期刊
BRAIN COMMUNICATIONS
卷 3, 期 2, 页码 -出版社
OXFORD UNIV PRESS
DOI: 10.1093/braincomms/fcab043
关键词
idiopathic intracranial hypertension; glymphatic system; cerebrospinal fluid; MRI; pulsatile intracranial pressure
资金
- Health South-East, Norway [2020068]
- Department of Neurosurgery, Oslo University Hospital-Rikshospitalet, Oslo, Norway
Idiopathic intracranial hypertension is a brain disease with unknown cause, characterized by cerebrospinal fluid disturbance, increased intracranial pressure, and visual failure. This study found impaired glymphatic function in several brain regions of patients with idiopathic intracranial hypertension, leading to altered tracer distribution and delayed clearance in grey and white matter. Further research is needed to investigate the implications of glymphatic failure in the progression of idiopathic intracranial hypertension.
Idiopathic intracranial hypertension is a brain disease incorporating cerebrospinal fluid disturbance, increased intracranial pressure and visual failure, but with unknown cause. This study examined a hypothesis that glymphatic function is impaired in idiopathic intracranial hypertension patients. The MRI contrast agent gadobutrol was utilized as a cerebrospinal fluid tracer following intrathecal administration. Consecutive standardized T1 MRI acquisitions over 48 h were done to assess tracer distribution within brain of 15 idiopathic intracranial hypertension patients and 15 reference individuals who were comparable in age and gender distribution. Using FreeSurfer software, we semi-quantified tracer level in multiple brain regions as T1 MRI signal change. The tracer enriched the entire brain of idiopathic intracranial hypertension and reference subjects. In idiopathic intracranial hypertension, tracer enrichment was increased and clearance of tracer delayed from a wide range of brain regions, including both grey and white matter. Differences were most evident in frontal and temporal regions. The pulsatile intracranial pressure was measured overnight and tracer propagation in brain compared between individuals with pathological and normal pulsatile intracranial pressure. In individuals with pathological pulsatile intracranial pressure, tracer enrichment was stronger and clearance from brain delayed, particularly in regions nearby large artery trunks at the brain surface. The present in vivo observations provide evidence for impaired glymphatic function in several brain regions of idiopathic intracranial hypertension patients. Glymphatic failure may imply altered clearance of metabolic byproducts, which may precede neurodegeneration. Further studies are needed to characterize glymphatic failure in idiopathic intracranial hypertension.
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