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In vivo distribution of cerebrospinal fluid tracer in human upper spinal cord and brain stem
Erik Melin, … , Per Kristian Eide, Geir Ringstad
Erik Melin, … , Per Kristian Eide, Geir Ringstad
Published December 8, 2023
Citation Information: JCI Insight. 2023;8(23):e173276. https://doi.org/10.1172/jci.insight.173276.
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Clinical Research and Public Health Neuroscience

In vivo distribution of cerebrospinal fluid tracer in human upper spinal cord and brain stem

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Abstract

BACKGROUND Intrathecal injection is an attractive route through which drugs can be administered and directed to the spinal cord, restricted by the blood-spinal cord barrier. However, in vivo data on the distribution of cerebrospinal fluid (CSF) substances in the human spinal cord are lacking. We conducted this study to assess the enrichment of a CSF tracer in the upper cervical spinal cord and the brain stem.METHODS After lumbar intrathecal injection of a magnetic resonance imaging (MRI) contrast agent, gadobutrol, repeated blood samples and MRI of the upper cervical spinal cord, brain stem, and adjacent subarachnoid spaces (SAS) were obtained through 48 hours. The MRI scans were then analyzed for tracer distribution in the different regions and correlated to age, disease, and amounts of tracer in the blood to determine CSF-to-blood clearance.RESULTS The study included 26 reference individuals and 35 patients with the dementia subtype idiopathic normal pressure hydrocephalus (iNPH). The tracer enriched all analyzed regions. Moreover, tracer enrichment in parenchyma was associated with tracer enrichment in the adjacent SAS and with CSF-to-blood clearance. Clearance from the CSF was delayed in patients with iNPH compared with younger reference patients.CONCLUSION A CSF tracer substance administered to the lumbar thecal sac can access the parenchyma of the upper cervical spinal cord and brain stem. Since CSF-to-blood clearance is highly individual and is associated with tracer level in CSF, clearance assessment may be used to tailor intrathecal treatment regimes.FUNDING South-Eastern Norway Regional Health and Østfold Hospital Trust supported the research and publication of this work.

Authors

Erik Melin, Are Hugo Pripp, Per Kristian Eide, Geir Ringstad

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Figure 3

Tracer enrichment in deep and superficial parts for reference patients.

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Tracer enrichment in deep and superficial parts for reference patients.
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(A–E)Percentage change in normalized T1-signal over time for mesencephalon, pons, medulla oblongata, C1 level of the spinal cord, and C3-level of the spinal cord for reference patients (n = 26). Red lines represent the superficial regions, and blue dotted lines represent the deep regions. The data presented as mean with error bars showing 95% CI (mixed-model analysis).

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