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Modeling CSF circulation and the glymphatic system during infusion using subject specific intracranial pressures and brain geometries
Department of Scientific Computing and Numerical Analysis, Simula Research Laboratory, Oslo, Norway; Department of Mathematics, University of Oslo, Oslo, Norway.
Umeå University, Faculty of Medicine, Department of Diagnostics and Intervention. Umeå University, Faculty of Science and Technology, Centre for Biomedical Engineering and Physics (CMTF).ORCID iD: 0000-0002-2031-722X
Department of Scientific Computing and Numerical Analysis, Simula Research Laboratory, Oslo, Norway; KG Jebsen Center for Brain Fluid Research, Oslo, Norway.
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Neurosciences.ORCID iD: 0000-0001-6451-1940
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2024 (English)In: Fluids and Barriers of the CNS, E-ISSN 2045-8118, Vol. 21, no 1, article id 82Article in journal (Refereed) Published
Abstract [en]

Background: Infusion testing is an established method for assessing CSF resistance in patients with idiopathic normal pressure hydrocephalus (iNPH). To what extent the increased resistance is related to the glymphatic system is an open question. Here we introduce a computational model that includes the glymphatic system and enables us to determine the importance of (1) brain geometry, (2) intracranial pressure, and (3) physiological parameters on the outcome of and response to an infusion test.

Methods: We implemented a seven-compartment multiple network porous medium model with subject specific geometries from MR images using the finite element library FEniCS. The model consists of the arterial, capillary and venous blood vessels, their corresponding perivascular spaces, and the extracellular space (ECS). Both subject specific brain geometries and subject specific infusion tests were used in the modeling of both healthy adults and iNPH patients. Furthermore, we performed a systematic study of the effect of variations in model parameters.

Results: Both the iNPH group and the control group reached a similar steady state solution when subject specific geometries under identical boundary conditions was used in simulation. The difference in terms of average fluid pressure and velocity between the iNPH and control groups, was found to be less than 6% during all stages of infusion in all compartments. With subject specific boundary conditions, the largest computed difference was a 75% greater fluid speed in the arterial perivascular space (PVS) in the iNPH group compared to the control group. Changes to material parameters changed fluid speeds by several orders of magnitude in some scenarios. A considerable amount of the CSF pass through the glymphatic pathway in our models during infusion, i.e., 28% and 38% in the healthy and iNPH patients, respectively.

Conclusions: Using computational models, we have found the relative importance of subject specific geometries to be less important than individual differences in resistance as measured with infusion tests and model parameters such as permeability, in determining the computed pressure and flow during infusion. Model parameters are uncertain, but certain variations have large impact on the simulation results. The computations resulted in a considerable amount of the infused volume passing through the brain either through the perivascular spaces or the extracellular space.

Place, publisher, year, edition, pages
BioMed Central (BMC), 2024. Vol. 21, no 1, article id 82
Keywords [en]
CSF circulation, CSF dynamics, Glymphatic pathway, Infusion test, Intracranial pressure, Paravascular flow
National Category
Neurosciences
Identifiers
URN: urn:nbn:se:umu:diva-231136DOI: 10.1186/s12987-024-00582-0ISI: 001332088000002PubMedID: 39407250Scopus ID: 2-s2.0-85206518102OAI: oai:DiVA.org:umu-231136DiVA, id: diva2:1909781
Funder
EU, Horizon 2020, 714892Swedish National Space Board, 193/17Swedish Foundation for Strategic ResearchThe Research Council of Norway, 300305The Research Council of Norway, 301013Available from: 2024-11-01 Created: 2024-11-01 Last updated: 2025-04-02Bibliographically approved

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Eklund, AndersMalm, JanQvarlander, SaraStoverud, Karen-Helene

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