The study of biomarkers in spondyloarthroparhy (SpA) has emerged to be a very important field of research. This is particularly because the two commonly used biomarkers, erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP), are of very low sensitivity and specificity. The second reason is, with advances in the treatment of SpA by the very expensive tumor necrosis factor-α (TNF-α) blockers, for cost-effectiveness, clinicians need to be much more accurate in predicting disease progression, evaluating disease activity and monitoring therapeutic efficacy. This review focuses on several biomarkers of promise: matrix metalloproteinases 3 (MMP-3), Type II collagen neoepitope (C2C and C1-2C), C-propeptide of Type II collagen (CPII), aggrecan 846 epitope, macrophage colony stimulating factor (M-CSF), serum amyloid A (SAA) and Interleukin-6 (IL-6). The results summarized in Table 1 call for a co-ordinated effort for systematic studies of existing biomarkers and for search for new candidates. © 2009 Landes Bioscience and Springer Science+Business Media.
CITATION STYLE
Chen, C. H., Yu, D. T. Y., & Chou, C. T. (2009). Biomarkers in spondyloarthropathies. Advances in Experimental Medicine and Biology, 649, 122–132. https://doi.org/10.1007/978-1-4419-0298-6_9
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