scholarly journals Role of subchondral bone properties and changes in development of load-induced osteoarthritis in mice

2017 ◽  
Vol 25 (12) ◽  
pp. 2108-2118 ◽  
Author(s):  
O.O. Adebayo ◽  
F.C. Ko ◽  
P.T. Wan ◽  
S.R. Goldring ◽  
M.B. Goldring ◽  
...  
2019 ◽  
Vol 27 (3) ◽  
pp. 535-543 ◽  
Author(s):  
N.L.A. Fell ◽  
B.M. Lawless ◽  
S.C. Cox ◽  
M.E. Cooke ◽  
N.M. Eisenstein ◽  
...  

2014 ◽  
Vol 33 (1) ◽  
pp. 63-70 ◽  
Author(s):  
Anik Chevrier ◽  
Ahou S. M. Kouao ◽  
Genevieve Picard ◽  
Mark B. Hurtig ◽  
Michael D. Buschmann

2014 ◽  
Vol 7 (5) ◽  
pp. 377-386 ◽  
Author(s):  
Stephen A. Brigido ◽  
Nicole M. Protzman ◽  
Melissa M. Galli ◽  
Scott T. Bleazey

Cystic talar shoulder defects are particularly challenging osteochondral lesions. A retrospective chart review was performed on 13 adults that previously failed microfracture, presented with medial cystic osteochondral lesions of the talus, and were treated with malleolar osteotomy and subchondral allograft reconstruction. The aim of the study was to evaluate the effect of a medial malleolar osteotomy and allograft subchondral bone plug on pain and function. We hypothesized that following surgery, pain and function would significantly improve. Compared with preoperative measures, pain (first step in the morning, during walking, at the end of the day) and function (descending the stairs, ascending the stairs, and ambulating up to 4 blocks) improved postoperatively at 6 and 12 months ( P ≤ .001). During each activity, pain improved postoperatively from 6 to 12 months ( P ≤ .006). Postoperatively, from 6 to 12 months, the level of disability improved while descending the stairs ( P = .004), and the level of disability experienced while ascending the stairs and ambulating up to 4 blocks was maintained ( P ≥ .02). Multiple regression analyses identified body mass index as a predictor of preoperative function ( R2 = .34, P = .04). No variables were identified as significant predictors of postoperative pain or function. With all osteotomies healing, no graft rejection, and a single deep venous thrombosis, allograft subchondral plugs appear to successfully treat osteochondral lesions of the talus with improvements in pain and function as well as an acceptable complication rate. Level of Evidence: Therapeutic, Level IV: Retrospective Case Series.


2016 ◽  
Vol 1383 (1) ◽  
pp. 58-66 ◽  
Author(s):  
Thomas R. Coughlin ◽  
Oran D. Kennedy

2018 ◽  
Vol 26 ◽  
pp. S118
Author(s):  
P. Chan ◽  
M. Au ◽  
W. Yang ◽  
C. Yan ◽  
K. Chiu ◽  
...  

Biomedicines ◽  
2021 ◽  
Vol 9 (11) ◽  
pp. 1593
Author(s):  
Yunfei Li ◽  
Yulia Liem ◽  
Zaitunnatakhin Zamli ◽  
Niall Sullivan ◽  
Enrico Dall’Ara ◽  
...  

Background: The purpose of this study was to investigate the relationship between the expression of key degradative enzymes by chondrocytes and the microarchitectural and mineral properties of subchondral bone across different stages of cartilage degradation in human hip osteoarthritis (OA). Methods: Osteochondral samples at different stages of cartilage degradation were collected from 16 femoral heads with OA. Osteochondral samples with normal cartilage were collected from seven femoral heads with osteoporosis. Microcomputed tomography was used for the investigation of subchondral bone microarchitecture and mineral densities. Immunohistochemistry was used to study the expression and distribution of MMP13 and ADAMTS4 in cartilage. Results: The microarchitecture and mineral properties of the subchondral plate and trabecular bone in OA varied with the severity of the degradation of the overlying cartilage. Chondrocytes expressing MMP13 and ADAMTS4 are mainly located in the upper zone(s) of cartilage regardless of the histopathological grades. The zonal expression of these enzymes in OA (i.e., the percentage of positive cells in the superficial, middle, and deep zones), rather than their overall expression (the percentage of positive cells in the full thickness of the cartilage), exhibited significant variation in relation to the severity of cartilage degradation. The associations between the subchondral bone properties and zonal and overall expression of these enzymes in the cartilage were generally weak or nonsignificant. Conclusions: Phenotypic changes in chondrocytes and remodelling of subchondral bone proceed at different rates throughout the process of cartilage degradation. Biological influences are more important for cartilage degradation at early stages, while biomechanical damage to the compromised tissue may outrun the phenotypic change of chondrocytes and is critical in the advanced stages.


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