IDEAS home Printed from https://ideas.repec.org/a/plo/pcbi00/1012882.html
   My bibliography  Save this article

Time-series modeling of epidemics in complex populations: Detecting changes in incidence volatility over time

Author

Listed:
  • Rachael Aber
  • Yanming Di
  • Benjamin D Dalziel

Abstract

Trends in infectious disease incidence provide important information about epidemic dynamics and prospects for control. Higher-frequency variation around incidence trends can shed light on the processes driving epidemics in complex populations, as transmission heterogeneity, shifting landscapes of susceptibility, and fluctuations in reporting can impact the volatility of observed case counts. However, measures of temporal volatility in incidence, and how volatility changes over time, are often overlooked in population-level analyses of incidence data, which typically focus on moving averages. Here we present a statistical framework to quantify temporal changes in incidence dispersion and to detect rapid shifts in the dispersion parameter, which may signal new epidemic phases. We apply the method to COVID-19 incidence data in 144 United States (US) counties from January 1st, 2020 to March 23rd, 2023. Theory predicts that dispersion should be inversely proportional to incidence, however our method reveals pronounced temporal trends in dispersion that are not explained by incidence alone, but which are replicated across counties. In particular, dispersion increased around the major surge in cases in 2022, and highly overdispersed patterns became more frequent later in the time series. These increases potentially indicate transmission heterogeneity, changes in the susceptibility landscape, or that there were changes in reporting. Shifts in dispersion can also indicate shifts in epidemic phase, so our method provides a way for public health officials to anticipate and manage changes in epidemic regime and the drivers of transmission.Author summary: Quantifying patterns in infectious disease incidence is crucial for understanding epidemic dynamics and for developing effective public health policy. Traditional metrics used to quantify incidence patterns often overlook variability as an important characteristic of incidence time series. Quantifying variability around incidence trends can elucidate important underlying processes, including transmission heterogeneity. We developed a statistical framework to quantify temporal changes in dispersion in time series of case counts and applied the method to COVID-19 case count data from U.S. counties. We found large shifts in incidence volatility (week-to-week variability in the numbers of new cases) that were synchronized across counties, and were not explained by broader-scale changes in mean incidence over time. Incidence dispersion increased around peaks in incidence such as the major surge in cases in 2022, and dispersion also increased as the pandemic progressed. These increases potentially indicate transmission heterogeneity, changes in the susceptibility landscape, or that there were changes in reporting. Shifts in dispersion can also indicate shifts in epidemic phase, so our method provides a way for public health officials to anticipate and manage changes in epidemic regime and the drivers of transmission.

Suggested Citation

  • Rachael Aber & Yanming Di & Benjamin D Dalziel, 2025. "Time-series modeling of epidemics in complex populations: Detecting changes in incidence volatility over time," PLOS Computational Biology, Public Library of Science, vol. 21(7), pages 1-12, July.
  • Handle: RePEc:plo:pcbi00:1012882
    DOI: 10.1371/journal.pcbi.1012882
    as

    Download full text from publisher

    File URL: https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1012882
    Download Restriction: no

    File URL: https://journals.plos.org/ploscompbiol/article/file?id=10.1371/journal.pcbi.1012882&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pcbi.1012882?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pcbi00:1012882. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: ploscompbiol (email available below). General contact details of provider: https://journals.plos.org/ploscompbiol/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.