Northwestern University Interdepartmental Neuroscience Program, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.
Department of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, MA, United States.
Brain Behav Immun. 2017 May;62:100-109. doi: 10.1016/j.bbi.2017.01.004. Epub 2017 Jan 10.
Despite improved survival due to combination antiretroviral therapy (cART), youth with perinatally-acquired HIV (PHIV) show cognitive deficits and developmental delay at increased rates. HIV affects the brain during critical periods of development, and the brain may be a persistent reservoir for HIV due to suboptimal blood brain barrier penetration of cART. We conducted structural magnetic resonance imaging (sMRI) and cognitive testing in 40 PHIV youth (mean age=16.7years) recruited from the NIH Pediatric HIV/AIDS Cohort Study (PHACS) who are part of the first generation of PHIV youth surviving into adulthood. Historical and current HIV disease severity and substance use measures were also collected. Total and regional cortical grey matter brain volumes were compared to a group of 334 typically-developing, HIV-unexposed and uninfected youth (frequency-matched for age and sex) from the Pediatric Imaging, Neurocognition, and Genetics (PING) study (mean age=16.1years). PHIV youth had smaller (2.8-5.1%) total and regional grey matter volumes than HIV-unexposed and uninfected youth, with smallest volumes seen among PHIV youth with higher past peak viral load (VL) and recent unsuppressed VL. In PHIV youth, worse cognitive performance correlated with smaller volumes. This pattern of smaller grey matter volumes suggests that PHIV infection may influence brain development and underlie cognitive dysfunction seen in this population. Among PHIV youth, smaller volumes were also linked to substance use (alcohol use: 9.0-13.4%; marijuana use: 10.1-16.0%). In this study, collection of substance use information was limited to the PHIV cohort; future studies should also collect substance use information in controls to further address interactions between HIV and substance use on brain volume.
尽管联合抗逆转录病毒疗法 (cART) 的应用提高了生存率,但在获得性人类免疫缺陷病毒 (PHIV) 的青年中,认知缺陷和发育迟缓的发生率仍较高。HIV 在大脑发育的关键时期对大脑产生影响,由于 cART 对血脑屏障的穿透性不理想,大脑可能是 HIV 的持续储存库。我们对来自 NIH 儿科 HIV/AIDS 队列研究 (PHACS) 的 40 名 PHIV 青年 (平均年龄为 16.7 岁) 进行了结构磁共振成像 (sMRI) 和认知测试,他们是第一代 PHIV 青年中存活到成年期的人。还收集了历史和当前的 HIV 疾病严重程度和物质使用情况的测量数据。将总皮质灰质脑容量和区域皮质灰质脑容量与来自儿科成像、神经认知和遗传学 (PING) 研究的 334 名未感染 HIV 的、未暴露于 HIV 的且发育正常的青年 (按年龄和性别匹配频率) 进行了比较 (平均年龄为 16.1 岁)。PHIV 青年的总皮质灰质脑容量和区域皮质灰质脑容量比未感染 HIV 的青年小 (2.8-5.1%),其中过去峰值病毒载量 (VL) 较高和最近未抑制 VL 的 PHIV 青年的脑容量最小。在 PHIV 青年中,认知表现越差与脑容量越小相关。这种较小的灰质体积模式表明,PHIV 感染可能会影响大脑发育,并导致该人群出现认知功能障碍。在 PHIV 青年中,较小的脑容量也与物质使用有关 (酒精使用:9.0-13.4%;大麻使用:10.1-16.0%)。在这项研究中,物质使用信息的收集仅限于 PHIV 队列;未来的研究还应在对照组中收集物质使用信息,以进一步探讨 HIV 和物质使用对脑容量的相互作用。