Osteoarthritis year 2012 in review: biomarkers

被引:130
作者
Mobasheri, A. [1 ]
机构
[1] Univ Nottingham, Fac Med & Hlth Sci, Sch Vet Med & Sci, Musculoskeletal Res Group, Loughborough LE12 5RD, England
基金
英国国家替代、减少和改良动物研究中心; 英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会; 英国惠康基金;
关键词
Osteoarthritis; Articular cartilage; Synovium; Inflammation; Biomarker; Biochemical marker; Proteomics; Complement; Chemotactic proteins; Adipokines; OLIGOMERIC MATRIX PROTEIN; FOLLISTATIN-LIKE PROTEIN-1; MEMBRANE ATTACK COMPLEX; BIOCHEMICAL MARKERS; RHEUMATOID-ARTHRITIS; KNEE OSTEOARTHRITIS; SYNOVIAL-FLUID; EXTRACELLULAR-MATRIX; RADIOGRAPHIC SEVERITY; INCREASED EXPRESSION;
D O I
10.1016/j.joca.2012.07.009
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
Purpose: Biomarkers provide useful diagnostic information by detecting cartilage degradation in osteoarthritis (OA), reflecting disease-relevant biological activity and predicting the course of disease progression. They also serve as surrogate endpoints in the drug discovery process. The aim of this narrative review was to focus on OA biomarker-related papers published between the osteoarthritis research society international (OARSI) 2011 meeting in San Diego and the OARS! 2012 meeting in Barcelona. Methods: The PubMed/MEDLINE and SciVerse Scopus bibliographic databases were searched using the keywords: 'biomarker' and 'osteoarthritis' and/or biomarker and 'proteomics'. Results: Ninety-eight papers were found with the keywords 'biomarker' and 'osteoarthritis'. Fifteen papers were found with the keywords 'biomarker' and 'proteomics'. Review articles were also included. The most relevant published studies focused on extracellular matrix (ECM) molecules in body fluids. Enrichment of the deamidated epitope of cartilage oligomeric matrix protein (D-COMP) suggests that OA disease progression is associated with post-translational modifications that may show specificity for particular joint sites. Fibulin-3 peptides (Fib3-1 and Fib3-2) have been proposed as potential biomarkers of OA along with follistatin-like protein 1 (FSTL1), a new serum biomarker with the capacity to reflect the severity of joint damage. The 'membrane attack complex' (MAC) component of complement has also been implicated in OA. Conclusion: Novel OA biomarkers are needed for sub-clinical disease diagnosis. Proteomic techniques are beginning to yield useful data and deliver new OA biomarkers in serum and urine. Combining biochemical markers with tissue and cell imaging techniques and bioinformatics (i.e., machine learning, clustering, data visualization) may facilitate the development of biomarker combinations enabling earlier detection of OA. (C) 2012 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1451 / 1464
页数:14
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