Cabello-Úbeda Alfonso, Baeza Alicia González, García Jesús Troya, de La Fuente Moral Sara, Mena María Novella, Martínez Adriana Pinto, Micán Rafael, Górgolas Miguel, Tascón Guillermo Cuevas, de Santiago Alberto Díaz, Morerno José Sanz, Crestelo David Rial, Arenzana Carmen Busca, Serna José Ignacio Bernardino, Almirón Mariana Díaz, Cano Joanna, Esteban Herminia, Pérez-Valero Ignacio
División de Enfermedades Infecciosas, Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
Departamento de Psicobiología, Facultad de Psicología, Universidad Autónoma de Madrid, Madrid, Spain.
Open Forum Infect Dis. 2022 Aug 6;9(9):ofac345. doi: 10.1093/ofid/ofac345. eCollection 2022 Sep.
Although switching antiretroviral therapy (ART) in people with human immunodeficiency virus experiencing insomnia due to dolutegravir-related neurotoxicity is well founded upon evidence, there is a lack of proof in regard to the outcome of stopping dolutegravir-based ART in people without insomnia but reporting poor sleep quality.
This is a randomized, multicenter, open-label study to evaluate the reversibility of patient-reported sleep disturbances in patients on dolutegravir/lamivudine/abacavir without insomnia after switching to darunavir/cobicistat/emtricitabine/tenofovir alafenamide. The participants were randomized to switch ART at baseline or at week 4 and then completed 8 weeks of darunavir/cobicistat/emtricitabine/tenofovir alafenamide. Our primary objective was to compare changes in sleep quality between arms at week 4. Secondary objectives were to compare changes in mood and neuropsychiatric symptoms (NS) at week 4 and 4 and 8 weeks after switching to darunavir/cobicistat/emtricitabine/tenofovir alafenamide. The participants completed a survey, including the Pittsburgh Sleep Quality Index (PSQI), the Hospital Anxiety and Depression scale (HADS), and specific questions to explore NS, at each visit to assess those objectives.
We included 72 participants. The results show that study arms were similar at baseline; however, at week 4, PSQI scores remained unchanged with dolutegravir/lamivudine/abacavir, whereas patients improved significantly after switching to darunavir/cobicistat/emtricitabine/tenofovir alafenamide. Similar differences between arms were also observed in HADS and NS changes. At weeks 4 and 8 after all participants switched to darunavir/cobicistat/emtricitabine/tenofovir alafenamide, we have observed significant improvements in PSQI and HAD scores and in NS.
In patients reporting subclinical sleep disturbances without insomnia, switching from dolutegravir/lamivudine/abacavir to darunavir/cobicistat/emtricitabine/tenofovir alafenamide was associated with better sleep quality and improvements in mood and NS.
尽管有证据表明,因多替拉韦相关神经毒性而出现失眠的人类免疫缺陷病毒感染者更换抗逆转录病毒疗法(ART)是有充分依据的,但对于没有失眠但报告睡眠质量差的患者停用基于多替拉韦的ART的结果,仍缺乏证据。
这是一项随机、多中心、开放标签研究,旨在评估在未出现失眠的接受多替拉韦/拉米夫定/阿巴卡韦治疗的患者换用达芦那韦/考比司他/恩曲他滨/替诺福韦艾拉酚胺后,患者报告的睡眠障碍的可逆性。参与者在基线或第4周随机更换ART,然后接受8周的达芦那韦/考比司他/恩曲他滨/替诺福韦艾拉酚胺治疗。我们的主要目标是比较第4周时两组之间睡眠质量的变化。次要目标是比较第4周以及换用达芦那韦/考比司他/恩曲他滨/替诺福韦艾拉酚胺后的第4周和第8周时情绪和神经精神症状(NS)的变化。参与者在每次就诊时完成一项调查,包括匹兹堡睡眠质量指数(PSQI)、医院焦虑抑郁量表(HADS)以及探索NS的特定问题,以评估这些目标。
我们纳入了72名参与者。结果显示,研究组在基线时相似;然而,在第4周时,使用多替拉韦/拉米夫定/阿巴卡韦时PSQI评分保持不变,而换用达芦那韦/考比司他/恩曲他滨/替诺福韦艾拉酚胺后患者有显著改善。在HADS和NS变化方面,两组之间也观察到类似差异。在所有参与者换用达芦那韦/考比司他/恩曲他滨/替诺福韦艾拉酚胺后的第4周和第8周,我们观察到PSQI和HAD评分以及NS有显著改善。
在报告有亚临床睡眠障碍但无失眠的患者中,从多替拉韦/拉米夫定/阿巴卡韦换用达芦那韦/考比司他/恩曲他滨/替诺福韦艾拉酚胺与更好的睡眠质量以及情绪和NS的改善有关。