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Reproducibility of a peripheral quantitative computed tomography scan protocol to measure the material properties of the second metatarsal

BACKGROUND: Peripheral quantitative computed tomography (pQCT) is an established technology that allows for the measurement of the material properties of bone. Alterations to bone architecture are associated with an increased risk of fracture. Further pQCT research is necessary to identify regions o...

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Autores principales: Chaplais, Elodie, Greene, David, Hood, Anita, Telfer, Scott, du Toit, Verona, Singh-Grewal, Davinder, Burns, Joshua, Rome, Keith, Schiferl, Daniel J, Hendry, Gordon J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108224/
https://www.ncbi.nlm.nih.gov/pubmed/25037451
http://dx.doi.org/10.1186/1471-2474-15-242
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author Chaplais, Elodie
Greene, David
Hood, Anita
Telfer, Scott
du Toit, Verona
Singh-Grewal, Davinder
Burns, Joshua
Rome, Keith
Schiferl, Daniel J
Hendry, Gordon J
author_facet Chaplais, Elodie
Greene, David
Hood, Anita
Telfer, Scott
du Toit, Verona
Singh-Grewal, Davinder
Burns, Joshua
Rome, Keith
Schiferl, Daniel J
Hendry, Gordon J
author_sort Chaplais, Elodie
collection PubMed
description BACKGROUND: Peripheral quantitative computed tomography (pQCT) is an established technology that allows for the measurement of the material properties of bone. Alterations to bone architecture are associated with an increased risk of fracture. Further pQCT research is necessary to identify regions of interest that are prone to fracture risk in people with chronic diseases. The second metatarsal is a common site for the development of insufficiency fractures, and as such the aim of this study was to assess the reproducibility of a novel scanning protocol of the second metatarsal using pQCT. METHODS: Eleven embalmed cadaveric leg specimens were scanned six times; three times with and without repositioning. Each foot was positioned on a custom-designed acrylic foot plate to permit unimpeded scans of the region of interest. Sixty-six scans were obtained at 15% (distal) and 50% (mid shaft) of the second metatarsal. Voxel size and scan speed were reduced to 0.40 mm and 25 mm.sec(-1). The reference line was positioned at the most distal portion of the 2(nd) metatarsal. Repeated measurements of six key variables related to bone properties were subject to reproducibility testing. Data were log transformed and reproducibility of scans were assessed using intraclass correlation coefficients (ICC) and coefficients of variation (CV%). RESULTS: Reproducibility of the measurements without repositioning were estimated as: trabecular area (ICC 0.95; CV% 2.4), trabecular density (ICC 0.98; CV% 3.0), Strength Strain Index (SSI) - distal (ICC 0.99; CV% 5.6), cortical area (ICC 1.0; CV% 1.5), cortical density (ICC 0.99; CV% 0.1), SSI – mid shaft (ICC 1.0; CV% 2.4). Reproducibility of the measurements after repositioning were estimated as: trabecular area (ICC 0.96; CV% 2.4), trabecular density (ICC 0.98; CV% 2.8), SSI - distal (ICC 1.0; CV% 3.5), cortical area (ICC 0.99; CV%2.4), cortical density (ICC 0.98; CV% 0.8), SSI – mid shaft (ICC 0.99; CV% 3.2). CONCLUSIONS: The scanning protocol generated excellent reproducibility for key bone properties measured at the distal and mid-shaft regions of the 2(nd) metatarsal. This protocol extends the capabilities of pQCT to evaluate bone quality in people who may be at an increased risk of metatarsal insufficiency fractures.
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spelling pubmed-41082242014-07-24 Reproducibility of a peripheral quantitative computed tomography scan protocol to measure the material properties of the second metatarsal Chaplais, Elodie Greene, David Hood, Anita Telfer, Scott du Toit, Verona Singh-Grewal, Davinder Burns, Joshua Rome, Keith Schiferl, Daniel J Hendry, Gordon J BMC Musculoskelet Disord Technical Advance BACKGROUND: Peripheral quantitative computed tomography (pQCT) is an established technology that allows for the measurement of the material properties of bone. Alterations to bone architecture are associated with an increased risk of fracture. Further pQCT research is necessary to identify regions of interest that are prone to fracture risk in people with chronic diseases. The second metatarsal is a common site for the development of insufficiency fractures, and as such the aim of this study was to assess the reproducibility of a novel scanning protocol of the second metatarsal using pQCT. METHODS: Eleven embalmed cadaveric leg specimens were scanned six times; three times with and without repositioning. Each foot was positioned on a custom-designed acrylic foot plate to permit unimpeded scans of the region of interest. Sixty-six scans were obtained at 15% (distal) and 50% (mid shaft) of the second metatarsal. Voxel size and scan speed were reduced to 0.40 mm and 25 mm.sec(-1). The reference line was positioned at the most distal portion of the 2(nd) metatarsal. Repeated measurements of six key variables related to bone properties were subject to reproducibility testing. Data were log transformed and reproducibility of scans were assessed using intraclass correlation coefficients (ICC) and coefficients of variation (CV%). RESULTS: Reproducibility of the measurements without repositioning were estimated as: trabecular area (ICC 0.95; CV% 2.4), trabecular density (ICC 0.98; CV% 3.0), Strength Strain Index (SSI) - distal (ICC 0.99; CV% 5.6), cortical area (ICC 1.0; CV% 1.5), cortical density (ICC 0.99; CV% 0.1), SSI – mid shaft (ICC 1.0; CV% 2.4). Reproducibility of the measurements after repositioning were estimated as: trabecular area (ICC 0.96; CV% 2.4), trabecular density (ICC 0.98; CV% 2.8), SSI - distal (ICC 1.0; CV% 3.5), cortical area (ICC 0.99; CV%2.4), cortical density (ICC 0.98; CV% 0.8), SSI – mid shaft (ICC 0.99; CV% 3.2). CONCLUSIONS: The scanning protocol generated excellent reproducibility for key bone properties measured at the distal and mid-shaft regions of the 2(nd) metatarsal. This protocol extends the capabilities of pQCT to evaluate bone quality in people who may be at an increased risk of metatarsal insufficiency fractures. BioMed Central 2014-07-19 /pmc/articles/PMC4108224/ /pubmed/25037451 http://dx.doi.org/10.1186/1471-2474-15-242 Text en Copyright © 2014 Chaplais et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Technical Advance
Chaplais, Elodie
Greene, David
Hood, Anita
Telfer, Scott
du Toit, Verona
Singh-Grewal, Davinder
Burns, Joshua
Rome, Keith
Schiferl, Daniel J
Hendry, Gordon J
Reproducibility of a peripheral quantitative computed tomography scan protocol to measure the material properties of the second metatarsal
title Reproducibility of a peripheral quantitative computed tomography scan protocol to measure the material properties of the second metatarsal
title_full Reproducibility of a peripheral quantitative computed tomography scan protocol to measure the material properties of the second metatarsal
title_fullStr Reproducibility of a peripheral quantitative computed tomography scan protocol to measure the material properties of the second metatarsal
title_full_unstemmed Reproducibility of a peripheral quantitative computed tomography scan protocol to measure the material properties of the second metatarsal
title_short Reproducibility of a peripheral quantitative computed tomography scan protocol to measure the material properties of the second metatarsal
title_sort reproducibility of a peripheral quantitative computed tomography scan protocol to measure the material properties of the second metatarsal
topic Technical Advance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108224/
https://www.ncbi.nlm.nih.gov/pubmed/25037451
http://dx.doi.org/10.1186/1471-2474-15-242
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