Laboratoire de Rétrovirologie, CIRMF, BP769, Franceville, Gabon.
J Int AIDS Soc. 2012 Nov 28;15(2):17985. doi: 10.7448/IAS.15.2.17985.
As antiretroviral treatment (ART) continues to expand in resource-limited countries, the emergence of HIV drug resistance mutations (DRMs) is challenging in these settings. In Gabon (central Africa), no study has yet reported the virological effectiveness of initial ART given through routine HIV care.
Following the World Health Organization (WHO) recommendations, a cross-sectional study with a one-time HIV-1 RNA viral load (VL) measurement was conducted in Gabon to assess virological failure (VF) defined by a VL result ≥1000 copies/ml and DRMs among adult patients living with non-B HIV-1 strains and receiving first-line non-nucleoside reverse transcriptase inhibitor (NNRTI)-based antiretroviral therapy for at least 12 months. Risk factors associated with VF and DRMs were assessed.
Between March 2010 and March 2011, a total of 375 patients were consecutively enrolled from two decentralized (one semirural and one rural) HIV care centres. Median time on ART was 33.6 months (range, 12-107). Overall, the rate of VF was 41.3% (36.4-46.4). Among viremic patients, 56.7% (80/141) had at least one DRM and 37.6% had dual-class resistance to nucleoside reverse transcriptase inhibitors (NRTIs) and NNRTIs. The most frequent DRMs were K103N/S (46.1%) and M184V/I (37.6%). Thymidine analogue mutations were found in 10.6%. Independent risk factors associated with VF were being followed up at the semirural centre (P=0.033), having experienced unstructured treatment interruptions (P=0.0044), and having low CD4+ counts at enrolment (P<0.0001). A longer time on ART (P=0.0008) and being followed up at the rural centre (P=0.021) were risk factors for DRMs.
This is the first study conducted in Gabon providing VF rates and DRM patterns in adult patients receiving first-line ART. In sub-Saharan Africa, where NNRTI-based regimens are recommended as the standard for first-line ART, strengthening virological monitoring together with preventing unplanned treatment interruptions are a global public health priority.
随着抗逆转录病毒治疗(ART)在资源有限的国家不断扩展,HIV 耐药突变(DRMs)的出现给这些环境带来了挑战。在加蓬(中非),尚无研究报告过通过常规 HIV 护理提供初始 ART 的病毒学疗效。
根据世界卫生组织(WHO)的建议,在加蓬进行了一项横断面研究,单次测量 HIV-1 RNA 病毒载量(VL),以评估定义为 VL 结果≥1000 拷贝/ml 的病毒学失败(VF)和非 B HIV-1 株的成年患者中接受至少 12 个月的一线非核苷逆转录酶抑制剂(NNRTI)为基础的抗逆转录病毒治疗的 DRMs。评估了与 VF 和 DRMs 相关的风险因素。
2010 年 3 月至 2011 年 3 月,连续从两个分散(一个半农村和一个农村)HIV 护理中心招募了 375 名患者。ART 的中位时间为 33.6 个月(范围,12-107)。总体而言,VF 发生率为 41.3%(36.4-46.4)。在病毒血症患者中,56.7%(80/141)有至少一种 DRM,37.6%有核苷逆转录酶抑制剂(NRTIs)和 NNRTIs 的双重耐药。最常见的 DRMs 是 K103N/S(46.1%)和 M184V/I(37.6%)。发现胸苷类似物突变占 10.6%。与 VF 相关的独立危险因素是在半农村中心就诊(P=0.033)、经历无计划的治疗中断(P=0.0044)和入组时 CD4+计数低(P<0.0001)。更长的 ART 时间(P=0.0008)和在农村中心就诊(P=0.021)是 DRM 的危险因素。
这是在加蓬进行的第一项研究,提供了接受一线 ART 的成年患者的 VF 率和 DRM 模式。在推荐 NNRTI 为一线 ART 标准的撒哈拉以南非洲,加强病毒学监测以及预防无计划的治疗中断是全球公共卫生的重点。