Pharmacotherapy of Bone Loss in Postmenopausal Women: Focus on Denosumab
ABSTRACT: Denosumab is a human monoclonal antibody against RANKL. This antibody decreases bone turnover markers and increases bone mineral density (BMD) in postmenopausal women. In phase 3 studies including more than 1100 women, denosumab achieved greater increases in lumbar spine, total hip, distal...
- Autores:
-
Román González, Alejandro
Ackerman, Kathryn E.
- Tipo de recurso:
- Review article
- Fecha de publicación:
- 2009
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/32170
- Acceso en línea:
- https://hdl.handle.net/10495/32170
- Palabra clave:
- Osteoporosis
Ligando RANK
RANK Ligand
Denosumab
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by-nc/2.5/co/
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Pharmacotherapy of Bone Loss in Postmenopausal Women: Focus on Denosumab |
| title |
Pharmacotherapy of Bone Loss in Postmenopausal Women: Focus on Denosumab |
| spellingShingle |
Pharmacotherapy of Bone Loss in Postmenopausal Women: Focus on Denosumab Osteoporosis Ligando RANK RANK Ligand Denosumab |
| title_short |
Pharmacotherapy of Bone Loss in Postmenopausal Women: Focus on Denosumab |
| title_full |
Pharmacotherapy of Bone Loss in Postmenopausal Women: Focus on Denosumab |
| title_fullStr |
Pharmacotherapy of Bone Loss in Postmenopausal Women: Focus on Denosumab |
| title_full_unstemmed |
Pharmacotherapy of Bone Loss in Postmenopausal Women: Focus on Denosumab |
| title_sort |
Pharmacotherapy of Bone Loss in Postmenopausal Women: Focus on Denosumab |
| dc.creator.fl_str_mv |
Román González, Alejandro Ackerman, Kathryn E. |
| dc.contributor.author.none.fl_str_mv |
Román González, Alejandro Ackerman, Kathryn E. |
| dc.contributor.researchgroup.spa.fl_str_mv |
Grupo Endocrinología y Metabolismo – GEM |
| dc.subject.decs.none.fl_str_mv |
Osteoporosis Ligando RANK RANK Ligand Denosumab |
| topic |
Osteoporosis Ligando RANK RANK Ligand Denosumab |
| description |
ABSTRACT: Denosumab is a human monoclonal antibody against RANKL. This antibody decreases bone turnover markers and increases bone mineral density (BMD) in postmenopausal women. In phase 3 studies including more than 1100 women, denosumab achieved greater increases in lumbar spine, total hip, distal 1/3 radius, and total BMD than alendronate 70 mg weekly. Recent data suggest that denosumab also decreases vertebral and non-vertebral fractures. This drug seems to be safe, although the most frequent side effects are arthralgia, back pain, and nasopharyngitis. No increased incidence of neoplasia has been found compared to placebo or alendronate. However, infections requiring inpatient treatment were more frequent in study groups treated with denosumab. These were common community acquired infections and were treated with standard antibiotics. No opportunistic infections were reported. Denosumab is a very promising new drug for the treatment of osteopenia and osteoporosis, and hopefully more long-term safety information and further fracture data will support its commercial use in the near future. |
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2009 |
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2009 |
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2022-11-21T16:09:50Z |
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2022-11-21T16:09:50Z |
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Artículo de revisión |
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1179-559X |
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https://hdl.handle.net/10495/32170 |
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10.4137/CMT.S1089 |
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1179-559X 10.4137/CMT.S1089 |
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| dc.language.iso.spa.fl_str_mv |
eng |
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eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Clin. Med. Insights. Ther. |
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1143 |
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1131 |
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1 |
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Clinical Medicine Insights: Therapeutics |
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Román González, AlejandroAckerman, Kathryn E.Grupo Endocrinología y Metabolismo – GEM2022-11-21T16:09:50Z2022-11-21T16:09:50Z20091179-559Xhttps://hdl.handle.net/10495/3217010.4137/CMT.S1089ABSTRACT: Denosumab is a human monoclonal antibody against RANKL. This antibody decreases bone turnover markers and increases bone mineral density (BMD) in postmenopausal women. In phase 3 studies including more than 1100 women, denosumab achieved greater increases in lumbar spine, total hip, distal 1/3 radius, and total BMD than alendronate 70 mg weekly. Recent data suggest that denosumab also decreases vertebral and non-vertebral fractures. This drug seems to be safe, although the most frequent side effects are arthralgia, back pain, and nasopharyngitis. No increased incidence of neoplasia has been found compared to placebo or alendronate. However, infections requiring inpatient treatment were more frequent in study groups treated with denosumab. These were common community acquired infections and were treated with standard antibiotics. No opportunistic infections were reported. Denosumab is a very promising new drug for the treatment of osteopenia and osteoporosis, and hopefully more long-term safety information and further fracture data will support its commercial use in the near future.COL003554713 páginasapplication/pdfengSAGE PublicationsThousand Oaks, Estados Unidoshttp://creativecommons.org/licenses/by-nc/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Pharmacotherapy of Bone Loss in Postmenopausal Women: Focus on DenosumabArtículo de revisiónhttp://purl.org/coar/resource_type/c_dcae04bchttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARTREVhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionOsteoporosisLigando RANKRANK LigandDenosumabClin. Med. Insights. 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