4.6 Article

A new straightforward method for semi-automated segmentation of trabecular bone from cortical bone in diverse and challenging morphologies

Journal

ROYAL SOCIETY OPEN SCIENCE
Volume 8, Issue 8, Pages -

Publisher

ROYAL SOC
DOI: 10.1098/rsos.210408

Keywords

trabecular segmentation; automatic segmentation; cortical bone; trabecular bone; thresholding; Avizo

Funding

  1. OA Tech+ Network [EP/N027264/1]
  2. Anatomical Society [SSD 011018SEAL-v1-011217]
  3. Great Ormond Street Hospital Charity Clinical Research Starter Grant [17DD46]
  4. European Commission via H2020-MSCA-RISE programme (BAMOS) [734156]
  5. Rosetrees Trust [A1184]
  6. Marie Curie Actions (MSCA) [734156] Funding Source: Marie Curie Actions (MSCA)

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This study developed a semi-automated protocol for separating trabecular and cortical compartments in bone images obtained through X-ray micro-CT scans. The method eliminates user bias, is user-friendly across various datasets, and has been validated for use in complex bone analyses, making it a widely applicable tool in the field of skeletal research.
Many physiological, biomechanical, evolutionary and clinical studies that explore skeletal structure and function require successful separation of trabecular from cortical compartments of a bone that has been imaged by X-ray micro-computed tomography (micro-CT) prior to analysis. Separation often involves manual subdivision of these two similarly radio-opaque compartments, which can be time-consuming and subjective. We have developed an objective, semi-automated protocol which reduces user bias and enables straightforward, user-friendly segmentation of trabecular from the cortical bone without requiring sophisticated programming expertise. This method can conveniently be used as a 'recipe' in commercial programmes (Avizo herein) and applied to a variety of datasets. Here, we characterize and share this recipe, and demonstrate its application to a range of murine and human bone types, including normal and osteoarthritic specimens, and bones with distinct embryonic origins and spanning a range of ages. We validate the method by testing inter-user bias during the scan preparation steps and confirm utility in the architecturally challenging analysis of growing murine epiphyses. We also report details of the recipe, so that other groups can readily re-create a similar method in open access programmes. Our aim is that this method will be adopted widely to create a reproducible and time-efficient method of segmenting trabecular and cortical bone.

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