Title of article
Indentation stiffness does not discriminate between normal and degraded articular cartilage
Author/Authors
Cameron P. Brown، نويسنده , , Ross W. Crawford، نويسنده , , Adekunle Oloyede، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2007
Pages
6
From page
843
To page
848
Abstract
Background
Relative indentation characteristics are commonly used for distinguishing between normal healthy and degraded cartilage. The application of this parameter in surgical decision making and an appreciation of articular cartilage biomechanics has prompted us to hypothesise that it is difficult to define a reference stiffness to characterise normal articular cartilage.
Methods
This hypothesis is tested for validity by carrying out biomechanical indentation of articular cartilage samples that are characterised as visually normal and degraded relative to proteoglycan depletion and collagen disruption. Compressive loading was applied at known strain rates to visually normal, artificially degraded and naturally osteoarthritic articular cartilage and observing the trends of their stress–strain and stiffness characteristics.
Findings
While our results demonstrated a 25% depreciation in the stiffness of individual samples after proteoglycan depletion, they also showed that when compared to the stiffness of normal samples only 17% lie outside the range of the stress–strain behaviour of normal samples.
Interpretation
We conclude that the extent of the variability in the properties of normal samples, and the degree of overlap (81%) of the biomechanical properties of normal and degraded matrices demonstrate that indentation data cannot form an accurate basis for distinguishing normal from abnormal articular cartilage samples with consequences for the application of this mechanical process in the clinical environment.
Keywords
Articular cartilage , Mechanical indentation , Stiffness , osteoarthritis , Cartilage degradation
Journal title
Clinical Biomechanics
Serial Year
2007
Journal title
Clinical Biomechanics
Record number
486766
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