Rationale and Objectives
To study the articular cartilage surface curvature determined automatically from magnetic resonance (MR) knee scans, evaluate accuracy of the curvature estimates on digital phantoms, and an evaluation of their potential as disease markers for different stages of osteoarthritis (OA).
Materials and Methods
Knee MR data were acquired using a low-field 0.18T scanner, along with posteroanterior x-rays for evaluation of radiographic signs of OA according to the Kellgren-Lawrence index (KL). Scans from a total of 114 knees from test subjects with KL 0–3, 59% females, ages 21–79 years were evaluated. The surface curvature for the medial tibial compartment was estimated automatically on a range of scales by two different methods: Euclidean shortening flow and boundary normal comparison on a cartilage shape model. The curvature estimates were normalized for joint size for intersubject comparisons. Digital phantoms were created to establish the accuracy of the curvature estimation methods.
Results
A comparison of the two curvature estimation methods to ground truth yielded absolute pairwise differences of 1.1%, and 4.8%, respectively. The interscan reproducibility for the two methods were 2.3% and 6.4% (mean coefficient of variation), respectively. The surface curvature was significantly higher in the OA population (KL > 0) compared with the healthy population (KLi = 0) for both curvature estimates, with P values of .000004 and .000006, respectively. The shape model based curvature estimate could also separate healthy from borderline OA (KL = 1) populations ( P = .005).
Conclusion
The phantom study showed that the shape model method was more accurate for a coarse-scale analysis, whereas the shortening flow estimated fine scales better. Both the fine- and the coarse-scale curvature estimates distinguished between healthy and OA populations, and the coarse-scale curvature could even distinguish between healthy and borderline OA populations. The highly significant differences between populations demonstrate the potential of cartilage curvature as a disease marker for OA.
Osteoarthritis (OA) is a disease characterized by degeneration of the articular cartilage and bone deformations in joints, is second to heart disease in causing work disability, and is associated with a large socioeconomic impact on health care systems ( ). Even though much effort has focused on development of disease modifying OA drugs, there is no standard clinical treatment of OA that can reverse cartilage degeneration. In clinical studies of new treatments, the ability to detect even small differences across populations receiving treatment or placebo could significantly reduce the cost of such studies. If OA can be detected at an early stage, patients that would be benefit from non medicinal intervention such as gait adjustment could be identified. Hence reliability and early OA detection are desirable features for OA disease markers.
Radiographs currently present the gold standard for measuring cartilage degradation in terms of joint space narrowing, and for determining the degree of OA using the Kellgren-Lawrence index (KL) ( ). However, standard radiographs are limited to a two-dimensional (2D) analysis of the joint and only measures the cartilage indirectly because it is not visible in the images. It is also sensitive to malpositioning, exposes test subjects to radiation, and is insensitive to small changes in the cartilage structure. Magnetic resonance imaging (MRI) has become one of the leading imaging modalities in osteoarthritis research because it allows for noninvasive, three-dimensional (3D) quantification of the articular cartilage ( ). Typical quantitative disease markers from MRI are the articular cartilage volume and thickness ( ) in which the volume on its own can be a relatively poor disease marker ( ).
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Materials and methods
Population and Image Acquisition
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Cartilage Segmentation
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Curvature Estimation
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Curvature Analysis by Shortening Flow
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in terms of derivatives of ϕ. The average mean curvature on the articular surface was calculated throughout the evolution and curvature estimates at the point during the flow that enables best separation between groups as described in Differentiation Between Populations and elsewhere ( ). The supersampling, making 5 × 5 × 5 voxels from each voxel before the evolution, was done to allow finer changes than the original voxel size. There was no smoothing involved in the supersampling, so the shortening flow will initially mainly reduce partial volume effects because it can be considered as a nonlinear smoothing process. In late stages of the flow, the object loses its cartilage like form and may even change topology. Figure 2 illustrates how a cartilage sheet deforms during mean curvature flow.
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Curvature Analysis by Shape Model
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Normalization of Curvature Estimates
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Analysis on Digital Phantoms
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Results
Evaluation on Phantoms
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Differentiation Between Populations
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Table 1
The Average Curvature Values for the Shortening Flow (Flow) and Shape Model (Shape) Curvature Estimation Methods in Different Populations Based on KL
Method KL = 0 KL = 1 KL = 2 KL = 3 Flow (m −1 ) 341 (± 29) 339 (± 29) 390 (± 46) 410 (± 46) Shape (m −1 ) 40 (± 5.4) 45 (± 7.3) 47 (± 7.1) 54 (± 13.6)
Values in parenthesis are standard deviations (SD).
KL: Kellgren-Lawrence index.
Table 2
Results Comparing the Performance of the Two Curvature Methods and Cartilage Volume and Thickness
Flow Shape Volume Thickness Average 360 (m −1 ) 45 (m −1 ) 1,900 (mm 3 ) 1.30 mm SD 32 (m −1 ) 9.6 (m −1 ) 440 (mm 3 ) 0.18 mm Maximum 465 (m −1 ) 100 (m −1 ) 3100 (mm 3 ) 1.70 mm Minimum 302 (m −1 ) 30 (m −1 ) 580 (mm 3 ) 0.79 mm Cartilage volume (%) 2.3 6.4 5.3 4.6 Diff (%) 3.3 9.0 7.5 6.4P (KL > 0) .00006 .000004 .004 .002P (KL > 1) .75 .005 .27 .32
Average curvature with standard deviation and maximum and minimum values are listed for the 114 evaluation scans, along with precision values, mean cartilage volume and absolute mean pairwise difference (diff), for the 31 scan-rescan pairs. P values for separation between the healthy population and osteoarthritis (OA) population (Kellgren-Lawrence index [KL] > 0) and borderline OA (KL = 1) are also listed.
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Discussion
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