来自病例对照、队列和横断面研究的人群归因风险的贝叶斯可信区间

Pub Date : 2022-01-17 DOI:10.1111/anzs.12352
Sarah Pirikahu, Geoffrey Jones, Martin L. Hazelton
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引用次数: 0

摘要

人口归因风险(PAR)和人口归因分数(PAF)在流行病学中用于预测从人群中去除危险因素的影响。直到最近,在文献中还没有计算置信区间或PAR方差的标准方法。之前,我们概述了一种完全贝叶斯方法,从横断面研究中为PAR和PAF提供可信的区间,其中数据以2×2表的形式呈现。但是,没有提供扩展以满足其他常用的研究设计。在本文中,我们提供了计算病例对照和队列研究的PAR和PAF可信区间的方法。此外,我们扩展了横断面的例子,以允许合并不确定性,当一个不完善的诊断测试是使用。在所有这些情况下,模型变得过度参数化或不可识别,这可能导致标准的“现成”马尔可夫链蒙特卡罗(MCMC)更新需要很长时间才能收敛,甚至完全失败。为了克服这一问题,我们采用了一种重要采样方法,并提出了一些考虑后脊形状的新型MCMC采样器,以帮助马尔可夫链收敛。
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Bayesian credible intervals for population attributable risk from case–control, cohort and cross-sectional studies

Population attributable risk (PAR) and population attributable fraction (PAF) are used in epidemiology to predict the impact of removing a risk factor from the population. Until recently, no standard approach for calculating confidence intervals or the variance for PAR in particular was available in the literature. Previously we outlined a fully Bayesian approach to provide credible intervals for the PAR and PAF from a cross-sectional study, where the data was presented in the form of a 2×2 table. However, extensions to cater for other frequently used study designs were not provided. In this paper we provide methodology to calculate credible intervals for the PAR and PAF for case–control and cohort studies. Additionally, we extend the cross-sectional example to allow for the incorporation of uncertainty that arises when an imperfect diagnostic test is used. In all these situations the model becomes over-parameterised, or non-identifiable, which can result in standard ‘off-the-shelf’ Markov Chain Monte Carlo (MCMC) updaters taking a long time to converge or even failing altogether. We adapt an importance sampling methodology to overcome this problem, and propose some novel MCMC samplers that take into consideration the shape of the posterior ridge to aid in the convergence of the Markov chain.

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