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Factors Associated with Incorrect Identification of Recent HIV Infection Using the BED Capture Immunoassay

机译:使用BED捕获免疫测定法无法正确识别近期HIV感染的相关因素

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摘要

The BED capture enzyme immunoassay (BED-CEIA) was developed for estimating HIV incidence from cross-sectional data. This assay misclassifies some individuals with nonrecent HIV infection as recently infected, leading to overestimation of HIV incidence. We analyzed factors associated with misclassification by the BED-CEIA. We analyzed samples from 383 men who were diagnosed with HIV infection less than 1 year after a negative HIV test (Multicenter AIDS Cohort Study). Samples were collected 2–8 years after HIV seroconversion, which was defined as the midpoint between the last negative and first positive HIV test. Samples were analyzed using the BED-CEIA with a cutoff of OD-n ≤0.8 for recent infection. Logistic regression was used to identify factors associated with misclassification. Ninety-one (15.1%) of 603 samples were misclassified. In multivariate models, misclassification was independently associated with highly active antiretroviral treatment (HAART) for >2 years, HIV RNA <400 copies/ml, and CD4 cell count <50 or <200 cells/mm3; adjusted odds ratios (OR) and 95% confidence intervals (CI) were 4.72 (1.35–16.5), 3.96 (1.53–10.3), 6.85 (2.71–17.4), and 11.5 (3.64–36.0), respectively. Among 220 men with paired samples, misclassification 2–4 years after seroconversion was significantly associated with misclassification 6–8 years after seroconversion [adjusted OR: 25.8 (95% CI: 8.17–81.5), p<0.001] after adjusting for race, CD4 cell count, HIV viral load, and HAART use. Low HIV viral load, low CD4 cell count, and >2 years of HAART were significantly associated with misclassification using the BED-CEIA. Some men were persistently misclassified as recently infected up to 8 years after HIV seroconversion.
机译:BED捕获酶免疫测定法(BED-CEIA)的开发是为了通过横截面数据估算HIV的发病率。该测定法将一些近期感染非近期感染的个体错误分类,导致对HIV发病率的高估。我们分析了与BED-CEIA错误分类有关的因素。我们分析了383名在HIV阴性试验后不到1年被诊断出感染HIV的男性的样本(多中心AIDS队列研究)。 HIV血清转化后2-8年收集了样本,这被定义为最后一次阴性和第一次阳性HIV检测之间的中点。使用BED-CEIA对样品进行分析,其OD-n≤0.8的临界值用于近期感染。 Logistic回归用于识别与错误分类相关的因素。 603个样本中有91个(15.1%)被错误分类。在多变量模型中,错误分类与高活性抗逆转录病毒治疗(HAART)持续2年以上,HIV RNA <400拷贝/ ml和CD4细胞计数<50或<200细胞/ mm 3 独立相关;调整后的优势比(OR)和95%置信区间(CI)分别为4.72(1.35-16.5),3.96(1.53-10.3),6.85(2.71-17.4)和11.5(3.64-36.0)。在220名配对样本的男性中,血清转换后2-4年的错误分类与血清转换后6-8年的错误分类显着相关[校正后的OR:25.8(95%CI:8.17-81.5),p <0.001],种族校正后,CD4细胞计数,HIV病毒载量和HAART使用情况。低HIV病毒载量,低CD4细胞计数和> 2年的HAART与使用BED-CEIA的错误分类显着相关。在HIV血清学转化后长达​​8年的时间里,有些男性一直被错误地归类为近期感染。

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