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Sclerostin Inhibition in the Management of Osteoporosis

The recognition of the importance of the Wnt-signaling pathway in bone metabolism and studies of patients with rare skeletal disorders characterized by high bone mass identified sclerostin as target for the development of new therapeutics for osteoporosis. Findings in animals and humans with scleros...

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Detalles Bibliográficos
Autores principales: Appelman-Dijkstra, Natasha M., Papapoulos, Socrates E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4824823/
https://www.ncbi.nlm.nih.gov/pubmed/27016922
http://dx.doi.org/10.1007/s00223-016-0126-6
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author Appelman-Dijkstra, Natasha M.
Papapoulos, Socrates E.
author_facet Appelman-Dijkstra, Natasha M.
Papapoulos, Socrates E.
author_sort Appelman-Dijkstra, Natasha M.
collection PubMed
description The recognition of the importance of the Wnt-signaling pathway in bone metabolism and studies of patients with rare skeletal disorders characterized by high bone mass identified sclerostin as target for the development of new therapeutics for osteoporosis. Findings in animals and humans with sclerostin deficiency as well as results of preclinical and early clinical studies with sclerostin inhibitors demonstrated a new treatment paradigm with a bone building agent for the management of patients with osteoporosis, the antifracture efficacy, and long-term tolerability of which remain to be established in on-going phase III clinical studies. In this article we review the currently available preclinical and clinical evidence supporting the use of sclerostin inhibitors in osteoporosis.
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spelling pubmed-48248232016-04-20 Sclerostin Inhibition in the Management of Osteoporosis Appelman-Dijkstra, Natasha M. Papapoulos, Socrates E. Calcif Tissue Int Review The recognition of the importance of the Wnt-signaling pathway in bone metabolism and studies of patients with rare skeletal disorders characterized by high bone mass identified sclerostin as target for the development of new therapeutics for osteoporosis. Findings in animals and humans with sclerostin deficiency as well as results of preclinical and early clinical studies with sclerostin inhibitors demonstrated a new treatment paradigm with a bone building agent for the management of patients with osteoporosis, the antifracture efficacy, and long-term tolerability of which remain to be established in on-going phase III clinical studies. In this article we review the currently available preclinical and clinical evidence supporting the use of sclerostin inhibitors in osteoporosis. Springer US 2016-03-26 2016 /pmc/articles/PMC4824823/ /pubmed/27016922 http://dx.doi.org/10.1007/s00223-016-0126-6 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Appelman-Dijkstra, Natasha M.
Papapoulos, Socrates E.
Sclerostin Inhibition in the Management of Osteoporosis
title Sclerostin Inhibition in the Management of Osteoporosis
title_full Sclerostin Inhibition in the Management of Osteoporosis
title_fullStr Sclerostin Inhibition in the Management of Osteoporosis
title_full_unstemmed Sclerostin Inhibition in the Management of Osteoporosis
title_short Sclerostin Inhibition in the Management of Osteoporosis
title_sort sclerostin inhibition in the management of osteoporosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4824823/
https://www.ncbi.nlm.nih.gov/pubmed/27016922
http://dx.doi.org/10.1007/s00223-016-0126-6
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