In a bivariate meta-analysis, the number of diagnostic studies involved is often very low so that frequentist methods may result in problems. Using Bayesian inference is particularly attractive as informative priors that add a small amount of information can stabilise the analysis without overwhelming the data. However, Bayesian analysis is often computationally demanding and the selection of the prior for the covariance matrix of the bivariate structure is crucial with little data. The integrated nested Laplace approximations method provides an efficient solution to the computational issues by avoiding any sampling, but the important question of priors remain. We explore the penalised complexity (PC) prior framework for specifying informative priors for the variance parameters and the correlation parameter. PC priors facilitate model interpretation and hyperparameter specification as expert knowledge can be incorporated intuitively. We conduct a simulation study to compare the properties and behaviour of differently defined PC priors to currently used priors in the field. The simulation study shows that the PC prior seems beneficial for the variance parameters. The use of PC priors for the correlation parameter results in more precise estimates when specified in a sensible neighbourhood around the truth. To investigate the usage of PC priors in practice, we reanalyse a meta-analysis using the telomerase marker for the diagnosis of bladder cancer and compare the results with those obtained by other commonly used modelling approaches. Copyright (c) 2017 John Wiley & Sons, Ltd.
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Univ Minnesota, Div Biostat, Minneapolis, MN 55455 USAUniv Minnesota, Div Biostat, Minneapolis, MN 55455 USA
Rudser, Kyle
Sutcliffe, Siobhan
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Washington Univ, Sch Med, Dept Surg, Div Publ Hlth Sci, St Louis, MO 63110 USAUniv Minnesota, Div Biostat, Minneapolis, MN 55455 USA
Sutcliffe, Siobhan
Markland, Alayne
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Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
Birmingham VA Med Ctr, Birmingham Geriatr Res Educ & Clin Ctr, Birmingham, AL USAUniv Minnesota, Div Biostat, Minneapolis, MN 55455 USA
Markland, Alayne
Brubaker, Linda
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Univ Calif San Diego, Dept Obstet Gynecol & Reprod Sci, Div Female Pelv Med & Reconstruct Surg, La Jolla, CA 92093 USAUniv Minnesota, Div Biostat, Minneapolis, MN 55455 USA
Brubaker, Linda
Gahagan, Sheila
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Univ Calif San Diego, Dept Pediat, Div Child Dev & Community Hlth, La Jolla, CA 92093 USAUniv Minnesota, Div Biostat, Minneapolis, MN 55455 USA
Gahagan, Sheila
Stapleton, Ann E.
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Univ Washington, Div Allergy & Infect Dis, Seattle, WA 98195 USAUniv Minnesota, Div Biostat, Minneapolis, MN 55455 USA
Stapleton, Ann E.
Chu, Haitao
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Univ Minnesota, Div Biostat, Minneapolis, MN 55455 USAUniv Minnesota, Div Biostat, Minneapolis, MN 55455 USA
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Univ Liverpool, Ctr Med Stat & Hlth Evaluat, Fac Med, Liverpool L69 3GS, Merseyside, EnglandUniv Liverpool, Ctr Med Stat & Hlth Evaluat, Fac Med, Liverpool L69 3GS, Merseyside, England
Riley, Richard D.
Dodd, Susanna R.
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Univ Liverpool, Ctr Med Stat & Hlth Evaluat, Fac Med, Liverpool L69 3GS, Merseyside, EnglandUniv Liverpool, Ctr Med Stat & Hlth Evaluat, Fac Med, Liverpool L69 3GS, Merseyside, England
Dodd, Susanna R.
Craig, Jean V.
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Univ Liverpool, RLC NHS Trust, Inst Child Hlth, Evidence Based Child Hlth Unit, Liverpool L69 3GS, Merseyside, EnglandUniv Liverpool, Ctr Med Stat & Hlth Evaluat, Fac Med, Liverpool L69 3GS, Merseyside, England
Craig, Jean V.
Thompson, John R.
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Univ Leicester, Dept Hlth Sci, Ctr Biostat & Genet Epidemiol, Leicester LE1 7RH, Leics, EnglandUniv Liverpool, Ctr Med Stat & Hlth Evaluat, Fac Med, Liverpool L69 3GS, Merseyside, England
Thompson, John R.
Williamson, Paula R.
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Univ Liverpool, Ctr Med Stat & Hlth Evaluat, Fac Med, Liverpool L69 3GS, Merseyside, EnglandUniv Liverpool, Ctr Med Stat & Hlth Evaluat, Fac Med, Liverpool L69 3GS, Merseyside, England