Evidence map›Paper›PMID 42290682›Full record

ArticleOsteoarthritis and cartilage open2026

Degeneration dependent changes in human knee cartilage mechanical properties revealed by synchrotron tomography based finite element modeling.

Viktor Jönsson, Lorenzo Grassi, Anna Gustafsson, Maria Pierantoni, Hector Dejea, Amanda Sjögren, Christian M Schlepütz, Martin Englund, Hanna Isaksson

Abstract read
In one paragraph

Article in Osteoarthritis and cartilage open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Viktor JönssonDepartment of Biomedical Engineering, Lund University, Lund, Sweden.
Lorenzo GrassiDepartment of Biomedical Engineering, Lund University, Lund, Sweden.
Anna GustafssonDepartment of Biomedical Engineering, Lund University, Lund, Sweden.
Maria PierantoniDepartment of Biomedical Engineering, Lund University, Lund, Sweden.
Hector DejeaDepartment of Biomedical Engineering, Lund University, Lund, Sweden.
Amanda SjögrenClinical Sciences Lund Orthopedics, Lund University, Lund, Sweden.
Christian M SchlepützSwiss Light Source, Paul Scherrer Institute, Villigen, Switzerland.
Martin EnglundClinical Sciences Lund Orthopedics, Lund University, Lund, Sweden.
Hanna IsakssonDepartment of Biomedical Engineering, Lund University, Lund, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Knee osteoarthritis (OA) is a chronic joint disease associated with pain and reduced function. The mechanisms underlying OA and how mechanical properties change with the disease are not fully understood, partly due to large variability during mechanical testing of cartilage. We characterized the mechanical properties of human femoral cartilage with varying levels of degeneration using a tissue constitution specific fibril-reinforced poroelastic (FRPE) material model. Method: We created sample-specific finite element (FE) models based on synchrotron-based x-ray tomography to reduce the variability caused by sample geometry. For comparison, idealized FE models were also created without tomography data. Cartilage samples (n = 15) were mechanically tested in compressive stress relaxation (two steps of 15% strain) with in-situ x-ray tomography. Adjacent tissue samples were histopathologically graded (OARSI). The FRPE parameters were optimized to minimize differences between experimental and simulated stress relaxation forces. Identified material parameters were analyzed with linear regression, with OARSI grade as independent variable. Results: We identified reductions in both collagen (-2x) and non-fibrillar matrix stiffness (-3x) accompanied by increased permeability (+5.5x) when comparing tissue with OARSI grade 1 and 5 in tomography-based FE models. At OARSI = 1, in idealized and tomography-based models, the collagen stiffness, non-fibrillar matrix stiffness and permeability differed 20, 110 and 55% respectively. Only collagen and non-fibrillar matrix stiffness were associated with OARSI grade in idealized models. Conclusion: Segmentation-based models were better at detecting degeneration-related mechanical changes than idealized models. The identified parameter changes match known OA tissue developments and can be used in predictive FE knee joint models.

Indexed as

Articular cartilageFibril-reinforced poroelasticOARSI gradeOsteoarthritisStress-relaxation

Identifiers

PMID42290682
PMCPMC13262150

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.