Department of Internal Medicine and Infectious Diseases, University Medical Centre Utrecht, Utrecht, The Netherlands.
Department of Internal Medicine and Infectious Diseases, Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands.
AIDS Res Hum Retroviruses. 2024 Oct;40(10):581-590. doi: 10.1089/AID.2022.0069. Epub 2023 Mar 16.
Functional magnetic resonance imaging (fMRI) studies have demonstrated that HIV-infection affects the fronto-striatal network. It has not been examined what impact efavirenz (EFV), an antiretroviral drug notorious for its neurocognitive effects, has on the reward system: a key subcomponent involved in depressive and apathy symptoms. Therefore, this study aims to investigate the effect of EFV on reward processing using a monetary incentive delay (MID) task. In this multicenter randomized controlled trial, asymptomatic adult participants stable on emtricitabine/tenofovirdisoproxil fumarate (FTC/TDF)/EFV were randomly assigned in a 2:1 ratio to switch to FTC/TDF/rilpivirine (RPV) ( = 30) or continue taking FTC/TDF/EFV ( = 13). At baseline and 12 weeks after therapy switch, both groups performed an MID task. Behavior and functional brain activity related to reward anticipation and reward outcome were assessed with blood-oxygen-level-dependent fMRI. Both groups were matched for age, education level, and time since HIV diagnosis and on EFV. At the behavioral level, both groups had faster response times and better response accuracy during rewarding versus nonrewarding trials, with no improvement resulting from switching FTC/TDF/EFV to FTC/TDF/RPV. No significant change in activation related to reward anticipation in the ventral striatum was found after switching therapy. Both groups had significantly higher activation levels over time, consistent with a potential learning effect. Similar activity related to reward outcome in the orbitofrontal cortex was found. Discontinuing FTC/TDF/EFV was not found to improve activity related to reward anticipation in asymptomatic people living with HIV, with similar cortical functioning during reward outcome processing. It is therefore likely that EFV does not affect motivational control. Further research is needed to determine whether EFV affects motivational control in HIV populations with different characteristics.
功能磁共振成像(fMRI)研究表明,HIV 感染会影响额纹状体网络。目前还没有研究过抗逆转录病毒药物依非韦伦(EFV)对奖励系统的影响:奖励系统是涉及抑郁和淡漠症状的关键子成分。因此,本研究旨在使用货币奖励延迟(MID)任务来研究 EFV 对奖励处理的影响。在这项多中心随机对照试验中,接受恩曲他滨/替诺福韦二吡呋酯(FTC/TDF)/EFV 治疗且无症状的成年参与者以 2:1 的比例随机分配至切换为 FTC/TDF/利匹韦林(RPV)( = 30)或继续服用 FTC/TDF/EFV( = 13)。在治疗转换前和 12 周后,两组均进行 MID 任务。使用基于血氧水平的 fMRI 评估与奖励预期和奖励结果相关的行为和功能性大脑活动。两组在年龄、教育程度和 HIV 诊断后时间以及 EFV 方面相匹配。在行为水平上,两组在奖励与非奖励试验中均具有更快的反应时间和更好的反应准确性,而从 FTC/TDF/EFV 切换到 FTC/TDF/RPV 并未改善。在治疗转换后,腹侧纹状体与奖励预期相关的激活没有发现显著变化。两组的激活水平随着时间的推移均显著增加,这与潜在的学习效应一致。在眶额皮质中发现了与奖励结果相关的相似活动。在无症状的 HIV 感染者中,停用 FTC/TDF/EFV 并未发现与奖励预期相关的活动得到改善,而在奖励结果处理过程中皮质功能相似。因此,EFV 可能不会影响动机控制。需要进一步的研究来确定 EFV 是否会影响具有不同特征的 HIV 人群的动机控制。