The Identifiability of Mathematical Models in Epidemiology: Tuberculosis, HIV, COVID-19

O. Krivorotko, S. Kabanikhin, V. Petrakova
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Abstract

The paper is devoted to the short review and application of sensitivity-based identifiability approaches for analyzing mathematical models of epidemiology and related processes described by systems of differential equations and agent-based models. It is shown that for structural identifiability of basic SIR models (describe the dynamic of Susceptible, Infected and Removed groups based on nonlinear ordinary differential equations) of epidemic spread and linear compartmental models it is possible to use a priori information about the process. It is demonstrated that a model can be structurally identifiable but be practically non-identifiable due to incomplete data. The paper uses methods for analyzing the sensitivity of parameters to data variation, as well as analyzing the sensitivity of model states to parameter variation, based on linear and differential algebra, Bayesian, and Monte Carlo approaches. It was shown that in the SEIR-HCD model of COVID-19 propagation, described by a system of seven ordinary differential equations and based on the mass balance law, the parameter of humoral immunity acquisition is the least sensitive to changes in the number of diagnosed, critical and mortality cases of COVID-19. The spatial SEIR-HCD model of COVID-19 propagation demonstrated an increase the sensitivity of the partial immunity duration parameter over time, as well as a decrease in the limits of change in the infectivity and infection parameters. In the case of the SEIR-HCD mean-field model of COVID-19 propagation, the sensitivity of the system to the self-isolation index and the lack of sensitivity of the stochastic parameters of the system are shown. In the case of the agent-based COVID-19 propagation model, the change in the infectivity parameter was reduced by more than a factor of 2 compared to the statistics. A differential model of co-infection HIV and tuberculosis spread with multiple drug resistance was developed and its local identifiability was shown.
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流行病学数学模型的可识别性:结核病、艾滋病毒、COVID-19
本文简要回顾了基于敏感性的可识别性方法在分析由微分方程系统和基于主体的模型描述的流行病学数学模型和相关过程中的应用。结果表明,对于传染病传播和线性区室模型的基本SIR模型(基于非线性常微分方程描述易感、感染和移除群体的动态)的结构可识别性,可以使用有关该过程的先验信息。结果表明,模型在结构上是可识别的,但由于数据不完整,在实际中是不可识别的。本文采用基于线性代数和微分代数、贝叶斯和蒙特卡罗方法分析参数对数据变化的敏感性,以及分析模型状态对参数变化的敏感性。结果表明,在基于质量平衡定律的7个常微分方程组描述的SEIR-HCD模型中,体液免疫获得参数对COVID-19诊断、危重和死亡病例数的变化最不敏感。新冠病毒传播的空间SEIR-HCD模型显示,部分免疫持续时间参数随时间的敏感性增加,传染性和感染参数的变化极限降低。以COVID-19的SEIR-HCD平均场模型为例,说明了系统对自隔离指数的敏感性和系统随机参数的不敏感性。在基于agent的COVID-19传播模型中,与统计数据相比,感染性参数的变化减少了2倍以上。建立了HIV -结核多重耐药联合感染的鉴别模型,并证明了其局部可识别性。
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来源期刊
Mathematical Biology and Bioinformatics
Mathematical Biology and Bioinformatics Mathematics-Applied Mathematics
CiteScore
1.10
自引率
0.00%
发文量
13
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