Kayinda Francis, Awor Phyllis, Mahaba Twaha, Muganzi Alex M, Kigozi Joanita, Olwedo Patrick Odong, Nasuuna Esther M, Mutumba Robert, Wanyenze Rhoda
Makerere University School of Public Health, Kampala, Uganda.
Infectious Diseases Institute, Makerere University College of Health science, Kampala, Uganda.
PLoS One. 2025 Aug 5;20(8):e0320623. doi: 10.1371/journal.pone.0320623. eCollection 2025.
HIV drug resistance (HIVDR) poses a challenge to managing people living with HIV (PLHIV), particularly among those experiencing virological failure (VF). The West-Nile region of Uganda faces HIV treatment challenges and has a high virological failure rate. We estimated the prevalence of HIV drug resistance, described the HIV drug resistance mutations and evaluated the factors associated with HIVDR among PLHIV with virological failure in the West-Nile region of Uganda.
We conducted a retrospective cross-sectional analysis of HIVDR data in the West-Nile region of Uganda across the 161 health facilities that offer comprehensive Anti-retroviral therapy (ART) services. All PLHIV, regardless of age, who had been on ART for at least one-year, experienced virological failure and underwent an HIVDR test between 1st January 2021-30th December 2023 were included in the study. Demographic and clinical data were extracted from the National HIVDR database. HIVDR was defined as having at least one mutation with a penalty score of ≥15. PLHIV were characterized based on age, gender and clinical history. Logistic regression models determined factors associated with HIVDR with a p-value of <0.05 considered significant.
A total 295 records were analyzed. Of these, majority were female (56.6%) and adults aged ≥20 years (49.2%). The median age was 19 (Inter quartile range [IQR]: 13-41) years, and median duration on ART was 8 (IQR: 5-10) years. Overall, 218 (73.9%) had HIVDR with 66% of subjects having Non-nucleoside reverse transcriptase (NNRTI) mutations. M184V/I (50%), K103N (34%) and TAMS (26%) were the commonest mutations. Resistance to Etravirine (27%) was higher than that of Dolutegravir (12%) and Darunavir (5%). After accounting for gender, age, Nucleoside reverse transcriptase inhibitor (NRTI) anchor drug, ART regimen type and World Health Organization (WHO) clinical stage of the participants; long duration on ART (aOR=; 1.15 95%CI 1.05-1.26 p = 0.003), adolescents failing on first line (aOR=; 3.80 95%CI 1.02-14.08 p = 0.046) and participants failing on 2nd line (aOR=; 3.64 95%CI 1.18-11.21 p = 0.024) as indications for the HIVDR test, and the year of HIVDR sample collection (aOR=; 0.21 95%CI 0.07-0.69 p = 0.010), were independently associated with HIVDR mutations.
The study found a high HIVDR prevalence strongly associated with long ART duration which is likely to lead to increased ART treatment failure rates. The high Etravirine resistance and increasing Dolutegravir resistance are likely to complicate future treatment options while low Darunavir resistance makes it a future third-line treatment option. Strengthening routine resistance surveillance, timely VL monitoring, and adherence support are critical to mitigating drug resistance and preserving ART effectiveness among PLHIV in the West-Nile region.
艾滋病毒耐药性(HIVDR)对艾滋病毒感染者(PLHIV)的管理构成挑战,尤其是在那些经历病毒学失败(VF)的人群中。乌干达西尼罗河地区面临艾滋病毒治疗挑战,且病毒学失败率很高。我们估计了乌干达西尼罗河地区病毒学失败的艾滋病毒感染者中艾滋病毒耐药性的流行情况,描述了艾滋病毒耐药性突变,并评估了与艾滋病毒耐药性相关的因素。
我们对乌干达西尼罗河地区161家提供全面抗逆转录病毒疗法(ART)服务的医疗机构的艾滋病毒耐药性数据进行了回顾性横断面分析。所有接受抗逆转录病毒治疗至少一年、经历病毒学失败且在2021年1月1日至2023年12月31日期间接受艾滋病毒耐药性检测的艾滋病毒感染者,无论年龄大小,均纳入研究。人口统计学和临床数据从国家艾滋病毒耐药性数据库中提取。艾滋病毒耐药性定义为至少有一个罚分≥15的突变。根据年龄、性别和临床病史对艾滋病毒感染者进行特征描述。逻辑回归模型确定与艾滋病毒耐药性相关的因素,p值<0.05被认为具有统计学意义。
共分析了295条记录。其中,大多数为女性(56.6%)和年龄≥20岁的成年人(49.2%)。中位年龄为19岁(四分位间距[IQR]:13 - 41岁),抗逆转录病毒治疗的中位持续时间为8年(IQR:5 - 10年)。总体而言,218例(73.9%)存在艾滋病毒耐药性,66%的受试者有非核苷类逆转录酶(NNRTI)突变。M184V/I(50%)、K103N(34%)和TAMS(26%)是最常见的突变。对依曲韦林的耐药性(27%)高于多替拉韦(12%)和达芦那韦(5%)。在考虑了参与者的性别、年龄、核苷类逆转录酶抑制剂(NRTI)基础药物、抗逆转录病毒治疗方案类型和世界卫生组织(WHO)临床分期后;抗逆转录病毒治疗时间长(调整后比值比[aOR]=1.15,95%置信区间[CI]1.05 - 1.26,p = 0.003)、一线治疗失败的青少年(aOR = 3.80,95%CI 1.02 - 14.08,p = 0.046)和二线治疗失败的参与者(aOR = 3.64,95%CI 1.18 - 11.21,p = 0.024)作为艾滋病毒耐药性检测的指征,以及艾滋病毒耐药性样本采集年份(aOR = 0.21,95%CI 0.07 - 0.69,p = 0.010),均与艾滋病毒耐药性突变独立相关。
该研究发现艾滋病毒耐药性流行率很高,且与抗逆转录病毒治疗时间长密切相关,这可能导致抗逆转录病毒治疗失败率增加。依曲韦林的高耐药性和多替拉韦耐药性的增加可能会使未来的治疗选择复杂化,而达芦那韦的低耐药性使其成为未来的三线治疗选择。加强常规耐药性监测、及时进行病毒载量监测和依从性支持对于减轻耐药性和维持乌干达西尼罗河地区艾滋病毒感染者的抗逆转录病毒治疗效果至关重要。