脑血流量与白质高密度化进展之间的关系

Frontiers in neuroimaging Pub Date : 2025-01-21 eCollection Date: 2024-01-01 DOI:10.3389/fnimg.2024.1463311
Siriluk Thammasart, Danielle J Harvey, Pauline Maillard, Charles DeCarli, Corinne A Donnay, Gregory J Wheeler, Audrey P Fan
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摘要

简介在老龄人口中,FLAIR MRI 序列上观察到的白质高密度(WMHs)是认知能力下降、运动障碍和血管风险增加的指标。然而,人们对 WMHs 的病理生理机制,包括病变内部和邻近病变的脑血流(CBF)的动态变化仍然知之甚少:我们的研究通过 3 特斯拉核磁共振成像的动脉自旋标记(ASL)检查了 300 名老年参与者的不同队列,分析了横断面和纵向数据。我们描述了不同病变位置(基于与脑室的距离)和脑组织类型(WMH 病变、半影和正常白质)的 CBF 与 WMH 发展之间的关系:结果:我们的研究结果表明,与半影、正常外观的白质和灰质相比,WMHs 的相对 CBF(rCBF)明显降低,其中并脑室 WMHs(JVWMH)的降低幅度最大。纵向来看,在两年内体积增大的 WMHs 的基线 rCBF 低于保持不变的 WMHs,尤其是在并脑室和脑室周围区域:本研究不仅强调了rCBF在WMH进展中的预测价值,还提供了WMH的特定位置血液动力学信息,可指导临床治疗与WMH相关的脑部病变及其临床表现。
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Associations between cerebral blood flow and progression of white matter hyperintensities.

Introduction: In an aging population, white matter hyperintensities (WMHs), observed on FLAIR MRI sequences, are indicators of cognitive decline, motor impairment, and increased vascular risk. However, the pathophysiological mechanisms underlying WMHs, including dynamic changes in cerebral blood flow (CBF) within and adjacent to lesions, remain poorly understood.

Methods: Our study examined a diverse cohort of 300 elderly participants through arterial spin labeling (ASL) on 3 Tesla MRI, analyzing both cross-sectional and longitudinal data. We characterized the relationship between CBF and WMH development in different lesion locations (based on distance from ventricles) and brain tissue types (WMH lesion, penumbra, and normal white matter).

Results: Our findings reveal that WMHs exhibit significantly lower relative CBF (rCBF) compared to penumbra, normal-appearing white matter, and gray matter, with juxtaventricular WMHs (JVWMH) displaying the most substantial reductions. Longitudinally, WMHs that increased in size over a two-year period had lower baseline rCBF than those that remained stagnant, particularly in juxtaventricular and periventricular regions.

Discussion: This study not only highlights the predictive value of rCBF in WMH progression but also provides location-specific hemodynamic information about WMHs that can guide clinical management of WMH-related brain changes and their clinical manifestations.

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