血管生成后脉络膜丛灌注及颅内脑脊液变化

Skylar E Johnson, C. McKnight, Sarah K. Lants, Meher R. Juttukonda, M. Fusco, R. Chitale, Paula C Donahue, D. Claassen, M. Donahue
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引用次数: 12

摘要

最近的研究表明,脑皮质缺血可能影响脉络膜丛的功能,这种交流可能通过传统的脑脊液循环途径和/或可能的淋巴途径介导。在这里,我们研究了新血管生成后动脉健康的改善改变(i)颅内脑脊液容量和(ii)脉络膜丛灌注的假设。非动脉粥样硬化性颅内狭窄患者(如Moyamoya)的脑脊液和组织体积测量通过t1加权MRI获得,皮层和脉络膜丛灌注通过灌注加权动脉自旋标记MRI获得。间接手术血运重建术后重复测量,引起血运重建术部位附近的皮质新生血管生成(n = 23;年龄= 41.8±13.4岁),或在两个时间点没有间隔手术的队列参与者(n = 10;年龄= 41.7±10.7岁)。回归分析用于评估灌注和体积对状态的依赖性(时间1 vs. 2)。术后,脑脊液和组织体积均未发生显著变化。手术患者术后皮层灌注增加,脉络膜丛灌注减少;在没有手术的参与者中,皮层灌注减少,脉络膜丛灌注增加。研究结果在稳态机制的背景下进行了讨论,即动脉健康、血管旁血流和/或缺血可以影响脉络膜丛灌注。
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Choroid plexus perfusion and intracranial cerebrospinal fluid changes after angiogenesis
Recent studies have provided evidence that cortical brain ischemia may influence choroid plexus function, and such communication may be mediated by either traditional CSF circulation pathways and/or a possible glymphatic pathway. Here we investigated the hypothesis that improvements in arterial health following neoangiogenesis alter (i) intracranial CSF volume and (ii) choroid plexus perfusion in humans. CSF and tissue volume measurements were obtained from T1-weighted MRI, and cortical and choroid plexus perfusion were obtained from perfusion-weighted arterial spin labeling MRI, in patients with non-atherosclerotic intracranial stenosis (e.g. Moyamoya). Measurements were repeated after indirect surgical revascularization, which elicits cortical neoangiogenesis near the revascularization site (n = 23; age = 41.8 ± 13.4 years), or in a cohort of participants at two time points without interval surgeries (n = 10; age = 41.7 ± 10.7 years). Regression analyses were used to evaluate dependence of perfusion and volume on state (time 1 vs. 2). Post-surgery, neither CSF nor tissue volumes changed significantly. In surgical patients, cortical perfusion increased and choroid plexus perfusion decreased after surgery; in participants without surgeries, cortical perfusion reduced and choroid plexus perfusion increased between time points. Findings are discussed in the context of a homeostatic mechanism, whereby arterial health, paravascular flow, and/or ischemia can affect choroid plexus perfusion.
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