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Abdominal aortic calcification, bone mineral density and fractures: a systematic review and meta-analysis protocol
INTRODUCTION: Abdominal aortic calcification (AAC) is associated with low bone mass and increased fracture risk. Two previous meta-analyses have investigated the association between AAC and fracture. However, these meta-analyses only identified articles until December 2016, undertook limited searche...
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/PMC6500258/ https://www.ncbi.nlm.nih.gov/pubmed/30944137 http://dx.doi.org/10.1136/bmjopen-2018-026232 |
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author | Rodríguez, Alexander J Leow, Kevin Szulc, Pawel Scott, David Ebeling, Peter Sim, Marc Wong, Germaine Lim, Wai H Schousboe, John T Kiel, Douglas P Prince, Richard L R Lewis, Joshua |
author_facet | Rodríguez, Alexander J Leow, Kevin Szulc, Pawel Scott, David Ebeling, Peter Sim, Marc Wong, Germaine Lim, Wai H Schousboe, John T Kiel, Douglas P Prince, Richard L R Lewis, Joshua |
author_sort | Rodríguez, Alexander J |
collection | PubMed |
description | INTRODUCTION: Abdominal aortic calcification (AAC) is associated with low bone mass and increased fracture risk. Two previous meta-analyses have investigated the association between AAC and fracture. However, these meta-analyses only identified articles until December 2016, undertook limited searches and did not explore potential sources of between-study heterogeneity. We aim to undertake a sensitive and comprehensive assessment of the relationship between AAC, bone mineral density (BMD) as well as prevalent and incident fractures. METHODS: We will search MEDLINE, EMBASE, Web of Science core collection and Google Scholar (top 200 articles sorted by relevance) from their inception to 1 June 2018. Reference lists of included studies and previous systematic reviews will be hand searched for additional eligible studies. Retrospective and prospective cohort studies (cross-sectional, case–control and longitudinal) reporting the association between AAC, BMD and fracture at any site will be included. At least two investigators will independently: (A) evaluate study eligibility and extract data, with a third investigator to adjudicate when discrepancies occur, (B) assess study quality by the Newcastle-Ottawa Scale for each cohort/study. The meta-analysis will be reported in adherence to the Meta-analysis of Observational Studies in Epidemiology criteria. AAC will be grouped as either: (1) AAC present or absent, (2) AAC categorised as ‘low’ (referent—lowest reported group) versus ‘high’ (all other groups) or (3) dose–response when AAC was assessed in ≥3 groups. Where primary event data were reported in individual studies, pooled risk differences and risk ratios with 95% CI will be calculated, from which, a summary estimate will be determined using DerSimonian-Laird random effects models. For the AAC and BMD pooled analyses, estimates will be expressed as standardised mean difference with 95% CI. We will examine the likelihood of publication bias and where possible, investigate potential reasons for between-study heterogeneity using subgroup analyses and meta-regression. ETHICS AND DISSEMINATION: The study will be submitted to a peer- reviewed journal and disseminated via research presentations. PROSPERO REGISTRATION NUMBER: CRD42018088019. |
format | Online Article Text |
id | pubmed-6500258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-65002582019-05-21 Abdominal aortic calcification, bone mineral density and fractures: a systematic review and meta-analysis protocol Rodríguez, Alexander J Leow, Kevin Szulc, Pawel Scott, David Ebeling, Peter Sim, Marc Wong, Germaine Lim, Wai H Schousboe, John T Kiel, Douglas P Prince, Richard L R Lewis, Joshua BMJ Open Rheumatology INTRODUCTION: Abdominal aortic calcification (AAC) is associated with low bone mass and increased fracture risk. Two previous meta-analyses have investigated the association between AAC and fracture. However, these meta-analyses only identified articles until December 2016, undertook limited searches and did not explore potential sources of between-study heterogeneity. We aim to undertake a sensitive and comprehensive assessment of the relationship between AAC, bone mineral density (BMD) as well as prevalent and incident fractures. METHODS: We will search MEDLINE, EMBASE, Web of Science core collection and Google Scholar (top 200 articles sorted by relevance) from their inception to 1 June 2018. Reference lists of included studies and previous systematic reviews will be hand searched for additional eligible studies. Retrospective and prospective cohort studies (cross-sectional, case–control and longitudinal) reporting the association between AAC, BMD and fracture at any site will be included. At least two investigators will independently: (A) evaluate study eligibility and extract data, with a third investigator to adjudicate when discrepancies occur, (B) assess study quality by the Newcastle-Ottawa Scale for each cohort/study. The meta-analysis will be reported in adherence to the Meta-analysis of Observational Studies in Epidemiology criteria. AAC will be grouped as either: (1) AAC present or absent, (2) AAC categorised as ‘low’ (referent—lowest reported group) versus ‘high’ (all other groups) or (3) dose–response when AAC was assessed in ≥3 groups. Where primary event data were reported in individual studies, pooled risk differences and risk ratios with 95% CI will be calculated, from which, a summary estimate will be determined using DerSimonian-Laird random effects models. For the AAC and BMD pooled analyses, estimates will be expressed as standardised mean difference with 95% CI. We will examine the likelihood of publication bias and where possible, investigate potential reasons for between-study heterogeneity using subgroup analyses and meta-regression. ETHICS AND DISSEMINATION: The study will be submitted to a peer- reviewed journal and disseminated via research presentations. PROSPERO REGISTRATION NUMBER: CRD42018088019. BMJ Publishing Group 2019-04-02 /pmc/articles/PMC6500258/ /pubmed/30944137 http://dx.doi.org/10.1136/bmjopen-2018-026232 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (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, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Rheumatology Rodríguez, Alexander J Leow, Kevin Szulc, Pawel Scott, David Ebeling, Peter Sim, Marc Wong, Germaine Lim, Wai H Schousboe, John T Kiel, Douglas P Prince, Richard L R Lewis, Joshua Abdominal aortic calcification, bone mineral density and fractures: a systematic review and meta-analysis protocol |
title | Abdominal aortic calcification, bone mineral density and fractures: a systematic review and meta-analysis protocol |
title_full | Abdominal aortic calcification, bone mineral density and fractures: a systematic review and meta-analysis protocol |
title_fullStr | Abdominal aortic calcification, bone mineral density and fractures: a systematic review and meta-analysis protocol |
title_full_unstemmed | Abdominal aortic calcification, bone mineral density and fractures: a systematic review and meta-analysis protocol |
title_short | Abdominal aortic calcification, bone mineral density and fractures: a systematic review and meta-analysis protocol |
title_sort | abdominal aortic calcification, bone mineral density and fractures: a systematic review and meta-analysis protocol |
topic | Rheumatology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6500258/ https://www.ncbi.nlm.nih.gov/pubmed/30944137 http://dx.doi.org/10.1136/bmjopen-2018-026232 |
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