ArticleScientific reports2025
Cartilage mechanical responses during gait as in silico biomarkers for medial knee OA progression.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
3 citing papers in PubMed.
- Finite element analysis in foot and ankle arthrodesis.Bone & joint research · 2026Article
- Mechanical Signatures of Tibiofemoral Cartilage Degeneration Identified by Unconfined Compression Testing: Implications for Early Osteoarthritis Risk in Athletes.Medicina (Kaunas, Lithuania) · 2026Article
- Hydrogel microspheres for osteoarthritis treatment: Fabrication strategies, smart responsiveness, and multimodal therapies.Journal of tissue engineeringReview
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Authors and funding
8 authors.
Funding
Abstract
Osteoarthritis (OA) is a common degenerative whole joint disorder characterized by articular cartilage breakdown, mostly often in the knee's medial compartment. Traditional attempts to predict structural progression have focused on biochemical markers from blood, synovia, or urine; however, these do not capture internal mechanical environments that drives cartilage degeneration. In silico modelling enables non-invasive, patient-specific estimation of internal joint loading, including contact pressure, compressive strain, fibril strain and maximum shear strain, as potential mechanical biomarkers for OA progression. This study developed a novel MSK-FE workflow linking gait kinematics to contact pressures and cartilage tissue strains. Subjects showing medial OA progression over 2 years exhibited elevated medial compartment contact pressures and a posterolateral location shift at baseline. Unsupervised k-means clustering of cartilage tissue strain histograms further distinguished progressors from non-progressors and controls. These results demonstrate the potential of computationally efficient mechanical biomarkers to identify patients at risk of OA progression, supporting early and targeted preventative treatment strategies.
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Registered trials
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