruction as determined by histology and serum COMP. Rheumatol (Oxford) 2004, 43:428-434.
  • [45]Skoumal M, Haberhauer G, Feyertag J, Kittl EM, Bauer K, Dunky A: Serum levels of cartilage oligomeric matrix protein (COMP): a rapid decrease in patients with active rheumatoid arthritis undergoing intravenous steroid treatment. Rheumatol Int 2006, 26:1001-1004.
  • [46]Weitoft T, Larsson A, Saxne T, Ronnblom L: Changes of cartilage and bone markers after intra-articular glucocorticoid treatment with and without postinjection rest in patients with rheumatoid arthritis. Ann Rheum Dis 2005, 64:1750-1753.
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