Chen Yi, Xu Xiaoshan, Chen Huanhuan, Zhang Xiangjun, Zhu Qiuying, Liang Shujia, Xing Hui, Liao Lingjie, Feng Yi, Shao Yiming, Ruan Yuhua, Lan Guanghua, Li Jianjun
The Guangxi Academy of Medical Sciences, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China.
State Key Laboratory of Infectious Disease Prevention and Control (SKLID), Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, National Center for AIDS/STD Control and Prevention (NCAIDS), Chinese Center for Disease Control and Prevention (China CDC), Beijing, People's Republic of China.
Infect Drug Resist. 2025 May 6;18:2311-2327. doi: 10.2147/IDR.S516513. eCollection 2025.
Discontinuation of antiretroviral treatment (ART) raised drug resistance and failure of Human Immunodeficiency Virus (HIV) virological suppression. The study aimed to assess the relationship between pretreatment drug resistance (PDR) and ART dropout, as well as the relationship between HIV treatment dropout and HIV secondary transmission.
This study included all eligible participants from a local surveillance database in southwestern China between 2014 and 2021. The PDR prevalence trend was assessed using trend Chi-square tests within a consecutive cross-sectional design (N = 3060). Cox proportional hazards model was used to investigate the relationship between PDR and the risk of treatment dropout within a cohort design. Generalized Estimating Equations model was applied to explore the association between treatment dropout and HIV secondary transmission within a longitudinal genetic network study design. (N = 5094).
The overall PDR prevalence was 6.2%, analyzing a study sample of 3060 individuals with HIV/AIDS. Specifically, the prevalence of PDR to non-nucleoside reverse transcriptase inhibitors (NNRTIs), nucleoside reverse transcriptase inhibitors (NRTIs), and protease inhibitors (PIs) was 3.6%, 1.4%, and 1.1%, respectively. Yearly difference in prevalence was not identified. The independent association between PDR to NNRTIs and treatment dropout was significant (adjusted hazard ratio: 2.55, 95% CI 1.52-4.29). Among 5094 newly diagnosed HIV cases, participants who dropped out did not show a significant difference in HIV secondary transmission compared to those not on ART (adjusted odds ratio: 1.15, 95% CI 0.74-1.79).
PDR to NNRTIs may contribute to HIV secondary transmission through treatment dropout. It is imperative to offer comprehensive and advanced HIV care for all individuals with HIV, enhance treatment and medication adherence, and closely monitor PDR prevalence.
停止抗逆转录病毒治疗(ART)会增加耐药性,并导致人类免疫缺陷病毒(HIV)病毒学抑制失败。本研究旨在评估治疗前耐药性(PDR)与ART停药之间的关系,以及HIV治疗停药与HIV二次传播之间的关系。
本研究纳入了2014年至2021年间来自中国西南部一个本地监测数据库的所有符合条件的参与者。在连续横断面设计(N = 3060)中,使用趋势卡方检验评估PDR患病率趋势。在队列设计中,使用Cox比例风险模型研究PDR与治疗停药风险之间的关系。在纵向遗传网络研究设计(N = 5094)中,应用广义估计方程模型探讨治疗停药与HIV二次传播之间的关联。
在对3060例HIV/AIDS个体的研究样本进行分析时,总体PDR患病率为6.2%。具体而言,对非核苷类逆转录酶抑制剂(NNRTIs)、核苷类逆转录酶抑制剂(NRTIs)和蛋白酶抑制剂(PIs)的PDR患病率分别为为3.6%、1.4%和1.1%。未发现患病率的年度差异。对NNRTIs的PDR与治疗停药之间的独立关联具有统计学意义(调整后的风险比:2.55,95%CI 1.52 - 4.29)。在5094例新诊断的HIV病例中,与未接受ART治疗的参与者相比,停药的参与者在HIV二次传播方面没有显著差异(调整后的优势比:1.15,95%CI 0.74 - 1.79)。
对NNRTIs的PDR可能通过治疗停药导致HIV二次传播。必须为所有HIV感染者提供全面和先进的HIV护理,提高治疗和用药依从性,并密切监测PDR患病率。