New therapeutic targets for osteoarthritis pain

Osteoarthritis (OA), the most common form of arthritis, causes pain and disability, as well as emotional distress. While total joint replacement is one of the most effective treatments available for improving the quality of life in people with severe OA, it is not suitable for all patients and all j...

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Main Authors: Walsh, David A., Stocks, Joanne
Format: Article
Published: Sage 2017
Subjects:
Online Access:https://eprints.nottingham.ac.uk/51924/
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author Walsh, David A.
Stocks, Joanne
author_facet Walsh, David A.
Stocks, Joanne
author_sort Walsh, David A.
building Nottingham Research Data Repository
collection Online Access
description Osteoarthritis (OA), the most common form of arthritis, causes pain and disability, as well as emotional distress. While total joint replacement is one of the most effective treatments available for improving the quality of life in people with severe OA, it is not suitable for all patients and all joints. Current pharmacological analgesics have limited efficacy, and their use is often restricted by adverse events. Medications that might reduce pain by slowing or preventing structural disease remain elusive. Our increasing understanding of the complex mechanisms that underlie OA pain offers a wide range of potential new treatment targets. New drugs for OA pain might come from repurposing those developed for other conditions, as well as novel compounds targeting pain mechanisms specific to the joint. Here we discuss the mechanisms of OA pain and its therapeutic implications. We explore evolving treatment modalities, including combination treatment. We review recent research and patents pointing to future OA therapies. We discuss the potential for biomarkers to facilitate drug development and targeting.
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spelling nottingham-519242020-05-04T18:49:12Z https://eprints.nottingham.ac.uk/51924/ New therapeutic targets for osteoarthritis pain Walsh, David A. Stocks, Joanne Osteoarthritis (OA), the most common form of arthritis, causes pain and disability, as well as emotional distress. While total joint replacement is one of the most effective treatments available for improving the quality of life in people with severe OA, it is not suitable for all patients and all joints. Current pharmacological analgesics have limited efficacy, and their use is often restricted by adverse events. Medications that might reduce pain by slowing or preventing structural disease remain elusive. Our increasing understanding of the complex mechanisms that underlie OA pain offers a wide range of potential new treatment targets. New drugs for OA pain might come from repurposing those developed for other conditions, as well as novel compounds targeting pain mechanisms specific to the joint. Here we discuss the mechanisms of OA pain and its therapeutic implications. We explore evolving treatment modalities, including combination treatment. We review recent research and patents pointing to future OA therapies. We discuss the potential for biomarkers to facilitate drug development and targeting. Sage 2017-06-06 Article PeerReviewed Walsh, David A. and Stocks, Joanne (2017) New therapeutic targets for osteoarthritis pain. Slas Discovery, 22 (8). pp. 931-949. ISSN 2472-5552 osteoarthritis pain inflammation osteoclasts peripheral sensitization central sensitizatio http://journals.sagepub.com/doi/10.1177/2472555217716912 doi:10.1177/2472555217716912 doi:10.1177/2472555217716912
spellingShingle osteoarthritis
pain
inflammation
osteoclasts
peripheral sensitization
central sensitizatio
Walsh, David A.
Stocks, Joanne
New therapeutic targets for osteoarthritis pain
title New therapeutic targets for osteoarthritis pain
title_full New therapeutic targets for osteoarthritis pain
title_fullStr New therapeutic targets for osteoarthritis pain
title_full_unstemmed New therapeutic targets for osteoarthritis pain
title_short New therapeutic targets for osteoarthritis pain
title_sort new therapeutic targets for osteoarthritis pain
topic osteoarthritis
pain
inflammation
osteoclasts
peripheral sensitization
central sensitizatio
url https://eprints.nottingham.ac.uk/51924/
https://eprints.nottingham.ac.uk/51924/
https://eprints.nottingham.ac.uk/51924/