Rationale and Objectives
Periprosthetic osteolysis is a disease attributed to the body’s reaction to fine polyethylene wear debris shed from total hip replacements. The purpose of this preliminary study was to investigate the ability of radiographic texture analysis (RTA) to characterize the trabecular texture patterns on pelvic images for osteolysis and normal total hip arthroplasty (THA) cases.
Materials and Methods
Fourier-based and fractal-based texture features were calculated for a database of digitized radiographs from 202 THA cases, 70 of which developed osteolysis. The features were calculated from regions of interest selected at two time points: less than 1 month after surgery, and at the first clinical indication of osteolysis (or randomly selected follow-up time for normal cases). Receiver operating characteristic (ROC) analysis was used to compare feature performance at baseline and follow-up for osteolysis and normal cases.
Results
Separation between the RTA features for osteolysis and normal cases was negligible at baseline and increased substantially for the follow-up images. The directional Fourier-based feature provided the best separation with an A z value from ROC analysis of 0.75 for the follow-up images, in the task of distinguishing between normal and osteolytic cases.
Conclusions
The results from this preliminary analysis indicate that qualitative changes in trabecular patterns from immediately after surgery to the eventual detection of osteolysis correspond to quantitative changes in RTA features. It therefore appears that RTA provides information that could potentially be useful to aid in the detection of this disease.
Periprosthetic osteolysis is a common long-term complication in total hip replacement surgeries. It is a man-made disease attributed to the body’s reaction to fine polyethylene wear debris shed by the artificial hip articulation ( ). The process begins when macrophages ingest submicron polyethylene debris particles, leading to the stimulation of osteoclasts and resorption of adjacent bone ( ). The disease strongly contributes to weakening of the surrounding bone and disappearance of its trabecular pattern. This continual destruction of bone and consequent bone weakening can eventually lead to severe fractures and bone destruction, often necessitating complex revision surgeries.
The biologic process causing osteolysis is initially asymptomatic, with major bone destruction often occurring in the early stages before any loosening of the components of the replacement ( ). As a result, the disease is typically diagnosed when a region of localized trabecular bone loss is visible radiographically ( ). However, osteolytic lesions tend to evolve in a slow process and radiographic evidence is not usually visually apparent on earlier postoperative radiographs ( Fig 1 ). Moreover, trabecular texture patterns are difficult for even experts to quantify radiographically. The disease, therefore, commonly goes unnoticed until severe bone loss and loosening of the hip replacement or fracture has occurred, making surgical reconstruction difficult and clinical outcomes poor.
Figure 1
Radiographic example of osteolysis. The baseline image (a) and the 4-year follow-up image (b) show no signs of the disease. The 14-year follow-up image (c) contains a large region of osteolysis indicated by the arrows.
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Materials and methods
Database
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Table 1
Database Summary for the Osteolysis ( n = 70 cases) and Normal ( n = 132 cases) Total Hip Arthroplasty Populations
Patient Age at Surgery (Years) Follow-up Time (Years) Osteolysis Normal Osteolysis Normal Mean 49.3 57.7 10.3 10.3 Range 23–78 26–83 2–17 2–17
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Region of Interest Selection
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Feature Calculation
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Data Analysis
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Results
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Nondirectional RTA Features
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Table 2
Results from ROC Analysis of the Three Features for Baseline and Follow-up Images in the Task of Distinguishing Between Normal and Osteolysis Cases
Baseline A z Follow-up A z ΔA z P Value FMP 0.52 0.69 0.08–0.27 <.001 Minimum FMP( θ ) 0.54 0.75 0.13–0.30 <.001 MINK g 0.59 0.67 0–0.17 .05
The 95% confidence intervals for the difference in A z values between follow-up and baseline are also listed, along with the P values for this difference.
FMP = first moment of the power spectrum; MINK g = global Minkowski dimension.
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Table 3
Average Feature Values for the Three Features from (a) Baseline and (b) Follow-up Images
(a) Baseline Osteolysis Average (95% CI) Normal Average (95% CI)P Value FMP (cycles/mm) 0.71 (0.66–0.75) 0.70 (0.67–0.72) .75 Min. FMP(θ) (cycles/mm) 0.41 (0.38–0.45) 0.42 (0.40–0.45) .70 MINK g 2.349 (2.335–2.363) 2.361 (2.354–2.369) .11
(b) Follow-up Osteolysis Average (95% CI) Normal Average (95% CI)P Value FMP (cycles/mm) 0.66 (0.63–0.69) 0.77 (0.74–0.80) <.001 Min. FMP(θ) (cycles/mm) 0.35 (0.32–0.38) 0.48 (0.45–0.51) <.001 MINK g 2.327 (2.316–2.339) 2.360 (2.351–2.368) <.001
Student’s t -tests were performed to determine the significance of the feature differences between osteolysis and normal cases. Corresponding P values are also shown.
See Table 2 for abbreviations.
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Directional RTA Feature
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Discussion
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Table 4
Average Values and 95% Confidence Intervals for the Three Features from Baseline Images and Follow-up Images for (a) Osteolysis and (b) Normal Cases
(a) Osteolysis Baseline Average (95% CI) Follow-up Average (95% CI)P Value FMP (cycles/mm) 0.71 (0.66, 0.75) 0.66 (0.63, 0.69) .08 Min. FMP(θ) (cycles/mm) 0.41 (0.38, 0.45) 0.35 (0.32, 0.38) .003 MINK g 2.349 (2.335, 2.363) 2.327 (2.316, 2.339) .002
(b) Normal Baseline Average (95% CI) Follow-up Average (95% CI)P Value FMP (cycles/mm) 0.70 (0.67, 0.72) 0.77 (0.74, 0.80) <.001 Min. FMP(θ) (cycles/mm) 0.42 (0.40, 0.45) 0.48 (0.45, 0.51) <.001 MINK g 2.361 (2.354, 2.369) 2.360 (2.351, 2.368) .61
Paired Student’s t -tests were performed to determine the significance of the feature differences between baseline and follow-up images and the resulting P values are shown in the table.
See Table 2 for abbreviations.
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Acknowledgments
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