| Literature DB >> 35222885 |
Yun Xin Teoh1, Khin Wee Lai1, Juliana Usman1, Siew Li Goh2, Hamidreza Mohafez1, Khairunnisa Hasikin1, Pengjiang Qian3, Yizhang Jiang3, Yuanpeng Zhang4, Samiappan Dhanalakshmi5.
Abstract
Knee osteoarthritis (OA) is a deliberating joint disorder characterized by cartilage loss that can be captured by imaging modalities and translated into imaging features. Observing imaging features is a well-known objective assessment for knee OA disorder. However, the variety of imaging features is rarely discussed. This study reviews knee OA imaging features with respect to different imaging modalities for traditional OA diagnosis and updates recent image-based machine learning approaches for knee OA diagnosis and prognosis. Although most studies recognized X-ray as standard imaging option for knee OA diagnosis, the imaging features are limited to bony changes and less sensitive to short-term OA changes. Researchers have recommended the usage of MRI to study the hidden OA-related radiomic features in soft tissues and bony structures. Furthermore, ultrasound imaging features should be explored to make it more feasible for point-of-care diagnosis. Traditional knee OA diagnosis mainly relies on manual interpretation of medical images based on the Kellgren-Lawrence (KL) grading scheme, but this approach is consistently prone to human resource and time constraints and less effective for OA prevention. Recent studies revealed the capability of machine learning approaches in automating knee OA diagnosis and prognosis, through three major tasks: knee joint localization (detection and segmentation), classification of OA severity, and prediction of disease progression. AI-aided diagnostic models improved the quality of knee OA diagnosis significantly in terms of time taken, reproducibility, and accuracy. Prognostic ability was demonstrated by several prediction models in terms of estimating possible OA onset, OA deterioration, progressive pain, progressive structural change, progressive structural change with pain, and time to total knee replacement (TKR) incidence. Despite research gaps, machine learning techniques still manifest huge potential to work on demanding tasks such as early knee OA detection and estimation of future disease events, as well as fundamental tasks such as discovering the new imaging features and establishment of novel OA status measure. Continuous machine learning model enhancement may favour the discovery of new OA treatment in future.Entities:
Mesh:
Year: 2022 PMID: 35222885 PMCID: PMC8881170 DOI: 10.1155/2022/4138666
Source DB: PubMed Journal: J Healthc Eng ISSN: 2040-2295 Impact factor: 2.682
Figure 1Knee OA continuum in terms of detection and intervention.
Figure 2Overview of this review study (“∗” indicates numbering of section where the topic will be discussed).
Figure 3Illustration of knee OA features and pathologies with respect to healthy knee.
Radiological OA features.
| OA features | Description |
|---|---|
| Joint space narrowing (JSN) [ | Usually asymmetric, commonly happens at medial tibiofemoral and patellofemoral compartments |
| Osteophyte formation [ | Formation of bone spurs |
| Cyst/geode formation [ | Formation of fluid-filled cavities when synovial fluid is forced into subchondral bone |
| Subchondral sclerosis [ | Increased bone density or thickening of bone when bone grows in the area originally belongs to cartilage |
| Coronal tibiofemoral subluxation [ | Misaligned joint surface, causing altered shape of femoral condyles and tibial plateau |
Imaging techniques for knee OA diagnosis.
| Imaging technique | Working principle | Pros | Cons | Detectable OA features | Grading scale |
|---|---|---|---|---|---|
| X-ray imaging/radiography/roentgenography | Ionizing radiation from X-ray passes through patient's body in one direction | (i) Low cost | (i) Mostly limited to 2D visualization | (i) Joint space narrowing | (i) Kellgren–Lawrence (KL) |
| (ii) Routine OA imaging in clinical practice | (ii) Less sensitive to change over time | (ii) Osteophyte formation | (ii) Ahlbäck | ||
| (iii) Allows bony structure visualization | (iii) Lack of soft tissue visualization | (iii) Cyst formation | (iii) Brandt | ||
| (iv) Subjects can be scanned in different positions, including supine, sitting, standing, fully extended, semiflexed, non-weight-bearing, and weight-bearing conditions | (iv) Prone to positioning errors | (iv) Subchondral sclerosis | (iv) Osteoarthritis Research Society International (OARSI) | ||
