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Article: Bone turnover and articular cartilage differences localized to subchondral cysts in knees with advanced osteoarthritis

TitleBone turnover and articular cartilage differences localized to subchondral cysts in knees with advanced osteoarthritis
Authors
KeywordsArticular cartilage
Bone remodeling
Bone structure
Osteoarthritis
Subchondral bone cyst
Issue Date2015
PublisherWB Saunders Co Ltd. The Journal's web site is located at http://www.elsevier.com/locate/joca
Citation
Osteoarthritis and Cartilage, 2015, v. 23 n. 12, p. 2174-2183 How to Cite?
AbstractObjective: To investigate changes in bone structure, turnover, and articular cartilage localized in subchondral bone cyst (SBC) regions associated with knee osteoarthritis (OA). Methods: Tibial plateaus (n ¼ 97) were collected from knee OA patients during total knee arthroplasty (TKA). SBCs were identified using micro-computed tomography, and the specimens were divided into non-cyst (n ¼ 25) and bone cyst (n ¼ 72) groups. Microstructure of subchondral bone was assessed using bone volume fraction (BV/TV), trabecular number (Tb.N), structure model index (SMI) and bone mineral density (BMD). In bone cyst group, the cyst subregion, which contained at least one cyst, and the pericyst subregion, which contained no cysts, were further selected for microstructure analysis. Articular cartilage damage was estimated using the Osteoarthritis Research Society International (OARSI) score. The numbers of TRAPþ osteoclasts, Osterixþ osteoprogenitors, Osteocalcinþ osteoblasts and expression of SOX9 were evaluated by immunohistochemistry. Results: Bone cyst group presented higher BV/TV, Tb.N and SMI at subchondral bone than non-cyst group. Furthermore, cyst subregion displayed increased BV/TV and Tb.N but lower BMD and SMI than peri-cyst subregion. Histology revealed a higher OARSI score in bone cyst group. SBC exhibited a weak relationship with BV/TV, etc. The numbers of TRAPþ osteoclasts, Osterixþ osteoprogenitors, Osteocalcinþ osteoblasts and expression of SOX9, were higher in bone cyst group. Conclusion: SBCs within knee OA are characterized by focally increased bone turnover, altered bone structure and more severe articular cartilage damage. The increased bone turnover possibly contributes to altered bone structure localized in SBC areas, and thus aggravates articular cartilage degeneration. © 2015 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/231201
ISSN
2021 Impact Factor: 7.507
2020 SCImago Journal Rankings: 1.974
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChen, Y-
dc.contributor.authorWang, T-
dc.contributor.authorGuan, M-
dc.contributor.authorZhao, W-
dc.contributor.authorLeung, FKL-
dc.contributor.authorPan, H-
dc.contributor.authorCao, X-
dc.contributor.authorGuo, XE-
dc.contributor.authorLu, WW-
dc.date.accessioned2016-09-20T05:21:23Z-
dc.date.available2016-09-20T05:21:23Z-
dc.date.issued2015-
dc.identifier.citationOsteoarthritis and Cartilage, 2015, v. 23 n. 12, p. 2174-2183-
dc.identifier.issn1063-4584-
dc.identifier.urihttp://hdl.handle.net/10722/231201-
dc.description.abstractObjective: To investigate changes in bone structure, turnover, and articular cartilage localized in subchondral bone cyst (SBC) regions associated with knee osteoarthritis (OA). Methods: Tibial plateaus (n ¼ 97) were collected from knee OA patients during total knee arthroplasty (TKA). SBCs were identified using micro-computed tomography, and the specimens were divided into non-cyst (n ¼ 25) and bone cyst (n ¼ 72) groups. Microstructure of subchondral bone was assessed using bone volume fraction (BV/TV), trabecular number (Tb.N), structure model index (SMI) and bone mineral density (BMD). In bone cyst group, the cyst subregion, which contained at least one cyst, and the pericyst subregion, which contained no cysts, were further selected for microstructure analysis. Articular cartilage damage was estimated using the Osteoarthritis Research Society International (OARSI) score. The numbers of TRAPþ osteoclasts, Osterixþ osteoprogenitors, Osteocalcinþ osteoblasts and expression of SOX9 were evaluated by immunohistochemistry. Results: Bone cyst group presented higher BV/TV, Tb.N and SMI at subchondral bone than non-cyst group. Furthermore, cyst subregion displayed increased BV/TV and Tb.N but lower BMD and SMI than peri-cyst subregion. Histology revealed a higher OARSI score in bone cyst group. SBC exhibited a weak relationship with BV/TV, etc. The numbers of TRAPþ osteoclasts, Osterixþ osteoprogenitors, Osteocalcinþ osteoblasts and expression of SOX9, were higher in bone cyst group. Conclusion: SBCs within knee OA are characterized by focally increased bone turnover, altered bone structure and more severe articular cartilage damage. The increased bone turnover possibly contributes to altered bone structure localized in SBC areas, and thus aggravates articular cartilage degeneration. © 2015 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.-
dc.languageeng-
dc.publisherWB Saunders Co Ltd. The Journal's web site is located at http://www.elsevier.com/locate/joca-
dc.relation.ispartofOsteoarthritis and Cartilage-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectArticular cartilage-
dc.subjectBone remodeling-
dc.subjectBone structure-
dc.subjectOsteoarthritis-
dc.subjectSubchondral bone cyst-
dc.titleBone turnover and articular cartilage differences localized to subchondral cysts in knees with advanced osteoarthritis-
dc.typeArticle-
dc.identifier.emailChen, Y: cy003@connect.hku.hk-
dc.identifier.emailLeung, FKL: klleunga@hkucc.hku.hk-
dc.identifier.emailPan, H: haobo@hku.hk-
dc.identifier.emailLu, WW: wwlu@hku.hk-
dc.identifier.authorityLeung, FKL=rp00297-
dc.identifier.authorityPan, H=rp01564-
dc.identifier.authorityLu, WW=rp00411-
dc.description.naturepostprint-
dc.identifier.doi10.1016/j.joca.2015.07.012-
dc.identifier.pmid26241776-
dc.identifier.scopuseid_2-s2.0-84960292643-
dc.identifier.hkuros264604-
dc.identifier.volume23-
dc.identifier.issue12-
dc.identifier.spage2174-
dc.identifier.epage2183-
dc.identifier.isiWOS:000366838900013-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl1063-4584-

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