整合酶抑制剂与HIV妇女的神经精神症状有关。

Leah H Rubin, Jane A O'Halloran, Dionna W Williams, Yuliang Li, Kathryn C Fitzgerald, Raha Dastgheyb, Alexandra L Damron, Pauline M Maki, Amanda B Spence, Anjali Sharma, Deborah R Gustafson, Joel Milam, Kathleen M Weber, Adaora A Adimora, Igho Ofotokun, Margaret A Fischl, Deborah Konkle-Parker, Yanxun Xu
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引用次数: 0

摘要

目的:由于包括神经精神症状在内的副作用,感染艾滋病毒(WWH)的妇女更有可能停止/改变抗逆转录病毒疗法(ART)。依法韦仑和整合酶链转移抑制剂(INSTIs)尤其令人担忧。我们重点研究了先前开发的WWH亚组中的这些ART药物和神经精神症状,这些亚组在关键的社会人口统计学因素以及纵向行为和临床特征上存在差异。如果妇女跨机构HIV研究的WWH有可用的ART数据,完成了感知压力量表-10和创伤后应激障碍检查表平民,则将其纳入研究。从2008年到2016年,每半年完成一次问卷调查。为了检验ART症状的相关性,通过惩罚最大似然的约束延续比率模型被拟合在WWH的5个亚组中。1882年WWH的数据共提供了4598次观测。353名女性先前被定义为主要患有控制良好的HIV和血管合并症,463名具有遗留影响(CD4最低点
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Integrase Inhibitors are Associated with Neuropsychiatric Symptoms in Women with HIV.

Objective: Women with HIV(WWH) are more likely to discontinue/change antiretroviral therapy(ART) due to side effects including neuropsychiatric symptoms. Efavirenz and integrase strand transfer inhibitors(INSTIs) are particularly concerning. We focused on these ART agents and neuropsychiatric symptoms in previously developed subgroups of WWH that differed on key sociodemographic factors as well as longitudinal behavioral and clinical profiles. WWH from the Women's Interagency HIV Study were included if they had ART data available, completed the Perceived Stress Scale-10 and PTSD Checklist-Civilian. Questionnaires were completed biannually beginning in 2008 through 2016. To examine ART-symptom associations, constrained continuation ratio model via penalized maximum likelihood were fit within 5 subgroups of WWH. Data from 1882 WWH contributed a total of 4598 observations. 353 women were previously defined as primarily having well-controlled HIV with vascular comorbidities, 463 with legacy effects(CD4 nadir < 250cells/mL), 274 aged ≤ 45 with hepatitis, 453 between 35-55 years, and 339 with poorly-controlled HIV/substance users. INSTIs, but not efavirenz, were associated with symptoms among key subgroups of WWH. Among those with HIV legacy effects, dolutegravir and elvitegravir were associated with greater stress/anxiety and avoidance symptoms(P's < 0.01); dolutegravir was also associated with greater re-experiencing symptoms(P = 0.005). Elvitegravir related to greater re-experiencing and hyperarousal among women with well-controlled HIV with vascular comorbidities(P's < 0.022). Raltegravir was associated with less hyperarousal, but only among women aged ≤ 45 years(P = 0.001). The adverse neuropsychiatric effects of INSTIs do not appear to be consistent across all WWH. Key characteristics (e.g., age, hepatitis positivity) may need consideration to fully weight the risk-benefit ratio of dolutegravir and elvitegravir in WWH.

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