A new method to monitor bone geometry changes at different spatial scales in the longitudinal in vivo μCT studies of mice bones.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 22 03 2019
accepted: 21 06 2019
entrez: 23 7 2019
pubmed: 23 7 2019
medline: 28 2 2020
Statut: epublish

Résumé

Longitudinal studies of bone adaptation in mice using in vivo micro-computed tomography (μCT) have been commonly used for pre-clinical evaluation of physical and pharmacological interventions. The main advantage of this approach is to use each mouse as its own control, reducing considerably the sample size required by statistical power analysis. To date, multi-scale estimation of bone adaptations become essential since the bone activity that takes place at different scales may be associated with different bone mechanisms. Measures of bone adaptations at different time scales have been attempted in a previous study. This paper extends quantification of bone activity at different spatial scales with a proposition of a novel framework. The method involves applying level-set method (LSM) to track the geometric changes from the longitudinal in vivo μCT scans of mice tibia. Bone low- and high-spatial frequency patterns are then estimated using multi-resolution analysis. The accuracy of the framework is quantified by applying it to two times separated scanned images with synthetically manipulated global and/or local activity. The Root Mean Square Deviation (RMSD) was approximately 1.5 voxels or 0.7 voxels for the global low-spatial frequency or local high-spatial frequency changes, respectively. The framework is further applied to the study of bone changes in longitudinal datasets of wild-type mice tibiae over time and space. The results demonstrate the ability for the spatio-temporal quantification and visualisation of bone activity at different spatial scales in longitudinal studies thus providing further insight into bone adaptation mechanisms.

Identifiants

pubmed: 31329619
doi: 10.1371/journal.pone.0219404
pii: PONE-D-19-08245
pmc: PMC6645529
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0219404

Subventions

Organisme : National Centre for the Replacement, Refinement and Reduction of Animals in Research
ID : NC/R001073/1
Pays : United Kingdom

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Yang Zhang (Y)

Department of Automatic Control and Systems Engineering, The University of Sheffield, Sheffield, United Kingdom.
INSIGNEO Institute for in Silico Medicine, The University of Sheffield, Sheffield, United Kingdom.

Enrico Dall'Ara (E)

INSIGNEO Institute for in Silico Medicine, The University of Sheffield, Sheffield, United Kingdom.
Department of Oncology & Metabolism, The University of Sheffield, Sheffield, United Kingdom.

Marco Viceconti (M)

Department of Industrial Engineering, Alma Mater Studiorum, University of Bologna, Bologna Area, Italy.
Medical Technology Lab, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.

Visakan Kadirkamanathan (V)

Department of Automatic Control and Systems Engineering, The University of Sheffield, Sheffield, United Kingdom.
INSIGNEO Institute for in Silico Medicine, The University of Sheffield, Sheffield, United Kingdom.

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Classifications MeSH