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Pediatric DXA: clinical applications
Normal bone mineral accrual requires adequate dietary intake of calcium, vitamin D and other nutrients; hepatic and renal activation of vitamin D; normal hormone levels (thyroid, parathyroid, reproductive and growth hormones); and neuromuscular functioning with sufficient stress upon the skeleton to...
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950217/ https://www.ncbi.nlm.nih.gov/pubmed/17431606 http://dx.doi.org/10.1007/s00247-007-0450-0 |
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author | Binkovitz, Larry A. Sparke, Paul Henwood, Maria J. |
author_facet | Binkovitz, Larry A. Sparke, Paul Henwood, Maria J. |
author_sort | Binkovitz, Larry A. |
collection | PubMed |
description | Normal bone mineral accrual requires adequate dietary intake of calcium, vitamin D and other nutrients; hepatic and renal activation of vitamin D; normal hormone levels (thyroid, parathyroid, reproductive and growth hormones); and neuromuscular functioning with sufficient stress upon the skeleton to induce bone deposition. The presence of genetic or acquired diseases and the therapies that are used to treat them can also impact bone health. Since the introduction of clinical DXA in pediatrics in the early 1990s, there has been considerable investigation into the causes of low bone mineral density (BMD) in children. Pediatricians have also become aware of the role adequate bone mass accrual in childhood has in preventing osteoporotic fractures in late adulthood. Additionally, the availability of medications to improve BMD has increased with the development of bisphosphonates. These factors have led to the increased utilization of DXA in pediatrics. This review summarizes much of the previous research regarding BMD in children and is meant to assist radiologists and clinicians with DXA utilization and interpretation. |
format | Text |
id | pubmed-1950217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-19502172007-08-20 Pediatric DXA: clinical applications Binkovitz, Larry A. Sparke, Paul Henwood, Maria J. Pediatr Radiol Review Normal bone mineral accrual requires adequate dietary intake of calcium, vitamin D and other nutrients; hepatic and renal activation of vitamin D; normal hormone levels (thyroid, parathyroid, reproductive and growth hormones); and neuromuscular functioning with sufficient stress upon the skeleton to induce bone deposition. The presence of genetic or acquired diseases and the therapies that are used to treat them can also impact bone health. Since the introduction of clinical DXA in pediatrics in the early 1990s, there has been considerable investigation into the causes of low bone mineral density (BMD) in children. Pediatricians have also become aware of the role adequate bone mass accrual in childhood has in preventing osteoporotic fractures in late adulthood. Additionally, the availability of medications to improve BMD has increased with the development of bisphosphonates. These factors have led to the increased utilization of DXA in pediatrics. This review summarizes much of the previous research regarding BMD in children and is meant to assist radiologists and clinicians with DXA utilization and interpretation. Springer-Verlag 2007-04-13 2007-07 /pmc/articles/PMC1950217/ /pubmed/17431606 http://dx.doi.org/10.1007/s00247-007-0450-0 Text en © Springer-Verlag 2007 |
spellingShingle | Review Binkovitz, Larry A. Sparke, Paul Henwood, Maria J. Pediatric DXA: clinical applications |
title | Pediatric DXA: clinical applications |
title_full | Pediatric DXA: clinical applications |
title_fullStr | Pediatric DXA: clinical applications |
title_full_unstemmed | Pediatric DXA: clinical applications |
title_short | Pediatric DXA: clinical applications |
title_sort | pediatric dxa: clinical applications |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950217/ https://www.ncbi.nlm.nih.gov/pubmed/17431606 http://dx.doi.org/10.1007/s00247-007-0450-0 |
work_keys_str_mv | AT binkovitzlarrya pediatricdxaclinicalapplications AT sparkepaul pediatricdxaclinicalapplications AT henwoodmariaj pediatricdxaclinicalapplications |