4.6 Article

Subchondral bone turnover, but not bone volume, is increased in early stage osteoarthritic lesions in the human hip joint

Journal

OSTEOARTHRITIS AND CARTILAGE
Volume 23, Issue 12, Pages 2167-2173

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.joca.2015.06.001

Keywords

Osteoarthritis; Cartilage alterations; Bone turnover; Subchondral cortical bone; Subchondral trabecular bone; Femoral head

Funding

  1. Danish Rheumatism Association [R109-A2610]

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Objective: The pathogenesis of osteoarthritis (OA) is not fully understood, but bone changes are suggested to be important. Bone turnover and bone volume (BV) in human hip OA were investigated in relation to the overlying cartilage degeneration using design-based stereological estimators. Materials and Methods: Femoral heads were obtained from 25 end-stage OA patients and 24 controls (CTL). Design-based stereological methods were used for sampling and quantification to obtain absolute estimates of volume and surface in the central trabecular and the subarticular bone region. The subarticular bone was further subdivided into regions according to the OARSI-score of the overlying articular cartilage in which erosion and osteoid surfaces were estimated. Results: In the subarticular region, bone volume (BV/TV) was 15.0% higher in OA patients compared to CTL; The fraction of erosive (ES/BS) and osteoid surfaces (OS/BS) were 56.2% and 72.8% higher in OA compared to CTL. In subarticular regions with none to mild cartilage degeneration (OARSI grade 0-2), ES/BS and OS/BS were 48.6% and 59.9% higher in OA compared to CTL, whereas BV/TV did not differ between OA and CTL. Conclusion: In human end-stage hip OA, BV and bone turnover correlate with the degree of local cartilage degeneration. Subarticular bone sclerosis was only present in regions corresponding to end-stage OA. However, in regions with only none to mild cartilage degeneration the underlying bone had significantly higher turnover in OA patients compared to the control group, suggesting that high bone turnover may contribute to the early pathogenesis of OA. (C) 2015 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.

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