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Paget’s disease: a review of the epidemiology, etiology, genetics, and treatment
Paget’s disease of bone (PDB) is the second most prevalent metabolic bone disorder worldwide, with a prevalence rate of 1.5%–8.3%. It is characterized by localized areas of accelerated, disorganized, and excessive bone production and turnover. Typically, PDB develops in the later stages of life, par...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10169728/ https://www.ncbi.nlm.nih.gov/pubmed/37180975 http://dx.doi.org/10.3389/fgene.2023.1131182 |
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author | Banaganapalli, Babajan Fallatah, Ibrahim Alsubhi, Fai Shetty, Preetha Jayasheela Awan, Zuhier Elango, Ramu Shaik, Noor Ahmad |
author_facet | Banaganapalli, Babajan Fallatah, Ibrahim Alsubhi, Fai Shetty, Preetha Jayasheela Awan, Zuhier Elango, Ramu Shaik, Noor Ahmad |
author_sort | Banaganapalli, Babajan |
collection | PubMed |
description | Paget’s disease of bone (PDB) is the second most prevalent metabolic bone disorder worldwide, with a prevalence rate of 1.5%–8.3%. It is characterized by localized areas of accelerated, disorganized, and excessive bone production and turnover. Typically, PDB develops in the later stages of life, particularly in the late 50s, and affects men more frequently than women. PDB is a complex disease influenced by both genetic and environmental factors. PDB has a complex genetic basis involving multiple genes, with SQSTM1 being the gene most frequently associated with its development. Mutations affecting the UBA domain of SQSTM1 have been detected in both familial and sporadic PDB cases, and these mutations are often associated with severe clinical expression. Germline mutations in other genes such as TNFRSF11A, ZNF687 and PFN1, have also been associated with the development of the disease. Genetic association studies have also uncovered several PDB predisposing risk genes contributing to the disease pathology and severity. Epigenetic modifications of genes involved in bone remodelling and regulation, including RANKL, OPG, HDAC2, DNMT1, and SQSTM1, have been implicated in the development and progression of Paget’s disease of bone, providing insight into the molecular basis of the disease and potential targets for therapeutic intervention. Although PDB has a tendency to cluster within families, the variable severity of the disease across family members, coupled with decreasing incidence rates, indicates that environmental factors may also play a role in the pathophysiology of PDB. The precise nature of these environmental triggers and how they interact with genetic determinants remain poorly understood. Fortunately, majority of PDB patients can achieve long-term remission with an intravenous infusion of aminobisphosphonates, such as zoledronic acid. In this review, we discuss aspects like clinical characteristics, genetic foundation, and latest updates in PDB research. |
format | Online Article Text |
id | pubmed-10169728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101697282023-05-11 Paget’s disease: a review of the epidemiology, etiology, genetics, and treatment Banaganapalli, Babajan Fallatah, Ibrahim Alsubhi, Fai Shetty, Preetha Jayasheela Awan, Zuhier Elango, Ramu Shaik, Noor Ahmad Front Genet Genetics Paget’s disease of bone (PDB) is the second most prevalent metabolic bone disorder worldwide, with a prevalence rate of 1.5%–8.3%. It is characterized by localized areas of accelerated, disorganized, and excessive bone production and turnover. Typically, PDB develops in the later stages of life, particularly in the late 50s, and affects men more frequently than women. PDB is a complex disease influenced by both genetic and environmental factors. PDB has a complex genetic basis involving multiple genes, with SQSTM1 being the gene most frequently associated with its development. Mutations affecting the UBA domain of SQSTM1 have been detected in both familial and sporadic PDB cases, and these mutations are often associated with severe clinical expression. Germline mutations in other genes such as TNFRSF11A, ZNF687 and PFN1, have also been associated with the development of the disease. Genetic association studies have also uncovered several PDB predisposing risk genes contributing to the disease pathology and severity. Epigenetic modifications of genes involved in bone remodelling and regulation, including RANKL, OPG, HDAC2, DNMT1, and SQSTM1, have been implicated in the development and progression of Paget’s disease of bone, providing insight into the molecular basis of the disease and potential targets for therapeutic intervention. Although PDB has a tendency to cluster within families, the variable severity of the disease across family members, coupled with decreasing incidence rates, indicates that environmental factors may also play a role in the pathophysiology of PDB. The precise nature of these environmental triggers and how they interact with genetic determinants remain poorly understood. Fortunately, majority of PDB patients can achieve long-term remission with an intravenous infusion of aminobisphosphonates, such as zoledronic acid. In this review, we discuss aspects like clinical characteristics, genetic foundation, and latest updates in PDB research. Frontiers Media S.A. 2023-04-26 /pmc/articles/PMC10169728/ /pubmed/37180975 http://dx.doi.org/10.3389/fgene.2023.1131182 Text en Copyright © 2023 Banaganapalli, Fallatah, Alsubhi, Shetty, Awan, Elango and Shaik. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Banaganapalli, Babajan Fallatah, Ibrahim Alsubhi, Fai Shetty, Preetha Jayasheela Awan, Zuhier Elango, Ramu Shaik, Noor Ahmad Paget’s disease: a review of the epidemiology, etiology, genetics, and treatment |
title | Paget’s disease: a review of the epidemiology, etiology, genetics, and treatment |
title_full | Paget’s disease: a review of the epidemiology, etiology, genetics, and treatment |
title_fullStr | Paget’s disease: a review of the epidemiology, etiology, genetics, and treatment |
title_full_unstemmed | Paget’s disease: a review of the epidemiology, etiology, genetics, and treatment |
title_short | Paget’s disease: a review of the epidemiology, etiology, genetics, and treatment |
title_sort | paget’s disease: a review of the epidemiology, etiology, genetics, and treatment |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10169728/ https://www.ncbi.nlm.nih.gov/pubmed/37180975 http://dx.doi.org/10.3389/fgene.2023.1131182 |
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