Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, California.
Imaging Genetics Center, Mark and Mary Stevens Neuroimaging and Informatics Institute, Keck School of Medicine, University of Southern California, Marina del Rey, California.
Hum Brain Mapp. 2019 Oct 15;40(15):4370-4380. doi: 10.1002/hbm.24708. Epub 2019 Jul 4.
Recent evidence suggests the aging process is accelerated by HIV. Degradation of white matter (WM) has been independently associated with HIV and healthy aging. Thus, WM may be vulnerable to joint effects of HIV and aging. Diffusion-weighted imaging (DWI) was conducted with HIV-seropositive (n = 72) and HIV-seronegative (n = 34) adults. DWI data underwent tractography, which was parcellated into 18 WM tracts of interest (TOIs). Functional Analysis of Diffusion Tensor Tract Statistics (FADTTS) regression was conducted assessing the joint effect of advanced age and HIV on fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD) along TOI fibers. In addition to main effects of age and HIV on WM microstructure, the interactive effect of age and HIV was significantly related to lower FA and higher MD, AD, and RD across all TOIs. The location of findings was consistent with the clinical presentation of HIV-associated neurocognitive disorders. While older age is related to poorer WM microstructure, its detrimental effect on WM is stronger among HIV+ relative to HIV- individuals. Loss of WM integrity in the context of advancing age may place HIV+ individuals at increased risk for brain and cognitive compromise.
最近的证据表明,HIV 会加速衰老过程。白质(WM)的退化与 HIV 和健康衰老都有独立的关联。因此,WM 可能容易受到 HIV 和衰老的共同影响。对 HIV 血清阳性(n=72)和 HIV 血清阴性(n=34)成年人进行了扩散加权成像(DWI)检查。DWI 数据经过轨迹分析,将其分为 18 个感兴趣的 WM 束(TOI)。采用弥散张量纤维束统计功能分析(FADTTS)回归评估年龄增长和 HIV 对各 TOI 纤维的各向异性分数(FA)、平均弥散度(MD)、轴向弥散度(AD)和径向弥散度(RD)的联合影响。除了年龄和 HIV 对 WM 微观结构的主要影响外,年龄和 HIV 的交互作用与所有 TOI 上 FA 降低和 MD、AD 和 RD 升高显著相关。研究结果的位置与 HIV 相关认知障碍的临床表现一致。虽然年龄增长与 WM 微观结构变差有关,但与 HIV-个体相比,HIV+个体的 WM 受到的不利影响更大。在年龄增长的背景下 WM 完整性的丧失可能会使 HIV+个体的大脑和认知功能受损风险增加。