Blood–Brain Barrier Disruption and Perivascular Spaces in Small Vessel Disease and Neurodegenerative Diseases: A Review on MRI Methods and Insights

血管周围间隙 磁共振成像 血脑屏障 疾病 神经科学 磁共振弥散成像 医学 认知障碍 病理 心理学 放射科 中枢神经系统
作者
Paulien Voorter,Maud van Dinther,Willemijn J. Jansen,Alida A. Postma,Julie Staals,Jacobus F.A. Jansen,Robert J. van Oostenbrugge,Merel M. van der Thiel,Walter H. Backes
出处
期刊:Journal of Magnetic Resonance Imaging [Wiley]
卷期号:59 (2): 397-411 被引量:35
标识
DOI:10.1002/jmri.28989
摘要

Perivascular spaces (PVS) and blood–brain barrier (BBB) disruption are two key features of cerebral small vessel disease (cSVD) and neurodegenerative diseases that have been linked to cognitive impairment and are involved in the cerebral waste clearance system. Magnetic resonance imaging (MRI) offers the possibility to study these pathophysiological processes noninvasively in vivo. This educational review provides an overview of the MRI techniques used to assess PVS functionality and BBB disruption. MRI‐visible PVS can be scored on structural images by either (subjectively) counting or (automatically) delineating the PVS. We highlight emerging (diffusion) techniques to measure proxies of perivascular fluid and its movement, which may provide a more comprehensive understanding of the role of PVS in diseases. For the measurement of BBB disruption, we explain the most commonly used MRI technique, dynamic contrast‐enhanced (DCE) MRI, as well as a more recently developed technique based on arterial spin labeling (ASL). DCE MRI and ASL are thought to measure complementary characteristics of the BBB. Furthermore, we describe clinical studies that have utilized these MRI techniques in cSVD and neurodegenerative diseases, particularly Alzheimer's disease (AD). These studies demonstrate the role of PVS and BBB dysfunction in these diseases and provide insight into the large overlap, but also into the differences between cSVD and AD. Overall, MRI techniques may provide valuable insights into the pathophysiological mechanisms underlying these diseases and have the potential to be used as markers for disease progression and treatment response. Level of Evidence 3 Technical Efficacy Stage 2
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