Jankiewicz Marcin, Holmes Martha J, Taylor Paul A, Cotton Mark F, Laughton Barbara, van der Kouwe André J W, Meintjes Ernesta M
Division of Biomedical Engineering, Department of Human Biology, University of Cape Town, Cape Town, South Africa.
Scientific and Statistical Computing Core, National Institutes of Health, Bethesda, MD, United States.
Front Neuroanat. 2017 Sep 29;11:88. doi: 10.3389/fnana.2017.00088. eCollection 2017.
Due to changes in guidelines and access to treatment, more children start combination antiretroviral therapy (ART) in infancy. With few studies examining the long-term effects of perinatal HIV infection and early ART on neurodevelopment, much is still unknown about brain maturation in the presence of HIV and ART. Follow-up studies of HIV infected (HIV+) children are important for monitoring brain development in the presence of HIV infection and ART. We use diffusion tensor imaging (DTI) to examine white matter (WM) in 65 HIV+ and 46 control (HIV exposed uninfected (HEU) and HIV unexposed uninfected (HU)) 7-year-old children. This is a follow up of a cohort studied at 5 years, where we previously reported lower fractional anisotropy (FA) in corticospinal tract (CST) and mean diffusivity (MD) increases in inferior/superior longitudinal fasciculi (ILF/SLF), inferior fronto-occipital fasciculus (IFOF) and uncinate fasciculus (UF) in HIV+ children compared to uninfected controls. In addition, we also found a difference in FA related to age at which ART was initiated. At 7 years, we found two regions in the left IFOF and left ILF with lower FA in HIV+ children compared to controls. Higher MD was observed in a similar region in the IFOF, albeit bilaterally, as well as multiple clusters bilaterally in the superior corona radiata (SCR), the anterior thalamic radiation (ATR) and the right forceps minor. Unlike at 5 years, we found no impact on WM of ART initiation. In HEU children, we found a cluster in the right posterior corona radiata with higher FA compared to HU children, while bilateral regions in the CST demonstrated reduced MD. At age 7, despite early ART and viral load (VL) suppression, we continue to observe differences in WM integrity. WM damage observed at age 5 years persists, and new damage is evident. The continued observation of regions with lower FA and higher MD in HIV+ children point to disruptions in ongoing white matter development regardless of early ART. Lastly, in HEU children we find higher FA and lower MD in clusters in the CST tract suggesting that perinatal HIV/ART exposure has a long-term impact on WM development.
由于指南的变化和治疗的可及性,越来越多的儿童在婴儿期开始接受抗逆转录病毒联合疗法(ART)。由于很少有研究探讨围产期HIV感染和早期ART对神经发育的长期影响,关于HIV和ART存在情况下的大脑成熟情况仍有很多未知之处。对HIV感染(HIV+)儿童的随访研究对于监测HIV感染和ART存在情况下的大脑发育很重要。我们使用扩散张量成像(DTI)对65名HIV+儿童和46名对照儿童(HIV暴露未感染(HEU)和HIV未暴露未感染(HU))进行了7岁时的白质(WM)检查。这是对一个5岁时研究的队列的随访,我们之前报告过,与未感染对照相比,HIV+儿童的皮质脊髓束(CST)中分数各向异性(FA)较低,而下/上纵束(ILF/SLF)、额枕下束(IFOF)和钩束(UF)中的平均扩散率(MD)增加。此外,我们还发现与开始ART的年龄相关的FA存在差异。在7岁时,我们发现与对照相比,HIV+儿童的左侧IFOF和左侧ILF中有两个区域的FA较低。在IFOF的类似区域观察到较高的MD,尽管是双侧的,并且在双侧的放射冠上部(SCR)、丘脑前辐射(ATR)和右侧小钳中有多个簇。与5岁时不同,我们发现开始ART对WM没有影响。在HEU儿童中,我们发现与HU儿童相比,右侧放射冠后部有一个簇的FA较高,而CST中的双侧区域显示MD降低。在7岁时,尽管早期进行了ART且病毒载量(VL)得到抑制,但我们继续观察到WM完整性存在差异。5岁时观察到的WM损伤持续存在,并且新的损伤很明显。在HIV+儿童中持续观察到FA较低和MD较高的区域,这表明无论早期ART如何,正在进行的白质发育都受到了干扰。最后,在HEU儿童中,我们发现CST束中的簇中FA较高且MD较低,这表明围产期HIV/ART暴露对WM发育有长期影响。