Kolbe Scott C, Gajamange Sanuji I, Cleary Jon O, Kilpatrick Trevor J
Department of Neuroscience, Central Clinical School, Prahran, VIC, Australia.
Walt and Eliza Hall Institute, Parkville, VIC, Australia.
Front Neurol. 2020 Jun 2;11:476. doi: 10.3389/fneur.2020.00476. eCollection 2020.
The white matter is highly vascularised by the cerebral venous system. In this paper, we describe a unique blood oxygen-level dependent (BOLD) signal within the white matter using functional MRI and spatial independent components analysis. The signal is characterized by a narrow peak frequency band between 0.05 and 0.1 Hz. Hypercapnia, induced transient increases in white matter venous BOLD that disrupted the oscillation indicative of a vasocontractile mechanism. Comparison of the white matter venous BOLD oscillations between 14 healthy subjects and 18 people with perivenular inflammation due to multiple sclerosis (MS), revealed loss of power in the white matter venous BOLD signal in the peak frequency band (patients = 6.70 ± 0.94 dB/Hz vs. controls = 7.64 ± 0.71 dB/Hz; = 0.006). In MS, lower power was associated with greater levels of neuroinflammatory activity ( = -0.64, = 0.006). Using a signal modeling technique, we assessed the anatomical distribution of white matter venous BOLD signal abnormalities and detected reduced power in the periventricular white matter, a region of known venous damage in MS. These results demonstrate a novel link between neuroinflammation and vascular physiological dysfunction in the cerebral white matter, and could indicate enduring loss of vascular compliance associated with imperfect repair of blood-brain barrier damage after resolution of acute neuroinflammation.
白质由脑静脉系统高度血管化。在本文中,我们使用功能磁共振成像和空间独立成分分析描述了白质内一种独特的血氧水平依赖(BOLD)信号。该信号的特征是在0.05至0.1Hz之间有一个狭窄的峰值频带。高碳酸血症可引起白质静脉BOLD的短暂增加,从而破坏了指示血管收缩机制的振荡。比较14名健康受试者和18名因多发性硬化症(MS)而患有静脉周围炎症的人的白质静脉BOLD振荡,发现峰值频带内白质静脉BOLD信号的功率下降(患者=6.70±0.94dB/Hz,对照组=7.64±0.71dB/Hz;P=0.006)。在MS中,较低的功率与更高水平的神经炎症活动相关(r=-0.64,P=0.006)。使用信号建模技术,我们评估了白质静脉BOLD信号异常的解剖分布,并检测到脑室周围白质(MS中已知的静脉损伤区域)的功率降低。这些结果表明脑白质中神经炎症与血管生理功能障碍之间存在新的联系,并可能表明急性神经炎症消退后,与血脑屏障损伤修复不完善相关的血管顺应性持续丧失。