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The Future of Osteoarthritis Therapeutics: Targeted Pharmacological Therapy

Osteoarthritis (OA) is one of the most common forms of degenerative joint disease and a major cause of pain and disability affecting the aging population. It is estimated that more than 20 million Americans and 35 to 40 million Europeans suffer from OA. Analgesics and non-steroidal anti-inflammatory...

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Autor principal: Mobasheri, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789888/
https://www.ncbi.nlm.nih.gov/pubmed/24061701
http://dx.doi.org/10.1007/s11926-013-0364-9
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author Mobasheri, A.
author_facet Mobasheri, A.
author_sort Mobasheri, A.
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description Osteoarthritis (OA) is one of the most common forms of degenerative joint disease and a major cause of pain and disability affecting the aging population. It is estimated that more than 20 million Americans and 35 to 40 million Europeans suffer from OA. Analgesics and non-steroidal anti-inflammatory drugs (NSAIDs) are the only therapeutic treatment options for OA. Effective pharmacotherapy for OA, capable of restoring the original structure and function of damaged cartilage and other synovial tissue, is urgently needed, and research into such disease-modifying osteoarthritis drugs (DMOADs) is in progress. This is the first of three reviews focusing on OA therapeutics. This paper provides an overview of current research into potential structure-modifying drugs and more appropriately targeted pharmacological therapy. The challenges and opportunities in this area of research and development are reviewed, covering the most up-to-date initiatives, trends, and topics.
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spelling pubmed-37898882013-10-04 The Future of Osteoarthritis Therapeutics: Targeted Pharmacological Therapy Mobasheri, A. Curr Rheumatol Rep Osteoarthritis (Mb Goldring, Section Editor) Osteoarthritis (OA) is one of the most common forms of degenerative joint disease and a major cause of pain and disability affecting the aging population. It is estimated that more than 20 million Americans and 35 to 40 million Europeans suffer from OA. Analgesics and non-steroidal anti-inflammatory drugs (NSAIDs) are the only therapeutic treatment options for OA. Effective pharmacotherapy for OA, capable of restoring the original structure and function of damaged cartilage and other synovial tissue, is urgently needed, and research into such disease-modifying osteoarthritis drugs (DMOADs) is in progress. This is the first of three reviews focusing on OA therapeutics. This paper provides an overview of current research into potential structure-modifying drugs and more appropriately targeted pharmacological therapy. The challenges and opportunities in this area of research and development are reviewed, covering the most up-to-date initiatives, trends, and topics. Springer US 2013-09-24 2013 /pmc/articles/PMC3789888/ /pubmed/24061701 http://dx.doi.org/10.1007/s11926-013-0364-9 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Osteoarthritis (Mb Goldring, Section Editor)
Mobasheri, A.
The Future of Osteoarthritis Therapeutics: Targeted Pharmacological Therapy
title The Future of Osteoarthritis Therapeutics: Targeted Pharmacological Therapy
title_full The Future of Osteoarthritis Therapeutics: Targeted Pharmacological Therapy
title_fullStr The Future of Osteoarthritis Therapeutics: Targeted Pharmacological Therapy
title_full_unstemmed The Future of Osteoarthritis Therapeutics: Targeted Pharmacological Therapy
title_short The Future of Osteoarthritis Therapeutics: Targeted Pharmacological Therapy
title_sort future of osteoarthritis therapeutics: targeted pharmacological therapy
topic Osteoarthritis (Mb Goldring, Section Editor)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789888/
https://www.ncbi.nlm.nih.gov/pubmed/24061701
http://dx.doi.org/10.1007/s11926-013-0364-9
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