2022
DOI: 10.1016/j.joca.2021.12.014
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Subchondral bone changes after joint distraction treatment for end stage knee osteoarthritis

Abstract: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article. Please note that, during the production process, errors may be discovered which could affect the content, a… Show more

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Cited by 13 publications
(10 citation statements)
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“…6 Knee osteoarthritis is a chronic progressive joint disorder involving the joint pain, swelling, deformity, muscle atrophy, and synovium, and tends to occur in middle-aged and elderly people; it is the most common kind of disabling arthritis. 12 Typical pathological modifications in OA include articular cartilage damage, abnormal subchondral bone remodeling and muscle loss. 13 Therefore, preventing joint destruction is essential for OA therapy.…”
Section: Discussionmentioning
confidence: 99%
“…6 Knee osteoarthritis is a chronic progressive joint disorder involving the joint pain, swelling, deformity, muscle atrophy, and synovium, and tends to occur in middle-aged and elderly people; it is the most common kind of disabling arthritis. 12 Typical pathological modifications in OA include articular cartilage damage, abnormal subchondral bone remodeling and muscle loss. 13 Therefore, preventing joint destruction is essential for OA therapy.…”
Section: Discussionmentioning
confidence: 99%
“…OA is a degenerative disease characterized by progressive cartilage loss and bone deterioration [ 86 ], whereas RA is a systemic, persistent inflammatory condition driven by an autoimmune response to stimuli in the environment mainly affecting the synovial joints [ 87 ]. Rapid loss of articular cartilage, degradation of collagen and proteoglycans, upregulation of matrix metalloproteinases—leukotrienes (particularly leukotriene B4)—and thickening of the subchondral plate are the main contributors to the OA and RA [ 88 , 89 , 90 , 91 , 92 , 93 , 94 ]. A study by Yamada et al reported that MMP-1, MMP-3, matrix degradation, and IL-1α-induced release of proteoglycans in cartilages of osteoarthritic rats was inhibited with esculetin treatment (10–100 µM) [ 95 ].…”
Section: Therapeutic Applications Of Esculetinmentioning
confidence: 99%
“…OA is a degenerative disease characterized by progressive cartilage loss and bone deterioration [64] whereas rheumatoid arthritis is a systemic, persistent inflammatory condition driven by an autoimmune response to stimuli in the environment mainly affecting the synovial joints [65]. Rapid loss of articular cartilage, degradation of collagen and proteoglycans, upregulation of matrix metalloproteinases, leukotrienes (particularly leukotriene B4), and thickening of the subchondral plate are the main contributors to the OA and RA [66][67][68][69][70][71][72]. Various studies have reported that esculetin acts on cartilage and results in the inhibition of matrix degradation by suppressing the MMP production, secretion, and its activity in rabbit joint cartilage, which serves as a lead therapeutic compound in the treatment of OA and RA [73,74].…”
Section: Esculetin In Arthritismentioning
confidence: 99%