Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montréal, Québec, Canada.
Department of Neurology, Washington University, St Louis, Missouri.
JAMA Neurol. 2018 Jan 1;75(1):72-79. doi: 10.1001/jamaneurol.2017.3036.
Despite the introduction of combination antiretroviral therapy (cART), HIV-associated neurocognitive disorders continue to be a problem for treated HIV-positive individuals. The cause of this impairment remains unclear.
To determine if detectable brain changes occur during a 2-year period in HIV-positive individuals who were aviremic and treated with cART.
DESIGN, SETTING, AND PARTICIPANTS: In this longitudinal case-control study, participants underwent neuroimaging and neuropsychological assessment approximately 2 years apart. Data were collected from October 26, 2011, to March 1, 2016. Data from 92 HIV-positive individuals were acquired at Washington University in St Louis from ongoing studies conducted in the infectious disease clinic and AIDS Clinical Trial Unit. A total of 55 HIV-negative control participants were recruited from the St Louis community and a research participant registry. A total of 48 HIV-positive individuals who were aviremic and treated with cART and 31 demographically similar HIV-negative controls met the study requirements and were included in the analyses.
Brain volumes were extracted with tensor-based and voxel-based morphometry and cortical modeling. Raw scores from neuropsychological tests quantified cognitive performance. Multivariable mixed-effects models assessed the effect of HIV serostatus on brain volumes and cognitive performance, and determined if HIV serostatus affected how these measures changed over time. With HIV-positive participants, linear regression models tested whether brain volumes and cognitive performance were associated with measures of infection severity and duration of infection.
The 2 groups were demographically similar (HIV-positive group: 23 women and 25 men; mean [SD] age, 47.7 [13.2] years; mean [SD] educational level, 13.3 [3.4] years; and HIV-negative group, 16 women and 15 men; mean [SD] age, 51.2 [12.9] years; mean [SD] educational level, 14.5 [2.1] years). The HIV-positive participants had poorer neuropsychological test scores compared with controls on the Trail Making Test Part A (5.9 seconds; 95% CI, 1.5-10.3; P = .01), Trail Making Test Part B (27.3 seconds; 95% CI, 15.0-39.6; P < .001), Digit Symbol Substitution Task (-12.5 marks; 95% CI, -18.9 to -6.0; P < .001), Letter-Number Sequencing (-2.5 marks; 95% CI, -3.7 to -1.3; P < .001), Letter Fluency (-6.6 words; 95% CI, -11.5 to -1.6; P = .01), and Hopkins Verbal Learning Test-Revised immediate recall (-2.4 words; 95% CI, -4.4 to -0.4; P = .05), after adjusting for age, sex, and educational level. Only changes in Trail Making Test Part A significantly differed between the groups. Cortical thickness and subcortical volumes were smaller in HIV-positive individuals compared with controls. However, changes in brain volume over time were similar between the groups.
These findings are consistent with the idea that cognitive and structural brain changes may occur early after seroconversion, and argue that maintaining aviremia with cART can prevent or minimize progressive brain injury.
尽管引入了联合抗逆转录病毒疗法(cART),但 HIV 相关神经认知障碍仍然是接受治疗的 HIV 阳性个体的一个问题。其病因仍不清楚。
确定在接受 cART 治疗且病毒载量抑制的 HIV 阳性个体中,在 2 年内是否会发生可检测到的脑变化。
设计、地点和参与者:在这项纵向病例对照研究中,参与者每隔约 2 年进行一次神经影像学和神经心理学评估。数据于 2011 年 10 月 26 日至 2016 年 3 月 1 日收集。来自圣路易斯华盛顿大学的 92 名 HIV 阳性个体的数据来自传染病诊所和艾滋病临床试验单位正在进行的研究中获得。共有 55 名 HIV 阴性对照参与者从圣路易斯社区和研究参与者登记处招募。共有 48 名 HIV 阳性个体符合研究要求,病毒载量抑制且接受 cART 治疗,31 名年龄、性别相匹配的 HIV 阴性对照被纳入分析。
利用张量和基于体素的形态计量学和皮质建模方法提取脑体积。神经心理学测试的原始分数量化了认知表现。多变量混合效应模型评估了 HIV 血清状态对脑体积和认知表现的影响,并确定了 HIV 血清状态是否影响这些指标随时间的变化。在 HIV 阳性个体中,线性回归模型测试了脑体积和认知表现是否与感染严重程度和感染持续时间的测量值相关。
两组在人口统计学上相似(HIV 阳性组:23 名女性和 25 名男性;平均[标准差]年龄 47.7[13.2]岁;平均[标准差]教育水平 13.3[3.4]年;HIV 阴性组:16 名女性和 15 名男性;平均[标准差]年龄 51.2[12.9]岁;平均[标准差]教育水平 14.5[2.1]年)。与对照组相比,HIV 阳性参与者在 Trail Making Test Part A(5.9 秒;95%CI,1.5-10.3;P=0.01)、Trail Making Test Part B(27.3 秒;95%CI,15.0-39.6;P<0.001)、数字符号替代测试(-12.5 分;95%CI,-18.9 至-6.0;P<0.001)、字母数字序列测试(-2.5 分;95%CI,-3.7 至-1.3;P<0.001)、字母流畅性测试(-6.6 个单词;95%CI,-11.5 至-1.6;P=0.01)和 Hopkins 言语学习测试修订版即时回忆测试(-2.4 个单词;95%CI,-4.4 至-0.4;P=0.05)方面的神经心理学测试分数较差,在调整年龄、性别和教育水平后。只有 Trail Making Test Part A 的变化在两组之间有显著差异。与对照组相比,HIV 阳性个体的皮质厚度和皮质下体积较小。然而,两组的脑体积随时间的变化相似。
这些发现与认知和结构脑变化可能在血清转换后早期发生的观点一致,并认为使用 cART 维持病毒载量抑制可以预防或最小化进行性脑损伤。