Chang Joy, de Sousa Amina, Sabatier Jennifer, Assane Mariamo, Zhang Guoqing, Bila Dulce, Vaz Paula, Alfredo Charity, Cossa Loide, Bhatt Nilesh, Koumans Emilia H, Yang Chunfu, Rivadeneira Emilia, Jani Ilesh, Houston James C
Centers for Disease Control and Prevention (CDC), Atlanta, GA, United States of America.
Instituto Nacional de Saúde (INS), Ministry of Health, Maputo, Mozambique.
PLoS One. 2017 Jul 13;12(7):e0181054. doi: 10.1371/journal.pone.0181054. eCollection 2017.
Quantitative plasma viral load (VL) at 1000 copies /mL was recommended as the threshold to confirm antiretroviral therapy (ART) failure by the World Health Organization (WHO). Because of ongoing challenges of using plasma for VL testing in resource-limited settings (RLS), especially for children, this study collected 717 DBS and paired plasma samples from children receiving ART ≥1 year in Mozambique and compared the performance of DBS using Abbott's VL test with a paired plasma sample using Roche's VL test. At a cut-off of 1000 copies/mL, sensitivity of DBS using Abbott DBS VL test was 79.9%, better than 71.0% and 63.9% at 3000 and 5000 copies/mL, respectively. Specificities were 97.6%, 98.8%, 99.3% at 1000, 3000, and 5000 copies/mL, respectively. The Kappa value at 1000 copies/mL, 0.80 (95% CI: 0.73, 0.87), was higher than 0.73 (95% CI: 0.66, 0.80) and 0.66 (95% CI: 0.59, 0.73) at 3000, 5000 copies/mL, respectively, also indicating better agreement. The mean difference between the DBS and plasma VL tests with 95% limits of agreement by Bland-Altman was 0.311 (-0.908, 1.530). Among 73 children with plasma VL between 1000 to 5000 copies/mL, the DBS results were undetectable in 53 at the 1000 copies/mL threshold. While one DBS sample in the Abbott DBS VL test may be an alternative method to confirm ART failure at 1000 copies/mL threshold when a plasma sample is not an option for treatment monitoring, because of sensitivity concerns between 1,000 and 5,000 copies/ml, two DBS samples may be preferred accompanied by careful patient monitoring and repeat testing.
世界卫生组织(WHO)建议将血浆病毒载量(VL)定量达到1000拷贝/毫升作为确认抗逆转录病毒疗法(ART)失败的阈值。由于在资源有限的环境(RLS)中,尤其是对儿童而言,使用血浆进行VL检测存在持续挑战,本研究收集了莫桑比克717份干血斑(DBS)样本以及接受ART≥1年的儿童的配对血浆样本,并将使用雅培VL检测的DBS性能与使用罗氏VL检测的配对血浆样本进行比较。在1000拷贝/毫升的临界值下,使用雅培DBS VL检测的DBS灵敏度为79.9%,分别优于3000拷贝/毫升和5000拷贝/毫升时的71.0%和63.9%。特异性在1000、3000和5000拷贝/毫升时分别为97.6%、98.8%、99.3%。1000拷贝/毫升时的Kappa值为0.80(95%置信区间:0.73,0.87),高于3000拷贝/毫升时的0.73(95%置信区间:0.66,0.80)和5000拷贝/毫升时的0.66(95%置信区间:0.59,0.73),也表明一致性更好。根据Bland-Altman法,DBS和血浆VL检测之间的平均差异及95%一致性界限为0.311(-0.908,1.530)。在73名血浆VL在1000至5000拷贝/毫升之间的儿童中,在1000拷贝/毫升的阈值下,53名儿童的DBS结果检测不到。虽然当血浆样本不适合用于治疗监测时,雅培DBS VL检测中的一份DBS样本可能是在1000拷贝/毫升阈值下确认ART失败的替代方法,但由于1000至5000拷贝/毫升之间的灵敏度问题,可能更倾向于采集两份DBS样本,并对患者进行仔细监测和重复检测。