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The relation between cartilage biomarkers (C2C, C1,2C, CS846, and CPII) and the long-term outcome of rheumatoid arthritis patients within the CAMERA trial

  • Marije F. Bakker
  • , Suzanne M. M. Verstappen
  • , Paco M. J. Welsing
  • , Johannes W. G. Jacobs
  • , Zalima N. Jahangier
  • , Maaike J. van der Veen
  • , Johannes W. J. Bijlsma
  • , Floris P. J. G. Lafeber
  • University Medical Center Utrecht
  • Department of Paediatrics, Tergooi Hospital, Blaricum, The Netherlands
  • Department of Medical Microbiology, St Jansdal Hospital, Harderwijk, The Netherlands

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Introduction: The aim of this study was to investigate whether serum biomarker levels of C2C, C1,2C, CS846, and CPII can predict the long-term course of disease activity and radiographic progression early in the disease course of rheumatoid arthritis (RA).Methods: In patients in the CAMERA trial, levels of biomarkers were evaluated at baseline and after 1 year of treatment. Relations of (changes in) biomarker values with the mean yearly radiographic progression rate and mean disease activity over a 5-year period were evaluated by using regression analysis. The added predictive value of biomarkers over established predictors for long-term outcome was analyzed by multiple linear regression analysis.Results: Of 133 patients, serum samples were available at baseline and after 1 year of treatment. In the regression analysis C1,2C at baseline, the change in C2C, C1,2C, and the sum of the standardized changes in C2C + C1,2C scores were statistically significantly associated with the mean yearly radiographic progression rate; the change in CPII was associated with the mean disease activity over 5 years of treatment. In the multiple linear regression analysis, only the change in C1,2C was of added predictive value (P = 0.004) for radiographic progression. Explained variances of models for radiographic progression and disease activity were low (0.28 and 0.34, respectively), and the biomarkers only marginally improved the explained variance.Conclusions: The change in C1,2C in the first year after onset of RA has a small added predictive value for disease severity over a 5-year period, but the predictive value of this biomarker combined with current predictive factors is too small to be of use for individual patients. © 2011 Bakker et al.; licensee BioMed Central Ltd.
Original languageEnglish
Article numberR70
JournalArthritis Research and Therapy
Volume13
Issue number3
DOIs
Publication statusPublished - 8 May 2011
Externally publishedYes

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