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Can digital X-ray radiogrammetry be an alternative for dual-energy X-ray absorptiometry in the diagnosis of secondary low bone quality in children?
Bone quality in children is generally measured with dual-energy X-ray absorptiometry (DXA). Digital X-ray radiogrammetry (DXR) uses BoneXpert to measure cortical bone quality on hand radiographs. This prospective study compared DXR and DXA results in children with high probability of secondary low b...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694095/ https://www.ncbi.nlm.nih.gov/pubmed/31352546 http://dx.doi.org/10.1007/s00431-019-03425-5 |
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author | Leijten, Alex D. Hampsink, Brieke Janssen, Marcel Klein, Willemijn M. Draaisma, Jos M. T. |
author_facet | Leijten, Alex D. Hampsink, Brieke Janssen, Marcel Klein, Willemijn M. Draaisma, Jos M. T. |
author_sort | Leijten, Alex D. |
collection | PubMed |
description | Bone quality in children is generally measured with dual-energy X-ray absorptiometry (DXA). Digital X-ray radiogrammetry (DXR) uses BoneXpert to measure cortical bone quality on hand radiographs. This prospective study compared DXR and DXA results in children with high probability of secondary low bone quality, defined as DXA of the lumbar spine (DXA(LS)) Z-score ≤ − 2.0. One hundred one children underwent both DXA and DXR assessment. DXA(LS)Z-scores were also adjusted for bone age. DXR Z-scores were compared with both DXA(LS)Z-scores, using Pearson correlations, Bland-Altman analysis, and sensitivity-specificity analysis. Mean bone age, DXR, and both DXA Z-scores were significantly impaired. Pearson correlation coefficients were significant between DXR Z-scores and both DXA(LS)Z-scores 0.507–0.564 (p < 0.001). Bland-Altman analysis showed a mean difference of 0.05–0.48 between DXR and both DXA Z-scores and showed more than 90% similarity for both DXA(LS)Z-scores ≤ − 2.0. DXR had a sensitivity of 67–71% and specificity of 77–83% compared to both DXA(LS)Z-scores. Conclusion: DXR correlates well with as well DXA(LS) as bone age-adjusted DXA(LS)Z-scores and shows good agreement with as well DXA(LS) as bone age-adjusted DXA(LS)Z-scores ≤ − 2.0. DXR shows best results when compared with DXA(LS)Z-scores. |
format | Online Article Text |
id | pubmed-6694095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-66940952019-08-28 Can digital X-ray radiogrammetry be an alternative for dual-energy X-ray absorptiometry in the diagnosis of secondary low bone quality in children? Leijten, Alex D. Hampsink, Brieke Janssen, Marcel Klein, Willemijn M. Draaisma, Jos M. T. Eur J Pediatr Original Article Bone quality in children is generally measured with dual-energy X-ray absorptiometry (DXA). Digital X-ray radiogrammetry (DXR) uses BoneXpert to measure cortical bone quality on hand radiographs. This prospective study compared DXR and DXA results in children with high probability of secondary low bone quality, defined as DXA of the lumbar spine (DXA(LS)) Z-score ≤ − 2.0. One hundred one children underwent both DXA and DXR assessment. DXA(LS)Z-scores were also adjusted for bone age. DXR Z-scores were compared with both DXA(LS)Z-scores, using Pearson correlations, Bland-Altman analysis, and sensitivity-specificity analysis. Mean bone age, DXR, and both DXA Z-scores were significantly impaired. Pearson correlation coefficients were significant between DXR Z-scores and both DXA(LS)Z-scores 0.507–0.564 (p < 0.001). Bland-Altman analysis showed a mean difference of 0.05–0.48 between DXR and both DXA Z-scores and showed more than 90% similarity for both DXA(LS)Z-scores ≤ − 2.0. DXR had a sensitivity of 67–71% and specificity of 77–83% compared to both DXA(LS)Z-scores. Conclusion: DXR correlates well with as well DXA(LS) as bone age-adjusted DXA(LS)Z-scores and shows good agreement with as well DXA(LS) as bone age-adjusted DXA(LS)Z-scores ≤ − 2.0. DXR shows best results when compared with DXA(LS)Z-scores. Springer Berlin Heidelberg 2019-07-27 2019 /pmc/articles/PMC6694095/ /pubmed/31352546 http://dx.doi.org/10.1007/s00431-019-03425-5 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Leijten, Alex D. Hampsink, Brieke Janssen, Marcel Klein, Willemijn M. Draaisma, Jos M. T. Can digital X-ray radiogrammetry be an alternative for dual-energy X-ray absorptiometry in the diagnosis of secondary low bone quality in children? |
title | Can digital X-ray radiogrammetry be an alternative for dual-energy X-ray absorptiometry in the diagnosis of secondary low bone quality in children? |
title_full | Can digital X-ray radiogrammetry be an alternative for dual-energy X-ray absorptiometry in the diagnosis of secondary low bone quality in children? |
title_fullStr | Can digital X-ray radiogrammetry be an alternative for dual-energy X-ray absorptiometry in the diagnosis of secondary low bone quality in children? |
title_full_unstemmed | Can digital X-ray radiogrammetry be an alternative for dual-energy X-ray absorptiometry in the diagnosis of secondary low bone quality in children? |
title_short | Can digital X-ray radiogrammetry be an alternative for dual-energy X-ray absorptiometry in the diagnosis of secondary low bone quality in children? |
title_sort | can digital x-ray radiogrammetry be an alternative for dual-energy x-ray absorptiometry in the diagnosis of secondary low bone quality in children? |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694095/ https://www.ncbi.nlm.nih.gov/pubmed/31352546 http://dx.doi.org/10.1007/s00431-019-03425-5 |
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