Case report: A multiple sclerosis patient with imaging features of glymphatic failure benefitted from CSF flow shunting

The derangement of CSF circulation impacts the functions of the glymphatic-lymphatic system (G-Ls), which regulates solute trafficking and immune surveillance in the CNS. The G-Ls failure leads to the dysregulation of clearance of waste molecules in the brain and to an altered CNS immune response. T...

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Published in:Frontiers in neuroscience Vol. 16
Main Authors: Scollato, Antonio, Lolli, Francesco, Lastrucci, Giancarlo, Repice, Anna, De Santis, Giuseppe, Nicoletti, Claudio, Porfirio, Berardino, Gallina, Pasquale
Format: Journal Article
Language:English
Published: Lausanne Frontiers Research Foundation 01-11-2022
Frontiers Media S.A
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Summary:The derangement of CSF circulation impacts the functions of the glymphatic-lymphatic system (G-Ls), which regulates solute trafficking and immune surveillance in the CNS. The G-Ls failure leads to the dysregulation of clearance of waste molecules in the brain and to an altered CNS immune response. The imaging features of dilated perivascular spaces imply the impairment of the G-Ls. We report on the case of a patient with primary progressive multiple sclerosis and dilatation of perivascular spaces, who transiently improved after CSF shunt diversions. The underlying mechanisms remain to be determined and at this stage, it is not possible to link CSF diversion to an effect on MS pathology. However, this observation provides the rationale to incentivize research in the largely unknown area of CSF dynamic disturbances on G-Ls failure and ultimately in neurodegeneration.
Bibliography:Reviewed by: Esmaeil Davoodi-Bojd, University of Illinois at Chicago, United States; Peter Kosa, National Institutes of Health (NIH), United States
Edited by: Arumugam R. Jayakumar, University of Miami, United States
This article was submitted to Neurodegeneration, a section of the journal Frontiers in Neuroscience
ORCID: Pasquale Gallina orcid.org/0000-0002-4672-101X
ISSN:1662-453X
1662-4548
1662-453X
DOI:10.3389/fnins.2022.863117