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Zoledronate in the prevention of Paget’s (ZiPP): protocol for a randomised trial of genetic testing and targeted zoledronic acid therapy to prevent SQSTM1-mediated Paget’s disease of bone
INTRODUCTION: Paget’s disease of bone (PDB) is characterised by increased and disorganised bone remodelling affecting one or more skeletal sites. Complications include bone pain, deformity, deafness and pathological fractures. Mutations in sequestosome-1 (SQSTM1) are strongly associated with the dev...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731944/ https://www.ncbi.nlm.nih.gov/pubmed/31488492 http://dx.doi.org/10.1136/bmjopen-2019-030689 |
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author | Cronin, Owen Forsyth, Laura Goodman, Kirsteen Lewis, Steff C Keerie, Catriona Walker, Allan Porteous, Mary Cetnarskyj, Roseanne Ranganath, Lakshminarayan R Selby, Peter L Hampson, Geeta Chandra, Rama Ho, Shu Tobias, Jon H Young-Min, Steven McKenna, Malachi J Crowley, Rachel K Fraser, William D Gennari, Luigi Nuti, Ranuccio Brandi, Maria Luisa Del Pino-Montes, Javier Devogelaer, Jean-Pierre Durnez, Anne Isaia, Giancarlo Di Stefano, Marco Guañabens, Núria Blanch, Josep Seibel, Markus J Walsh, John P Kotowicz, Mark A Nicholson, Geoffrey C Duncan, Emma L Major, Gabor Horne, Anne Gilchrist, Nigel L Boers, Maarten Murray, Gordon D Charnock, Keith Wilkinson, Diana Russell, R Graham G Ralston, Stuart H |
author_facet | Cronin, Owen Forsyth, Laura Goodman, Kirsteen Lewis, Steff C Keerie, Catriona Walker, Allan Porteous, Mary Cetnarskyj, Roseanne Ranganath, Lakshminarayan R Selby, Peter L Hampson, Geeta Chandra, Rama Ho, Shu Tobias, Jon H Young-Min, Steven McKenna, Malachi J Crowley, Rachel K Fraser, William D Gennari, Luigi Nuti, Ranuccio Brandi, Maria Luisa Del Pino-Montes, Javier Devogelaer, Jean-Pierre Durnez, Anne Isaia, Giancarlo Di Stefano, Marco Guañabens, Núria Blanch, Josep Seibel, Markus J Walsh, John P Kotowicz, Mark A Nicholson, Geoffrey C Duncan, Emma L Major, Gabor Horne, Anne Gilchrist, Nigel L Boers, Maarten Murray, Gordon D Charnock, Keith Wilkinson, Diana Russell, R Graham G Ralston, Stuart H |
author_sort | Cronin, Owen |
collection | PubMed |
description | INTRODUCTION: Paget’s disease of bone (PDB) is characterised by increased and disorganised bone remodelling affecting one or more skeletal sites. Complications include bone pain, deformity, deafness and pathological fractures. Mutations in sequestosome-1 (SQSTM1) are strongly associated with the development of PDB. Bisphosphonate therapy can improve bone pain in PDB, but there is no evidence that treatment alters the natural history of PDB or prevents complications. The Zoledronate in the Prevention of Paget’s disease trial (ZiPP) will determine if prophylactic therapy with the bisphosphonate zoledronic acid (ZA) can delay or prevent the development of PDB in people who carry SQSTM1 mutations. METHODS AND ANALYSIS: People with a family history of PDB aged >30 years who test positive for SQSTM1 mutations are eligible to take part. At the baseline visit, participants will be screened for the presence of bone lesions by radionuclide bone scan. Biochemical markers of bone turnover will be measured and questionnaires completed to assess pain, health-related quality of life (HRQoL), anxiety and depression. Participants will be randomised to receive a single intravenous infusion of 5 mg ZA or placebo and followed up annually for between 4 and 8 years at which point baseline assessments will be repeated. The primary endpoint will be new bone lesions assessed by radionuclide bone scan. Secondary endpoints will include changes in biochemical markers of bone turnover, pain, HRQoL, anxiety, depression and PDB-related skeletal events. ETHICS AND DISSEMINATION: The study was approved by the Fife and Forth Valley Research Ethics Committee on 22 December 2008 (08/S0501/84). Following completion of the trial, a manuscript will be submitted to a peer-reviewed journal. The results of this trial will inform clinical practice by determining if early intervention with ZA in presymptomatic individuals with SQSTM1 mutations can prevent or slow the development of bone lesions with an adverse event profile that is acceptable. TRIAL REGISTRATION NUMBER: ISRCTN11616770 |
format | Online Article Text |
