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揭示 COVID-19 发病率的空间时间序列趋势与人类流动性之间的关联:双向性和时空异质性分析。

Revealing associations between spatial time series trends of COVID-19 incidence and human mobility: an analysis of bidirectionality and spatiotemporal heterogeneity.

机构信息

Department of Geographical and Sustainability Sciences, University of Iowa, Iowa City, IA, USA.

出版信息

Int J Health Geogr. 2023 Nov 27;22(1):33. doi: 10.1186/s12942-023-00357-0.

Abstract

BACKGROUND

Using human mobility as a proxy for social interaction, previous studies revealed bidirectional associations between COVID-19 incidence and human mobility. For example, while an increase in COVID-19 cases may affect mobility to decrease due to lockdowns or fear, conversely, an increase in mobility can potentially amplify social interactions, thereby contributing to an upsurge in COVID-19 cases. Nevertheless, these bidirectional relationships exhibit variations in their nature, evolve over time, and lack generalizability across different geographical contexts. Consequently, a systematic approach is required to detect functional, spatial, and temporal variations within the intricate relationship between disease incidence and mobility.

METHODS

We introduce a spatial time series workflow to investigate the bidirectional associations between human mobility and disease incidence, examining how these associations differ across geographic space and throughout different waves of a pandemic. By utilizing daily COVID-19 cases and mobility flows at the county level during three pandemic waves in the US, we conduct bidirectional Granger causality tests for each county and wave. Furthermore, we employ dynamic time warping to quantify the similarity between the trends of disease incidence and mobility, enabling us to map the spatial distribution of trends that are either similar or dissimilar.

RESULTS

Our analysis reveals significant bidirectional associations between COVID-19 incidence and mobility, and we develop a typology to explain the variations in these associations across waves and counties. Overall, COVID-19 incidence exerts a greater influence on mobility than vice versa, but the correlation between the two variables exhibits a stronger connection during the initial wave and weakens over time. Additionally, the relationship between COVID-19 incidence and mobility undergoes changes in direction and significance for certain counties across different waves. These shifts can be attributed to alterations in disease control measures and the presence of evolving confounding factors that differ both spatially and temporally.

CONCLUSIONS

This study provides insights into the spatial and temporal dynamics of the relationship between COVID-19 incidence and human mobility across different waves. Understanding these variations is crucial for informing the development of more targeted and effective healthcare policies and interventions, particularly at the city or county level where such policies must be implemented. Although we study the association between mobility and COVID-19 incidence, our workflow can be applied to investigate the associations between the time series trends of various infectious diseases and relevant contributing factors, which play a role in disease transmission.

摘要

背景

先前的研究利用人类流动性作为社交互动的代理,揭示了 COVID-19 发病率和人类流动性之间存在双向关联。例如,由于封锁或恐惧,COVID-19 病例的增加可能会导致流动性下降,反之亦然,而流动性的增加可能会增加社交互动,从而导致 COVID-19 病例的激增。然而,这些双向关系在性质上存在差异,随时间演变,并且在不同的地理背景下缺乏普遍性。因此,需要采用系统的方法来检测疾病发病率和流动性之间复杂关系中的功能、空间和时间变化。

方法

我们引入了一种空间时间序列工作流程来研究人类流动性和疾病发病率之间的双向关联,研究这些关联如何在不同的地理空间和整个大流行的不同波次中有所不同。我们利用美国三次大流行期间的县级每日 COVID-19 病例和流动性数据,对每个县和波次进行双向 Granger 因果关系检验。此外,我们还采用动态时间扭曲来量化疾病发病率和流动性趋势之间的相似性,从而能够绘制出趋势相似或不相似的空间分布。

结果

我们的分析揭示了 COVID-19 发病率和流动性之间存在显著的双向关联,并提出了一种分类法来解释这些关联在波次和县之间的变化。总体而言,COVID-19 发病率对流动性的影响大于反之,但两者之间的相关性在初始波次中更强,随着时间的推移而减弱。此外,COVID-19 发病率和流动性之间的关系在不同波次和不同县之间的方向和重要性发生了变化。这些变化可以归因于疾病控制措施的改变和空间和时间上不断变化的混杂因素的存在。

结论

本研究深入了解了 COVID-19 发病率和人类流动性在不同波次之间的空间和时间动态。了解这些变化对于制定更有针对性和有效的医疗保健政策和干预措施至关重要,特别是在必须实施这些政策的城市或县一级。虽然我们研究了流动性和 COVID-19 发病率之间的关联,但我们的工作流程可以应用于研究各种传染病的时间序列趋势及其相关影响因素之间的关联,这些因素在疾病传播中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cacc/10683178/e97256ee7c69/12942_2023_357_Fig1_HTML.jpg

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