使用近期感染测试估计人群中的艾滋病毒感染率:问题、挑战和前进方向。

Timothy D Mastro, Andrea A Kim, Timothy Hallett, Thomas Rehle, Alex Welte, Oliver Laeyendecker, Tom Oluoch, Jesus M Garcia-Calleja
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引用次数: 0

摘要

导言:HIV 感染率是指随着时间的推移人群中新感染者的比率。艾滋病发病率是评估艾滋病在人群中流行的现状和趋势以及指导和评估预防干预措施效果所需的一个重要指标。 方法:目前有几种方法可用于估算人群中的 HIV 感染率:通过对新感染 HIV 的高危人群进行纵向追踪,直接观察 HIV 感染率;利用人群中 HIV 感染率和死亡率的数据,间接测量 HIV 感染率;利用近期感染测试 (TRI) 直接测量 HIV 感染率,该测试可根据横断面样本中的生物标志物区分 "近期 "和 "非近期 "感染。鉴于直接观察发病率测量的局限性以及间接测量发病率所需的假设,人们对用于艾滋病发病率监测以及项目监测和评估的 TRIs 的需求日益增加。 结果:自第一个 TRI 推出十多年来,一些低收入、中等收入和高收入国家已将这种方法纳入其 HIV 监测系统,以监测人群中的 HIV 感染率。然而,迄今为止,这些检测方法测量 HIV 感染率的准确性并不令人满意,这主要是由于检测方法将慢性感染误列为近期感染所致。为提高 TRI 测定发病率的准确性,建议各国采用基于病例的调整、使用当地校正因子的基于公式的调整或基于实验室的调整,以尽量减少与检测误分类有关的误差。可在近期感染检测算法(RITA)中使用多种检测方法,以获得更准确的艾滋病毒发病率估计值。 结论:目前仍然非常需要改进的 TRI 和 RITA,以监测 HIV 发病率、确定预防重点并评估干预措施的影响。目前的 TRIs 有明显的局限性,但经过适当调整并与其他流行病学数据并行解释后,仍可提供有关人群新感染情况的有用信息。需要新的 TRI 和 RITAs 来提高准确性和性能,应支持这些工具的开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Estimating HIV Incidence in Populations Using Tests for Recent Infection: Issues, Challenges and the Way Forward.

Estimating HIV Incidence in Populations Using Tests for Recent Infection: Issues, Challenges and the Way Forward.

Estimating HIV Incidence in Populations Using Tests for Recent Infection: Issues, Challenges and the Way Forward.

INTRODUCTION: HIV incidence is the rate of new infections in a population over time. HIV incidence is a critical indicator needed to assess the status and trends of the HIV epidemic in populations and guide and assess the impact of prevention interventions. METHODS: Several methods exist for estimating population-level HIV incidence: direct observation of HIV incidence through longitudinal follow-up of persons at risk for new HIV infection, indirect measurement of HIV incidence using data on HIV prevalence and mortality in a population, and direct measurement of HIV incidence through use of tests for recent infection (TRIs) that can differentiate "recent" from "non-recent" infections based on biomarkers in cross-sectional specimens. Given the limitations in measuring directly observed incidence and the assumptions needed for indirect measurements of incidence, there is an increasing demand for TRIs for HIV incidence surveillance and program monitoring and evaluation purposes. RESULTS: Over ten years since the introduction of the first TRI, a number of low-, middle-, and high-income countries have integrated this method into their HIV surveillance systems to monitor HIV incidence in the population. However, the accuracy of these assays for measuring HIV incidence has been unsatisfactory to date, mainly due to misclassification of chronic infections as recent infection on the assay. To improve the accuracy of TRIs for measuring incidence, countries are recommended to apply case-based adjustments, formula-based adjustments using local correction factors, or laboratory-based adjustment to minimize error related to assay misclassification. Multiple tests may be used in a recent infection testing algorithm (RITA) to obtain more accurate HIV incidence estimates. CONCLUSION: There continues to be a high demand for improved TRIs and RITAs to monitor HIV incidence, determine prevention priorities, and assess impact of interventions. Current TRIs have noted limitations, but with appropriate adjustments, interpreted in parallel with other epidemiologic data, may still provide useful information on new infections in a population. New TRIs and RITAs with improved accuracy and performance are needed and development of these tools should be supported.

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