| (v) Risk of radiation | (v) International Knee Documentation Committee (IKDC) | ||||
| (vi) Fair bank | |||||
| (vii) Jäger-Wirth | |||||
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| Magnetic resonance imaging (MRI) | Protons in patient's body are stimulated using magnetic fields | (i) Permits visualization of intra-articular structures and soft tissues | (i) Expensive | (i) Joint space narrowing | (i) Modified Outerbridge classification |
| (ii) Permits visualization of cartilage biochemical properties and pathological features | (ii) Intolerable to metal implant | (ii) Bone marrow lesions | (ii) Whole-Organ MRI Scoring (WORMS) | ||
| (iii) Allows 2D and 3D visualization | (iii) Risk of overdiagnosis | (iii) Knee Osteoarthritis Scoring System (KOSS) | |||
| (iv) Boston Leeds Osteoarthritis Knee Score (BLOKS) | |||||
| (v) MRI Osteoarthritis Knee Score (MOAKS) | |||||
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| Computed tomography (CT) | Ionizing radiation is passed through patient's body using motorized X-ray source before reaching the electronic detector | (i) Permits visualization of bony structure and calcified tissue (e.g., intra-articular calcium crystal deposition) | (i) Expensive | (i) Osteophyte formation | (i) OsteoArthritis Computed Tomography (OACT) |
| (ii) Allows study of osteoarthritic biomechanics using weight-bearing and kinematic four-dimensional CT | (ii) Risk of radiation | (ii) Cyst formation | |||
| (iii) Allows study of joint metabolism | (iii) Requires intra-articular injection of contrast material in the case of CT arthrography, may cause allergic reaction | (iii) Subchondral sclerosis | |||
| (iv) Potential image-guided therapy tools with CT arthrography | |||||
| (v) Allows 2D (slices) and 3D visualization | |||||
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| Nuclear medicine bone scan | Radioactive tracer is injected into patient's vein is absorbed by metabolically active cells and tissues | (i) Enables radiopharmaceutical localization | (i) Injection of radioactive tracer | (i) Osteophyte formation | Nil |
| (ii) Allows evaluation of injury status | (ii) Complicated procedures | (ii) Cyst formation | |||
| (iii) Differentiation of OA from bone metastases and osteomyelitis | (iii) No grading system for OA disease severity | (iii) Subchondral sclerosis | |||
| (iv) 2D and 3D visualization | (iv) Bone marrow lesions | ||||
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| Ultrasonography | Knee joint is scanned with sound waves | (i) Low cost | (i) Limited to 2D visualization | (i) Osteophyte formation | (i) Ultrasonographic grading scale |
| (ii) Evaluation of ligaments and synovium | (ii) Poor contrast caused by fat and air | ||||
| (iii) Real-time assessment | (iii) Limited to evaluation of the far inner margins of lateral and medial femorotibial joints | ||||
| (iv) Portable | (iv) Risk of overdiagnosis | ||||
| (v) Potential image-guided therapy tools | |||||
| (vi) Better spatial resolution | |||||
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| Optical coherence tomography (OCT) | Cartilage sample is scanned with infrared light | (i) Evaluation of articular cartilage at resolution up to micron scale at 4 to 20 | (i) Not applicable to in vivo assessment | (i) Cartilage surface roughness | (i) Degenerative joint disease (DJD) classification |
| (ii) Portable | (ii) Time-consuming | (ii) Degeneration of articular cartilage | |||
| (iii) Potential image-guided therapy tools | |||||
| (iv) 2D and 3D visualization | |||||
Summary of knee OA grading systems based on imaging modalities.
| Imaging modalities | OA grading system | Examined OA features | Pros | Cons |
|---|---|---|---|---|
| X-ray images | KL | (i) Osteophyte | (i) Universally accepted knee OA grading system | (i) Overemphasizes the significance of osteophytes as compared to JSN |
| (ii) JSN | (ii) Indicates OA changes in medial compartment better | (ii) Poor reliability for OA changes in lateral compartment | ||
| (iii) Bone end deformity | (iii) Poor inter- and intraobserver reliabilities | |||
| (iv) Subchondral sclerosis | ||||
| Ahlbäck | (i) JSN | (i) Greater emphasis on JSN than osteophytes by assuming the joint space reduction as an indirect sign of cartilage loss | (i) Poor inter- and intraobserver reliabilities | |
