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Sclerostin, an emerging therapeutic target for treating osteoporosis and osteoporotic fracture: A general review

Osteoporosis and its associated fracture risk has become one of the major health burdens in our aging population. Currently, bisphosphonate, one of the most popular antiresorptive drugs, is used widely to treat osteoporosis but so far still no consensus has been reached for its application in treatm...

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Detalles Bibliográficos
Autores principales: Suen, Pui Kit, Qin, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese Speaking Orthopaedic Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987014/
https://www.ncbi.nlm.nih.gov/pubmed/30035061
http://dx.doi.org/10.1016/j.jot.2015.08.004
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author Suen, Pui Kit
Qin, Ling
author_facet Suen, Pui Kit
Qin, Ling
author_sort Suen, Pui Kit
collection PubMed
description Osteoporosis and its associated fracture risk has become one of the major health burdens in our aging population. Currently, bisphosphonate, one of the most popular antiresorptive drugs, is used widely to treat osteoporosis but so far still no consensus has been reached for its application in treatment of osteoporotic fractures. However, in old patients, boosting new bone formation and its remodelling is essential for bone healing in age-related osteoporosis and osteoporotic fractures. Sclerostin, an inhibitor of the Wnt/β-catenin signalling pathway that regulates bone growth, has become an attractive therapeutic target for treating osteoporosis. In this review, we summarize the recent findings of sclerostin and its potential as an effective drug target for treating both osteoporosis and osteoporotic fractures.
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spelling pubmed-59870142018-07-20 Sclerostin, an emerging therapeutic target for treating osteoporosis and osteoporotic fracture: A general review Suen, Pui Kit Qin, Ling J Orthop Translat Review Article Osteoporosis and its associated fracture risk has become one of the major health burdens in our aging population. Currently, bisphosphonate, one of the most popular antiresorptive drugs, is used widely to treat osteoporosis but so far still no consensus has been reached for its application in treatment of osteoporotic fractures. However, in old patients, boosting new bone formation and its remodelling is essential for bone healing in age-related osteoporosis and osteoporotic fractures. Sclerostin, an inhibitor of the Wnt/β-catenin signalling pathway that regulates bone growth, has become an attractive therapeutic target for treating osteoporosis. In this review, we summarize the recent findings of sclerostin and its potential as an effective drug target for treating both osteoporosis and osteoporotic fractures. Chinese Speaking Orthopaedic Society 2015-09-12 /pmc/articles/PMC5987014/ /pubmed/30035061 http://dx.doi.org/10.1016/j.jot.2015.08.004 Text en © 2016 The Authors 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
Suen, Pui Kit
Qin, Ling
Sclerostin, an emerging therapeutic target for treating osteoporosis and osteoporotic fracture: A general review
title Sclerostin, an emerging therapeutic target for treating osteoporosis and osteoporotic fracture: A general review
title_full Sclerostin, an emerging therapeutic target for treating osteoporosis and osteoporotic fracture: A general review
title_fullStr Sclerostin, an emerging therapeutic target for treating osteoporosis and osteoporotic fracture: A general review
title_full_unstemmed Sclerostin, an emerging therapeutic target for treating osteoporosis and osteoporotic fracture: A general review
title_short Sclerostin, an emerging therapeutic target for treating osteoporosis and osteoporotic fracture: A general review
title_sort sclerostin, an emerging therapeutic target for treating osteoporosis and osteoporotic fracture: a general review
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987014/
https://www.ncbi.nlm.nih.gov/pubmed/30035061
http://dx.doi.org/10.1016/j.jot.2015.08.004
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