Evaluating the use of social contact data to produce age-specific short-term forecasts of SARS-CoV-2 incidence in England.

IF 4.3 2区 生物学 PLoS Computational Biology Pub Date : 2023-09-12 eCollection Date: 2023-09-01 DOI:10.1371/journal.pcbi.1011453
James D Munday, Sam Abbott, Sophie Meakin, Sebastian Funk
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引用次数: 2

Abstract

Mathematical and statistical models can be used to make predictions of how epidemics may progress in the near future and form a central part of outbreak mitigation and control. Renewal equation based models allow inference of epidemiological parameters from historical data and forecast future epidemic dynamics without requiring complex mechanistic assumptions. However, these models typically ignore interaction between age groups, partly due to challenges in parameterising a time varying interaction matrix. Social contact data collected regularly during the COVID-19 epidemic provide a means to inform interaction between age groups in real-time. We developed an age-specific forecasting framework and applied it to two age-stratified time-series: incidence of SARS-CoV-2 infection, estimated from a national infection and antibody prevalence survey; and, reported cases according to the UK national COVID-19 dashboard. Jointly fitting our model to social contact data from the CoMix study, we inferred a time-varying next generation matrix which we used to project infections and cases in the four weeks following each of 29 forecast dates between October 2020 and November 2021. We evaluated the forecasts using proper scoring rules and compared performance with three other models with alternative data and specifications alongside two naive baseline models. Overall, incorporating age interaction improved forecasts of infections and the CoMix-data-informed model was the best performing model at time horizons between two and four weeks. However, this was not true when forecasting cases. We found that age group interaction was most important for predicting cases in children and older adults. The contact-data-informed models performed best during the winter months of 2020-2021, but performed comparatively poorly in other periods. We highlight challenges regarding the incorporation of contact data in forecasting and offer proposals as to how to extend and adapt our approach, which may lead to more successful forecasts in future.

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评估使用社会接触数据对英格兰严重急性呼吸系统综合征冠状病毒2型发病率进行特定年龄的短期预测。
数学和统计模型可用于预测流行病在不久的将来可能如何发展,并构成疫情缓解和控制的核心部分。基于更新方程的模型允许从历史数据推断流行病学参数,并预测未来的流行病动态,而不需要复杂的机制假设。然而,这些模型通常忽略了年龄组之间的相互作用,部分原因是在参数化时变相互作用矩阵方面存在挑战。新冠肺炎疫情期间定期收集的社交接触数据提供了一种实时告知年龄组之间互动的手段。我们开发了一个特定年龄的预测框架,并将其应用于两个年龄分层的时间序列:根据全国感染和抗体流行率调查估计的严重急性呼吸系统综合征冠状病毒2型感染的发病率;以及,根据英国国家新冠肺炎仪表盘报告的病例。我们将我们的模型与CoMix研究的社会接触数据联合拟合,推断出一个时变的下一代矩阵,我们使用该矩阵来预测2020年10月至2021年11月期间29个预测日期后的四周内的感染和病例。我们使用适当的评分规则对预测进行了评估,并将性能与其他三个具有替代数据和规范的模型以及两个天真的基线模型进行了比较。总的来说,结合年龄相互作用改善了对感染的预测,CoMix数据知情模型是在两到四周的时间范围内表现最好的模型。然而,在预测案例时,情况并非如此。我们发现,年龄组的互动对于预测儿童和老年人的病例最为重要。接触数据表明,模型在2020-2021年冬季表现最好,但在其他时期表现相对较差。我们强调了在预测中纳入联系数据方面的挑战,并就如何扩展和调整我们的方法提出了建议,这可能会在未来带来更成功的预测。
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来源期刊
PLoS Computational Biology
PLoS Computational Biology 生物-生化研究方法
CiteScore
7.10
自引率
4.70%
发文量
820
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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