| (ii) Bone attrition | ||||
| Brandt | (i) Percentage of JSN | (i) Greater emphasis on JSN than osteophytes | (i) Poor inter- and intraobserver reliabilities | |
| (ii) JSN associated osteophytes | (ii) Good correlation with arthroscopic damage | |||
| (iii) JSN associated subchondral sclerosis | ||||
| (iv) JSN associated subchondral cysts | ||||
| OARSI | (i) Percentage of JSN | (i) Most widely used individual OA feature scale with example images | (i) Only focus on JSN feature | |
| IKDC | (i) Joint space width | (ii) Best combination of good interobserver reliability and medium correlation with arthroscopic findings | (i) Only focus on joint space width | |
| Fair bank | (i) Squaring of tibial margin | (i) Involves many radiographic features | (i) Limited to post-meniscectomy condition | |
| (ii) Flattening of femoral condyle | (ii) Lack of knowledge about its reliability | |||
| (iii) Sclerosis of tibial margin | ||||
| (iv) Hypertrophic changes | ||||
| (v) JSN | ||||
| Jäger-Wirth | (i) Osteophytes | (i) Involves many radiographic features. | (i) Lack of knowledge about its reliability | |
| (ii) JSN | ||||
| (iii) Arthrosis | ||||
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| MRI images | Modified Outerbridge classification | (i) Fat-saturated proton density sequences of chondromalacia patella and chondral surface | (i) Greater emphasis on cartilage morphology | (i) Require validation with arthroscopic examination |
| (ii) No bony assessment | ||||
| WORMS | (i) Cartilage | (i) Greater emphasis on cartilage and bone morphologies | (i) Tedious interpretation task | |
| (ii) Bone marrow lesions | ||||
| (iii) Subchondral cysts | ||||
| (iv) Bone attrition | ||||
| (v) Osteophytes | ||||
| (vi) Effusion synovitis | ||||
| (vii) Meniscal tears | ||||
| (viii) Ligaments | ||||
| (ix) Periarticular cysts | ||||
| (x) Bursitis | ||||
| (xi) Loose bodies | ||||
| KOSS | (i) Cartilage | (i) Greater emphasis on cartilage and bone morphologies | (i) Tedious interpretation task | |
| (ii) Bone marrow lesions | ||||
| (iii) Subchondral cysts | ||||
| (iv) Osteophytes | ||||
| (v) Effusion synovitis | ||||
| (vi) Synovial thickening | ||||
| (vii) Meniscal extrusion | ||||
| (viii) Meniscal tears | ||||
| (ix) Popliteal cysts | ||||
| BLOKS | (i) Cartilage | (i) Greater emphasis on cartilage and bone morphologies | (i) Tedious interpretation task | |
| (ii) Bone marrow lesions | ||||
| (iii) Osteophytes | ||||
| (iv) Effusion synovitis | ||||
| (v) Hoffa synovitis | ||||
| (vi) Meniscal extrusion | ||||
| (vii) Intrameniscal signal | ||||
| (viii) Meniscal tears | ||||
| (ix) Meniscal maceration | ||||
| (x) Meniscal cyst | ||||
| (xi) Ligaments | ||||
| (xii) Periarticular cysts | ||||
| (xiii) Bursitis | ||||
| (xiv) Loose bodies | ||||
| MOAKS | (i) Cartilage | (i) Greater emphasis on cartilage and bone morphologies | (i) Tedious interpretation task | |
| (ii) Bone marrow lesions | (ii) Cover most OA features | |||
| (iii) Osteophytes | ||||
| (iv) Effusion synovitis | ||||
| (v) Hoffa synovitis | ||||
| (vi) Meniscal extrusion | ||||
| (vii) Intrameniscal signal | ||||
| (viii) Meniscal tears | ||||
| (ix) Meniscal maceration | ||||
| (x) Meniscal cyst | ||||
| (xi) Hypertrophy | ||||
| (xii) Ligaments | ||||
| (xiii)Periarticular cysts | ||||
| (xiv) Bursitis | ||||
| (xv) Loose bodies | ||||
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| CT images | OACT | (i) JSN | (i) Emphasis on two knee compartments: tibiofemoral and patellofemoral joints | (i) Lack of validation result |
| (ii) Osteophytes | ||||
| (iii) Cysts | ||||
| (iv) Sclerosis | ||||
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| Ultrasonography | Ultrasonographic grading scale | (i) Osteophytes | (i) Depends on the shape of distal femoral osteophytes | (i) Features may be distorted by noise |
| (ii) Projection from femoral condyle | (ii) Limited to primary knee OA | |||
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| OCT images | DJD classification | (i) Cartilage surface irregularities | (i) Deep examination of cartilage | (i) Difficult to collect samples |
| (ii) Tissue disorganization in cartilage | (ii) Only focuses on cartilage changes | |||
| (iii) Fibrocartilaginous regeneration | ||||
| (iv) Cartilage erosion | ||||
Summary of automated knee OA diagnosis and prognosis.
