Osteoporosis in men: epidemiology and treatment with denosumab

Kristel M Sidlauskas, Emily E Sutton, Michael A Biddle Albany College of Pharmacy and Health Sciences-Vermont Campus, Colchester, VT, USA Abstract: Osteoporosis is a major public health care concern. Although often described as a disease affecting postmenopausal women, researchers and clinicians ha...

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Autores principales: Sidlauskas KM, Sutton EE, Biddle MA
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2014
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Men
Acceso en línea:https://doaj.org/article/d7f2f454f05a4b7caa35297f994f5d0d
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spelling oai:doaj.org-article:d7f2f454f05a4b7caa35297f994f5d0d2021-12-02T02:48:54ZOsteoporosis in men: epidemiology and treatment with denosumab1178-1998https://doaj.org/article/d7f2f454f05a4b7caa35297f994f5d0d2014-04-01T00:00:00Zhttps://www.dovepress.com/osteoporosis-in-men-epidemiology-and-treatment-with-denosumab-peer-reviewed-article-CIAhttps://doaj.org/toc/1178-1998Kristel M Sidlauskas, Emily E Sutton, Michael A Biddle Albany College of Pharmacy and Health Sciences-Vermont Campus, Colchester, VT, USA Abstract: Osteoporosis is a major public health care concern. Although often described as a disease affecting postmenopausal women, researchers and clinicians have emphasized its prevalence in men in recent years. The National Osteoporosis Foundation has stated that up to 25% of men over the age of 50 years will experience a fracture due to osteoporosis. Men who suffer from a major fracture have higher mortality rates than women. Pharmacologic therapy options for treating osteoporosis are limited for men as compared with women, so each medication approved for use in this population represents an important clinical option. In September 2012, the US Food and Drug Administration approved a new indication for denosumab to increase bone mass in men with osteoporosis at high risk for fracture. Denosumab is a fully human monoclonal antibody and novel antiresorptive agent that works by binding receptor activator of nuclear factor kappa-β ligand (RANKL) and inhibiting the signaling cascade that causes osteoclast maturation, activity, and survival. Ultimately, denosumab suppresses bone turnover and increases bone mineral density in both trabecular and cortical bone. Approval for treating osteoporosis in men was based on data from the ADAMO trial which displayed efficacy in increasing bone mineral density at the lumbar spine, total hip, femoral neck, hip trochanter, and one-third radius. Studies indicate that denosumab is effective and safe, and has superior adherence rates and patient satisfaction. Although long-term data and further research on fracture reduction rates in men should be explored, at this time denosumab is one of several appropriate first-line treatment options for men with osteoporosis. Keywords: denosumab, osteoporosis, men, treatmentSidlauskas KMSutton EEBiddle MADove Medical PressarticleDenosumabOsteoporosisMenTreatmentGeriatricsRC952-954.6ENClinical Interventions in Aging, Vol Volume 9, Pp 593-601 (2014)
institution DOAJ
collection DOAJ
language EN
topic Denosumab
Osteoporosis
Men
Treatment
Geriatrics
RC952-954.6
spellingShingle Denosumab
Osteoporosis
Men
Treatment
Geriatrics
RC952-954.6
Sidlauskas KM
Sutton EE
Biddle MA
Osteoporosis in men: epidemiology and treatment with denosumab
description Kristel M Sidlauskas, Emily E Sutton, Michael A Biddle Albany College of Pharmacy and Health Sciences-Vermont Campus, Colchester, VT, USA Abstract: Osteoporosis is a major public health care concern. Although often described as a disease affecting postmenopausal women, researchers and clinicians have emphasized its prevalence in men in recent years. The National Osteoporosis Foundation has stated that up to 25% of men over the age of 50 years will experience a fracture due to osteoporosis. Men who suffer from a major fracture have higher mortality rates than women. Pharmacologic therapy options for treating osteoporosis are limited for men as compared with women, so each medication approved for use in this population represents an important clinical option. In September 2012, the US Food and Drug Administration approved a new indication for denosumab to increase bone mass in men with osteoporosis at high risk for fracture. Denosumab is a fully human monoclonal antibody and novel antiresorptive agent that works by binding receptor activator of nuclear factor kappa-β ligand (RANKL) and inhibiting the signaling cascade that causes osteoclast maturation, activity, and survival. Ultimately, denosumab suppresses bone turnover and increases bone mineral density in both trabecular and cortical bone. Approval for treating osteoporosis in men was based on data from the ADAMO trial which displayed efficacy in increasing bone mineral density at the lumbar spine, total hip, femoral neck, hip trochanter, and one-third radius. Studies indicate that denosumab is effective and safe, and has superior adherence rates and patient satisfaction. Although long-term data and further research on fracture reduction rates in men should be explored, at this time denosumab is one of several appropriate first-line treatment options for men with osteoporosis. Keywords: denosumab, osteoporosis, men, treatment
format article
author Sidlauskas KM
Sutton EE
Biddle MA
author_facet Sidlauskas KM
Sutton EE
Biddle MA
author_sort Sidlauskas KM
title Osteoporosis in men: epidemiology and treatment with denosumab
title_short Osteoporosis in men: epidemiology and treatment with denosumab
title_full Osteoporosis in men: epidemiology and treatment with denosumab
title_fullStr Osteoporosis in men: epidemiology and treatment with denosumab
title_full_unstemmed Osteoporosis in men: epidemiology and treatment with denosumab
title_sort osteoporosis in men: epidemiology and treatment with denosumab
publisher Dove Medical Press
publishDate 2014
url https://doaj.org/article/d7f2f454f05a4b7caa35297f994f5d0d
work_keys_str_mv AT sidlauskaskm osteoporosisinmenepidemiologyandtreatmentwithdenosumab
AT suttonee osteoporosisinmenepidemiologyandtreatmentwithdenosumab
AT biddlema osteoporosisinmenepidemiologyandtreatmentwithdenosumab
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