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DOI 首次登记不等于接收或发表日期。部分更正、评论等条目没有独立摘要;缺少可靠材料时保留待补状态。

引用量采用 OpenAlex 单条关联记录,不合计多个记录;关联记录可能包含正式发表版本,不等于此版本单独引用。缺失不视为零,引用指标不代表论文质量。

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AI 根据所提供的论文材料归类:摘要研究疾病过程模拟的贝叶斯校准,未涉及经济行为结构模型,不能仅凭微观模拟归入结构估计。

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正在核对关联版本…

代码、数据与补充材料

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关注这篇论文的作者
Carolyn M. Rutter
James E. Savarino

微观模拟模型的贝叶斯校准

研究问题
研究疾病微观模拟模型中数据约束不足的参数如何校准,并同时反映多来源信息、参数可识别性和校准结果的不确定性。
方法与思路
作者提出基于 MCMC 的贝叶斯校准,将多个参数与多个数据来源联合处理,研究目标分布收敛并用于结直肠癌模拟模型。
材料陈述的贡献
摘要称方法可给出参数区间估计和可识别性描述;应用发现部分参数主要由先验识别,强调纳入多种不确定性来源。
阅读关注点
应核对校准数据与模拟输出之间的统计模型、先验敏感性、不同误差来源的处理,以及拟合良好是否意味着预测有效。
阅读边界
材料为版本未注明的 OpenAlex 索引摘要;未给出完整识别与收敛条件,校准拟合不能直接验证干预效应或推断刊本变化。

原文摘要

Microsimulation models that describe disease processes synthesize information from multiple sources and can be used to estimate the effects of screening and treatment on cancer incidence and mortality at a population level. These models are characterized by simulation of individual event histories for an idealized population of interest. Microsimulation models are complex and invariably include parameters that are not well informed by existing data. Therefore, a key component of model development is the choice of parameter values. Microsimulation model parameter values are selected to reproduce expected or known results though the process of model calibration. Calibration may be done by perturbing model parameters one at a time or by using a search algorithm. As an alternative, we propose a Bayesian method to calibrate microsimulation models that uses Markov chain Monte Carlo. We show that this approach converges to the target distribution and use a simulation study to demonstrate its finite-sample performance. Although computationally intensive, this approach has several advantages over previously proposed methods, including the use of statistical criteria to select parameter values, simultaneous calibration of multiple parameters to multiple data sources, incorporation of information via prior distributions, description of parameter identifiability, and the ability to obtain interval estimates of model parameters. We develop a microsimulation model for colorectal cancer and use our proposed method to calibrate model parameters. The microsimulation model provides a good fit to the calibration data. We find evidence that some parameters are identified primarily through prior distributions. Our results underscore the need to incorporate multiple sources of variability (i.e., due to calibration data, unknown parameters, and estimated parameters and predicted values) when calibrating and applying microsimulation models.

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