Am J Epidemiol. 2021 Feb 1;190(2):328-335. doi: 10.1093/aje/kwaa188.
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.
感染严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)后免疫的范围和持续时间是关于这种新型病毒流行病学的关键未解决问题,需要研究来评估血清阳性状态对再感染的影响。了解这些研究中潜在偏差的来源和减轻偏差的方法对于为其设计和分析提供信息很重要。在这种观察性研究中,个体水平风险因素的混杂相对容易理解。在这里,我们展示了地理结构和潜在的流行病自然动态如何也会引起非因果关系。我们采用在不受控制或受控制的流行情况下模拟血清学研究的方法,根据先前的感染是否确实或是否不能保护个体免受随后的感染做出不同的假设,并使用各种设计和分析方法来分析模拟数据。我们发现,在评估血清阳性是否对未来感染提供保护的研究中,通过在地理区域和入组时间上分层或匹配来比较具有相似感染暴露时间依赖性模式的血清阳性者和血清阴性者,对于防止偏差至关重要。