Crowell Claudia S, Maiga Almoustapha I, Sylla Mariam, Taiwo Babafemi, Kone Niaboula, Oron Assaf P, Murphy Robert L, Marcelin Anne-Geneviève, Traore Ban, Fofana Djeneba B, Peytavin Gilles, Chadwick Ellen G
From the *Department of Pediatrics, Division of Infectious Diseases, University of Washington, and †Seattle Children's Hospital, Seattle, Washington; ‡Unité d'Epidémiologie Moléculaire de la Résistance du VIH aux ARV, SEREFO, §University of Sciences, Techniques and Technologies of Bamako, and ¶Department of Pediatrics, University Hospital Gabriel Touré, Bamako, Mali; ‖Department of Medicine, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, Illinois; **Seattle Children's Research Institute, Children's Core for Biomedical Statistics, Seattle, Washington; ††Department of Virology, Sorbonne Université, UPMC Univ Paris 06, INSERM, Institut Pierre Louis d'épidémiologie et de Santé Publique, ‡‡Department of Pharmaco-Toxicology, APHP, Bichat-Claude Bernard Hospital, and §§Paris Diderot University, Sorbonne Paris Cité, IAME, INSERM UMR 1137, Paris, France; and ¶¶Department of Pediatrics, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine and Ann & Robert H. Lurie Children's Hospital, Chicago, Illinois.
Pediatr Infect Dis J. 2017 Nov;36(11):e258-e263. doi: 10.1097/INF.0000000000001575.
Limited data exist on drug resistance and antiretroviral treatment (ART) outcomes in HIV-1-infected children in West Africa. We determined the prevalence of baseline resistance and correlates of virologic failure (VF) in a cohort of ART-naive HIV-1-infected children <10 years of age initiating ART in Mali.
Reverse transcriptase and protease genes were sequenced at baseline (before ART) and at 6 months. Resistance was defined according to the Stanford HIV Genotypic Resistance database. VF was defined as viral load ≥1000 copies/mL after 6 months of ART. Logistic regression was used to evaluate factors associated with VF or death >1 month after enrollment. Post hoc, antiretroviral concentrations were assayed on baseline samples of participants with baseline resistance.
One-hundred twenty children with a median age 2.6 years (interquartile range: 1.6-5.0) were included. Eighty-eight percent reported no prevention of mother-to-child transmission exposure. At baseline, 27 (23%), 4 (3%) and none had non-nucleoside reverse transcriptase inhibitor (NNRTI), nucleoside reverse transcriptase inhibitor or protease inhibitor resistance, respectively. Thirty-nine (33%) developed VF and 4 died >1 month post-ART initiation. In multivariable analyses, poor adherence [odds ratio (OR): 6.1, P = 0.001], baseline NNRTI resistance among children receiving NNRTI-based ART (OR: 22.9, P < 0.001) and protease inhibitor-based ART initiation among children without baseline NNRTI resistance (OR: 5.8, P = 0.018) were significantly associated with VF/death. Ten (38%) with baseline resistance had detectable levels of nevirapine or efavirenz at baseline; 7 were currently breastfeeding, but only 2 reported maternal antiretroviral use.
Baseline NNRTI resistance was common in children without reported NNRTI exposure and was associated with increased risk of treatment failure. Detectable NNRTI concentrations were present despite few reports of maternal/infant antiretroviral use.
关于西非感染HIV-1的儿童的耐药性和抗逆转录病毒治疗(ART)结果的数据有限。我们确定了在马里开始接受ART的10岁以下未接受过ART的HIV-1感染儿童队列中的基线耐药率以及病毒学失败(VF)的相关因素。
在基线(ART前)和6个月时对逆转录酶和蛋白酶基因进行测序。耐药性根据斯坦福HIV基因型耐药数据库进行定义。VF定义为ART 6个月后病毒载量≥1000拷贝/mL。使用逻辑回归评估与VF或入组后1个月以上死亡相关的因素。事后,对具有基线耐药性的参与者的基线样本进行抗逆转录病毒药物浓度测定。
纳入了120名中位年龄为2.6岁(四分位间距:1.6 - 5.0)的儿童。88%报告未接受母婴传播预防措施。在基线时,分别有27名(23%)、4名(3%)和无儿童具有非核苷类逆转录酶抑制剂(NNRTI)、核苷类逆转录酶抑制剂或蛋白酶抑制剂耐药性。39名(33%)出现VF,4名在ART开始后1个月以上死亡。在多变量分析中,依从性差[比值比(OR):6.1,P = 0.001]、接受基于NNRTI的ART的儿童中的基线NNRTI耐药性(OR:22.9,P < 0.001)以及在无基线NNRTI耐药性的儿童中开始基于蛋白酶抑制剂的ART(OR:5.8,P = 0.018)与VF/死亡显著相关。10名(38%)具有基线耐药性的儿童在基线时可检测到奈韦拉平或依非韦伦水平;7名目前正在母乳喂养,但只有2名报告母亲使用了抗逆转录病毒药物。
在未报告有NNRTI暴露的儿童中,基线NNRTI耐药性很常见,并且与治疗失败风险增加相关。尽管很少有母亲/婴儿使用抗逆转录病毒药物的报告,但仍可检测到NNRTI浓度。