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Value of biomarkers in osteoarthritis: current status and perspectives

Osteoarthritis affects the whole joint structure with progressive changes in cartilage, menisci, ligaments and subchondral bone, and synovial inflammation. Biomarkers are being developed to quantify joint remodelling and disease progression. This article was prepared following a working meeting of t...

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Autores principales: Lotz, M, Martel-Pelletier, J, Christiansen, C, Brandi, M-L, Bruyère, O, Chapurlat, R, Collette, J, Cooper, C, Giacovelli, G, Kanis, J A, Karsdal, M A, Kraus, V, Lems, W F, Meulenbelt, I, Pelletier, J-P, Raynauld, J-P, Reiter-Niesert, S, Rizzoli, R, Sandell, L J, Van Spil, W E, Reginster, J-Y
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812859/
https://www.ncbi.nlm.nih.gov/pubmed/23897772
http://dx.doi.org/10.1136/annrheumdis-2013-203726
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author Lotz, M
Martel-Pelletier, J
Christiansen, C
Brandi, M-L
Bruyère, O
Chapurlat, R
Collette, J
Cooper, C
Giacovelli, G
Kanis, J A
Karsdal, M A
Kraus, V
Lems, W F
Meulenbelt, I
Pelletier, J-P
Raynauld, J-P
Reiter-Niesert, S
Rizzoli, R
Sandell, L J
Van Spil, W E
Reginster, J-Y
author_facet Lotz, M
Martel-Pelletier, J
Christiansen, C
Brandi, M-L
Bruyère, O
Chapurlat, R
Collette, J
Cooper, C
Giacovelli, G
Kanis, J A
Karsdal, M A
Kraus, V
Lems, W F
Meulenbelt, I
Pelletier, J-P
Raynauld, J-P
Reiter-Niesert, S
Rizzoli, R
Sandell, L J
Van Spil, W E
Reginster, J-Y
author_sort Lotz, M
collection PubMed
description Osteoarthritis affects the whole joint structure with progressive changes in cartilage, menisci, ligaments and subchondral bone, and synovial inflammation. Biomarkers are being developed to quantify joint remodelling and disease progression. This article was prepared following a working meeting of the European Society for Clinical and Economic Aspects of Osteoporosis and Osteoarthritis convened to discuss the value of biochemical markers of matrix metabolism in drug development in osteoarthritis. The best candidates are generally molecules or molecular fragments present in cartilage, bone or synovium and may be specific to one type of joint tissue or common to them all. Many currently investigated biomarkers are associated with collagen metabolism in cartilage or bone, or aggrecan metabolism in cartilage. Other biomarkers are related to non-collagenous proteins, inflammation and/or fibrosis. Biomarkers in osteoarthritis can be categorised using the burden of disease, investigative, prognostic, efficacy of intervention, diagnostic and safety classification. There are a number of promising candidates, notably urinary C-terminal telopeptide of collagen type II and serum cartilage oligomeric protein, although none is sufficiently discriminating to differentiate between individual patients and controls (diagnostic) or between patients with different disease severities (burden of disease), predict prognosis in individuals with or without osteoarthritis (prognostic) or perform so consistently that it could function as a surrogate outcome in clinical trials (efficacy of intervention). Future avenues for research include exploration of underlying mechanisms of disease and development of new biomarkers; technological development; the ‘omics’ (genomics, metabolomics, proteomics and lipidomics); design of aggregate scores combining a panel of biomarkers and/or imaging markers into single diagnostic algorithms; and investigation into the relationship between biomarkers and prognosis.
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spelling pubmed-38128592013-10-31 Value of biomarkers in osteoarthritis: current status and perspectives Lotz, M Martel-Pelletier, J Christiansen, C Brandi, M-L Bruyère, O Chapurlat, R Collette, J Cooper, C Giacovelli, G Kanis, J A Karsdal, M A Kraus, V Lems, W F Meulenbelt, I Pelletier, J-P Raynauld, J-P Reiter-Niesert, S Rizzoli, R Sandell, L J Van Spil, W E Reginster, J-Y Ann Rheum Dis Review Osteoarthritis affects the whole joint structure with progressive changes in cartilage, menisci, ligaments and subchondral bone, and synovial inflammation. Biomarkers are being developed to quantify joint remodelling and disease progression. This article was prepared following a working meeting of the European Society for Clinical and Economic Aspects of Osteoporosis and Osteoarthritis convened to discuss the value of biochemical markers of matrix metabolism in drug development in osteoarthritis. The best candidates are generally molecules or molecular fragments present in cartilage, bone or synovium and may be specific to one type of joint tissue or common to them all. Many currently investigated biomarkers are associated with collagen metabolism in cartilage or bone, or aggrecan metabolism in cartilage. Other biomarkers are related to non-collagenous proteins, inflammation and/or fibrosis. Biomarkers in osteoarthritis can be categorised using the burden of disease, investigative, prognostic, efficacy of intervention, diagnostic and safety classification. There are a number of promising candidates, notably urinary C-terminal telopeptide of collagen type II and serum cartilage oligomeric protein, although none is sufficiently discriminating to differentiate between individual patients and controls (diagnostic) or between patients with different disease severities (burden of disease), predict prognosis in individuals with or without osteoarthritis (prognostic) or perform so consistently that it could function as a surrogate outcome in clinical trials (efficacy of intervention). Future avenues for research include exploration of underlying mechanisms of disease and development of new biomarkers; technological development; the ‘omics’ (genomics, metabolomics, proteomics and lipidomics); design of aggregate scores combining a panel of biomarkers and/or imaging markers into single diagnostic algorithms; and investigation into the relationship between biomarkers and prognosis. BMJ Publishing Group 2013-11 2013-07-29 /pmc/articles/PMC3812859/ /pubmed/23897772 http://dx.doi.org/10.1136/annrheumdis-2013-203726 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Review
Lotz, M
Martel-Pelletier, J
Christiansen, C
Brandi, M-L
Bruyère, O
Chapurlat, R
Collette, J
Cooper, C
Giacovelli, G
Kanis, J A
Karsdal, M A
Kraus, V
Lems, W F
Meulenbelt, I
Pelletier, J-P
Raynauld, J-P
Reiter-Niesert, S
Rizzoli, R
Sandell, L J
Van Spil, W E
Reginster, J-Y
Value of biomarkers in osteoarthritis: current status and perspectives
title Value of biomarkers in osteoarthritis: current status and perspectives
title_full Value of biomarkers in osteoarthritis: current status and perspectives
title_fullStr Value of biomarkers in osteoarthritis: current status and perspectives
title_full_unstemmed Value of biomarkers in osteoarthritis: current status and perspectives
title_short Value of biomarkers in osteoarthritis: current status and perspectives
title_sort value of biomarkers in osteoarthritis: current status and perspectives
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812859/
https://www.ncbi.nlm.nih.gov/pubmed/23897772
http://dx.doi.org/10.1136/annrheumdis-2013-203726
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