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Osteoporotic profiles in elderly patients with symptomatic lumbar spinal canal stenosis

BACKGROUND: The osteoporosis and lumbar canal stenosis, in elderly patients are under diagnosed and under reported. We report a cross sectional study to demonstrate the osteoporotic profile in patients with lumbar spinal stenosis (LSS) and to determine the proportion of patients with LSS who need to...

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Autores principales: Lee, Byung Ho, Moon, Seong Hwan, Kim, Ho-Joong, Lee, Hwan Mo, Kim, Tae Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377137/
https://www.ncbi.nlm.nih.gov/pubmed/22719113
http://dx.doi.org/10.4103/0019-5413.96379
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author Lee, Byung Ho
Moon, Seong Hwan
Kim, Ho-Joong
Lee, Hwan Mo
Kim, Tae Hwan
author_facet Lee, Byung Ho
Moon, Seong Hwan
Kim, Ho-Joong
Lee, Hwan Mo
Kim, Tae Hwan
author_sort Lee, Byung Ho
collection PubMed
description BACKGROUND: The osteoporosis and lumbar canal stenosis, in elderly patients are under diagnosed and under reported. We report a cross sectional study to demonstrate the osteoporotic profile in patients with lumbar spinal stenosis (LSS) and to determine the proportion of patients with LSS who need to be treated for osteoporosis. MATERIALS AND METHODS: One hundred and six postmenopausal patients with symptomatic LSS were evaluated for osteoporotic profile, which included lumbar and hip bone mineral density (BMD), serum vitamin D concentration, bone resorption and formation markers. Demographic and disease related variables were analyzed to identify the association with the risk of osteoporosis or osteopenia. Statistical analysis used were multivariate logistic regression with a forward stepwise procedure. RESULTS: Twenty-four patients (22.6%) had osteoporosis and 60 (56.6%) had osteopenia. Overall, 84 patients (79.2%) with symptomatic LSS had osteoporosis or osteopenia. Fifty-nine patients (55.6%) had hypovitaminosis D. All bone turnover makers [alkaline phosphatase, osteocalcin, urinary-N-terminal telopeptide (u-NTx)] were demonstrated to be within normal range. Only age was associated with the risk of osteoporosis or osteopenia in the hip region. In the lumbar spine, all variables were not associated with osteoporosis or osteopenia. 44 patients (41.5%) required treatment for osteoporosis as per risk factors for osteoporosis. According to the guidelines from the Health Insurance Review Agency, however, only 20 patients (18.8% required) qualified for reimbursement for osteoporosis medications. CONCLUSIONS: LSS is associated with osteopenia, osteoporosis, and hypovitaminosis D, which should prompt careful screening and treatment in cases of osteoporosis and osteoarthritis.
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spelling pubmed-33771372012-06-20 Osteoporotic profiles in elderly patients with symptomatic lumbar spinal canal stenosis Lee, Byung Ho Moon, Seong Hwan Kim, Ho-Joong Lee, Hwan Mo Kim, Tae Hwan Indian J Orthop Original Article BACKGROUND: The osteoporosis and lumbar canal stenosis, in elderly patients are under diagnosed and under reported. We report a cross sectional study to demonstrate the osteoporotic profile in patients with lumbar spinal stenosis (LSS) and to determine the proportion of patients with LSS who need to be treated for osteoporosis. MATERIALS AND METHODS: One hundred and six postmenopausal patients with symptomatic LSS were evaluated for osteoporotic profile, which included lumbar and hip bone mineral density (BMD), serum vitamin D concentration, bone resorption and formation markers. Demographic and disease related variables were analyzed to identify the association with the risk of osteoporosis or osteopenia. Statistical analysis used were multivariate logistic regression with a forward stepwise procedure. RESULTS: Twenty-four patients (22.6%) had osteoporosis and 60 (56.6%) had osteopenia. Overall, 84 patients (79.2%) with symptomatic LSS had osteoporosis or osteopenia. Fifty-nine patients (55.6%) had hypovitaminosis D. All bone turnover makers [alkaline phosphatase, osteocalcin, urinary-N-terminal telopeptide (u-NTx)] were demonstrated to be within normal range. Only age was associated with the risk of osteoporosis or osteopenia in the hip region. In the lumbar spine, all variables were not associated with osteoporosis or osteopenia. 44 patients (41.5%) required treatment for osteoporosis as per risk factors for osteoporosis. According to the guidelines from the Health Insurance Review Agency, however, only 20 patients (18.8% required) qualified for reimbursement for osteoporosis medications. CONCLUSIONS: LSS is associated with osteopenia, osteoporosis, and hypovitaminosis D, which should prompt careful screening and treatment in cases of osteoporosis and osteoarthritis. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3377137/ /pubmed/22719113 http://dx.doi.org/10.4103/0019-5413.96379 Text en Copyright: © Indian Journal of Orthopaedics http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Byung Ho
Moon, Seong Hwan
Kim, Ho-Joong
Lee, Hwan Mo
Kim, Tae Hwan
Osteoporotic profiles in elderly patients with symptomatic lumbar spinal canal stenosis
title Osteoporotic profiles in elderly patients with symptomatic lumbar spinal canal stenosis
title_full Osteoporotic profiles in elderly patients with symptomatic lumbar spinal canal stenosis
title_fullStr Osteoporotic profiles in elderly patients with symptomatic lumbar spinal canal stenosis
title_full_unstemmed Osteoporotic profiles in elderly patients with symptomatic lumbar spinal canal stenosis
title_short Osteoporotic profiles in elderly patients with symptomatic lumbar spinal canal stenosis
title_sort osteoporotic profiles in elderly patients with symptomatic lumbar spinal canal stenosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377137/
https://www.ncbi.nlm.nih.gov/pubmed/22719113
http://dx.doi.org/10.4103/0019-5413.96379
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