TY - JOUR
T1 - Abdominal aortic calcification, bone mineral density and fractures
T2 - A systematic review and meta-Analysis protocol
AU - Rodríguez, Alexander J.
AU - Leow, Kevin
AU - Szulc, Pawel
AU - Scott, David
AU - Ebeling, Peter
AU - Sim, Marc
AU - Wong, Germaine
AU - Lim, Wai H.
AU - Schousboe, John T.
AU - Kiel, Douglas P.
AU - Prince, Richard L.
AU - Lewis, Joshua R.
PY - 2019/4/1
Y1 - 2019/4/1
N2 - 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 â € low' (referent-lowest reported group) versus â € 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.
AB - 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 â € low' (referent-lowest reported group) versus â € 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.
KW - abdominal aorta
KW - bone mineral density
KW - fracture
KW - vascular calcification
KW - vascular disease
UR - http://www.scopus.com/inward/record.url?scp=85064006713&partnerID=8YFLogxK
U2 - 10.1136/bmjopen-2018-026232
DO - 10.1136/bmjopen-2018-026232
M3 - Review article
C2 - 30944137
AN - SCOPUS:85064006713
SN - 2044-6055
VL - 9
JO - BMJ Open
JF - BMJ Open
IS - 4
M1 - e026232
ER -