Estimating Trends in Incidence, Time-to-Diagnosis and Undiagnosed Prevalence using a CD4-based Bayesian Back-calculation

P. Birrell, T. Chadborn, O. Gill, V. Delpech, Daniela, De Angelis
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引用次数: 17

Abstract

Abstract There has been much recent speculation regarding the potential for HIV test-and-treat strategies to provide control of the HIV endemic. In the UK, despite advanced HIV surveillance and the implementation of a number of testing initiatives and attempts to widen access to antiretroviral drugs, the number of new diagnoses persists at a high level having risen considerably over the course of the last ten years. The extent to which this high level of diagnosis is attributable to levels of HIV transmission or improved rates of testing and diagnosis is unclear. To disentangle these competing factors, we use a Bayesian back-calculation based on HIV and AIDS diagnosis data augmented by observed CD4 count levels at diagnosis. The CD4 count acts as a prognostic marker indicative of the time-since-infection for any new diagnosis. In addition to estimating time-dependent rates of infection and diagnosis, we exploit the model structure to estimate posterior distributions for a number of key epidemiological quantities such as trends in the time-to-diagnosis and the time-since infection distributions as well as the prevalence of undiagnosed infection. These quantities are stratified by CD4 count where possible. The proposed methodology is applied to HIV/AIDS surveillance data from England & Wales uncovering a decreasing trend in the time to diagnosis and stable levels of incidence in recent years.
使用基于cd4的贝叶斯反算估计发病率、诊断时间和未诊断患病率的趋势
最近有很多关于艾滋病毒检测和治疗策略的潜力的猜测,以提供艾滋病毒流行的控制。在英国,尽管进行了先进的艾滋病毒监测,实施了一些检测举措,并试图扩大获得抗逆转录病毒药物的机会,但在过去十年中,新诊断的数量仍然保持在较高水平,并大幅上升。目前尚不清楚这种高诊断率在多大程度上归因于艾滋病毒传播水平或检测和诊断率的提高。为了解开这些相互竞争的因素,我们使用基于HIV和AIDS诊断数据的贝叶斯反向计算,并在诊断时观察到CD4计数水平。CD4计数作为任何新诊断感染时间的预后标志物。除了估计感染和诊断率的时间依赖性外,我们还利用模型结构来估计一些关键流行病学数量的后验分布,例如诊断时间和自诊断时间以来感染分布的趋势以及未诊断感染的流行率。这些数量在可能的情况下按CD4计数分层。所提出的方法应用于英格兰和威尔士的艾滋病毒/艾滋病监测数据,发现近年来诊断时间呈下降趋势,发病率水平稳定。
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