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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
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.
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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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