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Assessment of the efficacy of MRI for detection of changes in bone morphology in a mouse model of bone injury. | LitMetric

AI Article Synopsis

  • The study aimed to evaluate the effectiveness of MRI in tracking bone healing changes compared to high-resolution μCT in a mouse model.
  • Different MRI pulse sequences were optimized, and a burr hole fracture was created in mouse tibias to assess healing over time using MRI and μCT, alongside histological validation.
  • Results indicated that the RARE sequence in MRI provided clear imaging of fractures and soft tissue changes not visible on μCT, suggesting MRI's potential as an effective tool for monitoring bone morphology changes.

Article Abstract

Purpose: To determine whether magnetic resonance imaging (MRI) could be used to track changes in skeletal morphology during bone healing using high-resolution micro-computed tomography (μCT) as a standard. We used a mouse model of bone injury to compare μCT with MRI.

Materials And Methods: Surgery was performed to induce a burr hole fracture in the mouse tibia. A selection of biomaterials was immediately implanted into the fractures. First we optimized the imaging sequences by testing different MRI pulse sequences. Then changes in bone morphology over the course of fracture repair were assessed using in vivo MRI and μCT. Histology was performed to validate the imaging outcomes.

Results: The rapid acquisition with relaxation enhancement (RARE) sequence provided sufficient contrast between bone and the surrounding tissues to clearly reveal the fracture. It allowed detection of the fracture clearly 1 and 14 days postsurgery and revealed soft tissue changes that were not clear on μCT. In MRI and μCT the fracture was seen at day 1 and partial healing was detected at day 14.

Conclusion: The RARE sequence was the most suitable for MRI bone imaging. It enabled the detection of hard and even soft tissue changes. These findings suggest that MRI could be an effective imaging modality for assessing changes in bone morphology and pathobiology.

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Source
http://dx.doi.org/10.1002/jmri.23876DOI Listing

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