论文标题

在没有风险转换的流行模型中,高风险群体未满足需求的贡献可能会被低估:机械建模分析

Contribution of high risk groups' unmet needs may be underestimated in epidemic models without risk turnover: a mechanistic modelling analysis

论文作者

Knight, Jesse, Baral, Stefan D., Schwartz, Sheree, Wang, Linwei, Ma, Huiting, Young, Katherine, Hausler, Harry, Mishra, Sharmistha

论文摘要

背景。传播性传播感染的流行模型通常用于表征风险群体对整体传播的贡献,通过预测归因于未满足预防的传播人群(TPAF)和风险群体内的治疗需求。但是,有证据表明,性传播感染风险在个人的性生活过程中是动态的,这表现为风险群体之间的离职。我们试图研究营业额影响高风险群体TPAF的模型投影的机制。方法。我们开发了一个统一的,数据引导的框架,以模拟确定性的隔离传输模型中的风险群体离职。我们将框架应用于STI的说明性模型,并检查了风险群体离职影响风险群体平衡率的机制。然后,我们将带有和没有营业额的模型拟合到相同的风险分层性传播感染患病率目标,并比较了这两个模型所预测的最高风险组的推断风险异质性和TPAF水平。结果。营业额对特定组的流行率的影响是由三个主要现象介导的:风险群体之间传染性个体的运动;改变牛群免疫力;以及不一致的伙伴关系的变化。更快的营业额导致最高风险组和最低风险组之间的性病患病率较小。与没有营业额的拟合模型相比,具有营业额的拟合模型推断出更大的风险异质性,并持续投射出更大的TPAF,随着时间的推移,最高风险组的最高风险组。含义。如果流行模型未捕获营业额,则可能会低估高风险群体的预计贡献,因此,将干预措施优先置于满足其需求的潜在影响。为了帮助下一代TPAF模型,应优先考虑以参数化风险组营业额来参数化风险组营业额的数据。

BACKGROUND. Epidemic models of STIs are often used to characterize the contribution of risk groups to overall transmission by projecting the transmission population attributable fraction (tPAF) of unmet prevention and treatment needs within risk groups. However, evidence suggests that STI risk is dynamic over an individual's sexual life course, which manifests as turnover between risk groups. We sought to examine the mechanisms by which turnover influences modelled projections of the tPAF of high risk groups. METHODS. We developed a unifying, data-guided framework to simulate risk group turnover in deterministic, compartmental transmission models. We applied the framework to an illustrative model of an STI and examined the mechanisms by which risk group turnover influenced equilibrium prevalence across risk groups. We then fit a model with and without turnover to the same risk-stratified STI prevalence targets and compared the inferred level of risk heterogeneity and tPAF of the highest risk group projected by the two models. RESULTS. The influence of turnover on group-specific prevalence was mediated by three main phenomena: movement of infectious individuals between risk groups; changes to herd immunity; and changes in discordant partnerships. Faster turnover led to a smaller ratio of STI prevalence between the highest and lowest risk groups. Compared to the fitted model without turnover, the fitted model with turnover inferred greater risk heterogeneity and consistently projected a larger tPAF of the highest risk group over time. IMPLICATIONS. If turnover is not captured in epidemic models, the projected contribution of high risk groups, and thus, the potential impact of prioritizing interventions to address their needs, could be underestimated. To aid the next generation of tPAF models, data collection efforts to parameterize risk group turnover should be prioritized.

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