scholarly journals Parathyroid hormone [1-34] improves articular cartilage surface architecture and integration and subchondral bone reconstitution in osteochondral defects in vivo

2013 ◽  
Vol 21 (4) ◽  
pp. 614-624 ◽  
Author(s):  
P. Orth ◽  
M. Cucchiarini ◽  
D. Zurakowski ◽  
M.D. Menger ◽  
D.M. Kohn ◽  
...  
2020 ◽  
Vol 8 (7_suppl6) ◽  
pp. 2325967120S0045
Author(s):  
Hailey Huddleston ◽  
Adam Yanke ◽  
Nozomu Inoue

Objectives: When performing a patellar osteochondral allograft, the patellar allograft is harvested from a similar anatomic location as the defect. This approach assumes that graft will have similar topography to the patellar defect. However, to our knowledge, no prior study has investigated the topography of the patella and what intrinsic factors of the graft and the recipient affect mismatch of the chondral and osseous layers between the graft and defect. Methods: Three-dimensional (3D) computed tomography (CT) models of the patella were created and exported into point-cloud models using a 3D reconstruction program (Mimics, Materialise Inc., Leuven, Belgium). Circular articular cartilage and subchondral bone defect models were created in each model of the recipient patella (diameter=18mm) at 3 locations: medial, distal, and lateral. Articular cartilage and subchondral bone graft models were created on all possible locations on the articular cartilage surface models of the donor patellae. 3D surface topographies of the articular cartilage surface and resulting subchondral bone surfaces were compared between graft and defect models. The graft models were virtually placed on the surface of the defect model. Least distances, defined as the shortest distance from the point in question to the corresponding point in space, where a perfect congruent match would equal a least distance of 0.00mm for given data points on the simulated articular cartilage surface, were calculated. A mean value of the least distances was calculated for each position of the graft model and for the subchondral bone surface, simultaneously. The graft model was then rotated 360° around the axis perpendicular to the articular cartilage surface in 1° increments, and the least distance of articular cartilage surface and least distance of subchondral bone surface were calculated at each rotating angle. This procedure was repeated for all points in the articular surface model of the donor patella. The 3D model creation and geometry matching were performed using a custom-written program coded by in Microsoft Visual C++ with Microsoft Foundation Class programming environment (Microsoft Corp., Redmond, WA). Multivariate linear regression analysis was conducted in SPSS (v26, IBM, Armonk, NY). Results: Chondral and osseous mismatch between the graft and defect were analyzed. ANOVA analysis on the multivariate linear regressions found significant predictors of cartilage mismatch for medial (p=0.002), lateral (p=0.022), and central (p=0.001) defects when testing 5 variables. However, no predicting variables were identified for osseous mismatch for medial (p=0.099), lateral (p=0.703), and central (p=0.641) defects. Differences in tibia width (p=0.005), bone width (p=0.004), and medial cartilage length (p=0.003) were predictive of mismatch in medial defects. When evaluating lateral defects, no variables were found to significantly effect mismatch, However, in this lateral defect group, the collinearity assumption of the regression was violated, as the VIF for bone width and lateral length were over 10. For the central group, difference in bone width (p=0.037), difference in percent of patella that was medial facet (p=0.001), and difference in tibial width (p=0.006) were predictive of mismatch. Conclusions: Differences between graft and recipient tibia width, bone width, and size of the medial or lateral facet are significant predictors of mismatch in patella allograft selection.


2020 ◽  
Vol 48 (12) ◽  
pp. 2836-2845 ◽  
Author(s):  
Paris Vakiel ◽  
Mehdi Shekarforoush ◽  
Christopher R. Dennison ◽  
Michael Scott ◽  
Cyril B. Frank ◽  
...  

