From the Brain Research Imaging Centre (G.W.B., M.J.T., Y.S., I.H., M.S., F.C., P.A., I.M., F.N.D., J.M.W.), Centre for Clinical Brain Sciences, University of Edinburgh, United Kingdom; UK Dementia Research Institute at The University of Edinburgh (G.W.B., M.J.T., Y.S., I.H., M.S., F.N.D., J.M.W.), Edinburgh Medical School, United Kingdom; Beijing Tiantan Hospital Affiliated to Capital Medical University (Y.S.), China; Institute of Cardiovascular and Medical Sciences (D.A.D.), University of Glasgow, United Kingdom; and Centre for Cognitive Ageing and Cognitive Epidemiology (J.M.W.), University of Edinburgh, United Kingdom.
Neurology. 2020 May 26;94(21):e2258-e2269. doi: 10.1212/WNL.0000000000009483. Epub 2020 May 4.
To investigate cerebrovascular reactivity (CVR), blood flow, vascular and CSF pulsatility, and their independent relationship with cerebral small vessel disease (SVD) features in patients with minor ischemic stroke and MRI evidence of SVD.
We recruited patients with minor ischemic stroke and assessed CVR using blood oxygen level-dependent MRI during a hypercapnic challenge, cerebral blood flow (CBF), vascular and CSF pulsatility using phase-contrast MRI, and structural magnetic resonance brain imaging to quantify white matter hyperintensities (WMHs) and perivascular spaces (PVSs). We used multiple regression to identify parameters associated with SVD features, controlling for patient characteristics.
Fifty-three of 60 patients completed the study with a full data set (age 68.0% ± 8.8 years, 74% male, 75% hypertensive). After controlling for age, sex, and systolic blood pressure, lower white matter CVR was associated with higher WMH volume (-0.01%/mm Hg per log10 increase in WMH volume, = 0.02), basal ganglia PVS (-0.01%/mm Hg per point increase in the PVS score, = 0.02), and higher venous pulsatility (superior sagittal sinus -0.03%/mm Hg, = 0.02, per unit increase in the pulsatility index) but not with CBF ( = 0.58). Lower foramen magnum CSF stroke volume was associated with worse white matter CVR (0.04%/mm Hg per mL increase in stroke volume, = 0.04) and more severe basal ganglia PVS ( = 0.09).
Lower CVR, higher venous pulsatility, and lower foramen magnum CSF stroke volume indicate that dynamic vascular dysfunctions underpin PVS dysfunction and WMH development. Further exploration of microvascular dysfunction and CSF dynamics may uncover new mechanisms and intervention targets to reduce SVD lesion development, cognitive decline, and stroke.
研究脑血管反应性(CVR)、血流、血管和 CSF 搏动及其与伴有 MRI 脑小血管病(SVD)证据的小缺血性卒中患者的 SVD 特征的独立关系。
我们招募了小缺血性卒中患者,并在高碳酸血症挑战期间使用血氧水平依赖 MRI 评估 CVR,使用相位对比 MRI 评估脑血流(CBF)、血管和 CSF 搏动,使用结构磁共振脑成像量化脑白质高信号(WMHs)和血管周围间隙(PVSs)。我们使用多元回归来确定与 SVD 特征相关的参数,同时控制患者特征。
在 60 名患者中,有 53 名完成了研究,获得了完整的数据(年龄 68.0%±8.8 岁,74%为男性,75%为高血压患者)。在控制年龄、性别和收缩压后,较低的脑白质 CVR 与较高的 WMH 容积相关(WMH 容积每增加 1 个对数,CVR 降低 0.01%/mmHg, = 0.02)、基底节 PVS(PVS 评分每增加 1 分,CVR 降低 0.01%/mmHg, = 0.02)和较高的静脉搏动性(上矢状窦 -0.03%/mmHg, = 0.02,脉动指数每增加 1 单位)相关,但与 CBF 无关( = 0.58)。后颅窝 CSF 搏动容积的降低与脑白质 CVR 的降低(搏动容积每增加 1mL,CVR 降低 0.04%/mmHg, = 0.04)和基底节 PVS 的加重( = 0.09)相关。
较低的 CVR、较高的静脉搏动性和较低的后颅窝 CSF 搏动容积表明,动态血管功能障碍是 PVS 功能障碍和 WMH 发展的基础。进一步探索微血管功能障碍和 CSF 动力学可能会发现新的机制和干预靶点,以减少 SVD 病变的发展、认知能力下降和卒中。