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Medical treatment of severe osteoporosis including new concept of advanced severe osteoporosis
Osteoporosis is a metabolic bone disease characterized by decreased bone strength, leading to an increased risk of fracture. The World Health Organization (WHO) defines osteoporosis as a bone mineral density (BMD) of 2.5 standard deviations below that of a young adults (T-score of −2.5 or lower). Se...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Osteoporosis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372737/ https://www.ncbi.nlm.nih.gov/pubmed/30775462 http://dx.doi.org/10.1016/j.afos.2016.02.003 |
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author | Choi, Han Seok Park, So Young Kim, Yoo Mee Kim, Se Hwa Kim, Kyoung Min Chung, Yoon-Sok |
author_facet | Choi, Han Seok Park, So Young Kim, Yoo Mee Kim, Se Hwa Kim, Kyoung Min Chung, Yoon-Sok |
author_sort | Choi, Han Seok |
collection | PubMed |
description | Osteoporosis is a metabolic bone disease characterized by decreased bone strength, leading to an increased risk of fracture. The World Health Organization (WHO) defines osteoporosis as a bone mineral density (BMD) of 2.5 standard deviations below that of a young adults (T-score of −2.5 or lower). Severe osteoporosis is differentiated from osteoporosis by the presence of one or more fragility fractures in addition to this T-score. However, the current WHO definition may be insufficient to reflect the diverse spectrum of osteoporosis or severe osteoporosis, which can encompass various number and severity of prevalent fractures. To overcome these shortcomings of the WHO definition of osteoporosis, we propose a concept of ‘advanced severe osteoporosis’, which is defined by the presence of proximal femur fragility fracture or two or more fragility fractures in addition to BMD T-score of −2.5 or less. Based on the previous clinical trials and post-hoc analyses, we recommend selective estrogen receptor modulators, bisphosphonates, receptor activator of nuclear factor kappa-B ligand (RANKL) monoclonal antibody, and parathyroid hormone for the medical treatment of severe osteoporosis. In cases of advanced severe osteoporosis or osteoporosis that does not respond to previous anti-osteoporotic treatments, we also recommend parathyroid hormone, bisphosphonates, and RANKL monoclonal antibody. In conclusion, we need more precise assessment of osteoporosis and further stratification of the disease by number of prevalent fractures in addition to BMD. More aggressive managements should be provided for those with advanced severe osteoporosis. |
format | Online Article Text |
id | pubmed-6372737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Society of Osteoporosis |
record_format | MEDLINE/PubMed |
spelling | pubmed-63727372019-02-15 Medical treatment of severe osteoporosis including new concept of advanced severe osteoporosis Choi, Han Seok Park, So Young Kim, Yoo Mee Kim, Se Hwa Kim, Kyoung Min Chung, Yoon-Sok Osteoporos Sarcopenia Review Article Osteoporosis is a metabolic bone disease characterized by decreased bone strength, leading to an increased risk of fracture. The World Health Organization (WHO) defines osteoporosis as a bone mineral density (BMD) of 2.5 standard deviations below that of a young adults (T-score of −2.5 or lower). Severe osteoporosis is differentiated from osteoporosis by the presence of one or more fragility fractures in addition to this T-score. However, the current WHO definition may be insufficient to reflect the diverse spectrum of osteoporosis or severe osteoporosis, which can encompass various number and severity of prevalent fractures. To overcome these shortcomings of the WHO definition of osteoporosis, we propose a concept of ‘advanced severe osteoporosis’, which is defined by the presence of proximal femur fragility fracture or two or more fragility fractures in addition to BMD T-score of −2.5 or less. Based on the previous clinical trials and post-hoc analyses, we recommend selective estrogen receptor modulators, bisphosphonates, receptor activator of nuclear factor kappa-B ligand (RANKL) monoclonal antibody, and parathyroid hormone for the medical treatment of severe osteoporosis. In cases of advanced severe osteoporosis or osteoporosis that does not respond to previous anti-osteoporotic treatments, we also recommend parathyroid hormone, bisphosphonates, and RANKL monoclonal antibody. In conclusion, we need more precise assessment of osteoporosis and further stratification of the disease by number of prevalent fractures in addition to BMD. More aggressive managements should be provided for those with advanced severe osteoporosis. Korean Society of Osteoporosis 2016-03 2016-03-16 /pmc/articles/PMC6372737/ /pubmed/30775462 http://dx.doi.org/10.1016/j.afos.2016.02.003 Text en © 2016 The Korean Society of Osteoporosis. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Article Choi, Han Seok Park, So Young Kim, Yoo Mee Kim, Se Hwa Kim, Kyoung Min Chung, Yoon-Sok Medical treatment of severe osteoporosis including new concept of advanced severe osteoporosis |
title | Medical treatment of severe osteoporosis including new concept of advanced severe osteoporosis |
title_full | Medical treatment of severe osteoporosis including new concept of advanced severe osteoporosis |
title_fullStr | Medical treatment of severe osteoporosis including new concept of advanced severe osteoporosis |
title_full_unstemmed | Medical treatment of severe osteoporosis including new concept of advanced severe osteoporosis |
title_short | Medical treatment of severe osteoporosis including new concept of advanced severe osteoporosis |
title_sort | medical treatment of severe osteoporosis including new concept of advanced severe osteoporosis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372737/ https://www.ncbi.nlm.nih.gov/pubmed/30775462 http://dx.doi.org/10.1016/j.afos.2016.02.003 |
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