在贝叶斯疾病模型校准中纳入额外证据作为先验信息以解决不可识别性问题

Daria Semochkina, Cathal Walsh
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引用次数: 0

摘要

背景:统计学家在评估筛查或疫苗接种等政策干预措施的影响时,需要使用疾病进展和传播的数学模型和计算模型。校准是确定这些模型参数的过程,贝叶斯框架提供了一种以概率方式完成校准的自然方法。马尔可夫链蒙特卡罗(MCMC)是进行校准时非常有用的计算工具之一。目标:特别是在复杂模型的背景下,出现的一个关键问题是不可识别性。在这种情况下,可以采用的一种方法是考虑并确保在联合参数空间上指定适当的信息先验。我们将举例说明在实践中如何解决这一问题。方法:使用一个基本的 SIS 模型,讨论校准过程和相关的不可识别性挑战。我们还说明了这一问题在 HPV 和宫颈癌的大型模型中是如何出现的。结果:在 SIS 模型中证明了解决不可识别性问题的条件。对于更大的 HPV 模型,还讨论了这对校准过程的影响。
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Incorporating additional evidence as prior information to resolve non-identifiability in Bayesian disease model calibration
Background: Statisticians evaluating the impact of policy interventions such as screening or vaccination will need to make use of mathematical and computational models of disease progression and spread. Calibration is the process of identifying the parameters of these models, with a Bayesian framework providing a natural way in which to do this in a probabilistic fashion. Markov Chain Monte Carlo (MCMC) is one of a number of computational tools that is useful in carrying out this calibration. Objective: In the context of complex models in particular, a key problem that arises is one of non-identifiability. In this setting, one approach which can be used is to consider and ensure that appropriately informative priors are specified on the joint parameter space. We give examples of how this arises and may be addressed in practice. Methods: Using a basic SIS model the calibration process and the associated challenge of non-identifiability is discussed. How this problem arises in the context of a larger model for HPV and cervical cancer is also illustrated. Results: The conditions which allow the problem of non-identifiability to be resolved are demonstrated for the SIS model. For the larger HPV model, how this impacts on the calibration process is also discussed.
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