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Bone loss in chronic liver diseases: Could healthy liver be a requirement for good bone health?

Given that the liver is involved in many metabolic mechanisms, it is not surprising that chronic liver disease (CLD) could have numerous complications. Secondary osteoporosis and increased bone fragility are frequently overlooked complications in CLD patients. Previous studies implied that up to one...

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Autores principales: Jadzic, Jelena, Djonic, Danijela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9932432/
https://www.ncbi.nlm.nih.gov/pubmed/36816627
http://dx.doi.org/10.3748/wjg.v29.i5.825
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author Jadzic, Jelena
Djonic, Danijela
author_facet Jadzic, Jelena
Djonic, Danijela
author_sort Jadzic, Jelena
collection PubMed
description Given that the liver is involved in many metabolic mechanisms, it is not surprising that chronic liver disease (CLD) could have numerous complications. Secondary osteoporosis and increased bone fragility are frequently overlooked complications in CLD patients. Previous studies implied that up to one-third of these individuals meet diagnostic criteria for osteopenia or osteoporosis. Recent publications indicated that CLD-induced bone fragility depends on the etiology, duration, and stage of liver disease. Therefore, the increased fracture risk in CLD patients puts a severe socioeconomic burden on the health system and urgently requires more effective prevention, diagnosis, and treatment measures. The pathogenesis of CLD-induced bone loss is multifactorial and still insufficiently understood, especially considering the relative impact of increased bone resorption and reduced bone formation in these individuals. It is essential to note that inconsistent findings regarding bone mineral density measurement were previously reported in these individuals. Bone mineral density is widely used as the “golden standard” in the clinical assessment of bone fragility although it is not adequate to predict individual fracture risk. Therefore, microscale bone alterations (bone microstructure, mechanical properties, and cellular indices) were analyzed in CLD individuals. These studies further support the thesis that bone strength could be compromised in CLD individuals, implying that an individualized approach to fracture risk assessment and subsequent therapy is necessary for CLD patients. However, more well-designed studies are required to solve the bone fragility puzzle in CLD patients.
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spelling pubmed-99324322023-02-17 Bone loss in chronic liver diseases: Could healthy liver be a requirement for good bone health? Jadzic, Jelena Djonic, Danijela World J Gastroenterol Minireviews Given that the liver is involved in many metabolic mechanisms, it is not surprising that chronic liver disease (CLD) could have numerous complications. Secondary osteoporosis and increased bone fragility are frequently overlooked complications in CLD patients. Previous studies implied that up to one-third of these individuals meet diagnostic criteria for osteopenia or osteoporosis. Recent publications indicated that CLD-induced bone fragility depends on the etiology, duration, and stage of liver disease. Therefore, the increased fracture risk in CLD patients puts a severe socioeconomic burden on the health system and urgently requires more effective prevention, diagnosis, and treatment measures. The pathogenesis of CLD-induced bone loss is multifactorial and still insufficiently understood, especially considering the relative impact of increased bone resorption and reduced bone formation in these individuals. It is essential to note that inconsistent findings regarding bone mineral density measurement were previously reported in these individuals. Bone mineral density is widely used as the “golden standard” in the clinical assessment of bone fragility although it is not adequate to predict individual fracture risk. Therefore, microscale bone alterations (bone microstructure, mechanical properties, and cellular indices) were analyzed in CLD individuals. These studies further support the thesis that bone strength could be compromised in CLD individuals, implying that an individualized approach to fracture risk assessment and subsequent therapy is necessary for CLD patients. However, more well-designed studies are required to solve the bone fragility puzzle in CLD patients. Baishideng Publishing Group Inc 2023-02-07 2023-02-07 /pmc/articles/PMC9932432/ /pubmed/36816627 http://dx.doi.org/10.3748/wjg.v29.i5.825 Text en ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Minireviews
Jadzic, Jelena
Djonic, Danijela
Bone loss in chronic liver diseases: Could healthy liver be a requirement for good bone health?
title Bone loss in chronic liver diseases: Could healthy liver be a requirement for good bone health?
title_full Bone loss in chronic liver diseases: Could healthy liver be a requirement for good bone health?
title_fullStr Bone loss in chronic liver diseases: Could healthy liver be a requirement for good bone health?
title_full_unstemmed Bone loss in chronic liver diseases: Could healthy liver be a requirement for good bone health?
title_short Bone loss in chronic liver diseases: Could healthy liver be a requirement for good bone health?
title_sort bone loss in chronic liver diseases: could healthy liver be a requirement for good bone health?
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9932432/
https://www.ncbi.nlm.nih.gov/pubmed/36816627
http://dx.doi.org/10.3748/wjg.v29.i5.825
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