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High Resolution X-Ray: A Reliable Approach for Quantifying Osteoporosis in a Rodent Model

Osteoporosis is the most common metabolic disease of bone, resulting in significant worldwide morbidity. Currently, there are insufficient imaging modalities available to evaluate osteoporotic bones in small animal models. Here, we demonstrate the feasibility of using high resolution X-ray imaging a...

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Autores principales: Velasco, Omar, James, Aaron W., Asatrian, Greg, Ajalat, Mark, Pritchard, Tyler, Novshadian, Siyouneh, Murthy, Anu, Bayani, Georgina, Zhang, Xinli, Ting, Kang, Soo, Chia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4120930/
https://www.ncbi.nlm.nih.gov/pubmed/25126483
http://dx.doi.org/10.1089/biores.2014.0017
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author Velasco, Omar
James, Aaron W.
Asatrian, Greg
Ajalat, Mark
Pritchard, Tyler
Novshadian, Siyouneh
Murthy, Anu
Bayani, Georgina
Zhang, Xinli
Ting, Kang
Soo, Chia
author_facet Velasco, Omar
James, Aaron W.
Asatrian, Greg
Ajalat, Mark
Pritchard, Tyler
Novshadian, Siyouneh
Murthy, Anu
Bayani, Georgina
Zhang, Xinli
Ting, Kang
Soo, Chia
author_sort Velasco, Omar
collection PubMed
description Osteoporosis is the most common metabolic disease of bone, resulting in significant worldwide morbidity. Currently, there are insufficient imaging modalities available to evaluate osteoporotic bones in small animal models. Here, we demonstrate the feasibility of using high resolution X-ray imaging as a comparable measure of bone degeneration to dual-energy X-ray absorptiometry (DXA) in an osteoporosis rodent model. At week 0, animals underwent either an ovariectomy (OVX) or sham procedure (SHAM). DXA analysis was performed weekly to confirm and compare the bone degenerative changes induced by OVX. A comparison using high resolution X-ray imaging (Faxitron(®)) was then performed postmortem due to need of soft tissue removal. Two regions of interest (ROIs) were utilized: the distal third of the femur and the lumbar spine (L4/L5). It was observed that SHAM animals maintained a relatively constant bone mineral density (BMD), in comparison to OVX animals, whereby a significant decrease in BMD was appreciated. Post mortem X-ray scans were performed and converted to 8-bit color and quantified. A high level of agreement with DXA quantifications was observed with X-ray quantifications, and a significant correlation between the radiopacity, visualized by color distributions, and the DXA BMD values between animal groups was evident. Our study demonstrates the applicability of high resolution X-ray imaging both qualitatively and quantitatively as a reliable approach for quantifying osteoporosis in rodent osteoporotic models. With DXA being a highly user dependent modality, our technique is a unique secondary methodology to verify DXA findings and minimize inter-observer variability.
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spelling pubmed-41209302014-08-14 High Resolution X-Ray: A Reliable Approach for Quantifying Osteoporosis in a Rodent Model Velasco, Omar James, Aaron W. Asatrian, Greg Ajalat, Mark Pritchard, Tyler Novshadian, Siyouneh Murthy, Anu Bayani, Georgina Zhang, Xinli Ting, Kang Soo, Chia Biores Open Access Technical Report Osteoporosis is the most common metabolic disease of bone, resulting in significant worldwide morbidity. Currently, there are insufficient imaging modalities available to evaluate osteoporotic bones in small animal models. Here, we demonstrate the feasibility of using high resolution X-ray imaging as a comparable measure of bone degeneration to dual-energy X-ray absorptiometry (DXA) in an osteoporosis rodent model. At week 0, animals underwent either an ovariectomy (OVX) or sham procedure (SHAM). DXA analysis was performed weekly to confirm and compare the bone degenerative changes induced by OVX. A comparison using high resolution X-ray imaging (Faxitron(®)) was then performed postmortem due to need of soft tissue removal. Two regions of interest (ROIs) were utilized: the distal third of the femur and the lumbar spine (L4/L5). It was observed that SHAM animals maintained a relatively constant bone mineral density (BMD), in comparison to OVX animals, whereby a significant decrease in BMD was appreciated. Post mortem X-ray scans were performed and converted to 8-bit color and quantified. A high level of agreement with DXA quantifications was observed with X-ray quantifications, and a significant correlation between the radiopacity, visualized by color distributions, and the DXA BMD values between animal groups was evident. Our study demonstrates the applicability of high resolution X-ray imaging both qualitatively and quantitatively as a reliable approach for quantifying osteoporosis in rodent osteoporotic models. With DXA being a highly user dependent modality, our technique is a unique secondary methodology to verify DXA findings and minimize inter-observer variability. Mary Ann Liebert, Inc. 2014-08-01 /pmc/articles/PMC4120930/ /pubmed/25126483 http://dx.doi.org/10.1089/biores.2014.0017 Text en Copyright 2014, Mary Ann Liebert, Inc.
spellingShingle Technical Report
Velasco, Omar
James, Aaron W.
Asatrian, Greg
Ajalat, Mark
Pritchard, Tyler
Novshadian, Siyouneh
Murthy, Anu
Bayani, Georgina
Zhang, Xinli
Ting, Kang
Soo, Chia
High Resolution X-Ray: A Reliable Approach for Quantifying Osteoporosis in a Rodent Model
title High Resolution X-Ray: A Reliable Approach for Quantifying Osteoporosis in a Rodent Model
title_full High Resolution X-Ray: A Reliable Approach for Quantifying Osteoporosis in a Rodent Model
title_fullStr High Resolution X-Ray: A Reliable Approach for Quantifying Osteoporosis in a Rodent Model
title_full_unstemmed High Resolution X-Ray: A Reliable Approach for Quantifying Osteoporosis in a Rodent Model
title_short High Resolution X-Ray: A Reliable Approach for Quantifying Osteoporosis in a Rodent Model
title_sort high resolution x-ray: a reliable approach for quantifying osteoporosis in a rodent model
topic Technical Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4120930/
https://www.ncbi.nlm.nih.gov/pubmed/25126483
http://dx.doi.org/10.1089/biores.2014.0017
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