Increased intra-cortical porosity reduces bone stiffness and strength in pediatric patients with osteogenesis imperfecta
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Updated: Apr 23, 2026

A Sectioning, Coring, and Image Processing Guide for High-Throughput Cortical Bone Sample Procurement and Analysis for Synchrotron Micro-CT
Published on: June 12, 2020
V Vardakastani1, D Saletti1, W Skalli1
1Institut de Biomécanique Humaine Georges Charpak, Arts et Metiers ParisTech (ENSAM), 151 Boulevard de l'Hôpital, 75013 Paris, France.
Insights
Osteogenesis imperfecta (OI) causes brittle bones due to disorganized collagen. This study found increased porosity in OI bone, directly correlating with reduced strength and suggesting new imaging methods for assessing bone fragility.
Area of Science:
- Biomaterials Science
- Orthopedics
- Skeletal Biology
Background:
- Osteogenesis imperfecta (OI) is a genetic disorder affecting collagen, leading to increased bone fragility.
- The precise mechanisms linking collagen mutations to fracture susceptibility in OI remain unclear.
- Understanding OI bone microstructure is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the cortical bone microstructure in OI patients using polarized light microscopy.
- To correlate microstructural findings with mechanical compression test results.
- To identify potential imaging biomarkers for assessing bone strength in OI.
Main Methods:
- Harvesting cortical bone specimens from OI patients during surgery.
- Utilizing polarized light microscopy to examine bone collagen architecture and porosity.
- Analyzing the correlation between areal porosity and previously measured mechanical properties (Young's modulus, compressive strength).
Main Results:
- Observed disorganized collagen architecture and significantly increased areal porosity in OI bone compared to healthy bone.
- Identified large, asymmetrical pores within the cortical bone structure.
- Demonstrated a strong correlation between increased areal porosity and reduced apparent Young's modulus and compressive strength in OI bone samples.
Conclusions:
- Increased intra-cortical porosity is a key factor contributing to the reduced mechanical integrity of OI cortical bone.
- In vivo imaging techniques with resolutions of approximately 100 μm or less may offer non-invasive assessment of bone strength in OI.
- Further research with larger cohorts is needed to fully elucidate the relationship between porosity and mechanical integrity in OI.
Abstract:
Osteogenesis imperfecta (OI) is a heritable disease occurring in one out of every 20,000 births. Although it is known that Type I collagen mutation in OI leads to increased bone fragility, the mechanism of this increased susceptibility to fracture is not clear. The aim of this study was to assess the microstructure of cortical bone fragments from patients with osteogenesis imperfecta (OI) using polarized light microscopy, and to correlate microstructural observations with the results of previously performed mechanical compression tests on bone from the same source. Specimens of cortical bone were harvested from the lower limbs of three (3) OI patients at the time of surgery, and were divided into two groups. Group 1 had been subjected to previous micro-mechanical compression testing, while Group 2 had not been subjected to any prior testing. Polarized light microscopy revealed disorganized bone collagen architecture as has been previously observed, as well as a large increase in the areal porosity of the bone compared to typical values for healthy cortical bone, with large (several hundred micron sized), asymmetrical pores. Importantly, the areal porosity of the OI bone samples in Group 1 appears to correlate strongly with their previously measured apparent Young's modulus and compressive strength. Taken together with prior nanoindentation studies on OI bone tissue, the results of this study suggest that increased intra-cortical porosity is responsible for the reduction in macroscopic mechanical properties of OI cortical bone, and therefore that in vivo imaging modalities with resolutions of ~100 μm or less could potentially be used to non-invasively assess bone strength in OI patients. Although the number of subjects in this study is small, these results highlight the importance of further studies in OI bone by groups with access to human OI tissue in order to clarify the relationship between increased porosity and reduced macroscopic mechanical integrity.
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