aDivision of Global Health and Infectious Diseases bDepartment of Epidemiology, UNC Gillings School of Global Public Health, University of North Carolina, Chapel Hill cDivision of HIV/AIDS, North Carolina Department of Public Health, Raleigh, North Carolina, USA.
AIDS. 2017 Oct 23;31(16):2235-2244. doi: 10.1097/QAD.0000000000001611.
We sought to define the prevalence of pretreatment integrase strand transfer inhibitor (INSTI) resistance and assess the transmission networks of those with pretreatment INSTI resistance.
A retrospective cohort study of HIV-positive patients with genotypic resistance testing sent to a single referral laboratory in North Carolina between 2010 and 2016.
We linked genotype and public health data for in-care HIV-positive individuals to determine the prevalence of INSTI resistance among treatment-naive (defined as those with a first genotype ≤3 months after diagnosis) and treatment-experienced (defined as those with a first genotype >3 months after diagnosis) patients. We performed molecular and phylogenetic analyses to assess whether pretreatment INSTI resistance mutations represented clustered HIV transmission.
Of 8825 individuals who contributed sequences for protease, reverse transcriptase, or INSTI genotypic resistance testing during the study period, 2784 (31%) contributed at least one sequence for INSTI resistance testing. Of these, 840 were treatment-naive individuals and 20 [2.4%, 95% confidence interval (CI): 1.5, 3.6%] had INSTI mutations; only two (0.2%, 95% CI: 0.02, 0.9%) had major mutations. Of 1944 treatment-experienced individuals, 9.6% (95% CI: 8.3, 11.0%) had any INSTI mutation and 7.0% (95% CI: 5.9, 8.3%) had major mutations; the prevalence of INSTI mutations among treatment-experienced patients decreased overtime (P < 0.001). In total 12 of 20 individuals with pretreatment INSTI mutations were part of 10 molecular transmission clusters; only one cluster shared identical minor mutations.
The prevalence of major pretreatment INSTI resistance is very low. Pretreatment INSTI mutations do not appear to represent clustered HIV transmission.
我们旨在确定治疗前整合酶抑制剂(INSTI)耐药的流行率,并评估具有治疗前 INSTI 耐药的患者的传播网络。
这是一项回顾性队列研究,纳入了 2010 年至 2016 年期间在北卡罗来纳州的一家转诊实验室进行基因耐药检测的 HIV 阳性患者。
我们将基因型和公共卫生数据进行了关联,以确定治疗初治(定义为诊断后首次基因型检测结果在 3 个月内)和治疗经验(定义为诊断后首次基因型检测结果在 3 个月后)患者中 INSTI 耐药的流行率。我们进行了分子和系统发生分析,以评估治疗前 INSTI 耐药突变是否代表了 HIV 聚集性传播。
在研究期间,共有 8825 名个体进行了蛋白酶、逆转录酶或 INSTI 基因型耐药检测,其中 2784 名(31%)至少进行了一次 INSTI 耐药检测。在这些患者中,840 名是治疗初治患者,其中 20 名(2.4%,95%置信区间[CI]:1.5,3.6%)有 INSTI 突变;仅有 2 名(0.2%,95%CI:0.02,0.9%)有主要突变。在 1944 名治疗经验患者中,9.6%(95%CI:8.3,11.0%)有任何 INSTI 突变,7.0%(95%CI:5.9,8.3%)有主要突变;治疗经验患者中 INSTI 突变的流行率随时间推移而降低(P < 0.001)。在总共 20 名治疗前 INSTI 耐药的患者中,有 12 名属于 10 个分子传播簇;仅有 1 个簇共享相同的次要突变。
主要的治疗前 INSTI 耐药的流行率非常低。治疗前 INSTI 突变似乎并不代表聚集性 HIV 传播。