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A longitudinal study of subchondral plate and trabecular bone in cruciate-deficient dogs with osteoarthritis followed up for 54 months

dc.contributor.authorDedrick, Dale K.en_US
dc.contributor.authorGoldstein, Steven A.en_US
dc.contributor.authorBrandt, K. D.en_US
dc.contributor.authorO'Connor, B. L.en_US
dc.contributor.authorGoulet, Robert W.en_US
dc.contributor.authorAlbrecht, M.en_US
dc.date.accessioned2006-04-28T16:25:00Z
dc.date.available2006-04-28T16:25:00Z
dc.date.issued1993-10en_US
dc.identifier.citationDedrick, D. K.; Goldstein, S. A.; Brandt, K. D.; O'Connor, B. L.; Goulet, R. W.; Albrecht, M. (1993)."A longitudinal study of subchondral plate and trabecular bone in cruciate-deficient dogs with osteoarthritis followed up for 54 months." Arthritis & Rheumatism 36(10): 1460-1467. <http://hdl.handle.net/2027.42/37796>en_US
dc.identifier.issn0004-3591en_US
dc.identifier.issn1529-0131en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/37796
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8216405&dopt=citationen_US
dc.description.abstractObjective. To evaluate the sequence of changes in articular cartilage, trabecular bone, and subchondral plate in dogs with osteoarthritis (OA), 3 months, 18 months, and 54 months after anterior cruciate ligament transection (ACLT). Methods. Specimens of the medial tibial plateau were analyzed with microscopic computed tomography (micro-CT) at a resolution of 60 Μm, and biochemical and morphologic changes in the femoral articular cartilage were assessed. Results. At 3 months and 18 months after ACLT, the articular cartilage in the unstable knee showed histologic changes typical of early OA and increased water content and uronic acid concentration; by 54 months, full-thickness ulceration had developed. Micro-CT analysis showed a loss of trabecular bone in the unstable knee, compared with the contralateral knee, at all time points. At both 18 and 54 months, the differences in trabecular thickness and surface-to-volume ratio were greater than at 3 months. Although the mean subchondral plate thickness, especially in the medial aspect of the medial tibial plateau, was greater in the OA knee than in the contralateral knee 18 months and 54 months after ACLT, these differences were not statistically significant; however, the difference was significantly greater at 54 months than at 3 months. Conclusion. Thickening of the subchondral bone is not required for the development of cartilage changes of OA in this model. The bony changes that develop after ACLT, however, could result in abnormal transmission of stress to the overlying cartilage and thereby contribute to the progression of cartilage degeneration.en_US
dc.format.extent777144 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherRheumatologyen_US
dc.titleA longitudinal study of subchondral plate and trabecular bone in cruciate-deficient dogs with osteoarthritis followed up for 54 monthsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeriatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumOrthopaedic Research Laboratories, Section of Orthopaedics, Department of Surgery, Multipurpose Arthritis and Musculoskeletal Disease Center, and Division of Rheumatology, Department of Internal Medicine, University of Michigan ; Orthopaedic Research Laboratories, Section of Orthopaedics, Department of Surgery, the Multipurpose Arthritis and Musculoskeletal Disease Center, and the Division of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor; and the Rheumatology Division, Department of Medicine, the Multipurpose Arthritis and Musculoskeletal Disease Center, and the Specialized Center of Research in Osteoarthritis, Indiana University School of Medicine, Indianapolis. ; Address reprint requests to Dale K. Dedrick, MD, Orthopaedic Research Laboratory, G0161 N.I.B., University of Michigan, 400 North Ingalls, Ann Arbor, MI 48109-0486en_US
dc.contributor.affiliationumOrthopaedic Research Laboratories, Section of Orthopaedics, Department of Surgery, Multipurpose Arthritis and Musculoskeletal Disease Center, University of Michigan ; Orthopaedic Research Laboratories, Section of Orthopaedics, Department of Surgery, the Multipurpose Arthritis and Musculoskeletal Disease Center, and the Division of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor; and the Rheumatology Division, Department of Medicine, the Multipurpose Arthritis and Musculoskeletal Disease Center, and the Specialized Center of Research in Osteoarthritis, Indiana University School of Medicine, Indianapolis.en_US
dc.contributor.affiliationumRheumatology Division, Department of Medicine, Multipurpose Arthritis and Musculoskeletal Disease Center, and Specialized Center of Research in Osteoarthritis, Indiana University School of Medicine ; Orthopaedic Research Laboratories, Section of Orthopaedics, Department of Surgery, the Multipurpose Arthritis and Musculoskeletal Disease Center, and the Division of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor; and the Rheumatology Division, Department of Medicine, the Multipurpose Arthritis and Musculoskeletal Disease Center, and the Specialized Center of Research in Osteoarthritis, Indiana University School of Medicine, Indianapolis.en_US
dc.contributor.affiliationumRheumatology Division, Department of Medicine, Multipurpose Arthritis and Musculoskeletal Disease Center, and Specialized Center of Research in Osteoarthritis, Indiana University School of Medicine ; Orthopaedic Research Laboratories, Section of Orthopaedics, Department of Surgery, the Multipurpose Arthritis and Musculoskeletal Disease Center, and the Division of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor; and the Rheumatology Division, Department of Medicine, the Multipurpose Arthritis and Musculoskeletal Disease Center, and the Specialized Center of Research in Osteoarthritis, Indiana University School of Medicine, Indianapolis.en_US
dc.contributor.affiliationumOrthopaedic Research Laboratories, Section of Orthopaedics, Department of Surgery, Multipurpose Arthritis and Musculoskeletal Disease Center, University of Michigan ; Orthopaedic Research Laboratories, Section of Orthopaedics, Department of Surgery, the Multipurpose Arthritis and Musculoskeletal Disease Center, and the Division of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor; and the Rheumatology Division, Department of Medicine, the Multipurpose Arthritis and Musculoskeletal Disease Center, and the Specialized Center of Research in Osteoarthritis, Indiana University School of Medicine, Indianapolis.en_US
dc.contributor.affiliationumRheumatology Division, Department of Medicine, Multipurpose Arthritis and Musculoskeletal Disease Center, and Specialized Center of Research in Osteoarthritis, Indiana University School of Medicine ; Orthopaedic Research Laboratories, Section of Orthopaedics, Department of Surgery, the Multipurpose Arthritis and Musculoskeletal Disease Center, and the Division of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor; and the Rheumatology Division, Department of Medicine, the Multipurpose Arthritis and Musculoskeletal Disease Center, and the Specialized Center of Research in Osteoarthritis, Indiana University School of Medicine, Indianapolis.en_US
dc.identifier.pmid8216405en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/37796/1/1780361019_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/art.1780361019en_US
dc.identifier.sourceArthritis & Rheumatismen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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