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Quantification of bone metabolic activity in the natural course of fractural lesions measured by quantitative SPECT/CT

OBJECTIVE(S): While increased uptake at the bone fractural site gradually decreases over time on bone scans, the rate of change has not been quantitatively evaluated. The purpose of this study was to quantify the extent of bone metabolic changes in fractural lesions on bone SPECT/CT. METHODS: We rev...

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Autores principales: Yamane, Tomohiko, Matsusaka, Yohji, Fukushima, Kenji, Seto, Akira, Matsunari, Ichiro, Kuji, Ichiei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803622/
https://www.ncbi.nlm.nih.gov/pubmed/36619183
http://dx.doi.org/10.22038/AOJNMB.2022.63484.1446
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author Yamane, Tomohiko
Matsusaka, Yohji
Fukushima, Kenji
Seto, Akira
Matsunari, Ichiro
Kuji, Ichiei
author_facet Yamane, Tomohiko
Matsusaka, Yohji
Fukushima, Kenji
Seto, Akira
Matsunari, Ichiro
Kuji, Ichiei
author_sort Yamane, Tomohiko
collection PubMed
description OBJECTIVE(S): While increased uptake at the bone fractural site gradually decreases over time on bone scans, the rate of change has not been quantitatively evaluated. The purpose of this study was to quantify the extent of bone metabolic changes in fractural lesions on bone SPECT/CT. METHODS: We reviewed bone scans acquired by dedicated SPECT/CT and chose those scans in which quantitative SPECT/CT of the same range was acquired twice or more. We set the region of interest on lesions of bone fracture and degeneration, and measured the maximum standardized uptake value (SUV(max)). From the SUV(max) of lesions and the interval between scans, a value for 30-day change in SUV(max) was calculated as ∆SUV(max)30d. The relationship between preSUV(max), SUV(max) for the first scan of the comparison, and ∆SUV(max)30d was evaluated utilizing a linear least-squares method. Furthermore, we assessed the ability to differentiate between fracture and degeneration using receiver operating characteristics (ROC) analysis and the Mann-Whitney U test. All cases were then categorized into five groups according to preSUV(max). Values of p <0.05 were considered statistically significant. RESULTS: We investigated 175 scans from 60 patients and analyzed scan combinations for 157 fractural lesions and 266 degenerative lesions. The relationship between preSUV(max) of fractural lesions and ∆SUV(max)30d was approximated as ∆SUV(max)30d =-0.15×preSUV(max) +1.35 (R(2)=0.60, p<0.0001). Area under the curves for all cases, 30≤ preSUV(max), 20≤ preSUV(max) <30, 15≤ preSUV(max) <20, 10≤ preSUV(max) <15, and preSUV(max) <10 were 0.73, 0.89, 0.86, 0.80, 0.91, and 0.59, respectively. Median ∆SUV(max)30d was significantly lower at fractural lesions than at degenerative lesions (-0.62 vs -0.04; p <0.0001). As for analyses of groups divided by preSUV(max), all median ∆SUV(max)30d for fractural lesions were significantly lower than those of degenerative lesions except for the group with preSUV(max) <10. CONCLUSION: The increased uptake at the fractural bone lesion observed in the quantitative bone SPECT/CT gradually decreased at the rate of SUV 0.15 per month, which showed a different trend with degenerative change.
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spelling pubmed-98036222023-01-07 Quantification of bone metabolic activity in the natural course of fractural lesions measured by quantitative SPECT/CT Yamane, Tomohiko Matsusaka, Yohji Fukushima, Kenji Seto, Akira Matsunari, Ichiro Kuji, Ichiei Asia Ocean J Nucl Med Biol Original Article OBJECTIVE(S): While increased uptake at the bone fractural site gradually decreases over time on bone scans, the rate of change has not been quantitatively evaluated. The purpose of this study was to quantify the extent of bone metabolic changes in fractural lesions on bone SPECT/CT. METHODS: We reviewed bone scans acquired by dedicated SPECT/CT and chose those scans in which quantitative SPECT/CT of the same range was acquired twice or more. We set the region of interest on lesions of bone fracture and degeneration, and measured the maximum standardized uptake value (SUV(max)). From the SUV(max) of lesions and the interval between scans, a value for 30-day change in SUV(max) was calculated as ∆SUV(max)30d. The relationship between preSUV(max), SUV(max) for the first scan of the comparison, and ∆SUV(max)30d was evaluated utilizing a linear least-squares method. Furthermore, we assessed the ability to differentiate between fracture and degeneration using receiver operating characteristics (ROC) analysis and the Mann-Whitney U test. All cases were then categorized into five groups according to preSUV(max). Values of p <0.05 were considered statistically significant. RESULTS: We investigated 175 scans from 60 patients and analyzed scan combinations for 157 fractural lesions and 266 degenerative lesions. The relationship between preSUV(max) of fractural lesions and ∆SUV(max)30d was approximated as ∆SUV(max)30d =-0.15×preSUV(max) +1.35 (R(2)=0.60, p<0.0001). Area under the curves for all cases, 30≤ preSUV(max), 20≤ preSUV(max) <30, 15≤ preSUV(max) <20, 10≤ preSUV(max) <15, and preSUV(max) <10 were 0.73, 0.89, 0.86, 0.80, 0.91, and 0.59, respectively. Median ∆SUV(max)30d was significantly lower at fractural lesions than at degenerative lesions (-0.62 vs -0.04; p <0.0001). As for analyses of groups divided by preSUV(max), all median ∆SUV(max)30d for fractural lesions were significantly lower than those of degenerative lesions except for the group with preSUV(max) <10. CONCLUSION: The increased uptake at the fractural bone lesion observed in the quantitative bone SPECT/CT gradually decreased at the rate of SUV 0.15 per month, which showed a different trend with degenerative change. Mashhad University of Medical Sciences 2023 /pmc/articles/PMC9803622/ /pubmed/36619183 http://dx.doi.org/10.22038/AOJNMB.2022.63484.1446 Text en © 2023 mums.ac.ir All rights reserved https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yamane, Tomohiko
Matsusaka, Yohji
Fukushima, Kenji
Seto, Akira
Matsunari, Ichiro
Kuji, Ichiei
Quantification of bone metabolic activity in the natural course of fractural lesions measured by quantitative SPECT/CT
title Quantification of bone metabolic activity in the natural course of fractural lesions measured by quantitative SPECT/CT
title_full Quantification of bone metabolic activity in the natural course of fractural lesions measured by quantitative SPECT/CT
title_fullStr Quantification of bone metabolic activity in the natural course of fractural lesions measured by quantitative SPECT/CT
title_full_unstemmed Quantification of bone metabolic activity in the natural course of fractural lesions measured by quantitative SPECT/CT
title_short Quantification of bone metabolic activity in the natural course of fractural lesions measured by quantitative SPECT/CT
title_sort quantification of bone metabolic activity in the natural course of fractural lesions measured by quantitative spect/ct
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803622/
https://www.ncbi.nlm.nih.gov/pubmed/36619183
http://dx.doi.org/10.22038/AOJNMB.2022.63484.1446
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