2001 ◽  
Vol 29 (6) ◽  
pp. 704-708 ◽  
Author(s):  
John G. Lane ◽  
Michael E. Amiel ◽  
Richard Greenfield ◽  
David Amiel

A long-term in vivo study was performed to assess biochemical changes after laser repair of articular cartilage. Forty New Zealand White rabbits were sacrificed 26 weeks after undergoing an articular cartilage chondroplasty with use of a holmium:yttrium-aluminum-garnet laser at 0.8 joules per pulse and a rate of 10 Hz. Glycosaminoglycan content in the repaired tissue decreased significantly with both perpendicular (19.59 ± 5.6 μg hexosamin/mg of dry tissue) and tangential delivery (14.78 ± 4.5 μg/mg) compared with the sham-treated tissue (39.6 ± 5.0 μg/mg). Cellular viability was also significantly decreased. Sulfate incorporation was decreased to 203 ± 142 cpm/mg of dry cartilage in the tangential mode and 461 ± 209 cpm/mg in the tangential mode, compared with the sham at 1845 cpm/mg. Uptake of [3H]thymidine decreased to 463 ± 473 cpm/mg of dry tissue and 455 ± 170 cpm/mg in the tangential and perpendicular modes, respectively, compared with 2465 cpm/mg in the sham tissue. There were no significant differences between the tangential and perpendicular delivery modes in any assessments performed. The short-term chondrocyte destruction previously noted in a 12-week study after laser treatment was not reversed during a longer-term 26-week study, and cellular viability was not recovered, suggesting that the loss of chondrocyte function may be permanent.


2021 ◽  
Vol 9 (10_suppl5) ◽  
pp. 2325967121S0032
Author(s):  
Hailey Huddleston ◽  
Theodore Wolfson ◽  
David Christian ◽  
Nozomu Inoue ◽  
Adam Yanke

Objectives: Patellar osteochondral allograft (OA) transplantation has been shown to be a successful treatment in patients with isolated patellar cartilage injury. Currently, there is minimal guidance in anatomic and sizing factors that portend similar patellar surface topography. The most commonly utilized patellar sizing criteria to match the donor and recipient is radiographic tibial width. Our hypothesis is that specific patella anatomic factors will better predict surface topography matching. To our knowledge, no prior study has investigated the topography of the patella and what intrinsic factors of the graft and the recipient affect matching of the chondral and osseous layers between the graft and defect. Methods: Computed tomography (CT) images of the specimens were acquired and three-dimensional (3D) CT models of the patella were then created and exported into point-cloud models using a 3D reconstruction software program. Circular articular cartilage and subchondral bone defect models were created in each point-cloud model of the recipient patella with a diameter of 18 mm and 22.5 mm at 3 locations: the medial, central, and lateral portions of the patellar surface. Circular articular cartilage and subchondral bone graft models were created on all possible locations on the articular cartilage surface models of the donor patellae (Figure 1). The graft models were virtually placed on the surface of the defect model. Orientation of the graft model was adjusted so that its axis matched that of the defect site. Least distances between the graft and the defect articular surface models were calculated and were defined as the shortest distance from the point in question to the corresponding point in space. A mean value of the least distances was calculated for each position of the graft model. The mean least distance of subchondral bone surface in each point was calculated simultaneously. The graft model was then rotated 360° around the axis perpendicular to the articular cartilage surface in 1° increments, and the least distance of articular cartilage surface and the resulting least distance of subchondral bone surface were calculated at each rotating angle. This procedure was repeated for all points in the articular surface model of the donor patella. Step-off was then calculated as the least mean square difference between the defect and graft along the periphery. Stepwise linear regression was used for each defect location to analyze which variables predict degree of mismatch in millimeters. Results: A total of 16 patella were utilized in analysis. Comparison of cartilage least mean square distances between locations demonstrated that the lateral location had significantly less surface incongruity compared to the other two locations (vs medial: p = .0038, vs central: p = .0046). In addition, significant differences in subchondral bone distances were observed between the locations (lateral vs medial: p = .0007, lateral vs central: p < .0001, medial vs central: p < .0001) (Table 1). The associations of six anatomic and morphologic variables with cartilage mismatch, bone mismatch, and step-off for 18 mm and 22.5 mm defects are presented in Tables 2 and Table 3. All variables were analyzed as the difference in value between the recipient and donor. For both lesion sizes, cartilage step-off was the most susceptible to variable differences. Compared to the 18 mm defect group, the 22.5 mm defects were more affected (higher coefficients) by the same differences in variables. Differences in tibial width were associated mismatch for central lesions (eg. 22.5mm defect coefficient: -0.026, p < .001), while cartilage width was associated with mismatch for lateral lesions. (eg. 22.5 mm defect coefficient: -0.034, p < .023). Conclusions: Multiple clinically relevant factors were found to affect graft and defect chondral mismatch and to a lesser extent osseous mismatch. For all three locations at both defect sizes, step-off was the most susceptible to differences in patellar morphology between the donor and recipient. In addition, differences in tibial width, a commonly used metric for patellar graft matching, did not significantly predict chondral mismatch for lateral and medial sized lesions. These findings should be considered when selecting and preparing the graft in a patella osteochondral allograft procedure.


