Correcting Structural Bias in Dynamical Models of Infectious Disease Using a Bayesian State-Space Framework.

IF 2.3 4区 数学 Q2 BIOLOGY
Miracle Amadi, José Carlos García-Merino, Heikki Haario
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引用次数: 0

Abstract

Deterministic dynamical models are widely used in infectious disease modelling, but they often become systematically biased when key drivers such as seasonality and random environmental variation are simplified or omitted. This paper proposes a practical way to account for structural bias while preserving the underlying mechanistic model. We model the observed time series as the sum of (i) a deterministic transmission component given by a reduced Ross malaria model and (ii) a latent stochastic seasonal component that captures unresolved seasonal forcing and other unmodelled variability. The seasonal component is defined as a mean-reverting stochastic differential equation with periodic forcing, which can be interpreted as a seasonally forced Ornstein-Uhlenbeck (OU) process and, at the same time, as a dynamically constrained model-discrepancy term. The combined model forms an additive Bayesian state-space system. A key challenge in additive decompositions is identifiability: many combinations of the deterministic and stochastic components can explain the same observations. We therefore use informative priors to stabilise this decomposition, together with a non-centred parameterisation (a reparameterisation that improves MCMC efficiency by sampling standardised noise terms instead of states directly) of the latent stochastic differential equation (SDE) states that enables efficient joint inference with Hamiltonian Monte Carlo (NUTS) in Stan. We validate the approach in three steps: (1) an OU example that contrasts parameter-only inference with latent state-space inference, (2) synthetic experiments that have a good agreement with the observed signal while highlighting the expected negative posterior dependence between components, and (3) an application to five years of monthly malaria case reports from Delta State, Nigeria. In the real-data analysis, the proposed additive ODE-SDE model produces a close fit with coherent uncertainty quantification and a flexible seasonal reconstruction, while keeping the mechanistic transmission model interpretable. Overall, the framework provides a flexible and transferable method for accounting for structural model discrepancy in misspecified dynamical models using a structured stochastic discrepancy.

利用贝叶斯状态空间框架修正传染病动力学模型中的结构偏差。
确定性动力学模型广泛应用于传染病建模,但当季节性和随机环境变化等关键驱动因素被简化或忽略时,它们往往会产生系统偏差。本文提出了一种实用的方法来解释结构偏差,同时保留潜在的机制模型。我们将观测到的时间序列建模为(i)由简化的Ross疟疾模型给出的确定性传播分量和(ii)捕获未解决的季节强迫和其他未建模变异性的潜在随机季节分量的总和。季节分量被定义为一个具有周期强迫的均值回归随机微分方程,它可以被解释为一个季节性强迫的Ornstein-Uhlenbeck (OU)过程,同时也是一个动态约束的模式差异项。组合模型形成了一个加性贝叶斯状态空间系统。加性分解的一个关键挑战是可识别性:确定性和随机成分的许多组合可以解释相同的观察结果。因此,我们使用信息先验来稳定这种分解,以及潜在随机微分方程(SDE)状态的非中心参数化(通过采样标准化噪声项而不是直接状态来提高MCMC效率的重新参数化),从而能够与Stan中的哈密顿蒙特卡罗(NUTS)进行有效的联合推理。我们通过三个步骤验证了该方法:(1)将仅参数推理与潜在状态空间推理进行对比的OU示例,(2)与观测信号非常一致的合成实验,同时突出了组件之间预期的负后验相关性,以及(3)应用于尼日利亚三角洲州5年的月度疟疾病例报告。在实际数据分析中,提出的可加性ODE-SDE模型在保持机制传递模型可解释性的同时,具有相干不确定性量化的紧密拟合和灵活的季节重建。总体而言,该框架提供了一种灵活和可转移的方法,用于使用结构化随机差异来计算错误指定的动态模型中的结构模型差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.90
自引率
8.60%
发文量
123
审稿时长
7.5 months
期刊介绍: The Bulletin of Mathematical Biology, the official journal of the Society for Mathematical Biology, disseminates original research findings and other information relevant to the interface of biology and the mathematical sciences. Contributions should have relevance to both fields. In order to accommodate the broad scope of new developments, the journal accepts a variety of contributions, including: Original research articles focused on new biological insights gained with the help of tools from the mathematical sciences or new mathematical tools and methods with demonstrated applicability to biological investigations Research in mathematical biology education Reviews Commentaries Perspectives, and contributions that discuss issues important to the profession All contributions are peer-reviewed.
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