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Osteoanabolic Agents for Osteoporosis

Medications for osteoporosis are classified as either antiresorptive or anabolic. Whereas antiresorptive agents prevent bone resorption, anabolic agents promote new bone formation. Anabolics should be considered in individuals with severe osteoporosis, failure of alternative osteoporosis agents, int...

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Detalles Bibliográficos
Autores principales: Haas, Andrea V, LeBoff, Meryl S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065487/
https://www.ncbi.nlm.nih.gov/pubmed/30087947
http://dx.doi.org/10.1210/js.2018-00118
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author Haas, Andrea V
LeBoff, Meryl S
author_facet Haas, Andrea V
LeBoff, Meryl S
author_sort Haas, Andrea V
collection PubMed
description Medications for osteoporosis are classified as either antiresorptive or anabolic. Whereas antiresorptive agents prevent bone resorption, anabolic agents promote new bone formation. Anabolics should be considered in individuals with severe osteoporosis, failure of alternative osteoporosis agents, intolerability or contraindications to other osteoporosis agents, and glucocorticoid-induced osteoporosis. There are currently two approved anabolic therapies, teriparatide and abaloparatide, and a third anabolic agent, romozosumab, is under review by the US Food and Drug Administration. Teriparatide and abaloparatide are administered as daily subcutaneous injections and have been shown to reduce vertebral and nonvertebral fractures significantly. The most common side effects are headache and nausea, but teriparatide and abaloparatide are generally well tolerated. The sequence of administration of anabolic therapy is important. Benefits of anabolics are attenuated in individuals with prior antiresorptive exposure; however, antiresorptive agents administered after anabolics consolidate bone mineral density gains.
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spelling pubmed-60654872018-08-07 Osteoanabolic Agents for Osteoporosis Haas, Andrea V LeBoff, Meryl S J Endocr Soc Mini-Reviews Medications for osteoporosis are classified as either antiresorptive or anabolic. Whereas antiresorptive agents prevent bone resorption, anabolic agents promote new bone formation. Anabolics should be considered in individuals with severe osteoporosis, failure of alternative osteoporosis agents, intolerability or contraindications to other osteoporosis agents, and glucocorticoid-induced osteoporosis. There are currently two approved anabolic therapies, teriparatide and abaloparatide, and a third anabolic agent, romozosumab, is under review by the US Food and Drug Administration. Teriparatide and abaloparatide are administered as daily subcutaneous injections and have been shown to reduce vertebral and nonvertebral fractures significantly. The most common side effects are headache and nausea, but teriparatide and abaloparatide are generally well tolerated. The sequence of administration of anabolic therapy is important. Benefits of anabolics are attenuated in individuals with prior antiresorptive exposure; however, antiresorptive agents administered after anabolics consolidate bone mineral density gains. Endocrine Society 2018-07-09 /pmc/articles/PMC6065487/ /pubmed/30087947 http://dx.doi.org/10.1210/js.2018-00118 Text en Copyright © 2018 Endocrine Society https://creativecommons.org/licenses/by-nc-nd/4.0/ This article has been published under the terms of the Creative Commons Attribution Non-Commercial, No-Derivatives License (CC BY-NC-ND; https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Mini-Reviews
Haas, Andrea V
LeBoff, Meryl S
Osteoanabolic Agents for Osteoporosis
title Osteoanabolic Agents for Osteoporosis
title_full Osteoanabolic Agents for Osteoporosis
title_fullStr Osteoanabolic Agents for Osteoporosis
title_full_unstemmed Osteoanabolic Agents for Osteoporosis
title_short Osteoanabolic Agents for Osteoporosis
title_sort osteoanabolic agents for osteoporosis
topic Mini-Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065487/
https://www.ncbi.nlm.nih.gov/pubmed/30087947
http://dx.doi.org/10.1210/js.2018-00118
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