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arXiv 1108.3137stat.APstat.CO
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自适应马尔可夫链蒙特卡罗正向模拟用于人乳头瘤病毒流行病学建模的统计分析

Adaptive Markov Chain Monte Carlo Forward Simulation for Statistical Analysis in Epidemic Modelling of Human Papillomavirus

Igor A. Korostil, Gareth W. Peters, Julien Cornebise, David G. Regan

摘要:

我们开发了一个贝叶斯统计模型和估计方法的基础上,前向投影自适应马尔可夫链蒙特卡罗,以执行校准的高维非线性系统的常微分方程代表的流行病模型的人乳头瘤病毒6型和11型(HPV-6,HPV-11)。该模型是分室的,涉及按年龄、性别和性活动组分层。开发这种模型和有效校准它的方法是相关的,因为HPV是一种非常多类型和常见的性传播感染,目前已知有100多种类型。本文研究的两种类型,6型和11型,引起约90%的肛门生殖器疣。我们扩展了人口的性别混合矩阵的发展,加内特和安德森首次提出的配方的基础上。特别是,我们考虑了一个随机混合矩阵框架,它允许我们共同估计未知的属性和参数的混合矩阵,以及参与校准的HPV流行病模型的参数。这个矩阵描述了所研究的人口成员之间的性互动,并依赖于几个先验未知的数量。开发的贝叶斯模型允许人们联合估计HPV-6和HPV-11流行病模型参数,例如传播概率、HPV潜伏期、感染持续时间、生殖器疣治疗持续时间、免疫持续时间、血清转换概率、性别、年龄组和性活动组,以及与生殖能力相关的未知性混合矩阵参数。我们的结论与模拟研究的合成和实际数据最近在澳大利亚进行的研究。

英文摘要:

We develop a Bayesian statistical model and estimation methodology based on Forward Projection Adaptive Markov chain Monte Carlo in order to perform the calibration of a high-dimensional non-linear system of Ordinary Differential Equations representing an epidemic model for Human Papillomavirus types 6 and 11 (HPV-6, HPV-11). The model is compartmental and involves stratification by age, gender and sexual activity-group. Developing this model and a means to calibrate it efficiently is relevant since HPV is a very multi-typed and common sexually transmitted infection with more than 100 types currently known. The two types studied in this paper, types 6 and 11, are causing about 90% of anogenital warts. We extend the development of a sexual mixing matrix for the population, based on a formulation first suggested by Garnett and Anderson. In particular we consider a stochastic mixing matrix framework which allows us to jointly estimate unknown attributes and parameters of the mixing matrix along with the parameters involved in the calibration of the HPV epidemic model. This matrix describes the sexual interactions between members of the population under study and relies on several quantities which are a-priori unknown. The Bayesian model developed allows one to estimate jointly the HPV-6 and HPV-11 epidemic model parameters such as the probability of transmission, HPV incubation period, duration of infection, duration of genital warts treatment, duration of immunity, the probability of seroconversion, per gender, age-group and sexual activity-group, as well as unknown sexual mixing matrix parameters related to assortativity. We conclude with simulation studies on synthetic and actual data from studies undertaken recently in Australia.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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