University of Colorado-Denver, Denver, Colorado, USA.
Department of Biostatistics and Bioinformatics, Colorado School of Public Health, Aurora, Colorado, USA.
AIDS Res Hum Retroviruses. 2023 Jan;39(1):33-37. doi: 10.1089/AID.2021.0218. Epub 2022 Nov 18.
The potency of modern antiretroviral therapy (ART) allows for greater forgiveness to missed doses while still achieving, and maintaining, viral suppression. However, imperfect ART adherence, even if sufficient to maintain viral suppression, has been associated with adverse clinical outcomes. ART adherence can be objectively quantified using tenofovir diphosphate (TFV-DP) in dried blood spots (DBS), a biomarker of cumulative adherence that is predictive of future viremia-even among persons with HIV (PWH) with an undetectable HIV viral load (VL). Within a prospective cohort of PWH on tenofovir disoproxil fumarate-including ART, mismatch between drug concentration and HIV VL (i.e., low concentrations of TFV-DP in DBS in the setting of viral suppression with subsequent viremia at the following visit) was observed more frequently in PWH who were Black (36% vs. 15%; = .04), had body mass index >30 kg/m (40% vs. 13%; = .01), and reported <100% 3 months (68% vs. 50%; = .005) and 30 days (56% vs. 31%; = .001) adherence, compared with PWH without mismatch. Identifying PWH at risk for future viremia could help clinicians implement targeted timely interventions before episodes of breakthrough viremia.
现代抗逆转录病毒疗法 (ART) 的疗效强大,即使漏服药物,仍能实现并维持病毒抑制。然而,即使足够维持病毒抑制,不完美的 ART 依从性仍与不良临床结局相关。通过检测干血斑(DBS)中的替诺福韦二磷酸(TFV-DP),可以客观地量化 ART 依从性,这是一种累积依从性的生物标志物,可预测未来的病毒血症,甚至在 HIV 病毒载量(VL)不可检测的 HIV 感染者(PWH)中也是如此。在一项包含使用富马酸替诺福韦二吡呋酯的 PWH 的前瞻性队列研究中,在药物浓度与 HIV VL 不匹配的情况下(即在病毒抑制的情况下 DBS 中 TFV-DP 浓度低,随后在下一次就诊时出现病毒血症),观察到黑人(36% vs. 15%;= 0.04)、身体质量指数 >30 kg/m (40% vs. 13%;= 0.01)和报告的 3 个月(68% vs. 50%;= 0.005)和 30 天(56% vs. 31%;= 0.001)依从性<100%的 PWH 中,这种不匹配更为常见。识别出有未来发生病毒血症风险的 PWH 可以帮助临床医生在突破性病毒血症发作之前及时实施有针对性的干预措施。