4.6 Article

Potential Biases Arising From Epidemic Dynamics in Observational Seroprotection Studies

期刊

AMERICAN JOURNAL OF EPIDEMIOLOGY
卷 190, 期 2, 页码 328-335

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/aje/kwaa188

关键词

bias (epidemiology); coronavirus disease 2019; epidemic dynamics; epidemics; immunity; SARS-CoV-2; seroprotection

资金

  1. National Institute of General Medical Sciences (National Institutes of Health) [U54GM088558]
  2. Centers for Disease Control and Prevention [U01IP001121]
  3. Office of Naval Research [N00014-19-1-2466]

向作者/读者索取更多资源

When studying the extent and duration of immunity following infection with SARS-CoV-2, it is important to consider individual risk factors and geographic structure as potential sources of bias. Stratifying or matching on geographic location and time of enrollment is essential in serological studies to prevent bias and ensure accurate results.
The extent and duration of immunity following infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are critical outstanding questions about the epidemiology of this novel virus, and studies are needed to evaluate the effects of serostatus on reinfection. Understanding the potential sources of bias and methods for alleviating biases in these studies is important for informing their design and analysis. Confounding by individual-level risk factors in observational studies like these is relatively well appreciated. Here, we show how geographic structure and the underlying, natural dynamics of epidemics can also induce noncausal associations. We take the approach of simulating serological studies in the context of an uncontrolled or controlled epidemic, under different assumptions about whether prior infection does or does not protect an individual against subsequent infection, and using various designs and analytical approaches to analyze the simulated data. We find that in studies assessing whether seropositivity confers protection against future infection, comparing seropositive persons with seronegative persons with similar time-dependent patterns of exposure to infection by stratifying or matching on geographic location and time of enrollment is essential in order to prevent bias.

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