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Age Related Osteoporosis: Targeting Cellular Senescence

Age-related chronic diseases are an enormous burden to modern societies worldwide. Among these, osteoporosis, a condition that predisposes individuals to an increased risk of fractures, substantially contributes to increased mortality and health-care costs in elderly. It is now well accepted that ad...

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Autores principales: Föger-Samwald, Ursula, Kerschan-Schindl, Katharina, Butylina, Maria, Pietschmann, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8910503/
https://www.ncbi.nlm.nih.gov/pubmed/35269841
http://dx.doi.org/10.3390/ijms23052701
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author Föger-Samwald, Ursula
Kerschan-Schindl, Katharina
Butylina, Maria
Pietschmann, Peter
author_facet Föger-Samwald, Ursula
Kerschan-Schindl, Katharina
Butylina, Maria
Pietschmann, Peter
author_sort Föger-Samwald, Ursula
collection PubMed
description Age-related chronic diseases are an enormous burden to modern societies worldwide. Among these, osteoporosis, a condition that predisposes individuals to an increased risk of fractures, substantially contributes to increased mortality and health-care costs in elderly. It is now well accepted that advanced chronical age is one of the main risk factors for chronical diseases. Hence, targeting fundamental aging mechanisms such as senescence has become a promising option in the treatment of these diseases. Moreover, for osteoporosis, the main pathophysiological concepts arise from menopause causing estrogen deficiency, and from aging. Here, we focus on recent advances in the understanding of senescence-related mechanisms contributing to age-related bone loss. Furthermore, treatment options for senile osteoporosis targeting senescent cells are reviewed.
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spelling pubmed-89105032022-03-11 Age Related Osteoporosis: Targeting Cellular Senescence Föger-Samwald, Ursula Kerschan-Schindl, Katharina Butylina, Maria Pietschmann, Peter Int J Mol Sci Review Age-related chronic diseases are an enormous burden to modern societies worldwide. Among these, osteoporosis, a condition that predisposes individuals to an increased risk of fractures, substantially contributes to increased mortality and health-care costs in elderly. It is now well accepted that advanced chronical age is one of the main risk factors for chronical diseases. Hence, targeting fundamental aging mechanisms such as senescence has become a promising option in the treatment of these diseases. Moreover, for osteoporosis, the main pathophysiological concepts arise from menopause causing estrogen deficiency, and from aging. Here, we focus on recent advances in the understanding of senescence-related mechanisms contributing to age-related bone loss. Furthermore, treatment options for senile osteoporosis targeting senescent cells are reviewed. MDPI 2022-02-28 /pmc/articles/PMC8910503/ /pubmed/35269841 http://dx.doi.org/10.3390/ijms23052701 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Föger-Samwald, Ursula
Kerschan-Schindl, Katharina
Butylina, Maria
Pietschmann, Peter
Age Related Osteoporosis: Targeting Cellular Senescence
title Age Related Osteoporosis: Targeting Cellular Senescence
title_full Age Related Osteoporosis: Targeting Cellular Senescence
title_fullStr Age Related Osteoporosis: Targeting Cellular Senescence
title_full_unstemmed Age Related Osteoporosis: Targeting Cellular Senescence
title_short Age Related Osteoporosis: Targeting Cellular Senescence
title_sort age related osteoporosis: targeting cellular senescence
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8910503/
https://www.ncbi.nlm.nih.gov/pubmed/35269841
http://dx.doi.org/10.3390/ijms23052701
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