Human brain clearance imaging: Pathways taken by magnetic resonance imaging contrast agents after administration in cerebrospinal fluid and blood

Author:

van Osch Matthias J. P.1ORCID,Wåhlin Anders234ORCID,Scheyhing Paul56,Mossige Ingrid78ORCID,Hirschler Lydiane1ORCID,Eklund Anders24ORCID,Mogensen Klara2ORCID,Gomolka Ryszard9ORCID,Radbruch Alexander56ORCID,Qvarlander Sara2ORCID,Decker Andreas6ORCID,Nedergaard Maiken910ORCID,Mori Yuki9ORCID,Eide Per Kristian1112ORCID,Deike Katerina56ORCID,Ringstad Geir1314ORCID

Affiliation:

1. C. J. Gorter MRI Center, Department of Radiology Leiden University Medical Center (LUMC) Leiden The Netherlands

2. Department of Radiation Sciences, Radiation Physics, Biomedical Engineering Umeå University Umeå Sweden

3. Department of Applied Physics and Electronics Umeå University Umeå Sweden

4. Umeå Center for Functional Brain Imaging Umeå University Umeå Sweden

5. Department of Neuroradiology, University Medical Center Bonn Rheinische Friedrich‐Wilhelms‐Universität Bonn Bonn Germany

6. German Center for Neurodegenerative Diseases (DZNE) Bonn Germany

7. Division of Radiology and Nuclear Medicine, Department of Physics and Computational Radiology Oslo University Hospital Oslo Norway

8. Institute of Clinical Medicine, The Faculty of Medicine University of Oslo Oslo Norway

9. Center for Translational Neuromedicine University of Copenhagen Copenhagen Denmark

10. Center for Translational Neuromedicine University of Rochester Medical Center Rochester New York USA

11. Department of Neurosurgery Oslo University Hospital‐Rikshospitalet Oslo Norway

12. KG Jebsen Centre for Brain Fluid Research, Institute of Clinical Medicine, Faculty of Medicine University of Oslo Oslo Norway

13. Department of Radiology Oslo University Hospital‐Rikshospitalet Oslo Norway

14. Department of Geriatrics and Internal Medicine Sorlandet Hospital Arendal Norway

Abstract

AbstractOver the last decade, it has become evident that cerebrospinal fluid (CSF) plays a pivotal role in brain solute clearance through perivascular pathways and interactions between the brain and meningeal lymphatic vessels. Whereas most of this fundamental knowledge was gained from rodent models, human brain clearance imaging has provided important insights into the human system and highlighted the existence of important interspecies differences. Current gold standard techniques for human brain clearance imaging involve the injection of gadolinium‐based contrast agents and monitoring their distribution and clearance over a period from a few hours up to 2 days. With both intrathecal and intravenous injections being used, which each have their own specific routes of distribution and thus clearance of contrast agent, a clear understanding of the kinetics associated with both approaches, and especially the differences between them, is needed to properly interpret the results. Because it is known that intrathecally injected contrast agent reaches the blood, albeit in small concentrations, and that similarly some of the intravenously injected agent can be detected in CSF, both pathways are connected and will, in theory, reach the same compartments. However, because of clear differences in relative enhancement patterns, both injection approaches will result in varying sensitivities for assessment of different subparts of the brain clearance system. In this opinion review article, the “EU Joint Programme – Neurodegenerative Disease Research (JPND)” consortium on human brain clearance imaging provides an overview of contrast agent pharmacokinetics in vivo following intrathecal and intravenous injections and what typical concentrations and concentration–time curves should be expected. This can be the basis for optimizing and interpreting contrast‐enhanced MRI for brain clearance imaging. Furthermore, this can shed light on how molecules may exchange between blood, brain, and CSF.

Funder

Norges Forskningsråd

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

Vetenskapsrådet

Alzheimer Nederland

Stiftelsen för Strategisk Forskning

Publisher

Wiley

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