| Task | Subtask | Area of OA management | Achievements | Future work suggestions | Machine learning techniques |
|---|---|---|---|---|---|
| Localization of knee joint | Detection of knee joint | Diagnosis | (i) Detected tibiofemoral joints on X-ray images [ | (i) Recognition of OA features | (i) Histogram of oriented gradients [ |
| (ii) Detected patellofemoral joints on X-ray images [ | (ii) Quantification of qualitative OA features | (ii) Local binary pattern [ | |||
| (iii) Random forest regression voting [ | |||||
| (iv) Fully convolutional neural network [ | |||||
| (iii) Detected cartilage X-ray images [ | (v) YOLOv2 network [ | ||||
| Segmentation of knee joint components | Diagnosis | (i) Segmented knee cartilage from 2D ultrasound images [ | (i) Area measurement | (i) Locally statistical level set method [ | |
| (ii) Segmented knee cartilage from 2D MRI images [ | (ii) Volumetric measurement | (ii) Automatic seed point detection [ | |||
| (iii) Segmented cartilage and meniscus from MRI images [ | (iii) Joint shape measurement | (iii) Random walker [ | |||
| (iv) Segmented subchondral bone from multiple 2D MRI images [ | (iv) Quantification of measurable OA features | (iv) Watershed | |||
| (v) Segmented distal femur and proximal tibia from X-ray images [ | (v) Reconstruction of 3D knee joint model for simulation and joint loading study | (v) Graph cut [ | |||
| (vi) Calculated joint space width on X-ray images [ | (vi) Finite element analysis | (vi) Support vector machine classifier [ | |||
| (vii) Segmented femoral condyle cartilage from ultrasound images [ | (vii) Utilization of statistical and computational models | (vii) Decision tree classifier [ | |||
| (viii) Segmented bones (femur and tibia) and cartilages (femoral and tibial cartilages) on MRI images [ | (viii) Active contour algorithm [ | ||||
| (ix) Segmented knee bones, cartilage, and muscle tissues on MRI images [ | (ix) U-Net [ | ||||
| (x) Segmented femoral cartilage and tibial cartilage from 3D MRI images [ | (x) Res-U-Net [ | ||||
| (xi) Siam-U-Net [ | |||||
| (xii) CUMed-Vision [ | |||||
| (xiii) DeepLabv3 [ | |||||
| (xiv) FC-DenseNet [ | |||||
| (xv) LinkNet [ | |||||
| (xvi) TernausNet [ | |||||
| (xvii) AlbuNet [ | |||||
| (xviii) Attention U-Net [ | |||||
| (xix) LadderNet [ | |||||
| (xx) Multi-atlas registration [ | |||||
| (xxi) CycleGAN [ | |||||
| (xxii) cGANs [ | |||||
| (xxiii) Connected conditional random field model [ | |||||
| (xxiv) Convolutional encoder-decoder model [ | |||||
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| Classification of knee OA severity | N/A | Diagnosis | (i) Discriminated osteoarthritic knee based on MRI features [ | (i) Risk stratification | (i) 3D-CNN [ |
| (ii) Discriminated patellofemoral OA based on X-ray images [ | (ii) Classification of OA features | (ii) Deep Siamese CNN [ | |||
| (iii) Classified meniscal lesion using MRI data [ | (iii) Classification of OA severity based on computational outcomes | (iii) CNN with LBP [ | |||
| (iv) Graded knee OA severity using X-ray images based on KL classification [ | (iv) CNN with HOG [ | ||||
| (v) ResNet [ | |||||
| (vi) VGG [ | |||||
| (vii) DenseNet [ | |||||
| (viii) InceptionV3 [ | |||||
| (ix) GooLeNet [ | |||||
| (x) ResNeXt [ | |||||
| (xi) MobileNetV2 [ | |||||
| (xii) Linear mixed-effects models [ | |||||
| (xiii) Elastic net [ | |||||
| (xiv) Support vector [ | |||||
| (xv) Random forest model [ | |||||
| (xvi) | |||||
| (xvii) Ensemble method using SE-ResNet-50 and SE-ResNet-50-32x4d [ | |||||
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| Prediction of knee OA disease progression | Without intervention | Prognosis | (i) Estimated future knee OA incidence | (i) Risk stratification | (i) Random forest classifier [ |
| (a) 30 months [ | (ii) Selection of data from suitable time points to indicate short-term and long-term OA changes | (ii) Logistic regression classifier [ | |||
| (b) 48 months [ | (iii) OA feature change detection | (iii) Support vector machine classifier [ | |||
| (c) 8 years | (iv) Discovery of pain-associated imaging features | (iv) XGBoost model [ | |||
| (ii) Predicted medial JSN progression [ | (v) Multilayer perceptron [ | ||||
| (iii) Predicted radiographic joint space loss progression [ | (vi) LASSO regression [ | ||||
| (iv) Predicted knee OA onset and knee OA deterioration [ | (vii) Artificial neural network [ | ||||
| (v) Discriminated between progressors and nonprogressors [ | (viii) Deep CNN [ | ||||
| (vi) Predicted pain [ | (ix) DenseNet CNN [ | ||||
| (vii) Predicted risk of progressive pain and structural change [ | (x) Gradient boosting machine [ | ||||
| (viii) Predicted total knee replacement (TKR) incidence [ | (xi) Duo classifier [ | ||||
| (xii) DeepSurv [ | |||||
| (xiii) Dynamic functional mixed-effects model [ | |||||