Alisch Joseph S R, Kiely Matthew, Triebswetter Curtis, Alsameen Maryam H, Gong Zhaoyuan, Khattar Nikkita, Egan Josephine M, Bouhrara Mustapha
Laboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States.
Front Aging Neurosci. 2021 Sep 17;13:734992. doi: 10.3389/fnagi.2021.734992. eCollection 2021.
The choroid plexus (CP) is an important cerebral structure involved in cerebrospinal fluid production and transport of solutes into the brain. Recent studies have uncovered the involvement of the CP in neurological disorders such as Alzheimer's disease and multiple sclerosis. However, our understanding of human age-related microstructural and functional changes in the CP with aging and neuropathology is limited. In this cross-sectional study, we investigated age and sex differences in the CP structure and function using advanced quantitative magnetic resonance imaging methodology in a large cohort ( = 155) of cognitively unimpaired individuals over a wide age range between 21 and 94 years. Our analysis included volumetric measurements, relaxometry measures ( and ), diffusion tensor imaging (DTI) measures of fractional anisotropy (FA) and mean diffusivity (MD), as well as measures of cerebral blood flow (CBF). Our results revealed that CP volume was increasing with advancing age. We conjecture that this novel observation is likely attributed to alterations in the CP microstructure or function as well as to ventriculomegaly. Indeed, we also found that CBF was lower with advanced age, while, consistent with previous studies, , and MD were higher, and FA was lower with advanced age. We attribute these functional and microstructural differences to a deteriorated CP structural integrity with aging. Furthermore, our relaxometry and DTI measures were found to be associated with differences in blood perfusion revealing lower microstructural integrity with lower CBF. Finally, in agreement with literature, sex-related differences in MD and CBF were statistically significant. This work lays the foundation for ongoing investigation of the involvement of CP in neurodegeneration.
脉络丛(CP)是一种重要的脑结构,参与脑脊液的生成以及溶质向脑内的转运。最近的研究发现脉络丛与阿尔茨海默病和多发性硬化症等神经系统疾病有关。然而,我们对脉络丛随年龄增长和神经病理学变化的人类年龄相关微观结构和功能变化的了解有限。在这项横断面研究中,我们使用先进的定量磁共振成像方法,对年龄在21至94岁之间的一大群(n = 155)认知未受损个体进行了研究,以调查脉络丛结构和功能的年龄和性别差异。我们的分析包括体积测量、弛豫测量(T1和T2)、扩散张量成像(DTI)的分数各向异性(FA)和平均扩散率(MD)测量,以及脑血流量(CBF)测量。我们的结果显示,脉络丛体积随着年龄的增长而增加。我们推测这一新发现可能归因于脉络丛微观结构或功能的改变以及脑室扩大。事实上,我们还发现,随着年龄的增长,脑血流量较低,而与先前的研究一致,T1、T2和MD较高,FA随着年龄的增长而较低。我们将这些功能和微观结构差异归因于随着年龄增长脉络丛结构完整性的恶化。此外,我们发现弛豫测量和DTI测量与血液灌注差异相关,表明脑血流量较低时微观结构完整性较低。最后,与文献一致,MD和CBF的性别相关差异具有统计学意义。这项工作为正在进行的关于脉络丛参与神经退行性变的研究奠定了基础。