id | pubmed-6731944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-67319442019-09-20 Zoledronate in the prevention of Paget’s (ZiPP): protocol for a randomised trial of genetic testing and targeted zoledronic acid therapy to prevent SQSTM1-mediated Paget’s disease of bone Cronin, Owen Forsyth, Laura Goodman, Kirsteen Lewis, Steff C Keerie, Catriona Walker, Allan Porteous, Mary Cetnarskyj, Roseanne Ranganath, Lakshminarayan R Selby, Peter L Hampson, Geeta Chandra, Rama Ho, Shu Tobias, Jon H Young-Min, Steven McKenna, Malachi J Crowley, Rachel K Fraser, William D Gennari, Luigi Nuti, Ranuccio Brandi, Maria Luisa Del Pino-Montes, Javier Devogelaer, Jean-Pierre Durnez, Anne Isaia, Giancarlo Di Stefano, Marco Guañabens, Núria Blanch, Josep Seibel, Markus J Walsh, John P Kotowicz, Mark A Nicholson, Geoffrey C Duncan, Emma L Major, Gabor Horne, Anne Gilchrist, Nigel L Boers, Maarten Murray, Gordon D Charnock, Keith Wilkinson, Diana Russell, R Graham G Ralston, Stuart H BMJ Open Rheumatology INTRODUCTION: Paget’s disease of bone (PDB) is characterised by increased and disorganised bone remodelling affecting one or more skeletal sites. Complications include bone pain, deformity, deafness and pathological fractures. Mutations in sequestosome-1 (SQSTM1) are strongly associated with the development of PDB. Bisphosphonate therapy can improve bone pain in PDB, but there is no evidence that treatment alters the natural history of PDB or prevents complications. The Zoledronate in the Prevention of Paget’s disease trial (ZiPP) will determine if prophylactic therapy with the bisphosphonate zoledronic acid (ZA) can delay or prevent the development of PDB in people who carry SQSTM1 mutations. METHODS AND ANALYSIS: People with a family history of PDB aged >30 years who test positive for SQSTM1 mutations are eligible to take part. At the baseline visit, participants will be screened for the presence of bone lesions by radionuclide bone scan. Biochemical markers of bone turnover will be measured and questionnaires completed to assess pain, health-related quality of life (HRQoL), anxiety and depression. Participants will be randomised to receive a single intravenous infusion of 5 mg ZA or placebo and followed up annually for between 4 and 8 years at which point baseline assessments will be repeated. The primary endpoint will be new bone lesions assessed by radionuclide bone scan. Secondary endpoints will include changes in biochemical markers of bone turnover, pain, HRQoL, anxiety, depression and PDB-related skeletal events. ETHICS AND DISSEMINATION: The study was approved by the Fife and Forth Valley Research Ethics Committee on 22 December 2008 (08/S0501/84). Following completion of the trial, a manuscript will be submitted to a peer-reviewed journal. The results of this trial will inform clinical practice by determining if early intervention with ZA in presymptomatic individuals with SQSTM1 mutations can prevent or slow the development of bone lesions with an adverse event profile that is acceptable. TRIAL REGISTRATION NUMBER: ISRCTN11616770 BMJ Publishing Group 2019-09-04 /pmc/articles/PMC6731944/ /pubmed/31488492 http://dx.doi.org/10.1136/bmjopen-2019-030689 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Rheumatology Cronin, Owen Forsyth, Laura Goodman, Kirsteen Lewis, Steff C Keerie, Catriona Walker, Allan Porteous, Mary Cetnarskyj, Roseanne Ranganath, Lakshminarayan R Selby, Peter L Hampson, Geeta Chandra, Rama Ho, Shu Tobias, Jon H Young-Min, Steven McKenna, Malachi J Crowley, Rachel K Fraser, William D Gennari, Luigi Nuti, Ranuccio Brandi, Maria Luisa Del Pino-Montes, Javier Devogelaer, Jean-Pierre Durnez, Anne Isaia, Giancarlo Di Stefano, Marco Guañabens, Núria Blanch, Josep Seibel, Markus J Walsh, John P Kotowicz, Mark A Nicholson, Geoffrey C Duncan, Emma L Major, Gabor Horne, Anne Gilchrist, Nigel L Boers, Maarten Murray, Gordon D Charnock, Keith Wilkinson, Diana Russell, R Graham G Ralston, Stuart H Zoledronate in the prevention of Paget’s (ZiPP): protocol for a randomised trial of genetic testing and targeted zoledronic acid therapy to prevent SQSTM1-mediated Paget’s disease of bone |
title | Zoledronate in the prevention of Paget’s (ZiPP): protocol for a randomised trial of genetic testing and targeted zoledronic acid therapy to prevent SQSTM1-mediated Paget’s disease of bone |
title_full | Zoledronate in the prevention of Paget’s (ZiPP): protocol for a randomised trial of genetic testing and targeted zoledronic acid therapy to prevent SQSTM1-mediated Paget’s disease of bone |
title_fullStr | Zoledronate in the prevention of Paget’s (ZiPP): protocol for a randomised trial of genetic testing and targeted zoledronic acid therapy to prevent SQSTM1-mediated Paget’s disease of bone |
title_full_unstemmed | Zoledronate in the prevention of Paget’s (ZiPP): protocol for a randomised trial of genetic testing and targeted zoledronic acid therapy to prevent SQSTM1-mediated Paget’s disease of bone |
title_short | Zoledronate in the prevention of Paget’s (ZiPP): protocol for a randomised trial of genetic testing and targeted zoledronic acid therapy to prevent SQSTM1-mediated Paget’s disease of bone |
title_sort | zoledronate in the prevention of paget’s (zipp): protocol for a randomised trial of genetic testing and targeted zoledronic acid therapy to prevent sqstm1-mediated paget’s disease of bone |
topic | Rheumatology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731944/ https://www.ncbi.nlm.nih.gov/pubmed/31488492 http://dx.doi.org/10.1136/bmjopen-2019-030689 |
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