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HCV avidity as a tool for detection of recent HCV infection: Sensitivity depends on HCV genotype

机译:HCV作为用于检测最近HCV感染的工具:敏感度取决于HCV基因型

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Accurate detection of incident hepatitis C virus (HCV) infection is required to target and evaluate public health interventions, but acute infection is largely asymptomatic and difficult to detect using traditional methods. Our aim was to evaluate a previously developed HCV avidity assay to distinguish acute from chronic HCV infection. Plasma samples collected from recent seroconversion subjects in two large Australian cohorts were tested using the avidity assay, and the avidity index (AI) was calculated. Demographic and clinical characteristics of patients with low/high AI were compared via logistic regression. Sensitivity and specificity of the assay for recent infection and the mean duration of recent infection (MDRI) were estimated stratified by HCV genotype. Avidity was assessed in 567 samples (from 215 participants), including 304 with viraemia (defined as ≥250?IU/mL). An inverse relationship between AI and infection duration was found in viraemic samples only. The adjusted odds of a low AI (30%) decreased with infection duration (odds ratio [OR] per week of 0.93; 95% CI:0.89‐0.97), and were lower for G1 compared with G3 samples (OR?=?0.14; 95% CI:0.05‐0.39). Defining recent infection as 26 weeks, sensitivity (at AI cut‐off of 20%) was estimated at 48% (95% CI:39‐56%), 36% (95% CI:20‐52%), and 65% (95% CI:54‐75%) and MDRI was 116, 83, and 152 days for all genotypes, G1, and G3, respectively. Specificity (≥52 weeks infection duration, all genotypes) was 96% (95% CI:90‐98%). HCV avidity testing has utility for detecting recent HCV infection in patients, and for assessing progress in reaching incidence targets for eliminating transmission, but variation in assay performance across genotype should be recognized.
机译:准确地检测入射丙型肝炎病毒(HCV)感染需要靶向和评估公共卫生干预,但急性感染在很大程度上无症状,难以使用传统方法检测。我们的目的是评估先前开发的HCV亲密测定以区分急性HCV感染。使用Avity测定测试从最近的两种大型澳大利亚群组中收集的血清转换对象中的血浆样品,并计算厌恶指数(AI)。通过逻辑回归比较低/高AI患者的人口统计学和临床​​特征。估计通过HCV基因型分层估计最近感染的测定的敏感性和特异性和最近感染(MDRI)的平均持续时间。在567个样品(来自215名参与者)中评估亲和力,其中包括病毒血症304(定义为≥250?IU / ml)。 AI和感染持续时间之间的反比关系仅在危令样本中发现。低ai(30%)的调节的几率随感染持续时间而降低(每周0.93的差距[或]; 95%Ci:0.89-0.97),与G3样品相比,G1较低(或?= ?0.14; 95%CI:0.05-0.39)。定义近期感染为& 26周,敏感性(AI截止值为20%)估计为48%(95%CI:39-56%),36%(95%CI:20-52%),和所有基因型,G1和G3分别为65%(95%CI:54-75%)和MDRI为116,83和152天。特异性(≥52周感染持续时间,所有基因型)为96%(95%CI:90-98%)。 HCV亲和力测试具有检测患者最近的HCV感染的实用性,以及评估达到消除速率的发病率的进展,但应识别出基因型的测定性能的变化。

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