Author(s):  
Sarah Davis ◽  
Marta Roldo ◽  
Gordon Blunn ◽  
Gianluca Tozzi ◽  
Tosca Roncada

Articular cartilage is a highly specialised connective tissue of diarthrodial joints which provides a smooth, lubricated surface for joint articulation and plays a crucial role in the transmission of loads. In vivo cartilage is subjected to mechanical stimuli that are essential for cartilage development and the maintenance of a chondrocytic phenotype. Cartilage damage caused by traumatic injuries, ageing, or degradative diseases leads to impaired loading resistance and progressive degeneration of both the articular cartilage and the underlying subchondral bone. Since the tissue has limited self-repairing capacity due its avascular nature, restoration of its mechanical properties is still a major challenge. Tissue engineering techniques have the potential to heal osteochondral defects using a combination of stem cells, growth factors, and biomaterials that could produce a biomechanically functional tissue, representative of native hyaline cartilage. However, current clinical approaches fail to repair full-thickness defects that include the underlying subchondral bone. Moreover, when tested in vivo, current tissue-engineered grafts show limited capacity to regenerate the damaged tissue due to poor integration with host cartilage and the failure to retain structural integrity after insertion, resulting in reduced mechanical function. The aim of this review is to examine the optimal characteristics of osteochondral scaffolds. Additionally, an overview on the latest biomaterials potentially able to replicate the natural mechanical environment of articular cartilage and their role in maintaining mechanical cues to drive chondrogenesis will be detailed, as well as the overall mechanical performance of grafts engineered using different technologies.


2012 ◽  
Vol 134 (10) ◽  
Author(s):  
M. L. Roemhildt ◽  
B. D. Beynnon ◽  
M. Gardner-Morse ◽  
K. Anderson ◽  
G. J. Badger

This study describes the first application of a varus loading device (VLD) to the rat hind limb to study the role of sustained altered compressive loading and its relationship to the initiation of degenerative changes to the tibio-femoral joint. The VLD applies decreased compressive load to the lateral compartment and increased compressive load to the medial compartment of the tibio-femoral joint in a controlled manner. Mature rats were randomized into one of three groups: unoperated control, 0% (sham), or 80% body weight (BW). Devices were attached to an animal’s leg to deliver altered loads of 0% and 80% BW to the experimental knee for 12 weeks. Compartment-specific material properties of the tibial cartilage and subchondral bone were determined using indentation tests. Articular cartilage, calcified cartilage, and subchondral bone thicknesses, articular cartilage cellularity, and degeneration score were determined histologically. Joint tissues were sensitive to 12 weeks of decreased compressive loading in the lateral compartment with articular cartilage thickness decreased in the peripheral region, subchondral bone thickness increased, and cellularity of the midline region decreased in the 80% BW group as compared to the 0% BW group. The medial compartment revealed trends for diminished cellularity and aggregate modulus with increased loading. The rat-VLD model provides a new system to evaluate altered quantified levels of chronic in vivo loading without disruption of the joint capsule while maintaining full use of the knee. These results reveal a greater sensitivity of tissue parameters to decreased loading versus increased loading of 80% BW for 12 weeks in the rat. This model will allow future mechanistic studies that focus on the initiation and progression of degenerative changes with increased exposure in both magnitude and time to altered compressive loads.


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