Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, P.O. Box 85500, 3508 GA Utrecht, The Netherlands.
Arthritis Res Ther. 2011 May 8;13(3):R70. doi: 10.1186/ar3331.
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).
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.
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.
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.
本研究旨在探究 C2C、C1,2C、CS846 和 CPII 的血清生物标志物水平是否可预测类风湿关节炎(RA)发病早期疾病活动度和放射学进展的长期病程。
在 CAMERA 试验中,在基线和治疗 1 年后评估生物标志物水平。通过回归分析评估生物标志物值(变化)与 5 年内平均每年放射学进展率和平均疾病活动度之间的关系。通过多元线性回归分析评估生物标志物对长期结局的既定预测因素的附加预测价值。
在 133 例患者中,有 133 例患者可获得基线和治疗 1 年后的血清样本。在回归分析中,基线时的 C1,2C、C2C 的变化、C2C、C1,2C 的变化之和与平均每年放射学进展率呈统计学显著相关;CPII 的变化与 5 年治疗期间的平均疾病活动度相关。在多元线性回归分析中,只有 C1,2C 的变化对放射学进展具有附加的预测价值(P = 0.004)。放射学进展和疾病活动模型的解释方差较低(分别为 0.28 和 0.34),生物标志物仅略微提高了解释方差。
RA 发病后第一年 C1,2C 的变化对 5 年内疾病严重程度具有较小的附加预测价值,但该生物标志物与当前预测因素结合的预测价值太小,无法用于个体患者。