Purpose

To evaluate the efficacy of novel biodegradable MAACP/n-HA composite artificial lamina for the prevention of postlaminectomy adhesions and lamina reconstruction.

Introduction

The cause of adolescent idiopathic scoliosis (AIS) is still not known. Although several candidate gene studies and linkage analyses have been done, no causal relationship has yet been established. To our knowledge, we report the first case-control based genome-wide association study (GWAS) for this trait.

Cam type femoro-acetabular impingement is defined by a reduced femoral head-neck offset and by excessive bone at antero-lateral femoral head-neck junction.

Reconstruction of the femoral head-neck offset by removing the femoral bony prominence is a common treatment for cam type impingement. In many cases, the goal of this treatment is to make the antero-lateral head-neck offset symmetrical to the postero-lateral offset. However, guidelines for bony removal are not well established. The objective of this study is to examine if the antero-lateral and postero-lateral femoral offsets are symmetrical in normal healthy hips.

CT analyses of the anatomic geometry of the femoral head and neck were performed. Hip joints with any evidence of cartilage defects and impingement were excluded. Eight cadaveric hips (3 right and 5 left hips) were examined. The average age of the cadavers was 65.1±15.1 years. A peripheral QCT scanner was used which provided 0.2 x 0.2 x 2 mm resolution. To improve the resolution of the final result, each hip joint was scanned in three different scanning directions (sagittal, coronal, and axial scanning planes). A custom imaging fixture was built to position a joint sample in three different scanning planes and a custom irrigation system supplied saline to protect the sample from dehydration. A custom segmentation program was developed to delineate the bony contours of the femoral head and neck in a fully automated manner. The segmentation data from the three differenent imaging planes were merged and a 3D solid model of each hip joint was created. The prominence of the femoral head was determined by the distance of the 3D head from an ideal sphere fitted into the 3D model.

All the femoral heads were found to be asymmetric. Prominence of posteromedial femoral head averaged 0.105 mm more than the antero-medial femoral head.

The antero-lateral head-neck junction was also found to be more prominent than the postero-lateral head-neck junction by an average of 1.09 mm. Asymmetry in the femoral head and femoral head-neck junction was a general finding in normal hip joints. The conventional approach of symmetric reconstruction of femoral head-neck junction may result in unnecessary removal of bone at the antero-lateral head-neck junction and potentially increase the risk of femoral neck fracture.

We implanted bone harvest chambers (BHCs) bilaterally in ten mature male New Zealand white rabbits. Polyethylene particles (0.3 ± 0.1 −m in diameter, 6.4×10¹² particles/ml) were implanted for two, four or six weeks bilaterally in the BHCs, with subsequent removal of the ingrown tissue after each treatment. In addition to the particles, one side also received 1.5 −g of recombinant transforming growth factor ß1 (TGFβ1).

At two weeks, the bone area as a percentage of total area was less in chambers containing TGFβ compared with those with particles alone (7.8 ± 1.3% v 16.9 ± 2.7% respectively; 95% confidence interval (CI) for difference -14.0 to -4.30; p = 0.002). At four weeks, the percentage area of bone was greater in chambers containing TGFβ compared with those with particles alone (31.2 ± 3.4% v 22.5 ± 2.0% respectively; 95% CI for difference 1.0 to 16.4; p = 0.03). There were no statistical differences at six weeks, despite a higher mean value with TGFβ treatment (38.2 ± 3.9% v 28.8 ± 3.5%; 95% CI for difference -4.6 to 23.3; p = 0.16). The number of vitronectin-receptor-positive cells (osteoclast-like cells) was greater in the treatment group with TGFβ compared with that with particles alone; most of these positive cells were located in the interstitium, rather than adjacent to bone.

TGFβ1 is a pleotropic growth factor which can modulate cellular events in the musculoskeletal system in a time- and concentration-dependent manner. Our data suggest that there is an early window at between two and six weeks, in which TGFβ may favourably affect bone ingrowth in the BHC model. Exogenous growth factors such as TGFβ may be a useful adjunct in obtaining osseointegration and bone ingrowth, especially in revisions when there is compromised bone stock and residual particulate debris.

Particulate wear debris is associated with periprosthetic inflammation and loosening in total joint arthroplasty. We tested the effects of titanium alloy (Ti-alloy) and PMMA particles on monocyte/macrophage expression of the C-C chemokines, monocyte chemoattractant protein-1 (MCP-1), monocyte inflammatory protein-1 alpha (MIP-1α), and regulated upon activation normal T expressed and secreted protein (RANTES). Periprosthetic granulomatous tissue was analysed for expression of macrophage chemokines by immunohistochemistry. Chemokine expression in human monocytes/macrophages exposed to Ti-alloy and PMMA particles in vitro was determined by RT-PCR, ELISA and monocyte migration.

We observed MCP-1 and MIP-1α expression in all tissue samples from failed arthroplasties. Ti-alloy and PMMA particles increased expression of MCP-1 and MIP-1α in macrophages in vitro in a dose- and time-dependent manner whereas RANTES was not detected. mRNA signal levels for MCP-1 and MIP-1α were also observed in cells after exposure to particles. Monocyte migration was stimulated by culture medium collected from macrophages exposed to Ti-alloy and PMMA particles. Antibodies to MCP-1 and MIP-1α inhibited chemotactic activity of the culture medium samples.

Release of C-C chemokines by macrophages in response to wear particles may contribute to chronic inflammation at the bone-implant interface in total joint arthroplasty.

The tissues surrounding 65 cemented and 36 cementless total joint replacements undergoing revision were characterised for cell types by immunohistochemistry and for cytokine expression by in situ hybridisation.

We identified three distinct groups of revised implants: loose implants with ballooning radiological osteolysis, loose implants without osteolysis, and well-fixed implants. In the cemented series, osteolysis was associated with increased numbers of macrophages (p = 0.0006), T-lymphocyte subgroups (p = 0.03) and IL-1 (p = 0.02) and IL-6 (p = 0.0001) expression, and in the cementless series with increased numbers of T-lymphocyte subgroups (p = 0.005) and increased TNFα expression (p = 0.04). For cemented implants, the histological, histochemical and cytokine profiles of the interface correlated with the clinical and radiological grade of loosening and osteolysis.

Our findings suggest that there are different biological mechanisms of loosening and osteolysis for cemented and cementless implants. T-lymphocyte modulation of macrophage function may be an important interaction at prosthetic interfaces.