Cargando…

Osteoporosis: From Molecular Mechanisms to Therapies 2.0

Osteoporosis is a common skeletal disorder, occurring as a result of an imbalance between bone resorption and bone formation, with bone breakdown exceeding bone building. Bone resorption inhibitors, e.g., bisphosphonates, have been designed to treat osteoporosis. Teriparatide, an anabolic agent, sti...

Descripción completa

Detalles Bibliográficos
Autor principal: Tang, Chih-Hsin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662323/
https://www.ncbi.nlm.nih.gov/pubmed/33126410
http://dx.doi.org/10.3390/ijms21218005
_version_ 1783609373406265344
author Tang, Chih-Hsin
author_facet Tang, Chih-Hsin
author_sort Tang, Chih-Hsin
collection PubMed
description Osteoporosis is a common skeletal disorder, occurring as a result of an imbalance between bone resorption and bone formation, with bone breakdown exceeding bone building. Bone resorption inhibitors, e.g., bisphosphonates, have been designed to treat osteoporosis. Teriparatide, an anabolic agent, stimulates bone formation and corrects the characteristic changes in the trabecular microarchitecture. However, these drugs are associated with significant side effects. It is therefore crucial that we continue to research the pathogenesis of osteoporosis and seek novel modes of therapy. This editorial summarizes and discusses the themes of the ten articles published in our Special Issue “Osteoporosis: From Molecular Mechanisms to Therapies 2.0”, a continuation of our 2019 Special Issue "Osteoporosis: From Molecular Mechanisms to Therapies" (https://www.mdpi.com/journal/ijms/special_issues/osteoporosis_ijms). These Special Issues detail important global scientific findings that contribute to our current understanding of osteoporosis.
format Online
Article
Text
id pubmed-7662323
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-76623232020-11-14 Osteoporosis: From Molecular Mechanisms to Therapies 2.0 Tang, Chih-Hsin Int J Mol Sci Editorial Osteoporosis is a common skeletal disorder, occurring as a result of an imbalance between bone resorption and bone formation, with bone breakdown exceeding bone building. Bone resorption inhibitors, e.g., bisphosphonates, have been designed to treat osteoporosis. Teriparatide, an anabolic agent, stimulates bone formation and corrects the characteristic changes in the trabecular microarchitecture. However, these drugs are associated with significant side effects. It is therefore crucial that we continue to research the pathogenesis of osteoporosis and seek novel modes of therapy. This editorial summarizes and discusses the themes of the ten articles published in our Special Issue “Osteoporosis: From Molecular Mechanisms to Therapies 2.0”, a continuation of our 2019 Special Issue "Osteoporosis: From Molecular Mechanisms to Therapies" (https://www.mdpi.com/journal/ijms/special_issues/osteoporosis_ijms). These Special Issues detail important global scientific findings that contribute to our current understanding of osteoporosis. MDPI 2020-10-28 /pmc/articles/PMC7662323/ /pubmed/33126410 http://dx.doi.org/10.3390/ijms21218005 Text en © 2020 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Editorial
Tang, Chih-Hsin
Osteoporosis: From Molecular Mechanisms to Therapies 2.0
title Osteoporosis: From Molecular Mechanisms to Therapies 2.0
title_full Osteoporosis: From Molecular Mechanisms to Therapies 2.0
title_fullStr Osteoporosis: From Molecular Mechanisms to Therapies 2.0
title_full_unstemmed Osteoporosis: From Molecular Mechanisms to Therapies 2.0
title_short Osteoporosis: From Molecular Mechanisms to Therapies 2.0
title_sort osteoporosis: from molecular mechanisms to therapies 2.0
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662323/
https://www.ncbi.nlm.nih.gov/pubmed/33126410
http://dx.doi.org/10.3390/ijms21218005
work_keys_str_mv AT tangchihhsin osteoporosisfrommolecularmechanismstotherapies20